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What are Chemotherapies? List from Cancer Survivors.

Breast Cancer Chemotherapies

What Breast Cancer Survivors said about their Chemotherapies.

2000 - Chemotherapy
Started chemo in May 2009, got a port so my viens are still good. Adriamycin: fatigue, hair losse, nausea, constipation. Taxol: PAIN, fatigue, chemo brain, PAIN.
Four months of dose-dense chemotherapy along with a shot of Neulasta after each session.
4 rounds of Adriamycin and Cyclophosphamide together every 2 weeks. I am done with those 4 rounds. 4 rounds of Taxol every 2 weeks I have 3 rounds left. Xeloda for a year, Gemzar and carbo still doing it once a month until I guess it stops working.
3 (months not sure of all the drug names. A/C and taxol i think. Round two,Cisplatin.
Started first round of AC on June 12th....will continue 3 more rounds and then on to Taxol.
Started chemo June 8 2006 and finished up Sept. 28. 2006. Side effects weren't to bad. Just did what I was suppose to so I wouldn't have many.. Biggest side effect.. Baldness but I got through that too.
AC was May to July 2014 (8 infusions, dose dense), Taxol was July to September 2014 (12 weekly infusions); suffered side effects from the chemo and the steroids: nausea, skin toxicity, weight gain, round face, hair loss (but saved most of it with cold caps!), nail discoloration, nail bed separation, hot flashes
4 treatments of taxotere and cytoxan, every 3 weeks began on January 12, 2011. I had a reaction to the second treatment. I was lucky with side effects. Shaved my head before the second treatment because it hurt, then the constipation started,nausea started after 3rd treatment, but never actually got sick. My fingernails hurt but never turned black or fell out. I felt like I had paper in my mouth for a few weeks. The booster shot made my bones ache. My back twitched after the first one so much that I could not get comfortable. And the steroids kept me awake.
Starting on 18th April, 2011
Had first treatment Sept 3rd. headaches really bad stomach, rash on my chest and face they just keep coming and changing really
I have completed 3 of my 6 cycles of chemo. I am on Taxotere, Cytoxin and Herceptin. I will finish up in September, with the completion of the Herceptin in May of 2012. I am also receiving a shot of Neulasta which makes my bones ache. The chemo this time has not been so bad except for the flu like symptoms and achiness in my bones. I am tired but this is due to the anemia.
First Chemo 9-8-2008. Side Effects - Pain, joint and bone pain, can't taste anything, headaches, bodyaches and my skin hurts and weight gain from the steroids.
26 weeks of chemo. 1X every other week for 8 weeks. Then weekly for 12 weeks. Continued with Herceptin drug Trail for 13 months, 1x every three weeks. Nausea to most foods and smells like coffee or strong perfumes. Wanted hot or cold things to eat....flu like symptoms showed up day 3-5 after chemo. No nuropothy! Did not throw up at all. Slept more days 2-3...weight loss but only a few lbs first 9 weeks then started to gain. Have gained 15 lbs since chemo ended due to hormone blockers I am on.
ACT from December 2010 - June 2011.
Started Chemotherapy on September 5, 2008; Taxotere, Carboplatin, and Herceptin - originally planned for 6 rounds (every three weeks). I completed 2 rounds and then my doctor stopped(my mass grew back). Side Effects - Nausea, diahrea, extreme fatigue, bone/joint pain, flu-like symptoms, hot flashes, numbing, weird taste in mouth, loss of appetite, hair loss I then did weekly Taxol and Herceptin started 10/17/08 for 6 weeks. Side effects included nausea, occasional diahrea, fatigue, muscle and joint pain, neuropathy, hot flashes. I started 5FU, Cytoxan, & Epirubicin on 12/02/08 (4 rounds every three week) while continuing with weekly Herceptin for 12 more weeks. Side effects - Nausea, vomiting, diarhea, hot flashes, mouth sore, fatigue, loss of appetite. I started Tykerb in Feb 2009. I will continue with Herceptin for at least 7 more months after surgery.
Chemo first out i overdosed and went right in hospital...oct 08 quite taking chemo jan 13, 09
Taxotere & herceptin weekly for the rest of my life.
12 rounds of chemo
It was called cef (which is cefuroxime, epirubicin, and cyclophosphomide). It is used only in a couple of Canadian provinces as it is very expensive.
through March 2008 CMF cocktail, 8 rounds. never lost my hair, nausea got pretty bad... three rounds in, I became a petulant child and announced I was NOT going back. A nurse family member asked my mom what kind of anti nausea meds I was given (don't remember) and told my mom to relay the following: "tell her to get pot, the pills suck" .... My resourceful husband came home with a surprise shortly after round 3. It PISSES me off that I had to break the law because the fact is, at least for me, IT WORKED and it was AMAZING.....
4 cycles starting 7-24-2014
Mom has changed chemotherapy a few times but has stopped treatment.
5/28 first treatment of clinical trial Gemzar with Avastin- was on this treatment for 6 months, it immediately reducedthe tumor on my liver and eventually totally got it. unfortuantely I had to stop Avastin due to high blood pressure and I experienced toxicity in my lungs with the high dose of Gemzar and had to stop. After 6months another liver tumor appeared. Now Phase One trial Irinotecan with PARP inhibitor. So far has shrunk the liver in my tumor in half.
None.

Prostate Cancer Chemotherapies

What Prostate Cancer Survivors said about their Chemotherapies.

none yet
RChop -six treatments, two weeks apart in Spring 2007.
taxater, didnt do anything,6 treatments, mitotaxatrine, still on it, barely any side effects due to the vit c drips
Docetaxel, 8 sessions in 2014; extreme fatigue, neuropathy, loss of hair
NONE!!
None
Taxotere, Jevtana

Lung Cancer Chemotherapies

What Lung Cancer Survivors said about their Chemotherapies.

3 days chemo every 21 days. Hydration as needed. Tiredness and nausea/vomiting at times.
Feb 08-Cisplatin/Etoposide- hideous vomiting diarreah Switched chemo drugs AND Hospital -April08-carbo/taxol/avastin. Tolerated well. Neulasta. Bone pain
I had my port-A-cath placement on November 9, 2010 for six cycles of Carbo/Alimta. The port-A-cath hurts just on its own, but chemo sucks, sucks, sucks! I cant say anything nice about chemo, other than hopefully it is killing those cancer cells! After each treatment I have extreme fatigue and appetite loss for 4-5 days following. My hair started falling out after the second cycle, which doesn't bother me compared to the fatigue. I hate not helping out around the house, or missing out on family time because all I want to do is sleep. My blood counts are also very low so the doctors and nurses check them every week, and they also check my kidney function. I'm on medicine for my anemia which helps a little with my fatigue. My kidneys should hang in there- I guess it paid off living a healthy life.
One a day pill forever (took 150 mg for 2 years). Down to 100 mg due to vertigo, fatigue. Other side effects, slow/non hair growth, rash, dry skin, dry mouth
carbo/taxol only effect has been being tired!! Verty low white cell counts, had to receive one transfusion, other wise has handled it well.
Alimta (Pemetrexed) Aug - Nov 2013, 6 cycles
Fatigue, acne, diarrhea, numbness and pain in fingers and feet, no appetite, foggy-brained, rheumatism, sensitive to sunlight, no taste, fungus in mouth and lung, partial loss of hair
None to date - The surgeon and oncologist felt that I should wait before starting chemo or radiation and be on the anti-fungal medication, indicating at least a year, to see if once the infection was gone, the remaining spots in my lungs would be gone. In January of 2010, I lost my job, medical insurance and the financial ability to continue the meds. I've recovered enough to find work and have been there long enough to receive medical insurance...now to find the courage to return to the doctor and take up where we left off, uhhh less the pre-existing conditions...to be continued...
3/2012 Adriamycin and dacarbazine 6 cycles 12/2012- 10/2013 votrient 600mg every day. 10/2013 - present gem/tax
Taxol and Carboplatin every 3 weeks for a total of 4-6 treatments. Have had 2. Nausea, fatigue, aches and pain in whole body. Also DVT.
avastin, alimta, carboplatrin 1/26/2015, fatigue, loss of appetite, dizziness, nausea; chemo not working; then Taxotere and Cyramza 4/20/2015
Carbo/Alimta 07.2008 Carbo/Taxol - Got taken off Avastin after pulmonary embolism. (nausea, vomiting, fatigue) 02.2009 Carbo/Alimta - Developed allergy to Taxol. (anemia, fatigue) Radiation therapy.
Cisplatin and Alimta and all of the side effects that ride with them. Four rounds in ten weeks.
1st series Aug'07 to Dec - 6 infusions - Carboplatin, Taxol and Avastin. Side effects, loss of all hair, fatigue, weight loss. 2nd series, 7 infusions - Sept '08 to Apr '09 - same coctail as above
Four treatments, most recent on 4 August, #5 scheduled for 25 August. Side Effects - minor nausea, extreme fatigue, loss of appetite and sense of taste and smell. carboplatin and Alimta (pemetrexed)for #'s 1-4. Provider stopped shipments of carboplatin so #5 and any remaining will be only the Alimta.
starting the 2nd week of August 2013
I begin chemotherapy on the April 8th. 4 rounds of 3 weeks each of Vinorelbine and Carboplatin. (Originally Cistoplatin but the doctor changed it cuz my ears were ringing)Worst side effects are feeling like lead and/or rubber, forgetfulness, weight gain, insomnia and aching bones, muscle and skin.
750ml & 500ml cisplatin & taxotere respectively on 12/10/09,12/31/09,1/20/10,2/11/10.i thought they were trying to kill me!
7/24/07 Taxol and Carboplatin 2 and a half days full of energy, 3rd day she is complaining of pain and flu like symptoms... She HAS NOT taken Claritin which her oncologist recommended for these symptoms.
Iressa (gefintib)
2007 April til present so far 5 rounds Taxotere Carboplatin Avastin Emend for nausea Aranesp for red blood Neulasta for white blood etc.....
December 6th, 2010 was first Chemo treatment... my mother is doing good..not neauseous, joint and leg pain, Hair started to hurt two weeks after first chemo treatment. Still playing golf...not eating much... get tired easily...gets cold easy
chemo fog.
will start on march 16 (tentative)
December 2004 - Present off and on. On Avastin and Tarceva currently, but stopping to start a new chemo.

Bladder Cancer Chemotherapies

What Bladder Cancer Survivors said about their Chemotherapies.

Foggy brain. Forgetfulness.

Non-Hodgkin Lymphoma Cancer Chemotherapies

What Non-Hodgkin Lymphoma Cancer Survivors said about their Chemotherapies.

RCHOPx6 started on 2/21/14 Some nausa and loss of appetite shortly after infusion, Some numbness in fingers after 4th infusion. Taste buds don't work for a few days after infusion
R-CHOP starts 8/26/10 Major Side Effects Day 1-3 Headache and Diarrhea Mouth Sores Days 3-6
RCHOP CHEMO
Chop 2002 Cop with Rituxan 2008. Hair loss, numbness (not bad this time), fatigue, insomnia from Prednosone.
Hyper CVAD, March through September 2007
Got temporary remission during some 16 months of various drugs, but no lasting remission
Rituxan 2001, Rituxan CHOP 2002, Rituxan 2003, TRM-1 (clinical trial) 2004-2005, Rituxan/Doxil 2006-2007. I have never reached a remission "yet" still hopeful!
Jaw pain, Gastritis, Mouth ulcer
R-CHOP R-ICE ESHAP
R-CHOP 25/11/11
R-Dhop 6 weeks. Every 21 days. Followed by Neulasta shot in stomach day after chemo. For those of you who have to have it. It hurts. It's not the needle it's the white blood cells going into your body. Burns badly. So, put ice pack on stomach before getting the shot. You'll thank me a million times. :) Had a picc line in upper right arm, leading a tube to my heart. Strong chemo. But, with all the other meds they put in it. I NEVER got sick. Everyone around me couldn't believe I had cancer. This is the last week before final treatment. Now body has said..."time to be fatigued." :)
Started11/15/2012, every 21 days until 03/06/2013. Had neuropathy, vincristine stopped for 2 cycles,better, then resumed 5th cycle. Had some issues with breathing-felt like I had eaten a lot of mints, treatment postponed for a week, got chest x ray, nothing wrong. Was tired with each cycle, but trudged through. Prednisone helped. Lost taste for some foods, but never lost my appetite!
Magrath protocol - R-CODOX-M and R-IVAC. Side effects - usual stuff + peripheral neuropathy, back pain (site of intrathecal/tumors?)
February 25th: R-CHOP. Mouth sores, nausea, fatigue, heartburn March 21st: R-CHOP. Mild nausea (it's only been two days, side effects showed up for me 4 days later)
R-CHOP
R-chop,
G-Chop 1/8/14 starting for 6 cycles, headache, jaw pain, hair loss
R-CHOP BEGINNING ON 12.21.2015
R-CHOP
Many different times beginning approx 1 year after spleen removal
RCHOP every two weeks. 6 times in total. Side effects were fatigue, nausea, complete loss of hair, dry mouth, weight gain, joint pain, weakening of bone density, etc....
R-CHOP14 to start on September 13 for six cycles.
1991 April to June MAKOP B, 12 months treatment plan administered weekly over 12 weeks, ulcers, nausea, tiredness, loss of nerve sensations in extremities, severe constipation, hair loss (lol)
12/8/14 R+Chop thrush, severe upper and lower abdominal pain, pain in muscles and joints, extreme fatigue, constipation, constant coughing, aspirating fluids into lungs. Gastric Reflux activated to point of juices flying up in throat even while on Omeprazole. Neuropathy-numbness and tingling hands and feet. Tongue is numb and can't taste anything. Hair loss 14 days post chemo. 12/29/14 - Severe Upper and lower abdominal pain, constant coughing, still aspirating fluids into lungs, lost my voice, vocal chords are fire engine red, the gastric reflux is so bad they had to add two more medications to my Omeprazole, Zantac, and Carafate. I have Flu symptoms, congestion, post nasal drip, pain in muscles and bones, numbness and tingling in hands and feet. Can't taste anything. Taste buds come back after 3 weeks. 1/19/15 -R+Chop- continue to have numbness and tingling in hands and feet. I drop things and can't feel things in my fingers. 1/20/14 Neulasta injection - exactly 24 hours after injection. Really sore muscles and joint pain all over. lower abdominal pain, constipation, extreme fatigue, coughing.
R-CHOP 21 Mouth Sores Steroid Withdrawl

Melanomas of the Skin Cancer Chemotherapies

What Melanomas of the Skin Cancer Survivors said about their Chemotherapies.

Fluorouracil treatment started Sept 2010 Fluorouracil treatment started Aug. 2011
Taxol, a pain in arm and in the Ass.

Kidney Cancer Chemotherapies

What Kidney Cancer Survivors said about their Chemotherapies.

no treatment yet?
Afinitor (everolimus) tablets daily, started on March 17, 2011
Votrient
4 months, Oct. 2010-Feb. 2011 Avastin and Interferon
My husband was on a trial for a new chamo for renal cancer called "Sutent". He made no progess and instead suffered significant side effects that we believe plunged him into a spiral of ever increasing side effects of his cancer.
On my third treatment and then will have a week off
50mg sunitinib/sutent on a 28/14 cycle. I've had minimal side effects, but I just finished my first four weeks "on".
As of 8/3/11 on second cycle of Sutent, 28 on 14 off
Did Xeloda and Gemcitabine with no results

Pancreas Cancer Chemotherapies

What Pancreas Cancer Survivors said about their Chemotherapies.

Start date November 14 th chemo drug called Folfirinox 8 weeks every other week to try and shrink tumor away from artery
6/2011 tiredness, nausea, dizziness
More harm than good; no chemo
Mar 4 _ Sept 15 2015(Folfirinox)Nausea, weakness, vomiting, low potassium, low platelets (despair)
5-Fluorouracil (5-FU) My sister gets chemo every other week. Her main side effect is diarrhea. She has had 3 chemo fusions so far. She has diabetes and the chemo she receives has glucose in it so when she receives the chemo her blood sugar level goes sky high and she gets severe headaches. She then takes additional insulin following the chemo to help bring down the sugar levels. I am amazed at the medications that help her symptoms. When told she was going to have "bone pain" after a shot to boost her platelet count, she was told to take "Claritin".
Initially 2 rounds of Folfirinox, that increased liver enzymes and CA-19-9
Carboplatin and Taxol started June 10, 2016 December 2015-April 2016 Cisplatin and Gemzar we only switched because he had 6 rounds of this. It did keep the cancer from growing.
Gemzar started Jan 2014. Once a week for three weeks then one week off for six rounds; liver function elevated and dehydration, fatigue , vision affected .
Folfirinox - 3 doses, Gem/Abraxane - 4 months
Extreme fatigue, some dry heaving, hair loss, neutropenia
Folfirinox Jan 2013 - Feb 2013, switched to Abraxane and Gemcitabine March 2013-current
1st session, September 20th. Once a week for 3 weeks then 1 week off. October 25th, white blood cell count was down for the 1st time, so they skipped chemo for that week. November 1, 2012, white blood cell count back up so they did chemo. December 2012 started 5 FU, Oxaliplatin and Leucovorin every 3 weeks to target the abdominal lining tumors that are continuing to grow. April 19, 2013, CT shows the chemo isn't working on the abdominal lining tumors, and they have given him the best chemo treatments they have, nothing more they can do. But will reduce the chemo he has been on to reduce painful sores in his mouth and side effects that were getting worse with each treatment, I think to keep the liver and pancreas tumors at bay and hopefully still give him pain relief.
Gemzar, 5-FU
Chemo #1 on 4/02/10: I was more tired then usual and had a "blah" moment after going outside for a few minutes.
Chemo once a week from 4/2/10 to 6/01/10: Was tired the next day with small "blah" moments.
Gemzar, Taxotere and Xeloda
Gemzar June, 2014. Nausea, weakness, fever, headache
every other week, cold sensitivity
started chemo 6/14. 18 treatments prescribed, currently going through chemo.
Gemcitabine (Gemzar)
Yes, decided to participate in a clinical study, began chemotherapy Tx on June 21, 2013, one month after Dx
Gemzar Jan 2008-May 2008 Sept 2009- Oct 2010
given up on dates the first time on chemo was 7 months and this time has been 9 months
Folfox mix of chemotherapy -nausea, vomiting, diahhrea , nil taste I food, shaking, mouth ulcers, dry skin
xeloda pills for two weeks then a week off.

Oral Cancer Chemotherapies

What Oral Cancer Survivors said about their Chemotherapies.

2 cisplatin 3/22/2011: nausea! and fatigue!
1st and 4th week of Radiotherapy treatment, chemotherapy was also performed. 24 x 5 delivery of 5FU with a Cisplatin infusion on second day of each of these weeks. Side effects included a 'Chemo crash' both weeks I had the treatment - second week worse than the first (required blood transfusions).
Cisplatin, hearing loss, ringing in ears
No Chemo
Cisplatoin 1x week for 7 weeks Dates: Aug 2011 through Nove 2011 Side Effects include; Nausea Hair loss from both radiation and chemotherapy Eyesight has deteriorated a little weak
Erbitux, once a week for 7 weeks, starting in August. Initially, severe tongue sensitivity (at one point even water was like battery acid). For most of the treatment time, daily nausea and and severe acid reflux with occasional vomiting. As of today: chemotherapy induced neuropathy of the right leg causing the inability to lift my toes or my ankle (currently wearing a brace), but expect this to improve; whatever contribution Erbitux has towards complete dry mouth and lact of taste.
3 total - week one - week three and week five easy to do - no issues during treatment lost my beard and hair - so I shaved it short to look like I did it on purpose - wore a crocheted cap - head was always cold.
We can cure this without Chemo. . . I'm going to do it!

Ovarian Cancer Chemotherapies

What Ovarian Cancer Survivors said about their Chemotherapies.

1st. Chemo July - August 2009 2nd. Chemo February 2010 ip.chemo 3rd. Chemo January 2011 ip.chemo
4 round of cisplatin, bleomycin and etoposide
My doctor said there wont be malignancy as the tumor was encapsulated, but it would be safe if i undergo 3sessions of chemotherapy. So i opted for chemo and had vomiting and hair loss while on therapy
3- one month cycles of cisplatin, bleomycin, and etoposide. Side effects: Nausea, hair loss (roughly 1 month after chemo began), fever
I was highly allergic to Taxil. When given I immediately stopped breathing. So I have had carbo and gemzar which didn't work and currently I am on Cytozan and Advastin.
cistplatin, bleomyocin, etopiside, numbness in hands and feet nausea and weakness major chemo brain
June 20, 2006, and every following 3 weeks...through August 29, 2006...then the last 2 of the 6 treatments - November 7, 2006 & November 28, 2006 Carboplatin & Taxol I really didn't know what to expect with the first treatment. Felt great for 24 hours after...but then I felt like a semi-truck had run over me about 10 times...or worse case of the flu X 20! Twelve days later, I had a reverse mohawk going on (hair falling out)and had my husband shave my head. The worst of it was losing my eyelashes and eyebrows!!!! You know your hair is going to go...but no one told me ALL of my body hair would go!!! Talk about being striped of your "womanhood"! I still wince when I think of those times! Numbness in my feet(Pins & Needles)...always worse by the end of the day.
The dates go for a couple of years. After I had suregery I think I started chemo about two weeks afterwards. It started with Taxol and Carboplatin through IV. I had 2 of those 3 weeks apart. Then I started the IV/IP with 24 hours of Taxol and then Cisplatin in the port. It went straight into my abdominal cavity. Then I went back the next week for Taxol in the port. I had one week off after that and then started the process over and did that four times. Then I had two more IV's of Taxol and Carboplatin. They took me off of chemo and supposedly I was good to go, but it came back and my CA 125 went back up two check ups later. Unfortunately, my doctor neglected to let me know. So when I ended up at the ER again I called MD Anderson. There I was approached about dong a study on Avastin and didn't make it because the previous doctor had taken me off of chemo too early. My insurance paid for it though so I went on IV - Taxol, Carboplatin and Avastin. All together I have had 28 rounds of chemo. My last was on 9-9-2009 - hopefully a very lucky date!
6 rounds of chemo, first one 3/9/11, last one 6/21/11. Side effects: constipation; sharp pains in legs and feet; metal taste in mouth; heavy limbs; pain in joints; jittery; loss of all body hair; eventual numbness and tingling on bottoms of feet; and a slew of other things.
March 9- June 24 2015
Taxol-2 doses until severe reaction Carboplatin- working trhough 6 doses, nausea, fatigue, forgetfulness!
14 treatments from December 2013 to current. weight loss, loss of appetite, hair loss, very tired all the time, loss of muscle tone.
i had 6 months of cemo, I did good I was determined to not let it get me down. I worked full time and went to the gym three days a week,
Started chemo July 7,2011--6 sessions of Taxotere and Carboplatin--first 2 treatments were horrible, nausea,got dehydrated, had to go to hospital for fluids and unable to eat or drink--started losing hair after 2nd treatment--hard to take--got nausea straight but still had metal taste in mouth and unable to drink or eat for about 2 weeks after chemo--couldn't really eat till the week before treatment time again--hardest thing I have ever gone thru in my life--and it still is chemo or not--finished chemo 10/18/11 & happy to say cancer free--still have side effects--the numbness and hair is taking it's time growing back--but I am happy to be here and alive.
To many to count. Nausea
taxol/carbo dec 2008-april2009 topotecan sept 2009/present
none the dr did a slice and dice SIDE AFFECTS WERE WEALINING OF HEART MUSCLES HAD A STROKE 2 YEARS LATER AND NEEDED A PACE MAKER PUT IN YES I AM THE BIONIC WOMAN HEAR ME ROAR ALSO HAVE NEROPATHY IN FEET AND LEGS
my chemo is cisplatin , etopside , and bleomyacin
There were eight cycles of chemotherapy: 4 before surgery and after surgery 4. My body responded well to chemotherapy and tumor marker (CA 125) decreased from 690 for 4.
Jan-May/06 6 Taxol/Carbo CA-124 = 7 May/06 neuropathy hit - severe damage to hands and feet. Hands are curled.. I can't move ankles or toes. Severe nerve pain - can walk 5-6 steps w/ walker
Paclitaxel (Taxol)/Carboplatin (Paraplatin)combination. 6 treatments. 21 days apart.
I started chemo on Dec 3, 2012. I need to complete 6 treatments of Carbo and Taxol. My treatements or given over a period of 3 weeks. The first week I receive the full carbo dose and 1/3 of the taxol. The next two weeks I recieve the remaining taxol. I am having trouble keeping my WBC up with the weekly treatments. I had to have Neupogen shots to help give them a boost.
10 rounds of chemo in 2004, hair loss weakness, nausea, you know the drill. 6 rounds of chemo in 2008, same effects
Taxol and carboplatin so far 8 treatments CA-125 is now down to 130
Taxol sucks!!!!! makes your hair fall out and makes breathing really difficult until i go into an anxiety attack. I dont like taxol

Thyroid Cancer Chemotherapies

What Thyroid Cancer Survivors said about their Chemotherapies.

HAD 7 TREATMENTS ONE A WEEK FOR 7 WEEKS SIDE EFFECTS WAS MINIMUM DID NOT LOOSE HAIR JUST WEAKNESS OR LARTHARGIC MOOD ...
Radioactive Iodine treatment, 8/09 - nausea
Thyrogen injection #1: 4/14/10 - stings #2 - didn't feel a thing RAI-131: 4/16/10 - 203.9 units - so far, so good.
RCHOP 21. Three rounds total. 11/2/0, 11/23/10, and 12/14/10. Worst effects so far: heartburn to point of esophageal spasms, constipation, headache, mouth tenderness and dryness, fatigue and hair loss. This was for the Lymphoma. No chemo (so far) for thyroid cancer.
Sutent currently

Stomach Cancer Chemotherapies

What Stomach Cancer Survivors said about their Chemotherapies.

Currently receiving- feeling bla- fatiqued- diarrhea
Original Chemo was Epirubicin, Cisplatin and 5-FU April-September 2nd Irinotecan and Taxane Current Fol Fox 4 + Avastin
4 months...not helping
Chemo every 2 weeks, nausea, vomitting.
Began chemo in July of '09 with camptosar, leucovrin, and 5-fu. this is over a 46 hour period. In January '10, they added avastin and zometa to the regimin and is ongoing.
cisplatine caused hearing damage, taxotere caused skin and nail damage and herceptin made my hands tingle. Xeloda wiped me out, and all of the above caused hair loss.
3/15/14 Began 10 session clinical trial at Memorial Sloan Kettering. Chemo iv (cisplatin and epirubicin + trial drug/placebo) every 3 weeks. 2000mg Xeloda pills daily. IV chemo is followed by two days of dextametazone (steroid pills) which give me a boost. Hair loss, dry hands - currently trying to prevent them from cracking, some fatigue. Trying to avoid pain meds because that seems to be the cause of constipation/discomfort.
No help says' the doctor.

Brain Cancer Chemotherapies

What Brain Cancer Survivors said about their Chemotherapies.

Temodor- 5 days on, 21 off- October 2009- June 2010 Avastin- Every 15 days- July 2010- Present Carboplatin- Every 30 days- July 2010- Present
Hair loss, fatigue, loss of appetite, bruising from all of the blood work, achy muscles and joints, off balance, loss of concentration.
7/08-1/09: I took pills for 5 days each month. The first month was fine. I thought, "this is going to be e-z." Boy, I wrong! After that month, it was horrible!
Temodal - started Aug 15, 2011
Temodar, 150 mg during radiation increased to 350 5 days/month for 3 months, then increased to 450/month at present Side effects: fatigue
Temodar April 2013
Tremador - First set - daily dose for 3 weeks Not able to continue to the next set. Nausea, weakness, loss of appetite, Sleeping constantly
i was supposed to get 8 chemo's. but i only received 7 because my blood count wasn't up in time. i had "Vincristine" (iv)every week. Cyclophosphamide(iv)every 6-8 weeks. Cisplatin (iv), every other chemo, and Lomustine (pill) every chemo.
Temodar 160 mg nightly began July 21, and continued during radiation treatments. Chris had to take Zofran with the Temodar, so he didn't get nauseous. He will finish the chemo up the chemo September 2, 2013. He will get 4 weeks off, and begin taking a double dose of the Temodar for the first five days of every month for the next six months.
3 Cycles of Chemo - Cyclophosphamide, Vincristine, Cisplatin - Dec to Feb. (3 weeks apart) - Foot Drops and trips and falls 3 Cycles of Intensive Chemo with Autologous Stem Cell Transplant - Carboplatin & Thiotepa - Feb to May (4 weeks apart) - Hearing Damage
low dose temodar- little to no side effects b/c of my use of supplements
Began 150mg Temodar on 1/3/2011 2nd Dose of Chemo to begin 3/17/2011
No chemo
temador nightly before bed. also on a target therapy trial of avastin which was researched at duke hosptiol
started 9/13/2010-7 days a week, temedar. nausea and vomiting forst two nights. was ok last night so we'll see.
Timodar Started in March 2006 and still ongoing. Side Effects: NAUSEA!
Chemo(Temador) 42 days - fatigue, memory loss,weak,nausea, no vomiting due to neausa pill taken 2 x day
I had oral chemotherapy. I started taking it when I started my radiation therapy. I finished my chemo in October 2011. I took it every night 21 out of 28 days. I had to wait 2-3 hrs after eating to take it and another hour after taking it to eat or take my other medications. (I took Zofran, a nausea medicine, half an hour before my chemo.) One positive is it broke my late night snacking. My chemo has random side effects and the possible side effects ranged from one thing to the opposite. For example, it could cause constipation or diarrhea. I didn't read all the possiblities until I was almost finished taking it. That explained why I cried so easily. It was a side effect not just stress from dealing with cancer.
May 2002-July 2003 hair loss, memory loss, hearing loss and growth deficiency
Temodar
Radiation & Temodar daily for 42 days then cycles of 5 days on 23 days off
1/12/12 - begin taking daily chemo pill Temador (not sure how to spell that) for up to 12 months.
Scheduled for first time chemo (Temodar) in July 2011
Started Temodar on 11-23-09 380mg to much dosage, went to Hospital for low platelets 12-18-09 My platelets were at 6K !!!
At first it was the same as radiation, but when they got aggressive in August, I was stuck to the couch for 2 weeks. Weakness, major nausea, muscle and bone pain, throat swelling, mouth sores, major shivers and shakiness, tremors, spinal and head pain, throbbing from head to lower spine...theres more but can't remember them all.

Multiple Myeloma Cancer Chemotherapies

What Multiple Myeloma Cancer Survivors said about their Chemotherapies.

began 12/1/14 - 4/30/15 (Velcade, dexamethasone and cytoxin), Cytoxin priming 6/5/15, Stem cell transplant6/16/15 and Malthalon 6/25/15 , also neuropathy (mild) in parts of hand and feet.
8/13/15 Cyclo,dexamethasone, velcaide, huge stomach, very nauseous,no life. After5 1/2 months fired oncologist and went to natural treating dr.
Velcade and Dexamethason from September 2010 to December 2010. Aredia once a month since October 2010. The biggest problem is weakness and dizziness, I fell twice since I was dizzy and weak.
January 2006 and May 2006 stem cell transplants with hi dose malthalon chemo resulting in malthalon misery - tired and more tired.
Revlamid, nausea, vomitting, loss of appetite and weight, fatigue, bone pain.
Velcade, Decadron, Revlemid. Mostly fatigue and a slight loss of appetite.
1st cycle December 2010. Loss of hair.
March to October 2010.Four treatments every 3 weeks. Velcade, Dex and Zometa. October 2010 went to 1 treatment every two weeks, same medication.Still on this schedule as of this date Mar 8, 2010
Revlamid - daily - ongoing
4 monthly rounds of VAD prior to allogenous bone marrow transplant.
Velcade, dexamethazone, since transplant just added revlamid
Started chemo Mar 1st 2009 Continued pain,a very few side effects to date-next treatmentApril 12
18 series VRDD and VRD so far
Thalomid: Fatigue. Red spots that eventually covered my entire body. Neuropathy in feet and hands. Revlimid: rash, upper body.

Colon and Rectal Cancer Chemotherapies

What Colon and Rectal Cancer Survivors said about their Chemotherapies.

im on xeloda and after the surgery ill have to do liquid iv chemo where i will have port inserted and i will have 16 weeks of 8 treatments where i walk around with the chemo for 48 hours.
No chemo ever.
6 weeks 3000mg xeoda pre surgery. 4 month 5000mg xelota post surgery. Oxi recommended. Tried but side effects too extreme. No hair loss. Tired and weak. Low energy with uncontrolled diarrhea.
I started chemo Sept 19,2006 minimal side effects I have had 20 treatments, and most people don`t realize I`m on chemo
FOLFOX started 2/11/2012 and ended on 7/18/12. The oxaliplatin in the FOLFOX caused peripheral neuropathy.
Neuropathy in toes arms diarreha constitpation pain when going. I have fissures now because of not being able to go which is causing bleeding and immense pain even hours after. Pain in jaw when I first eat. heart palpitations. No more mouth sores or fevers since I have been taking vitamins b and magnesium with zinc. Numbness in both hands and feet and cramping
First visit to oncologist 29th March.
Started FOLFOX Sept '11
Oral chemotherapy taken on radiation days 08/10/2011 - 09/19/2011 No side effects. Folfox - Begin 01/10/2012 - End date due to non-cancer complications: 4/18/2012. To date: lip numbness when I go in the cold for a couple of days after treatment. Cold sensitivity to foods and drinks for the first few days after treatment. No issue with fatique or nauseu to date. Xelox to replace Folfox: 05/02/2012 No side effects. End date due to non-cancer complications: 06/05/2012.
5-FU, and Eloxatin
November 1, 2006, Started with 5-FU, missing DPD enzyme causing life threatening toxicity issues and discontinuing the 5-FU. No additional chemo available to me for any treatment of this condition. Now in wait and see mode.
May 2010-July 2010: 24 hour, continuous 5FU infusion, Mondays-Fridays November 2010-January 2011 :Folfox December 2011-April 2012
3 treatments every two weeks with neupogen shots after every treatment. White blood cross ave been a problem but my platelets are what concern me. They have continued to decline and are not rebounding back between treatments. other concerns which are minor but irritating is the coldness everywhere especially the throat, hands and feet. Fatigue is manageable now after 3 months. Metal tasting mouth and bad breath right after treatment ....yuk! Lack of appetite seems to occur during the treatment week but subsides the following week.
One month off after the radiation concluded. I go in every third week to receive and IV of Oxilyplatin. I take 1650 mg of Xeloda twice daily starting with the date of iv, and lasting for 14 days. Thus far I've received 2 of six iv treatments. Side effects have been marginal and temporary. Sensitivity to cold lasts around 3 days. Some tingling in the hands and arm where the iv went in. Goes away after a few days.
Leucovorin, Oxaliplatin, 5-Flourouracil. Started September 19, 2009 for 12 bi-weekly infusions. Can't taste anything, eating or drinking anything cold makes me want to puke, cold air makes my throat close and I can't breath, pins and needles in hand, feet and any part of my body that gets cool, nausea, vomiting, diarrhea, constipation, cramping, headaches, major fatigue, depression.
FOLFOX plus Erbitux &
No Chemo in 2012. Now that its back, penidng Chemo therapy
Started June 23, 2008. Oxaluplapin, Leucovorin and Flourouracil. Side effects are extreme weakness, lack of appetite, many foods don't taste good, can't touch, eat or drink anything cold--needles & pins in fingertips & toes, and throat closes up. Needles & pins, needles & pins, if I drink or eat anything cold, MY breathing troubles begin!! smile
5-FU oxaliplatin and Avastin, due to start Nov 7, 2011
Pill form. Xeloda, 1800mil daily.
start chemo tomorrow jan 12, 2009 folfox
folfox + 5fu (dec 07-jan 08) folfiri + 5fu, avastin, cetuximab (jan 08-current)
May 2009 - Sept 2009 FolFox, peripheral nerve damage to hands and feet (used to unload dishwasher with ski gloves on cause touching plates etc felt like pickiing up glass!) All good now with help of Vit E and Alpha-lipoic acid suppliments. Xeloda - long term chemo. March 2010 til now and according to onologist, forever!! damages skin on my fingers and feet.
Bart has and still is undergoing Chemo. Bart has stage 4 Cancer. Bart's treatment of the tumor on his liver caused sloughing of the skin of his feet and hands. He is now on Erbotax. All tumors continue to shrink, and he feels great. Works most everyday he wants, as usual.
Inj Dacotine 150mg * Biovorine 600mg & 5FU 4600mg in 1000ml NS continuous infusion in two days. Inj Perinorm 10mg IV thrice a day Inj.

Liver Cancer Chemotherapies

What Liver Cancer Survivors said about their Chemotherapies.

11-19 chemo pellets not sure of the name, nausea,
On going chemo regiment and had one chemoembolization.
TACEdeb procedure begining of June....side effects... all haha vomitting, nausea, fever, pain, pancreatitis.
Nexavar 8/22/12 - forever, side effects all listed
Nexavar - Current (8 months)
First treatment was June 8th 7 hours between the other meds olus the chemo..Cisplatin and Gemzar.. Felt ok the day after but then started feeling very sick, achy, headache, ringing in ears, coulnt eat, weak, dizzy,tired,shaky all over I only felt well enough to go to the doctor on the 7th to have my blood drawn..saw dr and he said he would up my steroids next time and that should help second treatment was on the 8th, Just the gemzar.. Really tired and achy. Dizzy and weak. Had my shot of Lewnasta on Monday. Still fell tired and bone pain
every kind, all the time for the last 5 years
No chemo as no primary cancer found and chemo will only add a few months to life, yet these extra few months will be with the side-effects of chemo
7-2008 to present. Lethargic, no appetite, not able to focus for too long on anything, weight loss, strange thoughts, sleep seems to be all REM, dreams and or nightmares about Nam seem to pop up while I'm awake,anger, especially at the VA for not stepping up and admitting and approving my claims.
Tried Nexavar for one day, but decided against it; bad side effects--felt cloudy, nauseated like when I was on Interferon/Ribaviron and had rectal bleeding from the Nexavar; not worth it to buy a few more months of life; discontinued
i will tell you

Cervical Cancer Chemotherapies

What Cervical Cancer Survivors said about their Chemotherapies.

Cisplatin via port
8 rounds of a taxol, carboplatin, avastin combination every 3 weeks for 7 months then low dose cisplatin twice in 4 weeks with radiation. Side effects: nausea, vomiting, heartburn, fatigue, pain, depression, compromised immune system.
combination of xeloda and cisplatin- some loss of appetite, some naseau ( not too terrible), and some fatigue--started treatment in February 2006 cisplatin was administered once a week for four weeks and xeloda was taken orally Mon.-Fri. for 3 weeks, treatment was stopped early due to low blood counts
Metallic taste heart burn mild nausea ringing in ears
Cisplatin started 7/8/08
4 cycles (1 wk on 3 wks off) Cisplatin for 6 hours on day one, sent home with 5FU med pump for 96 hours. Side effects- nausea, diahrrea, agitation, black nail beds, hair thinning/loss, dehydration, irratation, moodiness, list goes on and on.........
Chemo not too bad with side effects. Im puffy. Numbness and tingling.
nauseousness....
I couldnt eat as much as I thought I would be hungry. Most food tasted terrible. I was able to watch much tv. I never watched tv since I was a kid. I am an active outdoor person, I felt it made me become lazy. lol I got the flu, lowered my immune system, however my red blood cell count always stayed very good!
Chemist Monday's only decadron steroids potassium
5 treatments of Cisplatin
N&V, Fatigue, Dulled mentation 12-15-09 to 1-30-10 SECOND ROUND OF CHEMO, CISPLATIN 01-01-11 to 02-17-11 LOTS OF VOMITING
Cisplatin
Cisplatin once a week In conjunction with the radiation. Then Five series with Etoposide.
Tirapazimine and cisplatin for 6 weeks...Metal taste in my mouth towards the end and thrush in my mouth for a couple of weeks which subsided with medication.
6 weeks of Cisplanin weekly Began 7/28/14 My babies 3rd birthday :{. terrible migraines intolerance to light nausea and vomiting and Menopause. were the worse of my Side effects.
methotrexate injections every other day via injection
Oct 07 to Dec 07 - Cisplatin chemo 1x a week with radiation;. Constant terrible nausea, very sensitive to tastes and smells. Ate only carbs, couldn't even stand the smell of my dog! Everything nauseated me. Aug 08 to Dec 08 - Carboplatin and Paclitaxel every 3 weeks x 6 doses. Hair gone by 2nd treatment, fluid overload on chemo days due to drugs being hard on kidneys - had to flush. About 2-3 days post chemo, horrible bone pain, numbness and tingling in hands and feet (peripheral neuropathy) and constipation that almost hospitalized me. Would last for a week or so and then settle down. Horrible fatigue, felt like lead. My hair started coming back really quickly after treatment stopped,but the neuropathy lasted almost a year, fatigue continues to be a problem. UPDATE Feb/10: Going back for another 6 rounds of the not so pretty poison. Carbo/Taxol once again. Gonna miss my hair...oh yeah, and the ability to feel human!
Done and it sucked
tahbso april 15,2013
Chemo was my biggest fear. Hearing so bad horror stories I was besid myself with fear. I actually have 1 more left to go and no problems except for a mild nausea about day 3 and thats it. Never really got too tired and never lost my hair. It really was like being pregnant as far physical problems with tired and nausea. It was a low dose cisplatin for 5 weeks.
i was put to sleep with benegril
I started Chemo in July. I went in with a positive attitude. My sister and I had done a lot of research about things to do to minimize side effects. I cannot stress the importance of drinking a lot of water (and I mean a lot!) before during and after the chemo. Rinse your mouth with a mouth wash specifically for dry mouth - thankfully I avoided sores and I think this was the reason. Rest as often as you can and don't ever feel guilty about it.
Chemo-has "chemo brain"
2 rounds of Taxol/carbo 11/2011 & 12/2011...Is being changed for 1/2012...not sure of new drugs yet

Larynx Cancer Chemotherapies

What Larynx Cancer Survivors said about their Chemotherapies.

Induction chemo for 2 months prior to radiation treatment - once a week during radiation; mouth sores for four days after first round, hair loss, fatigue, and some taste changes, but all in all, he did really well. Very little nausea.
12 total Erbitux sessions, once weekly, January 13 - March 31, 2011. Increasing fatigue and, ironically, insomnia following each session. From mid February through the end of treatments, somehow the Radiation/Erbitux mix seemed to spawn clusters of migraines.
Oct 8th- January 13th, 2010 Lost Hair after 21 days. Fatigue, dry mouth, muscle cramps that were very painful after 1st treatment. terrible rash on my head and neck the whole time I was taking chemo.

Acute Myeloid Leukemia Cancer Chemotherapies

What Acute Myeloid Leukemia Cancer Survivors said about their Chemotherapies.

Induction Theraphy Cytarabine and Doxorubicin for 8 days. I just start my Consolidation theraphy last March 30. Which is Doxorubicin for 1hour and vincristine(push) and cytarabine IT(so painful)
1/28/16 induction
11/2009. 1/2010. Neuro side effects. Vision compromised. Weakness. Nausea.
I've had 2 rounds of induction therapy and just finished my 4th round of consolidation therapy. Side effects have been different with each round. My hair only fell out my first round. Have experienced nausea, dizziness, weight loss, appetite loss, headaches, brain bleeds, metal-like taste in my mouth and food, lethargy, loss of endurance and stamina, chemo brain, grogginess and foggy brain, memory loss.
Induction round 12/22/14-1/19-15: nausea, vomiting, diarrhea, fatigue Consolidation February '15, Consolidation March '15, Consolidation April '15
the only side affect she has had is toxemia, and neuropothy.
started Chemo on 2/7/25 - 7 days straight - no side affects on day 4
First round of chemo started on the 03/03/15. Side effects were hair loss, nausea, night sweats, temperatures and fevers, weight loss, loss of appetite, depression, anxiety, rashes, diaroreah, constipation, chemo brain and memory loss. My second round of chemo started on the 01/04/15. The side effects were the same but lesser this time. Although my second round, I didn't get any temperatures or fevers.
Nausea, vomiting and fatigue. Zofran helped a lot!
Multiple protocols for ALL & AML.
1 cycle of 7+3 regimen of Cytarabine, Idarubicin, but still had more than 10% of blasts in system. Went on to have 10 intermediate doses of cytarabine, and was in remission. Doctor had me on low dose decitabine and sorafenib (but I did not continue with sorafenib due to strong side effects of face bloating/swelling and rashes)
I have been through my first month of Chemotherapy. I am now going to the Mayo Clinic daily as an outpatient taking doses of arsenic. No Fun!!!
photosensitivity, some nauesea
chronic vommiting ,hair loss tiredness
Started daunorubicin and cytarabine 7+3 therapy on January 10, 2015. I stayed in the hospital approximately thirty days. A bone marrow biopsy at the end of this stay confirmed remission. My nausea was not too bad, except for a time that they served some green beans from the cafeteria. I dry heaved several times, and then ate only food from home. I suffered diarrhea, hair loss, a neutropenia fever, an acute kidney injury, fatigue, and weight loss. I started my first round of consolidation chemotherapy in February, second round in March, and third round in April. I have been very fortunate to this point to avoid a bone marrow transplant.
3+7 idarubicin and cytarabine On day 4
High dose chemotherapy, March-June 2012. Side effects: Nausea, vomiting, weight loss, fatigue.
Atra, Mylotarg, arsenic trioxide
Round one: 7 days of continuous chemo. Round two: 5 days of 2 times a day chemo Round three: 2 days of 2 times a day chemo Followed by 3 days of 2 times a day total body radiation.
I had Etoposide, Daunorubicin and Cytarabine. I had it over 4 rounds, each round about 3 weeks apart. My hair fell out, I felt so sick and so so tired. With the first round, my legs got insanelt itchy because of the Etoposide. My tastes changed-I lost my sweet tooth! Nad things didn't have much taste. There is still a few foods that I just can't eat yet. Chemo brain! My memory is shocking and I'm easily distracted with basically no concentration ability at all.
Started induction chemotherapy for AML on 25th September with "7+3 for 24 hours. I got Daunorubicin for 15 minutes the first 3 days while getting cytarabine the rest of the 24 hours. After the 3 days, the cytarabine continued 24 hours for the balance of the rest of the 7 days. I was medicated with multiple medications to prevent some of the known side effects such as eye damage, nausea, vomiting, and acid reflux. After the chemotherapy stopped, the Nader effects kicked in about a week later which is when the white and red blood cell counts and platelets drop. I ended up with ecoli infection in the blood and pneumonia which nessitated the administration of IV antibiotics. I also required Neupogen shots daily to help increase the production of white blood cells. Multiple platelet and blood transfusions were needed to sustain my existence. During this time I also had petechiae due the low platelet count. Stem cell or bone marrow transplant was recommended however, in my case, no full donor match could be found. Therefore my option was to have additional consolidation which consisted of hi-dac chemo (high dose chemo days 1,3,5 for 4 hours twice on those days. Typically if transplant is not an option, 4 doses of hi-dac is recommended. Due to my difficulty with the chemo, we opted for only 2 consolidation treatments. Right now I'm in remission although my white blood cell count and platelet counts are only 1/2 of the normal range. Last bone marrow biopsy (6th one) showed no Leukemia. Currently I have monthly blood work to monitor blood levels.
3/07- induction and followed by 3 consolidations. High dose ara-c and danirubicin. SEs include alopecia, fatigue, headaches, n/v, chills/fevers,low blood counts.Remission for about 2yrs, then it came back. Currently rec'd more chemo, with an unsuccessful remission at this point. More chemo planned, then bone marrow transplant.
Since June 2012 - july induction, August consolidation, Sept. consolidation, december 2012 induction. Stem cell transplant now on hold.
i had three induction therapies spaced about 6 months apart. and just completed two consolidation therapies. i am preparing for a bone marrow transplant.
Had two induction rounds and two consolidation rounds.

Chronic Lymphocytic Leukemia Cancer Chemotherapies

What Chronic Lymphocytic Leukemia Cancer Survivors said about their Chemotherapies.

Rituxan with High Dose Steriods - 2009 Campath - 2009
Fludarabine - 8/7/06 - 8/11/06 -- tired and nausea Rituxan - 8/11/06 - "shake and bake"...you name it I felt it...dizzy, chills, threw up, nurses very good in giving me appropriate meds to counteract side effects

Testicular Cancer Chemotherapies

What Testicular Cancer Survivors said about their Chemotherapies.

My husband had 4 cycles of chemo. Aug 2005-Dec 2005. Son is having 3 cycles. Started 8th June 2010... next cycle 28th June 2010. Both lost hair.
Bleomycin, Etoposide, Cisplatn (March 07 - May 07) Cisplatin, Taxol, Ifosfamide (September 07 - November 07)
Loss of hair, loss of weight, loss of wife. LOL
had no treatment
I was on three types Cisplatin,Bleomycin,& Etoposide.I started treatment in 9/08 and finished 12/08,four cycles.Effects were real BAD..it sucked hair started coming out about two weeks after first treatment,rashes just sick most of the time.
Chemo Began 12/02/2013... Bleomycin-Cisplatin and Etoposide
Bleomycin, Etoposide, Cisplatin (BEP) 4 cycles Side Effects: Blood clots, low blood pressure, fever, neuropathy, vomiting, nausea, hair loss, weight loss
Four rounds of VIP. Ifosfamide, Cisplatin and Etopiside, one day Cytoxan to motivate marrow growth.

GIST (Gastro-Intestinal Stromal Tumors) Cancer Chemotherapies

What GIST (Gastro-Intestinal Stromal Tumors) Cancer Survivors said about their Chemotherapies.

Gleevec 400 mg. daily, nausea, taking anti nausea medication
taking Gleevec for life

Chronic Myeloid Leukemia Cancer Chemotherapies

What Chronic Myeloid Leukemia Cancer Survivors said about their Chemotherapies.

Chronic fatigue
Gleevec
I've been on Gleevec for 3 weeks. the first week was no different than the previous ones, lots of fatigue, but that is from the leukemia. In the second week, I started having more pain and some diahrrea. The diahrrea cleared up in a few days but the pains got worse. By week three, I have a lot of bone pain. I can get around and i can work, but it hurts quite a bit to move and my legs (thighs) are the worst. I often wake up with pain and my fatigue is not improving.

Acute Lymphocytic Leukemia Cancer Chemotherapies

What Acute Lymphocytic Leukemia Cancer Survivors said about their Chemotherapies.

2-CdA, 2-hour infusions, 5 days. October, 2002. Progressive fatigue during treatment week. Could barely have energy to walk on day 5. Week later, UTI, high fever and fear of no immune system put me in hospital (reverse isolation) for a week. 2 blood transfusions brought counts up enough to go home. Fatigue endured for two months. Was back on job (teaching) in January.
Hyper CVAD protocol. Started 3/22/10. None for the first 3 rounds of protocol. Last 4 rounds have had N/V, extreme faitigue, bone and joint pain.
Jacob began chemo in February of this year. Things went really well and the only side effects that mom and I could see were abrasive hair (prior to it falling out), weight fluctuations, some nausea, and an aversion to sweets.
I have 6 months of chemo: 1. Daunorubicin, Vincristine, Asparaginase, Prednisone 2. Cytarabine, Etoposide 3. Methotrexate months 4, 5, and 6 are a repeat of months 1, 2, and 3. I also had 6 doses of intrathecal methotrexate (chemo injected into my spine). I am getting cytarabine, methotrexate, and a steroid intrathecally. I think I'll also get one round of high-dose cytarabine intravenously prior to transplant.
I recieved Chemo in 2004-2006 with my first diagnosis of ALL. I relasped in June 2011 and started chemo on June 24-July 18. I will continue chemo until my Bone Marrow Transplant.
An assortment of chemo drugs administered through an IV, spine and orally from Oct. 2009 - June 2010: Vincristine PEG-aspariginase Doxorubicin Methotrexate Cytoxan Cytarabine 6-MP 6-TG Side-effects: Nausea, Vomiting, loss of appetite, EXTREME fatigue, loss of muscle mass, mouth-sores, headaches, inability to concentrate (a.k.a. Chemo-brain), hair-loss, altered mood, bone pain.
I didn't really focus on what chemo I've gotten/getting, but my main side effects were nausea and fatigue.
Vomiting, hair loss, fatigue, mouth sores, reduced immune function.
I'm not going to tell you anything you would be shocked by here. I'm bald - and have been for two years. 98% of anything I eat upsets my stomach in some way. I wish I could sleep all the time, but I have a 5 year old little girl, a full time job and a husband so that is possible. Other than that, Cancer sucks, Chemo sucks worse, but we will all get through it, right?
lots of dates, spinal chemo right now are every three months and that causes head ach pretty bad for her and also some nausea vincrisine she gets once a month and that hurts her jaw arms and knees. mostly the joints. mercaptiprine, is every day, that just gives her a weird rash. methotrexate makes her sleepy
I don't remember all of them, but cytotoxin was one of them
Methotrexate, Doxyrubicin, Vincristine, Vinblastine, Cytarabine, Etopomide

Anal Cancer Chemotherapies

What Anal Cancer Survivors said about their Chemotherapies.

Xeloda Monday thru Friday. Weekends off. Also had mytomycin Iv in the beginning and end of treatment.
No problems with chemo. Lots of itching from radiation
Picc line inserted Nov 17, 2010... 5fu/mitomycin started Monday Dec 6, 2010. Took a week off from radiation after second round of chemo due to unmanageable pain. Finished chemo Jan 7th, 2011 and finished radiation Feb 4, 2011.
June 28 - July 4. A single 1 hour mitomycin pump followed by 4 24/7 fluorouracil pump. I like to think that I got extremely lucky with side effects. I was seriously constipated the first 4 days and put on 8 pounds in the first 48 hours. The only other side effect to this point is incredibly red blotchy skin on the face, neck and chest. I can only hope that round 2 goes as smoothly. July 27 - August 1. Intended to be the same as week 1. The mitomycin was put on hold until my platelet levels got back to normal, but we got it done. 4 bags of fluorouracil. Again, I was extremely lucky with side effects. None to speak of really and this time I didn't get the red blotchy skin on the face, neck and chest.
2 weeks started 21 July 2016- 25 July 2016
1st round 9/28/15: Mitomycin infusion; 5FU drip for 4 days. Stupidly stopped taking anti-nausea med Zofran for a day because it was making me constipated and proceeded to get sick throughout the night. Started taking Compazine instead. Developed thrush/mouth sores once finished with chemo - they lasted a week. Next round of chemo coming up 10/19/15.
began Nov17 for 96 hours and again on Dec 15 for 96 hours absolute neutrophil got down to .05 on Nov 27 and spent 4 days in isolation in hospital some hair loss and fatigue
Began 5FU and cisplatin chemo on 1/4/10 and 2/1/10 for 1 wk cycles. Side effects: nausea, vomiting, diarrhea, mouth sores, and fatigue. Hospitalized after last day of 5fu infusions for 3wks for chemo toxicity, diarrhea, severe abdominal cramping, dehydration uncontrollable fever, etc. At least I had completed menopause at age 42 and did not have to deal with the emotional side of this. Stopped HRT during treatments only.
Mitomycin and f5u-begin 4/12/11. . . . I was EXTREMELY tired and became EXTREMELY short-of-breath (ended up with bronchitis, but I have asthma.) One of the meds, Mytomycin, I think, can adversely affect the lungs. My thyroid got messed up so I now take meds. Nodules on lungs, on CT . . . monitoring those.
12/7-10. Not too sick alot of mouth sores and counts were drastically low hospitalized 12/15 with new oncologist
Taking Xeloda- doing awesome on it!
Infusion of Mitomycin 10/27/14, plus 96 hours of 5-FU via PICC line and carry-home pouch. PICC line removed at the end of 96 hours. Repeat this procedure 12/1/14 thru 12/5/14, which is also my last week of radiation. Had really bad mouth sores and lip blisters after the 1st chemo round, but not so much after the 2nd round. The pelvic radiation burns are very painful and hard to manage. But, once the healing started (for me, 1-2 weeks after treatment ended), it happened quickly. Didn't completely lose my hair, but experienced severe all-over thinning (at least 50%).
Started March 3rd, mitomicin infusion first week, next week started Xeloda 5 days a week, last week mitomicin and zeloda. Some feet neuropathy, 1 week off of Zeloda due to very low wbc and platelets, very tired. Hard to tell what symptoms go with which treatment
mitomyacin and 5fu two times over two different weekends 2009 mouth sores, weight loss, nausea,hair thinning, lightheadedness, memory loss,
1st and 5th week for 4 days
Cisplatin infusion weekly for 7 weeks, 5FU 5 days a week through a picc line.
June 23 to August 4. Two rounds of Mitomycin C and 5FU( I know why they call it that!!)......Fatigue, mouth sores, loss of all hair.
june 15-August 6, 2015
Dates 1/31/15, 2/19/15 Type, F5
Mitromycin and 5FU via pump, 1st week and 4th week of treatment. Nausea - 4 week had to be hospitalized
She has had 2 full weeks of chemo. FU5 and mitocytin. The second one they reduced the dosage as she had a violent reaction. She will finish the 2nd week of chemo on 1/21.
2/8/10 - 2/12/10: 5-FU and Mytomycin. 3/8/10 - 3/12/10: 5-FU. Nausea, loss of appetite, weight loss, lethargy, weakness, late effect hair thinning.
Taking pills(xeloda) 2 x day only on radiation days. Mitomycin IV 1st day and 28th day of radiation treatment Some nausea/Anti nausea pills help
2 rounds via port, less than 96 hrs round 1 due to New Year's Eve infusion clinic closing, 96 hrs round 2, Low WBC, fatigue, port infection,
Gi toxicity, fatigue, bone marrow suppression lasting many months hair loss, went in the hospital for a fever of 104 with low white count

Pleura, Malignant Mesothelioma Cancer Chemotherapies

What Pleura, Malignant Mesothelioma Cancer Survivors said about their Chemotherapies.

On Chemo from April to Sept 2010. Main side effects were fatigue, weight gain, mouth sores occasionally.

Bone Cancer Chemotherapies

What Bone Cancer Survivors said about their Chemotherapies.

i cannot sleep..i cannot eat..i do vomiting
First time I did chemo was on May 2006 and I lost my hair, throwing up, rashes, weakness. Just pure hell.
A year of hell Ill never get back
6 bouts of intensive chemotherapy - April 2005-September 2005 6 bouts of a less intense chemotherapy - October 2005-February 2006

Nose, Nasal Cavity and Middle Ear Cancer Chemotherapies

What Nose, Nasal Cavity and Middle Ear Cancer Survivors said about their Chemotherapies.

See the Chemo Dr tomorrow, too. Don't know if I'm going to do it.

Nasopharyngeal Cancer Chemotherapies

What Nasopharyngeal Cancer Survivors said about their Chemotherapies.

Protocol #1: First of 3-21 day cycles of 5-FU, Cisplatin and Docetaxel started 10/7/13 - around the 2 or 3 week started losing hair and experiencing nausea, fatigue, weight loss, etc; Protocol #2: Eribtux and concurrent radiation for 6 weeks started ~12/10/13 - neuropathy in feetbegan a few months after treatment stopped and is still ongoing.
chemotherapy given from January to September Side effects: dehydration, vomiting, blood transfusions
3 x cycles of Cisplatin 80mg/m^2 over 9 weeks prior to Radiotherapy 3 x cycles of Xeloda (14 tablets) over 9 weeks prior to Radiotherapy Once weekly 40mg2 Cisplatin during Radiotherapy
3- 8 hr chemos mostly nausea.
Jan 2009-june 2009: lung nodules shrunk a bit and last CT scan end of june showed no growth: little nausea, tired all that stuff
Started weekly induction chemo on 9/5/13 with carboplatin and paclitaxel- soreness in mouth, slight nausea, dry skin (severe itching), acid reflux. Started chemo-radiation on 11/4/13 using cisplatin. Received 5 weekly cisplatin treatments until wbc count was too low.

Ureter Cancer Chemotherapies

What Ureter Cancer Survivors said about their Chemotherapies.

Taxol and Carboplatin. Started November 2008, should be completed March 25, 2008. Side effects some nausea with first treatment, leg pain and neuropathy.

Peritoneum, Omentum and Mesentery Cancer Chemotherapies

What Peritoneum, Omentum and Mesentery Cancer Survivors said about their Chemotherapies.

Carboplatin and Taxol once every three weeks, 6 times. Fatigue, faux sence of energy at first, couldn't sleep for two day after, then crashing with neuropathy pain and fatigue

Gastrointestinal Carcinoid Tumors Cancer Chemotherapies

What Gastrointestinal Carcinoid Tumors Cancer Survivors said about their Chemotherapies.

First & only dose: 09/05/08-5FU/Leucovorin/Oxaliplatin - side effects? fever, rash (?), edema, fatigue, neuropathy, dizziness, confusion (some); nausea, hand/foot - more, but can't remember them.
chemo side effects hair loss some weight loss vomitting sweats shakes hot cold pain emotional skin tone looked unhealthy

Esophagus Cancer Chemotherapies

What Esophagus Cancer Survivors said about their Chemotherapies.

Chemo is rough.
every 3 weeks, side effects: tinnitus and stomatitis after the last one
currently undergoing treatments
preadjuvant, and adjuvant, 12 week cycles with cisplatin, epirubicin and 5FU. For recurrence it was oxciliplatin, leukovorin and 5FU.
Too many chemo regimens and drugs to count. At present, I am on Xeloda, Herceptin and Avastin. One drug was damaging my liver, but okay now. Herceptin was damaging my heart, but it is okay now.
Carboplatin/Taxol, continuous 5FU drip March/April 2008 Taxotere July/August/September 2008 Cisplatin January/February 2009
Carboplatin and Taxol for 5 rounds. No side effects at all except tired on day 2 & 3 post treatment day. Tolerate chemo well.
june 13 2011. no side effects yet
Sysplatin that almost killed my it caused my kidneys to shut down. I cause me to become completely dependent on others. I didn't spell the Chemo right but it sounded like that. I don't know what the fed me after I was released from the hospital.
1-2 treatments per week for 6 weeks along with radiation
chemo from 2/98 through 9/98

Tonsil Cancer Chemotherapies

What Tonsil Cancer Survivors said about their Chemotherapies.

Hearing loss and ringing in my ears. 3 chemo treatments, first, fourth and 7 th week. Saliva got thicker then syrup,honey after treatments ended. Couldn't swallow and had to sleep sitting up in a recliner for weeks afterwards.
Chemotherapy Cisplatin. Vomiting started the first day of chemo and stopped two weeks after treatment complete (9 weeks of vomiting & vomiting).
Carboplatin - 6 Weekly infusions completed February 27
February 25, 2011 - Cysplatin (Cisplatyn) I don't know 4 of 8 weeks only as it ruined my throat way early and did it's job - according to the dr.
1st Chemo -Rituxan 6/12/13, CHO 6/13/13 with prednisone daily x 5 days, 6/14/13 Neulasta. Foods tasted sweet and had a slight headache but I did good until 5th day and I decreased my antiemetics and had nausea/vomiting and had to get IV fluids. I had some swelling in feet & hands. I worked several days but on the 7th day after neulasta I had back pain and had to take pain pills and a muscle relaxer, then I took Claritin and it did help. I still think I did good for my first chemo. 2nd Chemo- July 3 R-CHOP, July 4- Neulasta. I had swelling the first night in hands & feet. I feel weaker with this one and I'm having breathlessness. I called doctor and had labs but results were okay for chemo. I haven't worked after this one, yet.
Cisplatin ....nausea and fatigue
Started Treatment on May 24,2011... last Chemo July 5, 2011... hair thinning, but no sickness
April 4,2011, minor nausea April 12,2011, rash on upper lip
Began Erbitux November, once a week. Skipped December, resumed chemo January, I go weekly.
Cituximab Loading dose March 13th, High fever and severe headache. Second of 8 treatments March 21st. Only side effect was severe heartburn.
3 Cisplatin Chemo's, starting July 17, 2014
Cysplatin, Oct 6 thru Nov 18' 1ce a week
I will also start chemo on Monday, October 19th. That will be done after radiation every Monday for seven weeks. It's a combination of three drugs: Taxol, Carboplatine and Erbitux. Will be asking why once a week when it seems everyone else that I've read about get three treatments throughout those seven weeks.
Taxol and carboplatin. 6 weekly infusions.
Cisplatin gave my husband ringing in ears but much better now. Had complications each time after a chemo. Was hospitalized twice for them.
Chemo is Erbitux which I get once a week for 7 weeks.
after 1 chemo treatment I don't feel any reaction as of yet. Next treatment July 14.
Ciplatin 3 megadoses 3 weeks apart concurrent with radiation
Still waiting on Chemotherapy decision
cisplatin start 10/28/08
11 treatments ended about 11/07/2011
The first chemo treatment of Cisplatin was on 8/31 with another scheduled for 9/21 and 10/12.
CisPlatin 3 doses at weeks 1,3, 7 of radiation. Mild hearing loss of high frequency sounds after first dose; reduced dose on last 2 sessions to minimize additional hearing loss.
concurrent w/rad 3/19 3 weeks apart megadose cisplatin 100Mg/M² side effects have included peripheral neuropathy, hearing loss, ear ringing, fatigue, nausea, vomiting, slight hair loss, blurred vision, unexplained bruising, blood blisters on mucuos membranes, dizziness, destroyed vein and tendon damage near 2nd injection site(both probably permanent)
For details see my posting.

Mesothelioma Cancer Chemotherapies

What Mesothelioma Cancer Survivors said about their Chemotherapies.

carboplatin, alimta 8-27-09

Endometrial-Uterine Cancer Chemotherapies

What Endometrial-Uterine Cancer Survivors said about their Chemotherapies.

May 2010 Chemo Carboplatin/ Taxol, nausea, fatigue, hair loss
currently doing carbo/taxol every three weeks. Extreme fatigue, muscle aches, taste changes
I have had two rounds of chemo, and the next will take place on Jan 31, 2012. After that, three more rounds!
5/2010-tired, nausea 10/2014-tired, nausea,low blood countsand turned into mds 12/9/2015 start cgeno with doxil after mds in remission
Haven't started yet. Need advice.
See Surgery Description> apparently I cannot follow directions
Chemo start date 7/15/09 - Doxil infusion with Ativan and Compazine every 21 days...that was "potponed". Chemo, once started, was be Doxorubicin and Ifosfamide - 4 days of 24-hour infusions. Mom was having delirious thoughts from the chemicals, they took her off of food - the doc said she "had enough fat on her" to get by without food. She was in and out of sleep from the sedatives in between chemo.
4/17/15 Allergic reaction to Emend and Taxol
Lost hair not much else
Every week on Day 1 & 2 and Day 8.
Started my chemo on Sept 11th of 2008. I have to complete seven cycles. I receive cisplatin and adriamycin on the first day of treatment along with other pre-meds such as decadron and emend. Second day of treatment I receive Taxol and the following day I go back in to get a injection of neulasta.
Chemo came after radiation the first time, chemo only the second time, radiation only the 3rd time. Allergic reactions to almost all the drugs tried, but that was the second time. The ones that I didn't react to made me very sick, so I'd go in to be hydrated the day after chemo since I was unable to do that at home. It's hard to eat and drink when you're asleep. Another side effect of the drugs and certainly the pain killers for me.
little queasy tired bald last one nov 5th 2010 yesssssss!!
6 chemotherpay treatments. Cisplatin for 2 and Taxol/Carbo for 4. Stomach nausea,bone pain after Neulasta shot, constant dehydration, tired all the time & neuropathy in feet.
Cyclophosphamid Carpoplatin Taxol
Starting chemo (carboplatin and taxol) on 4/27/11. Will have 6 sessions, one every 3 weeks.
TBD but they definitely want to do it.
Taxol/carbo, starting Dec 12, 2007. Some joint pain, hair loss (boo-hoo) and slight stomach upset.
CarboPlatin & taxol w/ neuplasta at 3 wk intervals from Aug to Oct Severe constant leg pains, neuropathy in feet and hands, high heart rate. Unable to stand for more than 10 minutes, stumbling, dropping things regularly Treatment changing to CarboPlatin & doxil w/ neuplasta.
My symptoms became SO much worse after chemo: Pain, nausea, vomiting, mouth sores, chemical taste in mouth, fatigue, weight loss
First round of chemo on 7 May 09 Second round of chemo on 1 Jun 09 Third round of chemo scheduled for 21 Aug 09 My doctor is using a new "sandwich" approach to treatment. 2 rounds of chemo > then 25 days of radiation > then 2 more rounds of chemo. This is new and apparently works better than all chemo then radiation. I am in control and working to erradicate the cancer via chemo and radiation.
Finished Aug 23, 2011. 6 treatments completed. Zofran for anti-nausea worked but caused headaches.
recommended to start after radiation
Chemo 6/21/10, 7/12/10, 8/2/10, 8/24/10, 9/14/10 - nausea, fatigue, bone & joint pain, diarrhea, neuropathy; scheduled for 1 more round
Had a port put in August 2011, then started chemo. 2 drugs. Plan is 6 cycles, every 21 days. Have completed 3. Blood work ok, but almost unable to walk. No strength, can hardly stand, can't climb stairs well. Feet are numb, butt now numb. Had spinal MRI 11/11, #4 delayed a week.

Sarcoma Cancer Chemotherapies

What Sarcoma Cancer Survivors said about their Chemotherapies.

Doxorubicin Cisplation Methotrexate Ifosfomide Etoposide
cistoplatin made her very ill
Still to be determined.
Currently still undergoing chemotherapy. Started in October of 2010 and should be finished up just before or around early March of 2011.
IE and VAC treatment every 3 weeks. Lost weight and all my hair/ body hair
Currenly going through Ewings Sarcoma protocol for Chemotherapy. 14 total cycles.
Had AIM protocol (Adriamyacin, Ifosfamide and Mensa) for all of 2007, then in 2010 I had Yondelis, a clinical trial, also for a year. The AIM made me lose all my hair, had frequent need for transfusions of blood and platelets and I had many infections. The Yondelis did not make me lose hair, but the other side effects were the same.
Chemotherapy lasted from July 2010 - August 2011 His chemotherapy consisted of Vincristine, Doxorubicin, Cyclophosphamide, Ifosfamide, and Etoposide. Some vomiting and lots of nausea.
After 3 rounds of chemo and some radiation Nicole's doctor pronounced her freee and clear. This was not true and with Rhabdo, if you don't get it all and leave even a half of a cell the cancer comes back ten times stronger causing it to be incurable.
Doxorubicin and Ifosfamide: together from jan 2011 - april 2011. Bloating stomach, hair loss, skin darkened, gums darkened, bloated face, sore feet , palms and soles of feet became dark,tiredness, constant spitting. Trabectadin: Nov 2011 -Dec 2011 Didnt work. Constant spitting, skin darkened, gums darkened,face bloated, tiredness could not leave bed for one month. Just felt totally ill.
Adriamycin Dec 14/15 on going
Currently going through chemo... some of the side effects that I am experiencing are mouth sores, and sore GI tract. Definite tiredness, lunula turning black, of course hair falling out, complete loss of taste buds and smell during chemo but fine after.
Gleevec, vomiting, diarra, swollen eyes and ankles, cramping in hands feet arms legs, fatique, from 10/19/07 till 5/2013. Didn't work for me after awhile.
Chemotherapy started on 20th Dec 2008 and I chose to stop in June 2009 (I was meant to finish in Nov 2009, but when I found out my tumor was no longer shrinking, I physically could not deal with the side effects anymore). I lost my hair, which was by far not the worst side effect! Mouth sores, lost my sense of taste and smell. Horrendous constipation. Nauseous most of the time. Not able to eat. So completely exhausted, not even energy to stand up some days. Felt extreme cold, then major hot flushes, wake up drenched in sweat. Eyes always sore and watery. My chemotherapy was every 3 weeks, which took 5 days in hospital to administer IV - then every month when home I would spike a massive temp & have to be rushed into hospital for blood transfusions and isolated for neutronpenia! Chemo turned me into a shell of my former self, it destroyed my spirit and had me in tears most of the time. It was a hard, hard fight.
I have Chemo once a month. The Chemo caused the whites of my eyes to turn Fire Engine Red. It was a reaction that none of the nurses had ever seen. I was given IV Benedryl. The dose of the medicine knocked my butt out. That was my first treatment on May 21, 2012. I was set for 3 treatments. My Oncologist was not sure if the Chemo would work to begin with. Within the first treatment I could tell a difference. I was amazed. I could actually feel the mass and it was smaller. So, Dr. M ordered another 3 treatments for a total of six. I lost all my hair, eyebrows and eyelashes. Hey, they will grow back one day. I don't mind. I love all the scarves and hats I have bought and been given.
Chemotherapy to start in 2016
Chemotherapy started in September 2011 and continued every three weeks either daily for a week, or a single day dose of VAC - crappy crappy side effects, where do I start......numb finger tips, constipation, hair loss, loss of taste buds, thrush in mouth, lack of concentration, sooooo exhausted after each dose and weeks later. It is very true that the chemo is so much harder than the cancer to deal with.

Skin Cancer Chemotherapies

What Skin Cancer Survivors said about their Chemotherapies.

Photo Dynamic Therapy for any AKs... skin checks every three months

Throat Cancer Chemotherapies

What Throat Cancer Survivors said about their Chemotherapies.

Dry Mouth. Lost body hair, Sick at stomach, weight loss.
1997- Cisplatin/5FU - I wanted to die (permanent hearing loss & temporary vein loss) 2003 - Cisplatin/5FU - Extreme discomfort; bloating, burning, nausea, etc. I refused further treatment. 2005 - Taxol, 5FU, Carboplatin, Leucovorin - side effects so bad I quit 12 course regimen after 4th course 2007 - Taxol, 5FU, Carboplatin, Erbitux, Leucovorin - I wished I were dead! after 9th course I was not recognizable; the erbitux had caused my face and neck to break out with puss filled sores that burst and bled. I quit after 11th course.
May 7, May 14, May 24. (Now scheduled for June 1, 8 and 15). Side effects are fatigue and nausea. Taking anti-nausea meds. Worst part is we can't keep enough fluids in him to flush out the toxins due to chemo. We're told this is more common in throat cancer where food and fluids are taken through a feeding tube. Starting to lose patches of hair.
It seems that my side effects (nausea, tiredness) start a couple days after treatment. Emend and Zofran seem to be helping.
Start November 29, 2010. The drug was erbitux. No side effects with the weekly treatments except for after weeks four and five. After treatment I immediately had chronic chills and shakes in which I was given an injection of demorol and had to lie down for an additional hour until the effects subsided.
3 during 6 week radiation treatment (beginning middle & end.
Feb 14, 2011, Cisplatin, slightly tired immediately following treatment. March 7, 2011, same as treatement number 1. March 28th, 2011 - TBD
Months of daily treatment with both Cisplatin and Herbitux -- major side effects included a rash that covered me from head to toe, skin that was so dry that my scalped split open and bled when I vomited (which I did several times each day). Further side effects included hallucinations, tremors, chills, hot flashes, disturbed sleep patterns, fever, loss of hair, etc.
February - June 2009 Taxotere Cisplaten 5FU
Three rounds of Cisplatin - nausea, metallic taste and tired

Tongue Cancer Chemotherapies

What Tongue Cancer Survivors said about their Chemotherapies.

Three Cisplatin doses, Jan 4, Jan 26, Feb 16. Never got the Feb 16 dose as I was too sick from throwing up.
Erbitux for 6 weeks, no side effects.
second form of chemo 3 more weeks, no side effects
A 2 chemical soup every 3rd Monday and then a 24/5 fanny pack pump the same week as above. I have 1 week on and 2 weeks off treatment
For me Chemo was much easier than Radiation. Cisplatin and 5-FU 24/7 for which I was hospitalized. I refused my last chemo treatment because I was too sick, and honestly I thought it would take a lot more than chemo to save me from this beast called cancer. Yet I survived and have for the last 20 years.
Eurbitux caused a huge itchy red rash EVERYWHERE after week 3. I was almost hospitalized it was so severe, but huge IV bags of Benadryl saved the day.
Set for July 6 and July 21
I started the chemo the frist week in July 2010. I had a reaction to the first chemo which was Carboplatin and taxol so they changed it to Cisplatin and taxotere. They loaded me up on steroids and during the next treatment i had yet another reaction this one only worse than the first. So as a last ditch effort they changed again to cetuximab and honestly i cant remember what the second one they gave me with this was. I was ok with this drug but the side effects were aweful! I broke out all over my face with horrible acne and it made the radiation stronger which made the raidation burns worse.
Chemotherapy to be given concurrently, once a week. Began on 8/23/12.
3 bags of cisplatin
Do not know yet if I will have to go through Chemotherapy.

Hodgkins Lymphoma Cancer Chemotherapies

What Hodgkins Lymphoma Cancer Survivors said about their Chemotherapies.

Getting chemo doesn't hurt. I don't feel the chemo being injected, and I feel fine for 3 days after, minus the fatigue. Nausea, headaches, body aches, upset stomach are my most common side effects when my medications are done.
6cycles of Chemotherapy was planned that is a six montha duration.ABVD doses was induced in every fifteen days through veinflow during the first 3 cycles and later through picc line which was less painful. Side effects of chemo were many starting with gastritis, acidity, nausea, body pain,hair loss,fatigue...but this would be fine within a week after wbc count increases to normal level.
im doing an eight mounth treatment plan. every 21 days im back in the hospital for all the chemo they can give me.
Started chemotherapy on the 28th of September 2011. I first had really bad constipation, muscle and bone pain, fatigue, numbness in the tips of my fingers, hairloss, mouth ulcers, nails coming away from skin.
7/13/2012~ABVD
ABVD May 2008-October 2008 ICE January 2009-March 2009 BEAM April 2009
The usual - not a single strand of hair. But, the stomach was the killer. I would be on liquid diet for days during chemo period. Even after 1 year, I am still experience problems with stomach. Physically, the body has changed so much. Mentally and emotionally, I have changed too (hopefully for the better :))
Stanford V regimen - Weight gain, constipation, fatigue, hair loss.
8/23/12 - Hot-flash (minor) and a little fatigue 8/26/12 - Mouth sores.
4 Cylces (8 treatments) beginnning March 12. Second Session March 26, April 9th, April 23rd, May 7th, May 21st, June 4th and lastly June 18th!
4 cycles of chemotherapy ending in late August, radiation to follow depending on how the cancer responds.
ABVD for 6 cycles (12 treatments). Was quite well tolerated, tired for a few days after, hair loss, mild nausea but no vomiting, changes in bowel motions, mild rash on feet and arms, aching veins. MADEC (methotrexate, cytosine, dex, etoposide, cyclophosphamide) for 2 cycles, one week of chemo in hospital, 2 weeks to recover then repeat. Fatigue, mild nausea, hair loss. BEAM (carmustine, etoposide, cytosine, melphalan) prior to stem cell transplant. Have only just started this today, had carmustine and so far all good but I know this will change.
ABVD, started Feb. 13, 2009.
I had 6 x ABVD last summer. Now 3 x DHAP + stem cell transplantation in the future
ABVD 08/22/2014: Fatigue, jaw pain, swollen tongue/mouth, loss of taste, hiccups, sneezes, mood swings/anxiety attacks, bone pain, constipation, some nausea, loss of appetite, decreased white blood cells & fevers (resulting in ER visit & week-long hospitalization). ABVD 09/18/2014: Fatigue, hiccups, intense bone pain (pelvis & back), jaw pain, swollen tongue/mouth, loss of taste, emotional, loss of hair. ABVD 10/01/2014: Fatigue, painful bowels, jaw pain, hiccups, mild night sweats, bone pain, difficulty sleeping, mood swings, nausea, joint stiffness, mild skin rash, constipation & severe abdominal pain, decreased white blood cells & fevers (resulting in second ER visit & week-long hospitalization). ABVD (w/20% strength reduction) 10/15/2014: Fatigue, jaw pain, swollen tongue, loss of taste, bone pain, irregular bowels, some constipation, gassy, hiccups, mild night sweats, heart burns, sneezes, difficulty sleeping, mood swings
Clinical Trial-see below
12 rounds of ABVD. Side effects: hair loss, weight gain, nausea and fatigue
28 day cycle. Chemo on days 1 and 15. 6 cycles or 12 treatments
6 rounds of ABVD; vomiting, fatigue, diarea, insomnia, hair loss.
Started Chemotherapy (ABVD) on 30th March 2010. Found that the side effects of consist of bad heartburn & indigestion for a few days after chemo. My hair started to fall out about two weeks later and has slowly been falling out ever since, but not bald yet! Have had to give up fizzy drinks and spicy food, two thinks I enjoy. Unfortunately they cause uncomfortable consequences, like bloating, passing a lot of gas, nausea, heartburn, the list goes on.
Nausea, lightheaded, tired. First treatment was 8-13-15.
1/7/2014 and every 14 days thereafter - Nausea, jaw pain, loss of taste, hair loss, fatigue 6/10/2014 - chemo complete (6 cycles ABVD)
nausea, fatigue, anxiety, depression, dizziness, vomitting
About to start Chemotherepy. Very nervous. I was suppossed to start April 11th, but my insurance covers Lupron, so i can save my ovaries from the harmful drugs. Should be starting within the next week or so.
April 6th 2009 - Initial chemotherapy at the hospital. The immediate effect on the swollen nodes blew my mind. It was almost all gone 48 hours later. Several others that are chronicled in my blog.

Acute Lymphoblastic Leukemia Cancer Chemotherapies

What Acute Lymphoblastic Leukemia Cancer Survivors said about their Chemotherapies.

I'm getting three chemo a dont know what they're called but they all make me feel like crap. But whatever makes me better I guess. Fatigue, sick, swollen ankles, sensitive skin, pins and needles in finger tips. Bowel movements slow down. But speed up after a while
Started induction chemo within the first week of November. Integrating it with holistic therapies
From October 2014 until April 2015 I received heavy chemotherapy, which included Peg-Asparganase, Vincristine, Cytarabine, methotrexate, doxorubicin, daunorubicin, cyclophosphamide. April started maintenance therapy, which will last until January of 2017, and includes Vincristine(through IV), Cyarabine(through lumbar puncture), 6MP(mercaptopourine, a pill), methotrexate(pill form), and dexamethasone. in the very beginning of my treatment I also took prednisone for two weeks. Throughout my entire treatment I have taken Bactrim and Acyclovir to help prevent sickness, and also am prescribed Ativan, Zofran, and Phenagren for nausea. Also stool softners are prescribed. Side effects: Prednisone- uncontrollable fatigue during the day, couldn't sleep at night. Very very sore right around my middle. As if someone had put a huge rubber band around my lower abdomen/back and pulled it tight. My back hurt SO bad. My husband would rub it for hours in the middle of the night. Intrathecal methotrexate- nausea the day after for about a day. Vincristine- fatigue, mild nausea. Cyclophosphamide-extreme nausea for about 3-4 days. Methotrexate(pill form)- nausea a day later for about 12-14 hours. But not every dose. 6MP-horrible nausea; was relieved after dosage was lowered. Now it doesn't affect me at all! Dexamethasone-this is the worst one. I take this for 5 days once a month. Side effects hit anywhere from 3 days into the dosage, or 2-3 days after the dosage is done. Side effects include: Sensitive skin; so sensitive that I can't be touched. It feels like a severe sunburn. Always starts on the back of my neck, and moved its way down to my upper back, then shoulders, then lower back, sides, and sometimes it stops right there. Sometimes it will continue onto my outer thighs and butt. These effects come on fast, within 6 -8hours. Sometimes it is so severe I miss work, but when it's that bad, it only lasts 2-3 days. Other times the effects won't be as severe(I can still work) but they drag out for 7-8 days, and muscle fatigue is pretty bad. I do small excercises and run on the elliptical but when this is happening, I miss about 3-4 days of excercise because I hurt so much.
started Feb. 26, 2010 I was admitted to hospital every 3 weeks for a total of 6 rounds of treatment - Cycles A and B.
Hyper CVAD Protocol 6/1/2015-2/7/2016 including spinal chemo X 4
Fatigue, mouth sores, nausea
currently undergoing HYPER C-VAD
Started chemo once my pneumonia was under control which took 3 days after I was at the hospital(4/4/10 was start date). While in the hospital for a month getting very strong drugs I didn't have any sick-feeling side effects and ate like a horse. I did however lose a lot of muscle mass and after a bit I was barely able to walk and there were occasions where I passed out for various reasons and wasn't able to get myself back up. But I was on 150mg of prednisone at 7am and 7pm each and every day and the side effects from it were awful and probably the worst part about my hospital experience as it made me feel very strung out, nervous, antsy, you name it. Towards the end I started to feel as if I was starting to lose my mind which was more than likely just a chemo brain effect. However after my primary induction was over at the hospital, side effects became more prevalent doing chemo 5 days a week from May-July of 2010 where I passed out, god very sick, could barely eat, had no energy, was extremely depressed but that put me out of my second phase and into the long part, maintenance. I got to come home for maintenance which wasn't possible for the other treatments due to not having any blood cancer specialists where I live, but my doctor personally knew many of my doctors out of state and was who sent me to the group of doctors that he did. I was almost constantly vomiting, Intense chronic pain in my lower back, legs, shoulders, hands, feet, and various other parts of my body. Now I'm chemo free for two years from 2/26/13 but I still have very bad physical issues as well as PTSD, Depression, General Anxiety and other mental health related issues.
finished with induction therapy, now gonna begin with consolidation.
CALGB initial remission followed by 7 cycles HyperCVAD and 24 months maintenance vincristine, methotrexate, mercaptopurine
October 2010 - current; Unfortunately, I've had nearly every side effect from chemotherapy.

Bile Duct Cancer Chemotherapies

What Bile Duct Cancer Survivors said about their Chemotherapies.

HAIC 24/7 for two consecutive weeks of constant flow chemo delivered directly to the liver. Every two week chem, alt two weeks pump is filled with Saline. NO Side Effects
On my second round of 2 sessions each which are a week apart
Second time around: Fluorouracil (5-FU): given through a portable 48 hour pump Irinotecan (Campto): 1 hour iv, i think First time around: Gemcitabine: will be administered through IV for over an hour. Cisplatin: will be administered through IV for over an hour. He will have to rehydrate 4 ours before injection.

Leukemia Cancer Chemotherapies

What Leukemia Cancer Survivors said about their Chemotherapies.

January 6 2014 and February 15 2014

Myelodysplastic Syndrome Cancer Chemotherapies

What Myelodysplastic Syndrome Cancer Survivors said about their Chemotherapies.

too many to remember
Vidaza 5 day cycle once a month, side effects weight loss, erythema nodula,hair loss(slow), nail discoloration
rituxan, vidaza, and revlimid

Appendiceal Cancer Chemotherapies

What Appendiceal Cancer Survivors said about their Chemotherapies.

Fluorouracil (5-fu), Oxaliplatin, Avastin, leucovorin. 1/15-3/2? Side effects - Extreme fatigue, nausea, cold sensitivity, neuropathy
May 2013 to present. Nausea, tired, bloating, loss of concentration, neuropathy, diarrhea, jaw pain, high blood pressure, anxiety, sleep loss
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See full list of all Chemotherapies