What Breast Cancer Survivors said about their Chemotherapies.
4 rounds of taxotere & cytoxan every 3 weeks. Started 3/3/11. Second round completed 3/24/11; had allergic reactions to both drugs. Third round done without reactions (super slow drip) on 4/14/11. Fourth & FINAL round completed 5/5/11, and grateful for being finished!!
FEC and taxotere. Three treatments of each starting 2/11
Adriamycin-tore up my mouth and taste buds, cracked the corners of my mouth, leg pain/aches, fatigue, loss of hair, eyebrows and eyelashes.
My 1st chemo will be 2/14/11.
2000 - Chemotherapy
4/2009 Abraxane and Carboplatin 9/2009 Taxol and Avastin had an allergic reaction at the end of the run of Carboplatin Avastin caused my blood pressure to increase sharply, so it was discontinued
I have had 5FU, Adriamiacin, Taxol, Taxotere, Navalbine, Xeloda, Gemzar, Carboplatin, Abraxane
Taxotere & Cytoxan. Had violent allergic reaction to taxotere during treatment #2 on Dec. 10. This one wiped me out.
Sep-feb--The oncologist said it would be " hard going"--that would be one word for it.
I've taken chemo for 3 years now, many kinds of chemo, my "favorite" is Xeloda.
suffer to heal. stay mindful of what it means to be aware.
Chemo burnt a hole in my colon, so needed more surgery
This was the worst for me, seems like I stayed so sick & in the bed from being week & not being able to eat. It seemed that every time I tried to eat, I tried to throw up. I only had 6 wks. of chemo & only had to drive 55 miles for it. Again, the ride seemed to be the worst being sick on your stomach. When I was sick & could't eat, I drank Ensure, it's the only thing that I could hold down & Seemed to feel good on my stomach. Also gator aide helped with the strength. My white count got low several times & I had to give myself shots in my stomach to help bring it back up, but it wasen't to bad, cause I use to work for Dr.'s myself.
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.
may 4 2008,nausea,and alot of hand pain
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.
Started Adriamycin/Cytoxan on 6-4-09 dose dense. (1 dose every 2 weeks for total of 4 doses.) Felt fatigue, stomach upset,hair loss. Started Taxol 7-30-09 dose dense (1 dose every 2 weeks for total of 4 doses.) Felt achey, tired and depressed, hair loss.
from Aug to Dec nausa and tired and the hot flashes are unbearable
I will be recieving my port this week, and my chemo treatments should beginning by December 10.
4/06/11 met with medical oncologist who advised my Oncotype DX test results on my tumor were ER/PR positive, HER2 negative, High grade cancer, and determined to have an 11% chance of reoccurrence. Chemotherapy (cisplatin) was recommended for 4 cycles. Side effects and risks (known to cause malignant tumors 5-10 years out) were explained. After doing homework on internet and weighing the risks, quality of life vs. quantity, I declined chemotherapy. This was also based upon my extreme sensitivity and allergies to various medications (penicillin, morphine, demerol, codeine, iodine, sulpha to name a few). My surgeon, husband and family members have agreed/supported my decision. I will proceed with radiation therapy and will attempt hormone therapy.
Began Adreamycin/Cytoxin on Aug 30, 2007.Completed my last dose of Taxol on Jan. 30, 2008. My main side effects were the exhaustion and mouth ulceration and neuropathy in my toes and fingers with the Taxol.
Will have 4 rounds of chemo for preventative reasons. Taxotere & Cytoxan. Had my first dose 2 weeks ago. No nausea, just fatigue, some diarrhea. Thought I'd keep my hair until the next dose, but it just started falling out today.
AC followed by Taxol total 24 weeks beginning Oct 2009 Became very neutropenic (low white blood cells) A couple of mouth sores
Nausea, Diarrhea, Constipation, Fatigue, "Chemo-brain"
Finished February 21, 2010
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.
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
I begin chemotherapy on the April 8th. 4 rounds of 3 weeks each of Vinorelbine and Carboplatin. (Originally Cistoplatin but the doctor changed it cuz my ears were ringing)Worst side effects are feeling like lead and/or rubber, forgetfulness, weight gain, insomnia and aching bones, muscle and skin.
6 weeks, 3 weeks apart
carbo/taxol only effect has been being tired!! Verty low white cell counts, had to receive one transfusion, other wise has handled it well.
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...
Avastin-2008 and 2011, Cisplastin-2009 and 2011, and Tarceva-2011.
8 total cycles...6 while undergoing radiation (reduced rate) followed by 2 of triple dose after radiation.
Feb 08-Cisplatin/Etoposide- hideous vomiting diarreah Switched chemo drugs AND Hospital -April08-carbo/taxol/avastin. Tolerated well. Neulasta. Bone pain
I had my port-A-cath placement on November 9, 2010 for six cycles of Carbo/Alimta. The port-A-cath hurts just on its own, but chemo sucks, sucks, sucks! I cant say anything nice about chemo, other than hopefully it is killing those cancer cells! After each treatment I have extreme fatigue and appetite loss for 4-5 days following. My hair started falling out after the second cycle, which doesn't bother me compared to the fatigue. I hate not helping out around the house, or missing out on family time because all I want to do is sleep. My blood counts are also very low so the doctors and nurses check them every week, and they also check my kidney function. I'm on medicine for my anemia which helps a little with my fatigue. My kidneys should hang in there- I guess it paid off living a healthy life.
will start on march 16 (tentative)
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.
Chemo also started on 10/10/07 and its once a month for 3 days in a row.
Chemo began September, we are on third round of a four-round cycle. We expect five or six treatments will be needed. CT scan will tell us more after fourth round.
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...
Taxol and Carboplatin every 3 weeks for a total of 4-6 treatments. Have had 2. Nausea, fatigue, aches and pain in whole body. Also DVT.
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!
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
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.
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.
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
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.
Start Chemo May 18th 2007 Cisplaton and Etoposide
Alimta (Pemetrexed) Aug - Nov 2013, 6 cycles
What Bladder Cancer Survivors said about their Chemotherapies.
Foggy brain. Forgetfulness.
What Non-Hodgkin Lymphoma Cancer Survivors said about their Chemotherapies.
Chop 2002 Cop with Rituxan 2008. Hair loss, numbness (not bad this time), fatigue, insomnia from Prednosone.
RCHOP - 3 sessions. Start Aug 10 2012
CVP + R - 6 cycles and then two years of the "R" (Rituxan). stomach pain, diarrhea, fatigue for a week. Also, I receive an injection of Neulasta after each chemo which gives me bone pain but I am learning ways to stop that too and now go in for hydration the day after. I medicate myself for a few nights after the injection with Benadryl and Tylenol.
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.)
R-Chop, eight sessions one every 3 or 4 weeks, side effects, nausea, loss of appetite, some muscle aches
G-Chop 1/8/14 starting for 6 cycles, headache, jaw pain, hair loss
R-CHOP starts 8/26/10 Major Side Effects Day 1-3 Headache and Diarrhea Mouth Sores Days 3-6
RITUXIN 10-2010 - present Fludaraben 10-2010 R-chop 1-2011
R-CHOP 21 Mouth Sores Steroid Withdrawl
R-CHOP 14. RICE, and BEAM
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-CHOP 21 Round 1, July 19, 2010 (extreme drop in blood pressure, shortness of breath, chest pressure, swelling of hands, feet and face)
February 25th: R-CHOP. Mouth sores, nausea, fatigue, heartburn March 21st: R-CHOP. Mild nausea (it's only been two days, side effects showed up for me 4 days later)
R-CHOP every 3 weeks for 6 cycles
Bendamustien and Rituxen
R-chop 2005 breezed through it Rituxin 2007-2008 easy and effective Bexxar 2009 put me in ICU for 4 days but did well for years remission Bendamustine 2010 very easy and mild did very well but didn't last in remission very long R-ICE 2011 I had a transformation to large B-cell the treatment wasnvery very hard put me in the hospital isolated for 5 days with low blood counts needed transfusion of platelet and red blood I was in remission for 4 months only now it's back :( I'm going for R-GMOX now followed by SCT
11/2012-V-RCHOP....V-Velcade (Clinical trial drug) Side Effects: Headaches, hair loss, nausea, dehydration, neuropathy, & Fatigue
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
June 25, 2009--started chemo
Rituxan/Bendamustine (Summer 2010) - very little except fatigue. R-CHOP (summer 2011) - nausea, fatigue, hair loss
Rituximab cyclophosphamide vincristine Prednisolene every 3 weeks started 7th August 2012 x8 sessions then 2 years Rituximab control. So far, the only side affect is fatigue , normally towards the end of the day and the day after chemo. Hair still with me. Making sure I don't get an infection of any kind.
RCHOP six months - 2007, Rituxin maintenance two years
About to go for chemo number 3 on Friday, feb 22... bone pain, anxiousness, depression, numbness, random rashes, hair losss, constipation. RCHOP , nuelasta, etc
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.
Start date November 14 th chemo drug called Folfirinox 8 weeks every other week to try and shrink tumor away from artery
Yes, decided to participate in a clinical study, began chemotherapy Tx on June 21, 2013, one month after Dx
Gemzar weekly for two weeks and week off.
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.
Chemo once a week from 4/2/10 to 6/01/10: Was tired the next day with small "blah" moments.
Folfox mix of chemotherapy -nausea, vomiting, diahhrea , nil taste I food, shaking, mouth ulcers, dry skin
Chemo #1 on 4/02/10: I was more tired then usual and had a "blah" moment after going outside for a few minutes.
Gemazar.... So far, nausea and weakness
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 .
Gemzar Jan 2008-May 2008 Sept 2009- Oct 2010
Folfirinox Jan 2013 - Feb 2013, switched to Abraxane and Gemcitabine March 2013-current
Pill form chemo winter 2009...threw up at end of each round
March 22(3 types of chemo) i feel it lessened his quality of life, but for my dad he needed to fight back!!!
More harm than good; no chemo
will be starting after Christmas
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".
given up on dates the first time on chemo was 7 months and this time has been 9 months
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!
started chemo 6/14. 18 treatments prescribed, currently going through chemo.
June 2012-October 2012; Reported Lethargy, nausea, changes in taste, neuropathy in fingers, weight loss.
Gemzar, Taxotere and Xeloda
6/2011 tiredness, nausea, dizziness
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
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.
6 rounds of chemo, first one 3/9/11, last one 6/21/11. Side effects: constipation; sharp pains in legs and feet; metal taste in mouth; heavy limbs; pain in joints; jittery; loss of all body hair; eventual numbness and tingling on bottoms of feet; and a slew of other things.
Carbo/Taxol 4 treatments (didn't work) Then Doxil and a Trial Drug EC145 4 treatments (didn't work) Then Trial with Perisofone and Taxotere 3 treatments (again didn't work) Avstin and Cytoxan. Trial with Avastin/Torisel. I'm exhausted just typing all of this.
Ultimately decided not to have chemotherapy; my original gyn/onc strongly recommended it, but once my second one was strongly against it (I had my surgery done in one state but live in another), I decided to get a third and fourth opinion.
I'm on my 4th round of chemo treatment in 3 years time. This round is 2 days a week. Side effects are joint pain, nasea, vomiting, diarrhea, night sweats, loss of appetite, hair loss, irritability, exhaustion, and thankfulness for each day
First Chemotherapy was Monday, March 29, 2010 - The only medical side effect was a very red face in reaction to the steroid in one of the preparatory drugs. Main side effect was pronounced "blues". Mom stayed on the couch for three days and ate very little.
1. Chemo Sept- Oct.2010 2. Chemo Nov - dec. 2010 currently ip chemo
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 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...
4 round of cisplatin, bleomycin and etoposide
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.
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.
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.
Taxol sucks!!!!! makes your hair fall out and makes breathing really difficult until i go into an anxiety attack. I dont like taxol
Starting 4/24 - 6 rounds every 21 days
Start Jan 6, 2012 Six rounds of carboplatin and paclitaxel once every 3 weeks.
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.
Taxol+Carbo every 3 weeks, Taxol every week. Started March 2010. Hair loss, feeling tired.
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.
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?
my chemo is cisplatin , etopside , and bleomyacin
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
2/6/2009- Started Taxol and Carboplatnium cocktail. (6 sessions) 2/26/2009- Started GOG- 218 (Avastin Trial) Nurses/doctors notice side effects indicating she was actually receiving the drug.
3- one month cycles of cisplatin, bleomycin, and etoposide. Side effects: Nausea, hair loss (roughly 1 month after chemo began), fever
Jan-May/06 6 Taxol/Carbo CA-124 = 7 May/06 neuropathy hit - severe damage to hands and feet. Hands are curled.. I can't move ankles or toes. Severe nerve pain - can walk 5-6 steps w/ walker
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.
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
Chemo every 2 weeks, nausea, vomitting.
Began chemo in July of '09 with camptosar, leucovrin, and 5-fu. this is over a 46 hour period. In January '10, they added avastin and zometa to the regimin and is ongoing.
cisplatine caused hearing damage, taxotere caused skin and nail damage and herceptin made my hands tingle. Xeloda wiped me out, and all of the above caused hair loss.
3/15/14 Began 10 session clinical trial at Memorial Sloan Kettering. Chemo iv (cisplatin and epirubicin + trial drug/placebo) every 3 weeks. 2000mg Xeloda pills daily. IV chemo is followed by two days of dextametazone (steroid pills) which give me a boost. Hair loss, dry hands - currently trying to prevent them from cracking, some fatigue. Trying to avoid pain meds because that seems to be the cause of constipation/discomfort.
No help says' the doctor.
What Brain Cancer Survivors said about their Chemotherapies.
Temodar throughout radiation and now higher dosages (5 days on 23 days off). Fever, low platelets, fatigue
Dibromudocital, CCNU, 6-thioguanine, Vincristine
Tremador - First set - daily dose for 3 weeks Not able to continue to the next set. Nausea, weakness, loss of appetite, Sleeping constantly
Scheduled for first time chemo (Temodar) in July 2011
low dose temodar- little to no side effects b/c of my use of supplements
Temodar 28 Days on 5 Off. 14 Rounds. Nausea, vomiting, weakness, mouth sores, fatigue.
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 April 2013
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.
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.
Began 150mg Temodar on 1/3/2011 2nd Dose of Chemo to begin 3/17/2011
Hair loss, fatigue, loss of appetite, bruising from all of the blood work, achy muscles and joints, off balance, loss of concentration.
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.
Temodor- 5 days on, 21 off- October 2009- June 2010 Avastin- Every 15 days- July 2010- Present Carboplatin- Every 30 days- July 2010- Present
Start chemo 9/12/11 Temador
Temodar - hair loss - tired.
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.
started 9/13/2010-7 days a week, temedar. nausea and vomiting forst two nights. was ok last night so we'll see.
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!
Radiation & Temodar daily for 42 days then cycles of 5 days on 23 days off
I tooke Temodar pills from 08/2013 to 12/2013. The main side effects that I had were fatigue and nausea. I found that by taking my Zofran a half hour before bed and then taking the Temodar right before I went to sleep, I was able to sleep through most of the side effects.
Temodar, 12 month cycle with allergic reaction
Temodal - started Aug 15, 2011
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.
CAPOX 2006, FOLFIRI + AVASTIN 2007, TEGAFUR + AVASTIN 2008, FOLFIRI + AVASTIN 2010, XELODA + AVASTIN 2010 - ONGOING...........FOREVER....WHILST ITS WORKING
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.
FOLFOX started 2/11/2012 and ended on 7/18/12. The oxaliplatin in the FOLFOX caused peripheral neuropathy.
it was a bitch but everyone in the hospital oncology was very nice that helped alot.
Folfox and Avastin. Very debilitating, very fatigued and nauseated. Thinning hair.
Chemo-therapy of 5FU and Oxaliplatin started 3/12/2012 and finished 8/13/2012 administered every two weeks, and taking home an infusion pump of 5FU for two days.
June - August 2005: Side effects - Nausea; tunnel vision; fatigue; dry hands and feet; upset stomach; hair thinned; skin burned easily in the sun.
Pill form. Xeloda, 1800mil daily.
Started FOLFOX Sept '11
Started October 28, 2009 5FU 24/7
Very little after affects from the chemo other than slight nausea and some fatique. They had to cut the chemo treatments short in order to focus on the radiation treatments. Had a port-a-cath installed for future chemo treatments.
Erbitux Xeloda Oxalyplatin Avastin
He is going to start his first chemo treatment on August 12th. (Avastin, 5FU, Qxaliplatin, Neulasta, Leukine, and Neupogen).
Bi-weekly Chemo 6 months Oaxliplatin/ fluorouracil 5-fu
Each round of chemo consists of 3 weeks. Week 1 I get an Oxaliplatin infusion, weeks 2 & 3 I take oral chemo, Xeloda. Side effects are nerve pain (thanks I already had that), hand pain, fatigue, weakness, memory loss, confusion at times. Bla Bla Bla
Started 9 Nov on Poxy Oxy and capecitabine. Finding it tough, especially the first week. Been neutropenic on first 2 sessions so far which is causing delays.
Pre-surgery: Xeloda, oral chemo 28 days // Post-surgery: Folfox, infused through port in clinic, followed by 2 days of home infusion pump // Avastin also added // Folfiri for another 12 treatments started in May 2011 // back to Folfox for 3 mos// now to Irinotecan and Erbitux March 2012 / Xeloda June 2012 // Stivarga Dec 2012
24/7 pump 5fu.
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
March - August 2005 Luecovorin, 5fu, and Oxaliplatin. Had issues with joint and muscle pain, skin peeling, Neuroathy (with cold things/and taste) Minimum hair thinning and minimum nausea, fatigue was an issue. This was 3 days a week every other week both at office and home. 2008-Fulfury- was very very sick, constant nausea and vomiting, fatigue, only did two treatments and quit, because I was so sick it felt like the chemo was killing me. This was also a take home bag 3 days a week every other week. 2010- Urbetux (Erbitux) not sure of spelling with a benedryl cocktail pre-treatment to stave off allergic reactions,This is once a week for a few hours every week, has mainly caused skin issues, Acne like rash that has turned into cellulitis (skin infection) in some spots, I am now on antibiotics strong enough to fight MRSA just in case and pain meds as it is very painful, but it's getting better and in 2 weeks I will go back and we will see where it stands as far as do we have to cut my dosage back?
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.
June 2013 - December 2013
Chemo Wed, leave with bag, come back on Fri. Side effects neuropathy, fatigue, nausea, occasional constipation and/or diarhea
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.
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.
i was put to sleep with benegril
1 night a week, 12am-8am - December 2008/February 2009 Bedwetting, weight loss, nausea, fatigue, immuno-issues. (I caught the damn BIRD FLU!!)
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.........
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.
Rather not discuss
Chemist Monday's only decadron steroids potassium
1st chemo on 2/16 Cistplatin. had Headache for 2 days ??decadron given for nausea. mostly fatigue---but can't blame it all on the chemo. to have 6total treatments
tahbso april 15,2013
Cisplatin started 7/8/08
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.
5 chemotherapy sessions with cisplatin over 5 weeks
Done and it sucked
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 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!
Nausea and fatigue, Extreme Vomiting, Neuropathy
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 for 6 weeks Cisplatin & Topotecan for 4 21 day interval treatments. 3 day duration of treatment. CHEMOTHERAPY TREATMENTS are the treatments that made Aimee sicker: nausea, vomiting, diarrhea, and weight loss of 35#. She also had 10 blood transfusions during the 2 treatment plans because the cancer and chemo were killing her simultaneously. During her final treatment in January 2009 she had an allergic reaction and coded in the clinic. Treatment was discontinued and Palliative care began.
Extreme nausea, vomiting, some tingling in my toes.
Constipation. Fatigue. Nauseau. Metalic taste. Weight loss.
Weekly chemo for six weeks
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).
Chemotherapy is bi weekly on fridays! Side effects include Nausea, fatigue, and weakness, hair thinning
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.
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.
Commencing Chemo 28th April
Mitomycin given in one dose on June 28, followed by a week of infusion of 5FU. Four weeks later a second cycle of 5FU. Following the first treatment, severe mouth sores for 8 days - at the end could not swallow more than a teaspoon at a time. The second cycle had reduced mouth sores, but I did not have the Mitomycin as my blood count was too low. After the chemo ended, I developed a problem that my doctor and I identified as milk protein immune reaction. I was hospitalized twice for rehydration, following hours of vomiting and diarrhea, after eating ice cream (it's made with milk, who knew?) and a soup with light cream base, almost the same as milk. This turned me into a "food detective" when I ate away from home (what is in that sauce?). Finally, after a year, the oncologist suggested "challenges"with a fourth-teaspoon of the ice cream, followed by half-a teaspoon, etc., until I consumed the same size serving as the one that sent me to the hospital without any reaction. At last I could stop grilling my friends about what's in the food! At this point my only issue is the chile pepper question - if something is being cooked with hot chile peppers or flakes I have to leave the house or I start coughing. And eating them! Out of the question.
Starting Aug 27th 5FU and Mito C
April 2011 nausea and vomiting, weight loss,neutropenia,mouth sores, hair thinning April 2012 nausea, mouth sores, hair thinning
5 FU - through port for 5 days June 6th and again July 5th - survived first dose with severe sore throat, mouth sores and rash. Dreading July 5th
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
First Round: 9/3/2013 Received an injection (infusion?) of mitomycin, then was suited up with a mechanical pump, a bag of 5-FU, and an ugly, poorly designed fanny pack. I had to wear it for 5 days. Lots of nausea, no vomiting, very tired - which could have been caused by the anti-nausea meds that I took regularly. I basically slept my way through the first two days. I had a overall sensation of just not feeling well. After that, although I couldn't eat much, the nausea went away. On day 4, I felt really good - very slow, but good. Day 5, woke up feeling extremely weak and dreamlike. Noticed sore throat and bleeding gums (while brushing). Have developed a sore "spot" on the right side of my throat. More energy on day 6. NOTHING tasted good. :( Cramping, but no diarrhea.
Very fortunate to have had fairly mild chemo effects--mostly fatigue, some mouth sores etc. but not much nausea.
8-4-09 thru 8-7-09
Xeloda Monday thru Friday. Weekends off. Also had mytomycin Iv in the beginning and end of treatment.
mytomicin at beginning and end of 6 weeks 96 hours of 5FU at beginning and end doses halved for second cycle because of bad reaction to 5FU
12/7-10. Not too sick alot of mouth sores and counts were drastically low hospitalized 12/15 with new oncologist
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
Mitromycin and 5FU via pump, 1st week and 4th week of treatment. Nausea - 4 week had to be hospitalized
Mitomycin and 5 FU beginning 1/18/10
begun 26 September 2013
5-FU infusion mitomycin.. lss of appitite for a week, mouth sores.. feeling better when we took pump off.
9/97-12/97, 5-FU & Mitomycin. Side effects: Loss of appetite, some mouth sores, dry mouth, swollen tongue (once), loss of taste buds.
Having Chemo 1st a couple hours in Dr. Office + "buddy bag for 46 hours Started 1st treatment Dec 18-Friday Felt pretty good-till Sunday-Nausaus now alot of gas with new medicine
Cisplatin and 5FU, nausea and dizziness
Intravenous at day 1 and 30, during radiation in pill form - Mitomycin
weeks 1 & 5 Day 1 Mitomycin-C 10mg + 5FU 1000mg pump x 48hrs wk 1: bleeding gums, low wbc, anaemia, tiredness wk 5: nausea, low wbc, anaemia, onset of abdominal cramping, extreme fatigue hair-thinning, fatigue
No terrible side effects, the first round was heavy and I had mouth sores, but quickly learned to treat them. Little nausea, thank goodness. I was very grateful to have had the portacath rather than a picc line or the direct vain method. I watched others go through it while I was having my treatments and I felt it was easier for me to have the porta cath.
Mitomyscin and 5FU during first chemo round which began end of Sept. 2013. Shortness of breath, fatique, white and red blood cell count dropped
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.
Begin Erbitux treatments February 13 2012 and finished on May 2nd.
Begin weekly Erbitux 9/10/13
Hyporexia, nausea, tinntitus
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
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!!!
Chemotherapy Cisplatin. Vomiting started the first day of chemo and stopped two weeks after treatment complete (9 weeks of vomiting & vomiting).
Ciplatin 3 megadoses 3 weeks apart concurrent with radiation
2 Full Week Doses (M-F)
3 Cisplatin Chemo's, starting July 17, 2014
3 heavy does of cisplatin thankfully no hair loss or sickness just some constipation which was a pain oh and some weight loss
hearing loss and ringing in ear from chemo (cisplatin)
No side effects thankfully!
Hearing loss and ringing in my ears. 3 chemo treatments, first, fourth and 7 th week. Saliva got thicker then syrup,honey after treatments ended. Couldn't swallow and had to sleep sitting up in a recliner for weeks afterwards.
Cisplatin, 5-FU, Docetaxel
Cisplatin, 6 tx, every monday for 6 weeks, concurrent with radiation. Tolerated well and relieved all lupus symptoms. Last tx was 11/13/12.
Cituximab Loading dose March 13th, High fever and severe headache. Second of 8 treatments March 21st. Only side effect was severe heartburn.
The first chemo treatment of Cisplatin was on 8/31 with another scheduled for 9/21 and 10/12.
2/3/14 - 3/10/14 : 6 weekly Cisplatin doses @ 30mg/m^2 Side Effects - Ringing in ears (went from minor to moderate). Constipation. General "bad" feeling...like having a cold without the symptoms. Overall I think I did ok with the chemo though.
Cysplatin, Oct 6 thru Nov 18' 1ce a week
Low-dose chemotherapy (Cisplatin) coincided with radiation, 1 day per week, beginning December 7, 2009 and ending January 25, 2010. Side effects included nausea, fatigue, weakness, depression, low blood counts, increased age in appearance, loss of some hearing in the higher frequency range and tinnitus (ringing in both ears).
8 weeks of single dose of cisplatin...loss of taste, luckily I was on a PEG tube. I would strongly recommend the PEG to assue that enough protien uptake to support proper healing
Jan 21- vomit, headaches, fatigue, lack of sleep, sore throat, cold sores, dry mouth, weak, pain, dry skin, headaches
My cocktail included Fluorouracil and Cisplatin.
What Mesothelioma Cancer Survivors said about their Chemotherapies.
carboplatin, alimta 8-27-09
What Endometrial-Uterine Cancer Survivors said about their Chemotherapies.
Carbo/Taxol every 3 weeks, 6 cycles
currently doing carbo/taxol every three weeks. Extreme fatigue, muscle aches, taste changes
Cyclophosphamid Carpoplatin Taxol
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
Haven't started yet. Need advice.
May 2010 Chemo Carboplatin/ Taxol, nausea, fatigue, hair loss
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.
I have had two rounds of chemo, and the next will take place on Jan 31, 2012. After that, three more rounds!
felt sick all the time, metal icky taste, neuropathy, ruined joints >:( bone pain
Lost hair not much else
Finished Aug 23, 2011. 6 treatments completed. Zofran for anti-nausea worked but caused headaches.
recommended to start after radiation
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.
TBD but they definitely want to do it.
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 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.
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
little queasy tired bald last one nov 5th 2010 yesssssss!!
TAP regimen - 7 21 day cycles
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.
Chemotherapy Carboplatin, Taxol
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
Starting chemo (carboplatin and taxol) on 4/27/11. Will have 6 sessions, one every 3 weeks.
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: 8 Cycles (16 total treatments). My side effects were severe bone pain, fatigue, nausea, burning in my stomach, constipation, ileus, thinning hair
ABVD- no major side effects so far! Feel a little tired, otherwise ok. 1st treatment 10.11.12- at least 6 month course of treatment.
first round 09/08/11-ABVD-headache, swollen tongue, blisters on tongue, vomitting, nausea, bone aches.
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.
ABVD 11/30/2010-present Fatigue, weakness, dizziness, nausea, neuropathy, constipation, headaches, hair loss and chemo brain.
Started 6 cycle ABVD treatment on 8/16/11
hair loss... weight gain... nerve tingling... bad taste... feet pain... but no vomiting... so not all bad...
ABVD chemiotherapy, hair loss
I had 6 x ABVD last summer. Now 3 x DHAP + stem cell transplantation in the future
First round with chemo was brutal. Mustard Gas ... my grandfather got the purple-heart in World War 1 because of the genocide they used on our soldiers. The genocide they used was Mustard Gas … ironic huh? It was used in war to kill … it was used on me and so many others to try to save our lives. It was terrible stuff - if a drop of it got out of the vain, it could eat a whole on your skin. And so it did – so imagine what it was doing to the rest of my body. It was the throwing up for 24 hours, so violently that was so hard – especially when the poison itself only worked for 3 minutes…I believe. The rest of the time throwing up was just a bonus! It is easy to get lost amongst the chemo and radiation … but that is what family and friends are for.
About to start Chemotherepy. Very nervous. I was suppossed to start April 11th, but my insurance covers Lupron, so i can save my ovaries from the harmful drugs. Should be starting within the next week or so.
Clinical Trial-see below
I am having ABVD. Side effects: nausea, fatigue, hair loss, constipation, bone pain, fever, infection...
6 months of bs and stem cell transplant was life changing made me feel completley helpless
ABVD, hair loss, night sweats, depression, low white blood count, prone to bacterial infections.
started ABVD March 2011
ABVD- Side effect? UGH.
Yes, My chemotherapy treatment was ABVD.
ABVD, 6 cycles (or 12 treatments), self-administered neupogen shots, three ever other day following each treatment with EXTREME bone pain where vicoden did not help. PICC line inserted, had negative side effects to numbing agents used when placed. Shaved head three weeks after first treatment, but never was completely bald, eyelashes and eyebrows thinned a lot but thank god for makeup! Mouth pain, extreme fatigue, constant sick feeling, burning and tingling in arms the night after treatment. Toe nails on big toes bruised completely and lifted. Now they are starting to grow back and are painful (feels like ingrown toe nails). Super dry skin, especially heels - cracked heels... brittle fingernails that kept breaking, CHEMO BRAIN!, scars from tiny scratches that would have healed normally otherwise, but chemo made them stay A LOT LONGER!, new stretch marks, etc... so many more, just can't remember all of them.
ABVD- October 22, 2010-
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!
6 rounds of ABVD; vomiting, fatigue, diarea, insomnia, hair loss.
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.
ABDV-Adriamycin, bleomycin, dacarbazine, and vinblastine. Research Drug- Phase II Trial of Rituximab (Rituxan)-ABVD for Classical Hodgkin Lymphoma
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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