What Breast Cancer Survivors said about their Chemotherapies.
Taxotere & Carboplatin 6/30/11- 10/13/11 All classic symptoms
Red Devil, cytoxan, taxol....May 2002....Bone pain, tired all the time!...Gained weight
AC dose dense,then taxotere all for 5.5 months.Lots of lousy side effects you name it I had it!
First time: Taxol, Taxotere - Jan - June 2001 - had adverse reaction to taxotere & stopped breathing. Otherwise, the regular side effects like nausea, fatigue, mouth sorers, hair lost, & nerve damage to hands & feet. Second time: Abraxane, Avastin Oct '07 to May '09. Still on Zometa - indefinitely. Regular side effects: nausea, fatigue, hair lost. Worse one: medical port became infected & had open wound for 6 mons because it could not heal.
Dec 10- Feb ? 4 sessions 3 wks apart; lost hair after 1st treatment; threw up once, nauseous but controlled by anti nausea meds. Weak, tired, got horrible staff infection. I now have alot of bone and muscle pain
breast cancer, Breast exam, breast check,breast screening,self breast exam,breast screening device, breast awareness, breast cancer, self breast examination, self breast check, breast cancer awareness, breast examination, breast cancer screening, breast cancer symptoms
suffer to heal. stay mindful of what it means to be aware.
Double chemo infusions, including "red devil", during the first round of chemo over eight weeks every two weeks. This was from late Oct 2014 thru mid Dec 2014. Side effects included hair loss, sensitive finger tips and toe nails, painful mouth and tongue with half my throat swollen by end of treatment, constipation and over all brain fog. The hardest to get used to is the stuffy nose and nose bleed when it clears. Single chemo included Taxol, Herceptin, steroids, benadryl, and anti-nausea medication. Side effects were a continuation of tender nails till they have started to detatch from their nail beds. Sore mouth with base of tongue muscle having difficulty moving food around in my mouth, which has gotten worse as therapy has progressed. Constipation is still an issue unless I forget to eat my bowl of raw veggies every day. Brain fog or mushiness has been an issue throughout this entire experience, hopefully this will discontinue with the ending of chemo. Tiredness has been my constant companion throughout this entire experience also. Also, my constant stuffy nose that clears off and on and bleeds every time. I'm often awakened by my nose bleeding.
September 2007-February 2008 - fatigue was the worst part; no nausea; started losing hair on 13th day after first treatment. Hair began to return about 3 months after chemo and was long enough to be a "really short hairstyle" after 3 more months.
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.
Infusion #1 - 09-22-09. Severe joint pain in lower back, knees, and ankles. Intense nausea. Infusion #2 - Intense nausea. Severe joint pain. Darkening of my fingernails. Severe headaches. Infusion #3 and #4 - Intense nausea lasting my entire two week cycle. Headaches. Continued darkening of my nails. Taxol infusions #1-12 - Slow physical changes to my finger and toe nails, intense nail bed pain which has been cumulative. Big drop in counts at infusion #10, nausea, fatigue.
Began chemotherapy in 3'06. Side effects were mouth sores, nausea and vomiting. Bone pain, neuropathy in fingers and feet. Nail beds turned black.
ACT from December 2010 - June 2011.
Had first treatment Sept 3rd. headaches really bad stomach, rash on my chest and face they just keep coming and changing really
To start in Two Weeks
6 treatments, 3 weeks apart, fatigue, muscle aches, dizziness
Six rounds. Finished in April 2010.
6 Treatments - 3 week cycle 3 - FEC 3 - Taxoteer Sept. 7, 2006 through Dec. 21, 2006
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.
Nausea, vomiting, bad headache, fatigue, mouth soreness, hair loss.
4 cycles starting 7-24-2014
Chemo once every other Friday, eight prescribed. First four: Doxorubicin (a.k.a. Adriomicine) AND Cytoxin; last four Taxol. Nuelasta with every infusion prescribed. See post "I'm just sayin'" for side effects from first 4 infusions.
Started first round of AC on June 12th....will continue 3 more rounds and then on to Taxol.
What Prostate Cancer Survivors said about their Chemotherapies.
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
What Lung Cancer Survivors said about their Chemotherapies.
6 weeks, 3 weeks apart
Start Chemo May 18th 2007 Cisplaton and Etoposide
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 days chemo every 21 days. Hydration as needed. Tiredness and nausea/vomiting at times.
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
2007 April til present so far 5 rounds Taxotere Carboplatin Avastin Emend for nausea Aranesp for red blood Neulasta for white blood etc.....
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.
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!
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
Chemotherapy started on March 1st
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...
Feb 08-Cisplatin/Etoposide- hideous vomiting diarreah Switched chemo drugs AND Hospital -April08-carbo/taxol/avastin. Tolerated well. Neulasta. Bone pain
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
3/2012 Adriamycin and dacarbazine 6 cycles 12/2012- 10/2013 votrient 600mg every day. 10/2013 - present gem/tax
2/26/08to 5/28/08 - 6 cycles Taxol, carboplatin and Avastin for lung ca. Hair loss and peripheral neuropathy - some fatigue.
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.
starting the 2nd week of August 2013
December 2004 - Present off and on. On Avastin and Tarceva currently, but stopping to start a new chemo.
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.
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.
will start on march 16 (tentative)
Avastin-2008 and 2011, Cisplastin-2009 and 2011, and Tarceva-2011.
What Bladder Cancer Survivors said about their Chemotherapies.
Foggy brain. Forgetfulness.
What Non-Hodgkin Lymphoma Cancer Survivors said about their Chemotherapies.
June 25, 2009--started chemo
About to go for chemo number 3 on Friday, feb 22... bone pain, anxiousness, depression, numbness, random rashes, hair losss, constipation. RCHOP , nuelasta, etc
R-CHOP 14 See blog for side-effects which were many and awful.
Hyper CVAD, March through September 2007
R-CHOP I've gotten about every side effect possible.....start date was 5-27-2011
R-CHOP R-ICE ESHAP
R-CHOP, 4 cycles, side effects: nausea, fatigue
R-CHOP, (I know it as "rituxin" "the red stuff," "the clear stuff," and "the god damn prednisone pills" -- lazy, I know) started Oct 15, 2009. So far just a bit of fatigue, crankiness, and I think my body fluids may be like dinosaur acid right now. Also I hate taking my pills but have to do it because of, um, you know, long term survival and all that.
R Chop 6 cycles
8/6/2010 RCHOP - no major side effects with first treatment.
RCHOP six months - 2007, Rituxin maintenance two years
RITUXIN 10-2010 - present Fludaraben 10-2010 R-chop 1-2011
Several months of CHOP+Bleo. Got very bloated from Prednazone. Total body baldness, of course. My skin actually got quite beautiful and baby smooth. Toenails fell off. Heart and lung damage from Bleo. My mouth and throat were scarred by sores and from vomiting. Kidneys have been very vulnerable ever since. (Just want to add, I HAVE NO COMPLAINTS ABOUT ANY OF THIS. I lived! It was worth it.)
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.
GoSH, so many. Six cycles of RCHOP. side effects... 1) affected my eyesight since the 3rd cycle, never got better. It was the first time i feel how its like to be a blind person. Luckily was blind for only a day, and got better but never totally cured. 2) Shingles! yes i repeat shingles! its seriosly the worst thing to get when ur immunocompromised!!!the itch is so intense! 3) FATIGUE--> never seem to end, but sometimes i think its because im lazy
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 - 10/21/2010, 11/11/2010, 12/2/2010, 12/22/2010, 1/13/2011, and 2/16/2011 - was scheduled for 8 sessions but reduced to 6 sessions due to being determined NED, or in remission, per PET scan results dated 1/11/2011
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.
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.
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
What Pancreas Cancer Survivors said about their Chemotherapies.
Folfirinox Jan 2013 - Feb 2013, switched to Abraxane and Gemcitabine March 2013-current
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".
Gemazar.... So far, nausea and weakness
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.
Gemzar Jan 2008-May 2008 Sept 2009- Oct 2010
Chemo #1 on 4/02/10: I was more tired then usual and had a "blah" moment after going outside for a few minutes.
6/2011 tiredness, nausea, dizziness
June 2012-October 2012; Reported Lethargy, nausea, changes in taste, neuropathy in fingers, weight loss.
March 22(3 types of chemo) i feel it lessened his quality of life, but for my dad he needed to fight back!!!
Gemzar, Taxotere and Xeloda
Folfox mix of chemotherapy -nausea, vomiting, diahhrea , nil taste I food, shaking, mouth ulcers, dry skin
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 weekly for two weeks and week off.
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 .
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!
Yes, decided to participate in a clinical study, began chemotherapy Tx on June 21, 2013, one month after Dx
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
Pill form chemo winter 2009...threw up at end of each round
Chemo once a week from 4/2/10 to 6/01/10: Was tired the next day with small "blah" moments.
given up on dates the first time on chemo was 7 months and this time has been 9 months
Start date November 14 th chemo drug called Folfirinox 8 weeks every other week to try and shrink tumor away from artery
More harm than good; no chemo
will be starting after Christmas
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).
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.
What Ovarian Cancer Survivors said about their Chemotherapies.
1st. Chemo Feb. - March 2009 2nd. Chemo Nov - Dec. 2009 3rd. Chemo ip. Aug.-Sept.2010
my chemo is cisplatin , etopside , and bleomyacin
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.
bleomycin/etoposide/cisplatin Started 1/09 Hair loss, nausea, loss of energy
Had 2 courses of CarboPlatin and Taxol via vascualr Port; followed by 4 courses of IP chemo with Cisplatin and Taxol, one course every 3 weeks, requiring 3 days in hospital each time. Could only tolerate 4 courses because side effects were too severe: nausea, vomiting, constipation and diarrhea, ototoxicity resulting in some permanent hearing loss in left ear and also tinitus, tingling, numbness and pain in hands and feet (apparently permanent), and "chemo brain" - no short term memory, fogginess, confusion, and exhaustion. Serious loss of weight as well. Last 2 courses of chemo were via vascular port and the same as the first 2, and were tolerated fairly well.
Starting 4/24 - 6 rounds every 21 days
Combined carboplatin and taxol, both administered systemically by IV started August 10, 2011, with last cycle administered November 23, 2011. Side effects included: nausea that was only gotten under control after the second administration using about 5 drugs; intense fatigue; muscle and joint pains that were reduced with tylenol and later greatly reduced with gabopentin; intense neuropathy in hands and feet, but even lips and chin until the gabopentin took the edge off that, too. Neuropathy still intense in first week of every cycle. Other side effects included intense fatigue, weakness, vision problems on two occasions (blindness in one eye when reading lying on side), severe constipation, and cognitive effects (short term memory dysfunction, inability to solve puzzles, inability to multitask or withstand multiple stimuli at once). There's talk of giving me a PARP-inhibitor for maintenance therapy in 2012. Constipation for 9 months! No, wait. Make that FOREVER! Seriously. Til my dying day.
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.
Taxol/Carbo x 8
Taxol/Carbo 12/02-5/03 (with 2 Gemzar treatments) Avastin 8/06- 5/07 Etoposide / Avastin 8/08- Present
Carbo/Taxol every 3 weeks for 6 cycles from 6/10 - 10/10. Side effects: loss of hair, neuropathy, nausea, vomiting, fatigue. Carbo/Gemzar (wk 1 combo, wk 2 Gemzar alone, wk. 3 off) for recurrence 3/12 - 8/12. Side effects: naausea, fatigue, muscle aches.
I was aiming for Thursday (Day 22) and I just managed it by having the port (Yoda) installed on Day 21. Hurray! Scheduled for 6 rounds of carboplatin and taxol - 3 weeks apart. Thursdays worked out great - there all day (7 hours) for infusion with the world's greatest chemo nurses; worked on Fridays (felt fine); okay for 1/2 day on Saturdays... then YUCKY from Saturday afternoon until Sunday night (tired, tummy troubles, etc.) I did not get constipated as many of my fellow survivors complained of...for me, it was important to be very close to the bathroom on that weekend following chemo! Fortunately no nausea. Fine to go back to work on Monday. This lasted throughout my chemo, so I was truly blessed. Right on time at the 10 day mark, I started shedding like a Golden Retriever and immediately shaved my head. It felt so-o-o-o good to get rid of that hair. I wore a wig one time when I returned to work and ended up tossing it on my desk! Stuck to hats after that when my head felt cold. Chemo ended in September, 2012. Officially NED and in remission in October, 2012. Currently maintaining status quo..May, 2014. Yoda (my Bard Power Port) was removed on 05/09/14, exactly 2 years from my initial cancer surgery.
4 round of cisplatin, bleomycin and etoposide
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.
<b>February 2009:</b> CA125 level was around 3500. She began treatment with Taxol/Carbo with Avastin. Within two weeks, she lost all of her gorgeous red hair. Energy level dropped significantly. She continued having "maintenance" chemo. <b>June 2009:</b> CA125 dropped to 32, and then to 16 later that month. Oncologist decided to stop chemo- as there was no sign of cancer! <b>March 2010:</b> Having chest pain/shortness of breath. CT scan showed fluid in her lungs. Testing after thoracentesis revealed cancerous cells in the fluid. CA125 was back up to 300. It is now referred to as "RECURRENT CANCER" She began chemo again: Cisplatin and Gemzar. Cisplatin was causing tinnitus. Oncologist decided to discontinue to avoid permanent hearing damage. The Gemzar would usually burn during infusion. Side effects: headaches, intense nausea and often uncontrollable vomiting. Drastic decrease in appetite (and weight: about 70lbs) Last time it was checked, her CA12 was hovering around 86. I'm guessing it's currently off the charts.
Taxol and Carboplatin - 6 rounds beginning August 2010. Side effects included body/joint pains/aches, loss of hair, itchy skin, constipation, headaches.
I had my first chemo treatment on 04/07/2005 (my little brother's birthday) and I went for 6 hours a day, once every 3 weeks...
Bleomycin, Cisplatin, Etoposide for six months. Nausea and blood loss.
Taxol and carboplatin so far 8 treatments CA-125 is now down to 130
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"
taxol and platins - 9 treatments completed 4/1/10 (3 of which included IP cisplatin)
Nausea, fatigue/sleepiness, "Chemo brain" (inability to concentrate), dry skin, no nail growth, hair loss. January - May as of now
First chemo carbo/taxol on May 7th. so far, a bit of joint and bone pain, nothing else
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.
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!
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.
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.
What Brain Cancer Survivors said about their Chemotherapies.
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.
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!
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.
Temodar - hair loss - tired.
low dose temodar- little to no side effects b/c of my use of supplements
Start chemo 9/12/11 Temador
Temodar April 2013
Began 150mg Temodar on 1/3/2011 2nd Dose of Chemo to begin 3/17/2011
Scheduled for first time chemo (Temodar) in July 2011
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
Temodor- 5 days on, 21 off- October 2009- June 2010 Avastin- Every 15 days- July 2010- Present Carboplatin- Every 30 days- July 2010- Present
Temodar, 12 month cycle with allergic reaction
Chemo(Temador) 42 days - fatigue, memory loss,weak,nausea, no vomiting due to neausa pill taken 2 x day
Nothing early on with the low dose, extreme fatigue with the high dose/ On his 4th round, sleeps 15 hours or more a day. Little appetite. Has been nauseated on and off.
Temodal - started Aug 15, 2011
Timodar Started in March 2006 and still ongoing. Side Effects: NAUSEA!
Temodar throughout radiation and now higher dosages (5 days on 23 days off). Fever, low platelets, fatigue
Started Temodar on 11-23-09 380mg to much dosage, went to Hospital for low platelets 12-18-09 My platelets were at 6K !!!
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.
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.
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.
temodar 42 straight days
Temodar 28 Days on 5 Off. 14 Rounds. Nausea, vomiting, weakness, mouth sores, fatigue.
1/12/12 - begin taking daily chemo pill Temador (not sure how to spell that) for up to 12 months.
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.
What Colon and Rectal Cancer Survivors said about their Chemotherapies.
First circle two times for one week during radiation, second circle stopped after the first week because of acute leucopenia.
5FU, Leucovorin and Oxiplatin. Typcial symtoms could not tolorate cold after treatment, slept alot. I worked full time through chemo. Felt exhausted and don't remember too much in this time period. Work and slept.
I really don't recall the chemo drugs I was on but I never lost my hair and never was nauseous. I had little appetite which caused a huge weight loss.
Xeloda (oral chemo) for two and a half weeks. I was supposed to have it for five weeks, but my platelet counts wouldn't stay up. I was diagnosed with Chronic ITP (an auto-immune platelet disease) shortly after I finished treatment.
24/7 pump 5fu.
May 2010-July 2010: 24 hour, continuous 5FU infusion, Mondays-Fridays November 2010-January 2011 :Folfox December 2011-April 2012
I've been on some sort of chemotherapy for 21 months now. I've been lucky that the side effects haven't been too horrible. I would get a little sick here and there but everything was mostly tolerable and I've been able to function quite well.
4 treatments done... 8 more to go. Mom had her port put in and about a week later went for her first treatment. She spends about 6 hours at the cancer treatment center and has her "chemical purse" with her for 48 hours. Side effects: pain in feet occasionally and colder than usual.
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
Bi-weekly Chemo 6 months Oaxliplatin/ fluorouracil 5-fu
Feb 15th - march 19. Severe nausea.
Lecovorin, Oxiaplatin causes extreme neuoropathy in the hands and feet, He does not have finger prints now. 5-FU causes nausea, makes the hands and fet worse and soooo tired, like having the flu everyday with intense stomach cramping. Can not concentrate, chemobrain I guess they call it. Three days of intense chemo, then sick pass out for hrs. can't do anything but lay down or sit, there is nothing to help ease this...
started FOLFOX on 4th Dec 2011. Active treatment for 48 hours every 2 weeks. Lots of nausea, some mouth soreness, altered taste and smell
severe dehydration, potassium def. diarrhea
FOLFOX 8 treatments split into two rounds - one round before radiation and the other round post radiation Feb 3 - July 18, 2011 Neuropathy, hair thinning, blisters on fingers and feet, diarrhea, constipation, nausea,
I started Chemo on December 19,2008. I had a port put in to administer the treatment. For my lifestyle the port makes most sence. Have the pump hooked up was a bit invastive, but I have great nurses who have a trementious amount to compassion and skill
Started October 28, 2009 5FU 24/7
Just began 5FU 5 days ago. First round.
sisnce |July 2010 - ongoing
have the Powere Port for 5Fu chemo Pump removed 02/18/09 The port is a bit uncomfortable if I try to sleep on right side. The port itself still looks very unattractive, but hey if t helps, i won't complain.
Flu like symptoms and fatigue.
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
Oxalipilatin/5FU/Leucovorin/Avastin Feb 2011- Aug 2011 with use of pump at home. Now on 5FU/Leucovorin/Avastin weekly. Side effects peripheral neuropathy, vomiting, behavioral changes
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.
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
What Cervical Cancer Survivors said about their Chemotherapies.
8 rounds of an taxol, carboplatin, avastin combination every 3 weeks for 7 months then low dose cisplatin every week for 4 weeks with radiation. Side effects: nausea, vomiting, heartburn, fatigue, pain, depression, compromised immune system.
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.
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.
5 treatments of Cisplatin
Extreme nausea, vomiting, some tingling in my toes.
Loss of hair and nausea
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.
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!
Cisplatin once a week In conjunction with the radiation. Then Five series with Etoposide.
Chemo-has "chemo brain"
Had cisplatin for 6 weeks during radiation, now am on my 5th of 6 treatments every three weeks (taxol and cisplatin)
Constipation. Fatigue. Nauseau. Metalic taste. Weight loss.
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.........
Cisplatin started 7/8/08
Paclitaxel, Cisplatin, Bevacizumab, Avastin
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
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!
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.
1 night a week, 12am-8am - December 2008/February 2009 Bedwetting, weight loss, nausea, fatigue, immuno-issues. (I caught the damn BIRD FLU!!)
Cisplatin: Took 2 treatments, 1 week apart. Tolerated well. No nausea, though stomach very "acidy" feeling. Eating bland foods often throughout the day helped. Did have some tiredness. No loss of hair. Had to stop Cisplatin for a while due to frequent ringing in ears. Cisplatin can lead to permanent hearing loss. Was able to complete last 4 Cisplatin after a break. Have some hearing loss, but not much. Will be using an experimental drug-Avastin, as well. Avastin: no loss of hair. Felt a coldness in the core of the body and extremities. Combined with Cisplatin, usually left me feeling poor and unable to work for about 5 days. Starting Taxol, Carboplatin, and Avastin again next week.
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.
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!!
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.
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
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.
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!!!
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
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.
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
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.
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
What Anal Cancer Survivors said about their Chemotherapies.
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.
side effects; weakness, fatigue, occasional nausea.
2 rounds.. mouth sores
Flu type feeling... Fatigue Nausea ( took the meds every 8 hours to control) Hair thinning
Mitomycin and 5 FU beginning 1/18/10
7/15/13 1st round of chemo with Mitomycin and 96 hr (5 day) pump of 5-FU. Nausea, mouth sores, lack of appetite, weight loss. 8/12/13 2nd round of chemo ... same medication and side effects as 1st. Starting 7/18/14 Cisplatin, 5-FU. Every 3 weeks. Nausea, mouth sores 9/22 Carboplatin, 5-FU Every 3 weeks. Nausea, mouth changes
5/21/12 first week via port 7/2/12 2nd week via port Every third week 11/26/12 to 3/11/13, 5 hr drip
Nausea, diarrhea, low white blood cells, low red blood cells, low potassium
1st round was delayed because they could not find a vein, so I had to have a pick line surgically put in for the full time and treatment was delayed a full week as a result. I developed a very bad rash from my chest up a few days later. Overall feeling of unwell. Felt sick when I ate. I ended up in the hospital following second round of chemo. It effected my blood badly and I had to have blood and platelet transfusions and 5 days of intravenous full spectrum antibiotics. I lost about 80% of my hair, but very late compared to most people. It got especially bad for about 4 months after my last chemo.
PICC line surgically inserted for take away 24/7 chemo, replaced weekly. skin rash on chest, drop in blood pressure, drop in red cell count requiring x3 blood tranfusions, nausea, dizziness, alternating constipation through pain meds and diarrhea from chemo/radiation combo, mouth sores, lack of appetite.
Mitomycin C and 5FU infused for 96 hours (4 days) during week one and week 5 of 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.
start chemo on Jan 12 and then again on Feb 9th
Cisplatin infusion weekly for 7 weeks, 5FU 5 days a week through a picc line.
9/97-12/97, 5-FU & Mitomycin. Side effects: Loss of appetite, some mouth sores, dry mouth, swollen tongue (once), loss of taste buds.
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
8/13 - CADD Pump Infusion 8/14 - slight nausea, light headedness, constipation 8/15 - slight nausea, light headedness, aching teeth 8/16 - slight nausea, light headedness, aching teeth, swollen gums, sore mouth, red/sore/burning skin around nasal folds and chin 8/17 - slight nausea, light headedness, aching teeth, swollen gums, sore mouth, red/sore/burning skin around nasal folds and chin, sore throat, headache. Pump comes off today and hopefully will begin to feel better. Beginning to feel slight burning from radiation.
First week and final week of radiation treatments. Chemo pump. Itchy head and chest rash within 4 days after treatment started. Minor mouth sore 1 week after. Diarrehea two weeks after. Hairloss and drop in blood counts 3 weeks after.
PICC line put in 10/25/2010 intital large dose of Mitomycin, weekly infusion of FU5, disconnected every Friday, then started back on Monday 5 1/2 weeks. By 3rd week, severe stomach pains(lasted 1 week) diarrhea, no appetite, weakness , because of blood count did not take scheduled last dose of Mitomycin
Starting Chemo 19 April 2011. Will be doing a 5 day Infusion 5fu for 3-4 weeks.
8-4-09 thru 8-7-09
2/09/10 mitomycin & 5fu
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.
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.
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
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.
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
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.
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
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
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
What Tonsil Cancer Survivors said about their Chemotherapies.
Chemo coming up
after 1 chemo treatment I don't feel any reaction as of yet. Next treatment July 14.
Chemotherapy Cisplatin. Vomiting started the first day of chemo and stopped two weeks after treatment complete (9 weeks of vomiting & vomiting).
3 Cisplatin mega doses, 100 units per time, 6 hour chemos
3 treatments. Cisplatin at first but had terrible digestive side effects so used erbitux for last 2 treatments
hearing loss and ringing in ear from chemo (cisplatin)
11/9, 11/30, 12/21 - loss of appetite, cold, "chemo head" (loss of concentration and short term memory)
Cisplatin= 1 day a week for 7 weeks
Starting march 12 2009
5 treatments of cisplatin one a week commencing 14th July. Mocositis, fatigue WBC count dropped dramatically after last treatment
Cisplatin gave my husband ringing in ears but much better now. Had complications each time after a chemo. Was hospitalized twice for them.
Jan 21- vomit, headaches, fatigue, lack of sleep, sore throat, cold sores, dry mouth, weak, pain, dry skin, headaches
2 Full Week Doses (M-F)
03/05/14 Chemo 1-Chills & sweat & nausea the next 4 days.. 03/26/14 Chemo 2-Chills & sweat & un able to eat the next 4 days.
1st one today 26-April-2010 Slight nausea, headache and heart burn so far so good 2 more to go 3 weeks apart. 2nd was uneventful opted for the 3rd one while throwing up in the sink in the corner of my Rad-Oncs offce. Mucus was triggering my gag reflex something fierce by then, was going to hospital getting hydrated 1 or 2 full bags to lessen mucus knew how important that third dose was and made it to the end was glad I did. Didn't have many side effects from the chemo had tinnitus going in so when they asked I said i didn't care I have it already go for it. Was no cake walk and have talked to many others who have had tons of side effects so I guess I was lucky
Chemo - Cisplatin - Day 1 of week 1 / week 4 / week 7
GREAT NEWS!!! No Cisplatin treatment!! Only going to use Cetuximab! which means I will not be getting all the side effects of Chemo type treatments!!!
Cisplatin, 3 treatments , hair thinned, loss of hearing, nausia, ringing and static in my ears.
April 9, 2012 (Only made it through 4 treatments as it made me incredibly sick.)
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.
Start on March 29th 2011.
Carboplatin - 6 Weekly infusions completed February 27
Cisplatin. Lots of nausea. Some hair loss.
Chemo is Erbitux which I get once a week for 7 weeks.
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.)
What Mesothelioma Cancer Survivors said about their Chemotherapies.
carboplatin, alimta 8-27-09
What Endometrial-Uterine Cancer Survivors said about their Chemotherapies.
TAP regimen - 7 21 day cycles
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.
Taxol/carbo, starting Dec 12, 2007. Some joint pain, hair loss (boo-hoo) and slight stomach upset.
Haven't started yet. Need advice.
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 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
little queasy tired bald last one nov 5th 2010 yesssssss!!
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.
Finished Aug 23, 2011. 6 treatments completed. Zofran for anti-nausea worked but caused headaches.
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.
Chemotherapy Carboplatin, Taxol
TBD but they definitely want to do it.
My symptoms became SO much worse after chemo: Pain, nausea, vomiting, mouth sores, chemical taste in mouth, fatigue, weight loss
Lost hair not much else
Starting chemo (carboplatin and taxol) on 4/27/11. Will have 6 sessions, one every 3 weeks.
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.
See Surgery Description> apparently I cannot follow directions
felt sick all the time, metal icky taste, neuropathy, ruined joints >:( bone pain
I have had two rounds of chemo, and the next will take place on Jan 31, 2012. After that, three more rounds!
Carbo/Taxol every 3 weeks, 6 cycles
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.
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.
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.
What Skin Cancer Survivors said about their Chemotherapies.
Photo Dynamic Therapy for any AKs... skin checks every three months
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
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.
What Hodgkins Lymphoma Cancer Survivors said about their Chemotherapies.
ABVD- nausea, fatigue, wooziness, thinning hair ICE- nausea, fatigue, wooziness, total hair loss, bleeding gums and mouth sores GND- some fatigue, mouth sores
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.
nausea, neutropenia, anxiety, extreme fatigue, mouth sores and dry mouth
ABVD 12 rounds, 6 months
ABVD - six 4-week cycles (June-November) Prednisone Procarbizine
6 months of bs and stem cell transplant was life changing made me feel completley helpless
first round 09/08/11-ABVD-headache, swollen tongue, blisters on tongue, vomitting, nausea, bone aches.
AVD (Dr. says I don't need the B) constipation, nausia, jaw tingle, red hot face, tired, dizziness
Started ABVD November 20th~ a little nauseous, headaches, and a little tired..
ABVD regimen. First session was one day after diagnosis. #1:05/20/2010, #2:06/07/2010 (delayed by neutropenia), #3:07/01/2010 (delayed by neutropenia). Side effects: Hair loss, negligible neuropathy.
Delayed until I deliver my baby.
ABVD: 8 Cycles (16 total treatments). My side effects were severe bone pain, fatigue, nausea, burning in my stomach, constipation, ileus, thinning hair
ABVD, started Feb. 13, 2009.
ABVD chemiotherapy, hair loss
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.
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)
Initial treatment: ABVD/MOPP (8/92-12/92). I received 6 cycles with complete response. The chemo was relatively well-tolerate. Salvage treatment: DECAL (Dexamethasone, Etoposide, Cisplatin, Ara-C, L-Asparaginase) 9/92-12/92. One brutal regimen! Cisplatin was the worse. Three cycles with complete response followed by stem cell transplant.
started ABVD March 2011
Yes, My chemotherapy treatment was ABVD.
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 :))
ABVD started in December 2011-May 2012. Hair loss, nauscia, weakness. ICE July 2012-August 2012 Hair loss, nausea, weakness
I am having ABVD. Side effects: nausea, fatigue, hair loss, constipation, bone pain, fever, infection...
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.
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!
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.
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.
What Leukemia Cancer Survivors said about their Chemotherapies.
January 6 2014 and February 15 2014
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
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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