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What are Chemotherapies? List from Cancer Survivors.

Breast Cancer Chemotherapies

What Breast Cancer Survivors said about their Chemotherapies.



AC x4 Tax x4 recieved every two wks first chemo 29th April '10 last 5th august '10 side effects varied from the usual hair loss, vomiting to swelling of my chest wall, 19 of my 20 nails fell off (this happened a couple of weeks after the chemo finished) nose bleeds the list is endless but I got through it
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.
Feb 2011 - April 2011 every 3 weeks Side effects - tried slept about 5 days straight Neulasta Side Effects - Painful legs and joints
No chemo
Hair loss Fatigue mouth thrush low blood counts infection/ fever
I had Cytozen(I remember it burning badly)I had three months of chemo before surgery, and three months after surgery, total of six months,side effects nausea, fatigue, mouth sores hair loss
Had first treatment Sept 3rd. headaches really bad stomach, rash on my chest and face they just keep coming and changing really
AC dose dense,then taxotere all for 5.5 months.Lots of lousy side effects you name it I had it!
AC, 3-2-11 lots of nausea, hurt to breathe through nose, blinding headaches (3-4 through 3-6), all-over weakness through the first week, leg and tailbone area pain.
Pending. I have only been told of what the drugs of choice will be and I can plan on being bald.
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.
Dec - 2010 Jan - 2011... so far Feb
First Taxol 1.5.11, once a week for 12 weeks, FAC once every 3 weeks from 3.30 - 6.1.11. Taxol made me feel like I was wearing a lead raincoat and concrete shoes. FAC was far more discouraging. Lots of digestive issues, couldn't eat, everything taste nasty. It was horrible.
Taxotere, Carboplatin, Herceptin Dec 08 through Dec. 09 Nausea Migraines Loose fingernails/toenails, MRSA infections x 8, auto immune allergic reactions Hair loss allergies developed Loss of menses (early menopause)
Oral chemo twice a day, administerd first in January of this year, two weeks on and one week off then back to hospital for blood test and back we go again. Chemo has been reduced as my system is not strong enough to take the original dose now.
Started chemo just before Christmas of 2009. Was given cytoxin and taxotere. Extreme fatigue, nauseousness, no tomato foods first few days after chemo, and no burning food allowed in the house! Had my last chemo February 20. Took 2 months FMLA during chemo. Early chemo-induced menopause.
2013-2014: 1st chemo; Taxol, no help. 2nd chemo:Doxil, no help. 3rd and current chemo: Gemzar & Cisplatin. I also get Zometa injection every 4 weeks. I started Chemo on June 19, 2008 and as of today 7/7/08 I have only had 1 treatment. My second treatment is this week on Wednesday, July 9, 2008. I will have 6 chemo treatments, 3 weeks apart. The worst side effect I had was from the Nulasta shot I had the day after chemo. The bone and body aches really kicked my butt. I was fortunate and did not experience any nausea. On day 14 I started loosing my hair. It was coming out by the handfuls!! By day 16 I couldn't stand it anymore so I buzzed it all off.
I've taken chemo for 3 years now, many kinds of chemo, my "favorite" is Xeloda.
Every three weeks after first diagnosis (Nov. 2009) until "remission". Every two weeks after recurrence (Nov. 2011). Food tastes chemically. According to test results my wife unknowingly suffered a minor heart attack in 2012 (I believe due to long term use of Herceptin in her chemo sessions)
4 cycles dose dense Doxorubicin and Cyclophosphamide, then 4 cycles dose dense Paclitaxel to start 12/09/08
4 treatments 1 every 2 weeks started late March-May 2008
I had 5fu, Methotrexate and Cytoxan. I had the 5fu and Methotrexate in an IV push the first and second Tuesday of each month. The third week I took Cytoxan pills and rested the fouth week. This was for a total of six months.
I had my 4 cycles of chemotherapy a month after my surgery and had the neupogen injection.
AC and Taxol
Breast cancer 1 2004: FEC - started throwing up after session 2 and it just got progressively worse. Breast cancer 2 2011: TAC - minor heartburn, some nausea, some reaction to lenograstim injections, but apart from a little nausea, no sickness (hooray!). Complete hair loss with both types of chemo.

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
NONE!!
None

Lung Cancer Chemotherapies

What Lung Cancer Survivors said about their Chemotherapies.

Chemo also started on 10/10/07 and its once a month for 3 days in a row.
Started with nine drops of Taxol and had an allergic reaction that caused me to stop breathing. Then switched to Gemzar and Carboplatin. Had some nausea but started taking Emend....VERY tired.
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
Avastin-2008 and 2011, Cisplastin-2009 and 2011, and Tarceva-2011.
3 days chemo every 21 days. Hydration as needed. Tiredness and nausea/vomiting at times.
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.
Feb 08-Cisplatin/Etoposide- hideous vomiting diarreah Switched chemo drugs AND Hospital -April08-carbo/taxol/avastin. Tolerated well. Neulasta. Bone pain
Iressa (gefintib)
Nov 2013, jaundice, gas, diarrhea, constipation, hair loss, swelling of feet, bloating, weight loss, loss of appetite, metallic taste, dry mouth, mouth sores. Now on round 8 of chemo
December 2004 - Present off and on. On Avastin and Tarceva currently, but stopping to start a new chemo.
Carboplatin - my first treatment of chemo (started 2th of august 2010), no side effects so far (lucky me), gives good hope for second (heavier) chemo combined with radiation therapy
carbo/taxol only effect has been being tired!! Verty low white cell counts, had to receive one transfusion, other wise has handled it well.
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.
3/2012 Adriamycin and dacarbazine 6 cycles 12/2012- 10/2013 votrient 600mg every day. 10/2013 - present gem/tax
Dont know
chemo fog.
Start Chemo May 18th 2007 Cisplaton and Etoposide
Taxol, Carbo, Avastin (pain, nausea and vomiting, fatigue, confusion). Zofran was the BEST anti-nausea drug and I tried them all. Broken pelvic bone, NEUROPATHY (very bad so I am on an anti-seizure drug to control it). Tarceva, Alimptor...
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.
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
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.
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...
Chemotherapy 12/09 to 2/10- loss of hair, weight, blood clot, fatigue, low white blood cell count and nausea neuropathy in finger and toes. 6/10 to 1/11 same symptoms as previously noted except for no blood clots.
Alimta (Pemetrexed) Aug - Nov 2013, 6 cycles
2007 April til present so far 5 rounds Taxotere Carboplatin Avastin Emend for nausea Aranesp for red blood Neulasta for white blood etc.....

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.

1st treatment, August 23rd, 2011...which is tomorrow, so I don't know what side effects I'm going to have.
Rituxan-CVP
Began a course of Hyper C-Vad July 4th weekend. Rixutin was the first drug administered and it caused me to stop breathing very frightening. Other side effects extreme tiredness, mouth ulcers, nausea, and hair loss.
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." :)
R-CHOP 08/2008-12/2008 R-ICE 01/2009 ESHAP 02/2009-03/2009 BEAM 05/2009
R-CHOP R-ICE ESHAP
R-CHOP 25/11/11
R-CHOP every 3 weeks for 6 cycles
R-CHOP;
R-Chop, eight sessions one every 3 or 4 weeks, side effects, nausea, loss of appetite, some muscle aches
R-CHOP began 8/21/12, then 9/14,10/2, 10/23, 11/13, 12/4. vomiting, nausea, taste & smell changes, nueropathy, hair loss, depresssion
Rchop ---Lost of hair-tired-cold
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!
2 R-chops, with at least 4 more to go. Also, no one ever wants to give you the negative, as if I would fall to my knees and scream why. I am a "know the worst, plan for the best" kinda gal...but they don't seem to believe me. So far, the fatigue, headaches and random pain is bringing me down, along with the Prednisone crash I experience after each session.
4/2007-7/2007: 6 cycyles of EPOCH (Etoposide, doxorubicin, cincristine, prednisone, and cycolophosphamide). Side effects include hair loss, nausea, diahrrea, neutropenia, weight loss, mouth sores, and more
R-Hyper CVAD (6 cycles) followed by High-dose Methotrexate (2 cycles)
Start R-Chop on July 23,2013.
R-CHOP I've gotten about every side effect possible.....start date was 5-27-2011
6 cycles of r- chop 5/1/13 felt good just some tiredness, 5/29 pretty much the same as last treatment, 6/5 this round kicked my butt extremely tired very achy steriods had me feeling pretty crazy asked to have dosage lowered.
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)
R-CHOP 14 See blog for side-effects which were many and awful.
RCHOP - 6 sessions May - October 2011 Metaxtrate - 3 sessions on my brain May - October 2011 R- ICE - 3 sessions Feb 2012 Mini Beam -2 sessions December 2012 and January 2013 R- GDP -3 sessions March - April 2012 Side effects - My hair fell out 100% not one hair left. Completely bald! A feeling of sickness twenty four hours a day without actually getting physically sick. Tiredness and becoming neutropenic regularly.
General feeling of being unwell for 3 to 5 days...nausea / heartburn...not too bad...better with meds, light meals, tums
R-CHOP side effects are nausea, fatigue, hair loss, and chronic diarrhea. I lost 15 pounds - no complaints about that! Ativan was very effective in treating the nausea, but made me very sleepy.
non yet

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
Sutent (7/20/12 - 8/31/12), weight loss, skin rash, severe nausea, vomiting, diarrhea, gas, dry mouth, and overall misery. Switched to Torisel (9/8/12 - 10/13/12), fatigue, nausea, skin rash, itchiness, headache, constipation, heart racing. Switched to Votrient (10/27/12 - 12/21/12) muscle pain, increased BP, nausea, vomiting, taste changes, fatigue, myelosupression, stomach cramps, lack of appetite Zometa (present) nausea, vomiting, bone pain, fever Switched to Inlyta (12/22/12 - August 2013) Gemcitabine and Sutent (8/11/13 - Present)
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.

March 22(3 types of chemo) i feel it lessened his quality of life, but for my dad he needed to fight back!!!
Gemzar Jan 2008-May 2008 Sept 2009- Oct 2010
6/2011 tiredness, nausea, dizziness
Chemo once a week from 4/2/10 to 6/01/10: Was tired the next day with small "blah" moments.
started chemo 6/14. 18 treatments prescribed, currently going through chemo.
given up on dates the first time on chemo was 7 months and this time has been 9 months
Yes, decided to participate in a clinical study, began chemotherapy Tx on June 21, 2013, one month after Dx
Gemzar, Taxotere and Xeloda
Pill form chemo winter 2009...threw up at end of each round
Gemzar, 5-FU
will be starting after Christmas
Folfirinox Jan 2013 - Feb 2013, switched to Abraxane and Gemcitabine March 2013-current
Gemcitabine (Gemzar)
I do not remember all of the names. The chemo was a combination of four different chemo drugs. It did not work. My father experienced nausea and could not taste anything so lost his appetite. He also was very sensitive to temperature. We are still waiting to start a trial chemotherapy drug! Pray, pray, pray!
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 .
Folfox mix of chemotherapy -nausea, vomiting, diahhrea , nil taste I food, shaking, mouth ulcers, dry skin
More harm than good; no chemo
He had 7 types of Chemo I am not good with names, and he had two chemo embolization in which one nearly killed him because he got an abcess in his liver and it developed Sepsis back in 2007
Start date November 14 th chemo drug called Folfirinox 8 weeks every other week to try and shrink tumor away from artery
Gemazar.... So far, nausea and weakness
Gemzar weekly for two weeks and week off.
Gemcitibine plus Xeloda started March 2010 continuing through August 2010. The disease was in remission until August 2012, when metastases to the lungs was diagnosed, and the cancer progressed to Stage 4. Gemcitibine plus Xeloda followed until a chemo break in May 2013 was prescribed due to indolent nature of lung mets and hand/foot syndrome. With increasing size of lung mets, January 2014 began with chemo consisting of Abraxane plus Gemcitibine again.
June 2012-October 2012; Reported Lethargy, nausea, changes in taste, neuropathy in fingers, weight loss.
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".
Chemo #1 on 4/02/10: I was more tired then usual and had a "blah" moment after going outside for a few minutes.

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).
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
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.

Ovarian Cancer Chemotherapies

What Ovarian Cancer Survivors said about their Chemotherapies.

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
Paclitaxel(Taxol)/Carboplatin(Paraplatin) combination, intravenous, 4 treatments total, 3 weeks apart. My first treatment was Oct. 17th. The side effects weren't been too horrible. Days 3-6 I felt really bad, but I never vomited! I just felt VERY weak, and VERY sick. I was so pale I scared myself in the mirror, and sometimes I felt so bad I couldn't even talk. I had HORRIBLE constipation like never before, and I still have heartburn, which I never got before.
3- one month cycles of cisplatin, bleomycin, and etoposide. Side effects: Nausea, hair loss (roughly 1 month after chemo began), fever
cistplatin, bleomyocin, etopiside, numbness in hands and feet nausea and weakness major chemo brain
Taxol+Carbo every 3 weeks, Taxol every week. Started March 2010. Hair loss, feeling tired.
I just started the chemo on Monday January 12th. I am on a 5 day a week regimen which occuers every 3 weeks. On my "off" weeks I need to come in 1 day a week to get an injection. Towards the end of this first week I am feeling very tired and very nauseous.
Carboplatin started 2007, however I became allergic in 2008, so had to have it changed to Gemzar and Advastin then. Been on and off of chemo since for chronic cancer outbreaks.
Taxol/Carbo every 3 weeks. At 2nd round, Avastin was added to the mix & will receive for round 3 & 4 as well.
6 rounds of Carbo Platinum and Taxol from 3/18/05-7/8/05 major side effect after the chemo was stopped: fatigue, memory loss Started chemo again in October of 2008. Taxol, Carbo Platinum and Avastin. Switched the taxol to taxotere after four rounds because of neuropathy. Major symptoms, nausea, fatigue, nose bleeds, low white blood cells, memory loss, did I mention fatigue?
IP chemo. Taxol and Cisplatin. She has suffered from the following effects: fatigue, nausea, heart burn, pain in her lower abdomen, numbness/tingling in her hands, legs, feet and "chemo brain"
July 24,2009 first treatment taxol and carboplatin. The only problem I had was my own fault. I got sick that night because I came home and ate stewed tomatoes and chased it down with a Pepsi! Big mistake because I quickly learned that Chemo and acid DON'T mix. Treatments 2,3, bought feet itching, loss of smell and taste. Treatment 4 was not to bad slight big toe bleeds but manageable, slight problem with vision seeing bright white spaces from within my eyes. Treatment 5 I had a mouth bleed, neuropthy more consistant. Treatment 6 manageable but eyes still have the spots. Neuropthy worsens, still itching.
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.
Start Jan 6, 2012 Six rounds of carboplatin and paclitaxel once every 3 weeks.
Mar.2007-taxol & carboplantinum (8 treatments) July 2008-taxol & carboplantinum (7 treatments) The first 2 rounds left me weak, loss of hair, nausea and vomiting Oct 2009-Doxil for six months. Side effects not so bad
intraperitoneal taxol and cisplatin, 6 - 10/06 (heinous, too long to describe); HIPeC something-or-other intraoperatively 10/07 (really ghastly); IV carboplatin and gemcytabine, 2 - 5/08 (some hair loss, fatigue); sunitinib clinical trial 2/09 (painful hands and feet, fatigue); doxil, 3/09 (fatigue); taxol and carboplatin 5 - 9/09 (hair loss, fatigue, neuropathy, tinnitus); Avastin 10/09 to present (runny nose)
Taxol sucks!!!!! makes your hair fall out and makes breathing really difficult until i go into an anxiety attack. I dont like taxol
July - November 2008: 6 rounds IP Cisplatin and IV taxol. Side effects: You name it, it happened... hair loss, nerve damage, mouth sores, drop in red blood cells which required a transfusion, high creatin, low magnesium and potassium, diarrhea, constipation... I still blame the nurse for not making sure my dexamethosone was added to the chemo! Next Monday I start 6 rounds of IV Carboplatin and Doxil.
I have had chemo in 2004, 2009, and 2012. each chemo has been different than the one before. With my most recent round I was very nauseous and sick. Lost my hair with all of them and had muscle and bone pain. I also developed an orbital pseudotumer as a reaction to the carboplatin and had to be put on prednisone steroids. This will now be required anytime I am on carbo. It started as a twitching and watery eye almost like with allergies. The eye then swelled shut and was very painful.
Carbo/taxol Doxil Carbo/Taxol Topotecan Gemzar and experimental drug Taxotere and Avastin
One treatment so far on 3/23. Side effects for two days included exhaustion beyond sleepiness, nausea and depression. I'm so glad it only lasted 2 days! Constipation and painful bowel movements.
march-june 08: 6 taxotere/carboplatin november-april 09: 6 taxol/carboplatin oktober-? 09: started caelyx/carboplatin every side affect you can imagine
Paclitaxel (Taxol)/Carboplatin (Paraplatin)combination. 6 treatments. 21 days apart.
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.
Taxol-2 doses until severe reaction Carboplatin- working trhough 6 doses, nausea, fatigue, forgetfulness!
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.

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.
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
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.

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
temodar 42 straight days
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.
Temodar 28 Days on 5 Off. 14 Rounds. Nausea, vomiting, weakness, mouth sores, fatigue.
Hair loss, fatigue, loss of appetite, bruising from all of the blood work, achy muscles and joints, off balance, loss of concentration.
Started Temodar on 11-23-09 380mg to much dosage, went to Hospital for low platelets 12-18-09 My platelets were at 6K !!!
No chemo
1/12/12 - begin taking daily chemo pill Temador (not sure how to spell that) for up to 12 months.
Temodar throughout radiation and now higher dosages (5 days on 23 days off). Fever, low platelets, fatigue
Mom had Temodar - just fatigue. Dad tried chemo (IV) - and wound up nearly dying from it. Placed in hospital twice and determined his body just could not handle it.
low dose temodar- little to no side effects b/c of my use of supplements
Start chemo 9/12/11 Temador
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.
Dibromudocital, CCNU, 6-thioguanine, Vincristine
Taking a Temodar pill for 2 months.more fatigue, and sickness.
Temodar
Started temodar on November 9, 2011 140mg a day for 6 weeks - there has not been much happen in terms of side affects yet, some nausea
What more can I say other than YUCK! It has been very difficult thus far. Upon my first treatment I left the hospital, only to return a few hours later vomiting non-stop. Zofran hasn't helped. The only thing that does anything at all to combat the nausea is to drink plain green tea. I know it sounds weird, but it sometimes works.
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.
Undergoing chemotherapy in Chennai, India. Started on July 12, 2009. Total 12 doses. Hair loss, vomiting, fatigue, loss of appetite, etc
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.
Scheduled for first time chemo (Temodar) in July 2011
Timodar Started in March 2006 and still ongoing. Side Effects: NAUSEA!
Began 150mg Temodar on 1/3/2011 2nd Dose of Chemo to begin 3/17/2011

Multiple Myeloma Cancer Chemotherapies

What Multiple Myeloma Cancer Survivors said about their Chemotherapies.

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.
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
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.

Xeloda during radiation and again mid-June to July along with Oxaliplatin- only able to receive two treatments after surgery due to severe dehydration, malnutrition, immuno-suppression. Since July have had severe pain in joints- especially shoulders- now diagnosed with frozen shoulders. Beginning PT this week.
2/1/2010-3/11/2010 F5U pump 24/7 5 day/week, combined with the radiation, tiring. 7/23/2010 start, 12 treatments every 2 weeks. 5-FU, Eloxatin,leucovorin calcium; side effects - inconsistent energy, more emotional 2/2012 FOLFIRI; side effects diarrhea alternated with constipation, hemorrhoids, nausea, Tired
5f-u and Oxaliplatin start 10-19-2010~On June 13, 2011 I had an allergic reaction to Oxaliplatin and my Doctor made the decision to take me off of that for good. Nothing will take it's place as of now. I will remain on 5f-u and Leucovorin.
start chemo tomorrow jan 12, 2009 folfox
Chemo was 1 day a week for 5 weeks and I went after I had my radiation treatment. They made me very tired and weak feeling. Some days I just had to go home and go to bed. Was only sick a couple of times but kept diarrhea the whole time I was having the chemo treatments, going to the bathroom some days as many as 11-12 times.
Xeloda 3000mg by mouth twice a day for 5 1/2 weeks. Some skin issues with ears peeling, body aches & pain, very tired.
5FU Begining 1-18-11, 5 days on, weekends off...
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
started FOLFOX on 4th Dec 2011. Active treatment for 48 hours every 2 weeks. Lots of nausea, some mouth soreness, altered taste and smell
folfox 4 for 6 months...Oxaliplatin caused permanent, extreme peripheral neuropathy. Imagine your feet telling your brain that they are in severe pain 24x7 and that they are cold no matter how hot they are. The brain cannot handle that constant messaging and the results are not pretty...mentally and physically
Xeloda, taken during my radiation treatment (adjunct therapy) Started Folfox the last week of June 2010
I started chemo Sept 19,2006 minimal side effects I have had 20 treatments, and most people don`t realize I`m on chemo
5-fu orally before surgery 11/12 - 12/12. The oral chemo did a number on my stomach lining. After surgery did 8 FOLFOX treatments 3/13 - 7/13, side effects were sensitivity to cold, some nausea but not bad, and tired.
started with leucovorin, oxaliplatin, avastin, folfox pump, then camptosar, erbitux, folfuri pump, currently undergoing clinical trial with Xeloda and maybe or maybe not perifosine few side effects, I guess I've been lucky
6 Months starting Dec 2, 2011. 5 hours every other week. 5-FU, Oxaliplatin and leucovorin. Will bring home 5-Fu in a bag for the weekend will run through port and bag removed on Mondays
Chemotherapy started 7/31/08. I feel as though I have had every nasty side effect. I have heard it is not that bad but I feel rotten throughout the entire cycle.
5FU and Oxaliplatin. Started July 15 2009, every other week. Lots of fatigue neuropathy from the Oxaliplatin getting worse with each treatment, tingling, numbness, burning, shooting pains.
severe dehydration, potassium def. diarrhea
None, but for me I am receiving my medicine through a port in my chest, I have a small pump with a bag that they change once a week. my medicine is 5fu. The only side effect that I have is that I am alway hungry, I can not seem to get enough to eat. No nausea or cramping, no mouth sores or peeling skin. Just extremely hungry all the time.
FOLFOX every two weeks for 12 treatments total through a port installed in my chest. Started 3/17/14. Main side effects are fatigue and bouts of nausea. Catheter from my port ruptured 2 months into treatment. Port replaced 7/3/14.
5FU Portable Pump
Folfox6 November 13, 2012. 12 treatment cycles over 6 months, end date April 18, 2013. Oxaliplatin-allergic reaction, tongue numbness, profuse sweating, numbness in hands. Benadryl for two days. Immediate neuropathy in hands and feet, sensitivity to cold, very weak, chest pressure, numbness and tingling in limbs. 5FU- nausea' headache, diarrhea, itchy skin, no appetite, vision problems, dizziness
May 2010-July 2010: 24 hour, continuous 5FU infusion, Mondays-Fridays November 2010-January 2011 :Folfox December 2011-April 2012
I've had two rounds of chemo (carbo-taxol and FOLFOX, Avastin), neither of which were effective.
Will be starting chemo on April 27th. Getting 12 treatments over six months of 5Fu with leucovorin and oxaliplatin via a medi port. Had the port put in this week.

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.

2 rounds of Taxol/carbo 11/2011 & 12/2011...Is being changed for 1/2012...not sure of new drugs yet
Nausea and fatigue, Extreme Vomiting, Neuropathy
1 night a week, 12am-8am - December 2008/February 2009 Bedwetting, weight loss, nausea, fatigue, immuno-issues. (I caught the damn BIRD FLU!!)
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
Rather not discuss
Paclitaxel, Cisplatin, Bevacizumab, Avastin
Cisplatin
Had cisplatin for 6 weeks during radiation, now am on my 5th of 6 treatments every three weeks (taxol and cisplatin)
Cisplatin started 7/8/08
cisplatin, felt and tasted every drug they put in my body. It was very yucky. I am incredibly sensitive to the medications and was eventually given Ativan to help me sleep through it all. Lasix was fun though at the end of treatment peeing every 5 minutes!!
I had 6 chemotherapies. I would go once a week and sit for 7 hours. I had sisplatin(?). I would feel fine the day of but the next day I was very sick and in bed for the following 3 days weak, and throwing up. I would lose 3-5lbs each week.
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!
Cisplatin (40 units) every Monday for five weeks, beginning April 26, 2010. Hair thinned; veins hardened; steroid acne; acid reflux; turned yellow after treatments (that was odd).
Cisplatin weekly 10 weeks delayed nausea that was almost impossible to control. Change in texture of hair minimal loss of hair. Mostly just thinning.
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
Sept 6-Nov 6 2008: every three weeks for 6 hours. Side effects: hair loss, tired, and sore from the Nuesta shot, but overall not as bad as it could have been.
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.
That also starts withen the next 3 weeks.
Cisplatin 2009 six weekly treatments
tahbso april 15,2013
5 treatments of Cisplatin
Have had 5 chemo treatments. Took 5 hour "naps" afterwards. Some foods tasted nasty! Normally a huge water drinker but water nauseated me. Required at home IV infusions of Potassium and Magnesium for 8 hours/day for total of 15 days, also received a few infusions at the clinic for dehydration and low electrolytes. Anti-nausea meds didn't work on me.
Extreme nausea, vomiting, some tingling in my toes.
Cisplatin low dose for 5 cycles once a week. Tolerated it well just very tired. Considering I had concurrent radiation and chemo it was hard to tell what was causing all my nausea and vomiting but we think it was the radiation.
Had external and internal (brachytherapy) radiation over a six week schedule. 28 external rounds and 5 internal rounds. Radiation was concurrent with chemotherapy (cisplatin) for 6 weeks once a week. Seriously fatigued for at least six months post treatment.

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.

hydrea - 02/2009 little/to no side effects
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.
Oct 14th- 7 days Vidaza Nov 23rd- 7 plus 3 Dec 25th- fludarabine and busulfan
i had three induction therapies spaced about 6 months apart. and just completed two consolidation therapies. i am preparing for a bone marrow transplant.
first round for 5 days 2 times a day 2nd round a month later every other day 2 times a day for 5 days 3rd round was right before transplant 7 days of 3 differant chemo non stop the worst chemo was this one .....
the only side affect she has had is toxemia, and neuropothy.
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.
oct induction chemo, Nov another bout of induction chemo as first did not work. Jan: consolidation chemo Apr: additional chemo to prepare for bone marrow transplant.
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.
11/2009. 1/2010. Neuro side effects. Weakness. Nausea.
Always sleepy or nausous
Since June 2012 - july induction, August consolidation, Sept. consolidation, december 2012 induction. Stem cell transplant now on hold.
photosensitivity, some nauesea
idarubicin and atra began in april 2008 vomiting,diarhea,blood and platelet transfusions many transfusions
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.
I have been taking low dose chemotherapy via and infusion pump. I may need a bone marrow transplant at some point.
High dose chemotherapy, March-June 2012. Side effects: Nausea, vomiting, weight loss, fatigue.
chronic vommiting ,hair loss tiredness
Nausea, vomiting and fatigue. Zofran helped a lot!
1st round-12/09/2011Atromycin for 3 days nd Cytosar. for 7 days.
Multiple protocols for ALL & AML.
Ive been on too many chemos to describe. Generally though I handle them well. You will feel the nausea and the fatigue for sure. Mouthsores and hairloss come later. I usually go feverish at some point too.
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!!!

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.

Chronic Myeloid Leukemia Cancer Chemotherapies

What Chronic Myeloid Leukemia Cancer Survivors said about their Chemotherapies.

Interferon from onset- continued hospital admissions,recurrent infections, suppressed immune system Gleevec May 2001 to April 2010, minimal side effects, mostly nausea, malaise. April 2010- Present 800 mg. Tasigna daily requires weekly EKG due to this drug has been linked to A-Fib
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.

First round June 24, 2013. Vague feeling of unwell, horrible burping, relieved by Omeprazole, one and 1/2 days of sole pain, then resolved. Mouth sores began 6/29/13, peaked on 07/04/13. Second round July 22, Mitomycin reduced by half because of my WBC response the first time. Same feeling of unwell, anorexia, chemo created constipation for me, not diarrhea.
Standard protocol of 2 rounds of mitomycin & 5FU (8/13 & 9/13)
I will begin receiving 5-FU continuous infusion Mon.-Fri. for 6wks with Mitomycin added days 1&29.
1st Mitomycin on Nov 18, 2013. 1st 5FU Nov 18 - Nov 22, 2013. 2nd Mitomycin on Dec 16, 2013. 2nd 5FU Dec 16 - Dec 20, 2013. Similar side effects both times: fatigue, mouth sores, gum bleeding, cramps, body pain, nausea, some vomiting, decrease white and red blood cells, some hair shedding after treatments; but much hair shedding suddenly began again two months later (not thyroid).
completed the first of chemo, mouth sores are terrible, otherwise feel ok
Scheduled to begin 10/18/10, Fluorouracil and Mitomycin, 1st and 5th week
* Jul 27/09: met with Oncologist * Aug 4/09: chemo (portable pump: 5-FU) for weeks 1 and 5 until Sep 15/09; Mitomycin day 1 only of weeks 1 and 5
Cisplatin and 5FU, nausea and dizziness
Commencing Chemo 28th April
Jan 7th week -1st round of chemo - severe nausea, dehydration, and mouth sores. For 2nd round 5 weeks later, started Lysine powder 1 week prior with mouthwash so no sores.
8-4-09 thru 8-7-09
dehydration, some mouth sores, not bad, lost some hair, ruined my hairstyle, intestinal pain, tiredness, low white blood cell count and platelets, hospitalized for 11 days
mitomyacin and 5fu two times over two different weekends 2009 mouth sores, weight loss, nausea,hair thinning, lightheadedness, memory loss,
start chemo on Jan 12 and then again on Feb 9th
Mitomycin and 5-FU. 75% of standard Mito dose on 1/4 due to elevated creatinine levels. Standard 5-FU dose over 5 days through chest portacath.
Mitomycin C and 5FU infused for 96 hours (4 days) during week one and week 5 of radiation
March 19-23, 2012 and April 16-20, 2012: 4 days chemo (Fluorouracil and Mitomycin C)through chest port.
5-FU & Mito-3 for 4 days March 2010 and April 2010
First round 3/17-20/14, 5-FU and Mytomycin. Nausea, fatigue, severe mouth sores (lips, mouth, tongue, throat) and white blood cell count down as low as .7. Second round postponed to 8th week due to C. Diff. infection. 1/2 dose with no severe side effects.
2/09/10 mitomycin & 5fu
Chemo doable. Nausea, constipation (turned out my gall bladder wasnt funtioning but had to wait for surgery until long after completed therapy.)Dehydrated one time (walked for hour outdoors as it was a lovely day) so badly home nurse came to house to hook me up to fluids and it worked immediately. Radiation was more difficult in that I knew, due to light skin, that I would be much more burned. I was surprised when the treatment was over that I continued to be radiated though I wasn't receiving radiation but felt I was receiving it daily for approximately two more weeks.
5FU infusion for 96 hours the first and last week of radiation. Mitomycin the first day of radiation and the first day of the last week of radiation through a PICC line
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.
April 2011 nausea and vomiting, weight loss,neutropenia,mouth sores, hair thinning April 2012 nausea, mouth sores, hair thinning
2 rounds (5 day hopsitalization each cisplatin and 5FU) mouth sores, some hair loss, changes in taste and smell, weight loss 6 rounds Hepatic artery infusion (oxaliplatin)avastin 3 month Jakafi (oral) 22 treatmentsof unknown trial drug current trial cisplatin and gemcitabine

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

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.

chemotherapy given from January to September Side effects: dehydration, vomiting, blood transfusions
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

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.
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.

Hyporexia, nausea, tinntitus
Ciplatin 3 megadoses 3 weeks apart concurrent with radiation
3 treatments. Cisplatin at first but had terrible digestive side effects so used erbitux for last 2 treatments
yes, cisplatin treatment was needed as the lymph node in right neck lump broke through the cell wall; attempted 3 chemo treatments {large doses} every 21 days followed by 2 days of 2 hour treatments of iv saline soutions to wash out the chemo and lessen its effects on my kidney, though my body had too intense side effects..the chemo treatments changed to weekly for remaining 7 weeks with smaller doses of cisplantin
2 Full Week Doses (M-F)
7sessions, once weekly Metal tasting food, general lousy feeling 2 days after treatment.
Cisplatin, 6 tx, every monday for 6 weeks, concurrent with radiation. Tolerated well and relieved all lupus symptoms. Last tx was 11/13/12.
Two induction treatments then weekly chemo. Hospitalized eight times due to vomiting and fatigue
Start on March 29th 2011.
3 cisplatin treatments, concurrent with radiation treatments
Cisplatin - I was sick every day. Had to take anti-nausea medicine every 2 hours.
fatigue, nauseous, loss of hair, very very weak.
Cetuximab - Brand name: Erbitux - April 1, 2010 - so far just really really tired. I was told later a rash and other stuff could happen. ( 5/1/10 - rash did appear including itching. Scalp was the worst. Lying down felt like pins sticking my head. I was told if not rash, med is not working. After they know it was working, I got med to help the rash and itch.)
September 5 - 3 rounds
Chemo start date 10/5/09, three sessions, one every three weeks (cisplatin)
11 treatments ended about 11/07/2011
Cysplatin; 3 treatments; lost hair on face, massive vomiting and dehydration
Chem with Cisplatin, taxotere and 5-FU in pump.
5 treatments of cisplatin one a week commencing 14th July. Mocositis, fatigue WBC count dropped dramatically after last treatment
3 doses of Cisplatin.
3 heavy dose (8 hours each) chemo. sessions.
Taxol and carboplatin. 6 weekly infusions.
cysplatin
Chemo (Cisplatin) is anticipated to begin the second week in July. Treatment plan will include 6 chemo sessions (2 sessions every 21 days). Will complete chemo concurrently with radiation.
11/9, 11/30, 12/21 - loss of appetite, cold, "chemo head" (loss of concentration and short term memory)

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.

Lost hair not much else
little queasy tired bald last one nov 5th 2010 yesssssss!!
Starting chemo (carboplatin and taxol) on 4/27/11. Will have 6 sessions, one every 3 weeks.
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.
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.
6 rounds of chemo; every three weeks March - June 2014; few side effects; some joint and bone pain for a couple of days after each treatment; some neuropathy in my feet
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.
May 2010 Chemo Carboplatin/ Taxol, nausea, fatigue, hair loss
INITIALLY TOLD NONE NEEDED 7/6/09 MY DOCTORS REISDENT CALLED AND SAID NONE NEEDED BUT AT THIS POINT I DO NOT TRUST MY DOCTORS AND WILL SEEK NEW HELP SURGERY 8/6/09 REMOVAL 27 NODES NO CANCER...SO NO CHEMO WILL BE NEEDED
Start in mid October.
See Surgery Description> apparently I cannot follow directions
My symptoms became SO much worse after chemo: Pain, nausea, vomiting, mouth sores, chemical taste in mouth, fatigue, weight loss
I have had two rounds of chemo, and the next will take place on Jan 31, 2012. After that, three more rounds!
November 2011-December 2011--6 administrations of Taxol and Carboplatin; strong allergic reaction to Taxol (could not breathe and it felt like my back had been struck by a car) handled with heavy doses of Benadryl and slow infusion; lost hair all over my body slowly during treatment and over several months after treatment; painful tingling in feet and hands; fatigue; bloody nose daily; ridges across nails on hands; skin toughened on backs of hands and tops of feet; hair on my head hurts sometimes months after treatment.
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.
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.
Every week on Day 1 & 2 and Day 8.
Taxol/carbo, starting Dec 12, 2007. Some joint pain, hair loss (boo-hoo) and slight stomach upset.
Cyclophosphamid Carpoplatin Taxol
Haven't started yet. Need advice.
recommended to start after radiation
None required
TBD but they definitely want to do it.
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.

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.
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 current.
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.

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.
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
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.
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.

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.
ABVD- Side effect? UGH.
started chemo in 2010 6 months on an off, finally had stem cell transplant at Mass General Boston n March of 2012 remission lasted one year :(
ABVD treatment; my nausea was well-controlled with prescriptions, but I was often tired in the days following chemo. I went every other Friday so I could recuperate over the weekend and be ready to go back to school Tuesday-Thursday.
hair loss... weight gain... nerve tingling... bad taste... feet pain... but no vomiting... so not all bad...
Started ABVD November 20th~ a little nauseous, headaches, and a little tired..
ABVD chemiotherapy, hair loss
nausea, neutropenia, anxiety, extreme fatigue, mouth sores and dry mouth
first round 09/08/11-ABVD-headache, swollen tongue, blisters on tongue, vomitting, nausea, bone aches.
ABVD: 8 Cycles (16 total treatments). My side effects were severe bone pain, fatigue, nausea, burning in my stomach, constipation, ileus, thinning hair
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.
ABVD, started Feb. 13, 2009.
im doing an eight mounth treatment plan. every 21 days im back in the hospital for all the chemo they can give me.
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.
I had 6 x ABVD last summer. Now 3 x DHAP + stem cell transplantation in the future
ABVD- nausea, fatigue, wooziness, thinning hair ICE- nausea, fatigue, wooziness, total hair loss, bleeding gums and mouth sores GND- some fatigue, mouth sores
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.
ABDV-Adriamycin, bleomycin, dacarbazine, and vinblastine. Research Drug- Phase II Trial of Rituximab (Rituxan)-ABVD for Classical Hodgkin Lymphoma
ABVD May 2008-October 2008 ICE January 2009-March 2009 BEAM April 2009
Abvd every other week.
So far only 1 Session- 01/10/12
ABVD 12 rounds, 6 months
Brutal! I was sick (mostly fatigue, headachey, flu type symptoms) for a week after treatments, would get my energy back the second week and then start the cycle all over again!
ABVD started in December 2011-May 2012. Hair loss, nauscia, weakness. ICE July 2012-August 2012 Hair loss, nausea, weakness

Acute Lymphoblastic Leukemia Cancer Chemotherapies

What Acute Lymphoblastic Leukemia Cancer Survivors said about their Chemotherapies.

Started induction chemo within the first week of November. Integrating it with holistic therapies
started Feb. 26, 2010 I was admitted to hospital every 3 weeks for a total of 6 rounds of treatment - Cycles A and B.
currently undergoing HYPER C-VAD
finished with induction therapy, now gonna begin with consolidation.

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

Appendecial Cancer Chemotherapies

What Appendecial Cancer Survivors said about their Chemotherapies.

Fluorouracil (5-fu), Oxaliplatin, Avastin, leucovorin. 1/15-3/2? Side effects - Extreme fatigue, nausea, cold sensitivity, neuropathy
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Full list of all Chemotherapies