What are Chemotherapies? List from Cancer Survivors

The below is a list that has been posted by the bloggers in this cancer community. There are 7115 cancer fighters that are members here. This is what they said, not what the doctors or nurses will tell you.

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Breast Cancer Chemotherapies

What Breast Cancer Survivors said about their Chemotherapies.

Starting A/C on December 6, 2011. Will have chemo every 2 weeks for 4 months.
Cocktail: Taxotere (wasn't mentioned above), lots of anti-nausea meds!, Neulasta/Pegfilgrastim/G-CSF (the Purgatory Shot)(not mentioned above), Cytoxan. Dude and Dudesses, I have lost 10 lbs!!! Yee haw! Crappy way to lose it but it is lost!
AC dose dense,then taxotere all for 5.5 months.Lots of lousy side effects you name it I had it!
My 1st chemo will be 2/14/11.
8 sessions, sweats, nausea, constipation, de hydration, low white cell counts. joint, bone, muscle, numbness, tingling, pain from Taxol during and post-chemo. Peripheral neuropathy has been diagnosed.
Pamidronate or otherwise known as Aredia. Assists in replenishing bone loss. Given via IV monthly. Tired, headache after treatment, diarrehia, bones ache all over. MAR/08 New treatment - Clasteon - 4 pills/day but NO IV. HOORAY. No side effects except bone pain. I went on the internet to find an alternative cause it took 6 jabs every time with the IV and I just hated the thought of doing that for the rest of my life.
I was on a novel agent in a clinical trial. With Taxol for 12 weeks. Its was horrible diarreha, but it shrunk the tumors. Hooraay
I have completed 3 of my 6 cycles of chemo. I am on Taxotere, Cytoxin and Herceptin. I will finish up in September, with the completion of the Herceptin in May of 2012. I am also receiving a shot of Neulasta which makes my bones ache. The chemo this time has not been so bad except for the flu like symptoms and achiness in my bones. I am tired but this is due to the anemia.
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!!
Waiting for the biopsy result of er pr her2
Chemo sucked! It's a crazy way to slowly poison yourself and destroy every muscle that you have spent the last ten years working on. Chemo is barbaric and I will cheer the day when this is gone. Obviously, I don't work or support any drug companies.
Started Adriamycin/ Cytoxan infusions every 3 weeks, June 28, 2011. Would keep me pretty much bedridden for 2 of the 3 weeks.
through March 2008 CMF cocktail, 8 rounds. never lost my hair, nausea got pretty bad... three rounds in, I became a petulant child and announced I was NOT going back. A nurse family member asked my mom what kind of anti nausea meds I was given (don't remember) and told my mom to relay the following: "tell her to get pot, the pills suck" .... My resourceful husband came home with a surprise shortly after round 3. It PISSES me off that I had to break the law because the fact is, at least for me, IT WORKED and it was AMAZING.....
First Taxol 1.5.11, once a week for 12 weeks, FAC once every 3 weeks from 3.30 - 6.1.11. Taxol made me feel like I was wearing a lead raincoat and concrete shoes. FAC was far more discouraging. Lots of digestive issues, couldn't eat, everything taste nasty. It was horrible.
no chemo
FEC and taxotere. Three treatments of each starting 2/11
To date, I have not had chemotherapy.
AC 8 weeks staring 8/10/2017 followed by 12 weeks of Taxol. Nausea on AC. Terrible muscle and bone pain in Taxol.
Taxotere and Cytoxan - Four Treatments - 2 down 2 to go 10/24/11 Herceptin - 1 Year
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.
Abraxane & Avastin Both drugs on week 1 just Abraxane on week 2 Both drugs on week 3 week 4 I get a break. The chemo went that was for 4 months now I get a ct scan of the chest then he decides if I need more chemo or we start the hormone therapy. My oncologist decided since I was having a hard time with my insurance. (they cut me off for a month) & I couldn't get the ct scan to see if I start the Tamoxifen that I should do another month of chemo.
Taxotere & herceptin weekly for the rest of my life.
Things I wish someone had told me- You feel the worst on days 3-5. Even though you're nauseous you can still eat with enough drugs (I never threw up!) Get your hair buzzed as soon as it starts to come out, and your scalp hurts, you will feel much better. Don't shave it until your scalp stops hurting. Your nose runs because you have no nose hair to catch it A little infection will knock you on your ass. Claritin can fight some of the neulasta side effects Glutamine and vitamin B can help with the Taxol tingle Ugg makes flip flops- AHHH big help with the Taxol tingle Some people lose their fingernails with Taxol (but mine are intact- I have chemo rings, though)
May 23rd 2007 started 6 sessions 3 x F.E.C 3 X Taxotere Ulcers in my mouth, sickness, diarrhoea, thrush, joint pain, loss of finger and toe nails, peeling skin on hands and feet,
8 rounds - 4 A/C - 4 Taxol Hair loss on 13th day, bone pain from Taxol, rhematoid arthritis outcome

Prostate Cancer Chemotherapies

What Prostate Cancer Survivors said about their Chemotherapies.

none yet
taxater, didnt do anything,6 treatments, mitotaxatrine, still on it, barely any side effects due to the vit c drips
Docetaxel, 8 sessions in 2014; extreme fatigue, neuropathy, loss of hair
N/A Chemo poisons; cannabis brings about programmed cell death.
NONE!!
Taxotere, Jevtana

Lung Cancer Chemotherapies

What Lung Cancer Survivors said about their Chemotherapies.

Started chemo on July 7, 2016 - May 5, 2017 Side effects - nausea, vomiting, mouth sores
chemo fog.
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
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.
2007 April til present so far 5 rounds Taxotere Carboplatin Avastin Emend for nausea Aranesp for red blood Neulasta for white blood etc.....
2/26/08to 5/28/08 - 6 cycles Taxol, carboplatin and Avastin for lung ca. Hair loss and peripheral neuropathy - some fatigue.
Had 4 exhaustive chemo therapies. Found that they are not effective on NSCL as it came back in other lung. Targeted therapy of Tarceva put it in remission.
October 18 th and every 3 weeks for 4 treatments. Nausea and joint cramping, some neuropathy.
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...
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.
carbo/taxol only effect has been being tired!! Verty low white cell counts, had to receive one transfusion, other wise has handled it well.
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.
Iressa (gefintib)
Feb 08-Cisplatin/Etoposide- hideous vomiting diarreah Switched chemo drugs AND Hospital -April08-carbo/taxol/avastin. Tolerated well. Neulasta. Bone pain
carboplation and alimpta 4 treatment rounds, a lot of pain and nausea and increasing weakness
8 total cycles...6 while undergoing radiation (reduced rate) followed by 2 of triple dose after radiation.
One a day pill forever (took 150 mg for 2 years). Down to 100 mg due to vertigo, fatigue. Other side effects, slow/non hair growth, rash, dry skin, dry mouth
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.
December 2004 - Present off and on. On Avastin and Tarceva currently, but stopping to start a new chemo.
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.
Avastin-2008 and 2011, Cisplastin-2009 and 2011, and Tarceva-2011.
Start Chemo May 18th 2007 Cisplaton and Etoposide
3 days chemo every 21 days. Hydration as needed. Tiredness and nausea/vomiting at times.
Cisplatin & Etoposide May/18-August/18. Four rounds of treatment 3-4 weeks apart. Side effects- Hair loss, nausea, weakness & fatigue, weight loss
one treatment . switching to Afatinib

Bladder Cancer Chemotherapies

What Bladder Cancer Survivors said about their Chemotherapies.

Had Chemo biweekly starting Oct. 13, 2016 ending 1/20/17. Main side effects were fatigue, amnesia, hair loss, constipation. I do not know the drugs they used. It was a cocktail.

Non-Hodgkin Lymphoma Cancer Chemotherapies

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

Rituximab, Cyclophosphamide, Vincristine, Prednisone on 3 week cycles. Started 1st September 2010. Side effects - constipation, mild nausea, night sweats, tiredness, mood swings.
tired and sick feeling
R-CHOP 25/11/11
Stopping R-Chop Chemo on December 5th 2012. Cancer growing. Started a new Chemo Regimen on Dec 10th 2012.B-R( Rituximab and Bendamustine)Stopped Rituximab and Bendamustine regimen on February 18th,2013 due to developing PML in the brain. Started back on ( Rituximab and Bendamustine) PML cleared. Started in Nov 2013 on Tremsirolimus
August 3, 2015 - September 23, 2015 - High dose Methoreaxate and Rituximab September 30 - February 2016 - R+EPOC
6 Rounds R-Epoch
RCHOP every two weeks. 6 times in total. Side effects were fatigue, nausea, complete loss of hair, dry mouth, weight gain, joint pain, weakening of bone density, etc....
Rchop ---Lost of hair-tired-cold
11/2012-V-RCHOP....V-Velcade (Clinical trial drug) Side Effects: Headaches, hair loss, nausea, dehydration, neuropathy, & Fatigue
RCHOP
R-CHOP Four cycles, three weeks apart. March 26 thru July 7 2015. Minimal thru first stage thus far.
R Chop for my NHL, but not for the Breast cancers
R-CHOP, six session, three weeks apart, starting on June 29, 2012 and ending on October 16, 2012. Had some minor nausea on the night of the chemo sessions, but nothing too major. About 80% of hair fell out by the third chemo session.
6 treatments of R-CHOP, 3 weeks apart.
R-CHOP BEGINNING ON 12.21.2015
Dose adjusted R-EPOCH. Six rounds. 21 day cycles. Chemo administered as an inpatient. Started chemo December 19, 2011. Finished April 26, 2012.
R+Chop, 1/4/2012-4/23/2012
R-Chop, eight sessions one every 3 or 4 weeks, side effects, nausea, loss of appetite, some muscle aches
4 rounds of chemotherapy "R-CHOP", every 3 weeks for 12 weeks. 1 round of radiation therapy. Nauseated, feeling like am in a fog. I chew on ice chips prior to and during the administer of Adriamycin (red devil) to prevent mouth sores. So far it works!!!
R-Chop
1991 April to June MAKOP B, 12 months treatment plan administered weekly over 12 weeks, ulcers, nausea, tiredness, loss of nerve sensations in extremities, severe constipation, hair loss (lol)
I am on the ICE chemo therapy currently. it's a 3 day stay in the hospital for the treatment. mostly intravenous chemicals. having side effects of most being very tired and having blood numbers that should be high being low and vice versa. i have some numbness in my fingertips and night sweats.
R CHOP, effectiveness stalled after 5 treatments GDP, 2 treatments ineffective ICE, to begin asap
RITUXIN 10-2010 - present Fludaraben 10-2010 R-chop 1-2011
Chemotherapy & Radiation 2003 - Breast Cancer , Chemotherapy - Folecular Lymphoma Stage IV 2014 -RCHOP

Melanomas of the Skin Cancer Chemotherapies

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

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

Kidney Cancer Chemotherapies

What Kidney Cancer Survivors said about their Chemotherapies.

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

Pancreatic Cancer Chemotherapies

What Pancreatic Cancer Survivors said about their Chemotherapies.

Gemcitabine (Gemzar)
I do not remember all of the names. The chemo was a combination of four different chemo drugs. It did not work. My father experienced nausea and could not taste anything so lost his appetite. He also was very sensitive to temperature. We are still waiting to start a trial chemotherapy drug! Pray, pray, pray!
Extreme fatigue, some dry heaving, hair loss, neutropenia
Oxaliplatin,Calcium Leucovorin,Camptosar,Florouracil
Extreme fatigue, delerium
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. Metastases to peritoneum diagnosed in September 2015. Progression of metastases in May 2016 led to a determination that gemcitibine-based chemotherapy had ceased to be effective, and a new regimen of Onivyde plus 5-FU with leucovorin commenced. BRCA-1 mutation discovered and so the PARP inhibitor Olaparib was started in early 2017.
Started July 12. Two weeks on, 1 week off. Plan is 6 cycles. Side Effects - Can’t sleep (steroid pretreatment). Terrible constipation (Nausea meds), Very tired, mild fever, irritability on Day 2-3 post chemo.
More harm than good; no chemo
given up on dates the first time on chemo was 7 months and this time has been 9 months
Started 12.1t.16
5fu from 11/8/16 until 1/5/17. Five hour infusion then wore a pump home for 48 hours. Was supposed to do 8 cycles but only got to 4 when my white cell count dropped and we had to stop. The side effects of this treatment are horrendous. Pain, nausea/vomiting, fatigue, neuropathy in hands and feet, hair loss, cold sensitivity, shaky hands and lips, constipation, night sweats, mouth sores.
Folfirinox 10/17-3/2018; Gemzar 4/18-7/2018; Xeloda 8/18-9/2018
One round of Flourouracil but side effects were severe and patient chose to discontinue. Side effects were nausea, uncontrollable diarrhea
FOLFIRINOX and Gemcitabine/Abraxane
Gemzar, Taxotere and Xeloda
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 .
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.
Folfox mix of chemotherapy -nausea, vomiting, diahhrea , nil taste I food, shaking, mouth ulcers, dry skin
Mar 4 _ Sept 15 2015(Folfirinox)Nausea, weakness, vomiting, low potassium, low platelets (despair)
mid july to November 2015 Gemzar eight treatments, xeloda for 28 days on radiation days. Started Folfox regimen 09/20/2017 for recurrence.
every other week, cold sensitivity
Abraxane and Genzar
Started Chemo - Gemzar & Xeloda - in November 2016. 6 cycles planned. Side effects pretty mild - some nausea and tiredness
xeloda pills for two weeks then a week off.
6/2011 tiredness, nausea, dizziness

Oral Cancer Chemotherapies

What Oral Cancer Survivors said about their Chemotherapies.

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

Ovarian Cancer Chemotherapies

What Ovarian Cancer Survivors said about their Chemotherapies.

18 consecutive weeks of chemo with Taxol and carboplaten then 2 treatments of Doxil
My doctor said there wont be malignancy as the tumor was encapsulated, but it would be safe if i undergo 3sessions of chemotherapy. So i opted for chemo and had vomiting and hair loss while on therapy
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.
Carboplatin started 2007, however I became allergic in 2008, so had to have it changed to Gemzar and Advastin then. Been on and off of chemo since for chronic cancer outbreaks.
6 treatments chemotherapy (carbo/placing/Avastin
Declined chemotherapy
Carboplatin, taxol, avastin, and a PARP inhibitor for 6 rounds, then remission for about 7 months. Then more carboplatin and taxol for 3 more treatments until I became resistant, then onto the MEK/Milo trial. Failed that after 2 months, now looking into immunotherapy
I have had chemo in 2004, 2009, and 2012. each chemo has been different than the one before. With my most recent round I was very nauseous and sick. Lost my hair with all of them and had muscle and bone pain. I also developed an orbital pseudotumer as a reaction to the carboplatin and had to be put on prednisone steroids. This will now be required anytime I am on carbo. It started as a twitching and watery eye almost like with allergies. The eye then swelled shut and was very painful.
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...
I just started the chemo on Monday January 12th. I am on a 5 day a week regimen which occuers every 3 weeks. On my "off" weeks I need to come in 1 day a week to get an injection. Towards the end of this first week I am feeling very tired and very nauseous.
4 months of chemo. Made me achy like having the flu but much worse especially in my legs, naseous, food tasted bad, water tasted bad, low energy.
I had three rounds of chemo in three week cycles. Week 1: 5 days of treatment (admitted in hospital) Week 2: Recovery in hospital Week 3: Recovery at home I experienced low blood pressure, dehydration, nausea, fatigue and anaemia. I still have fatigue after treatment, muscle atrophy and peripheral neuropathy.
<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.
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
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.
six infusions of carbo/taxol every 3 weeks from 3/13 to 6/13 six more infusions carbo/taxol every 3 weeks from 1/15 to 4/15 three infusions doxy every 3 weeks from 8/15 - severe rash - discontinued several infusions every week gemzar from 10/15 to 2/16 tanked white count and increased acities - discontinued avastin/taxol every 3 weeks from 3/16 to present
I have a three prong chemo, which takes place every three weeks. I suffer from extreme nausea, vomiting, fatigue, hair loss, chemo acne and pain at the IV site.
Dizziness and low blood pressure
First time,6sessions of paclitaxel and carboplatin followed by 12 monthly sessions of paclitaxel. Second time 12 sessions of paclitaxel and uniplatin. Periperal nueropathy and weight loss which i'm unable to regain despite healthy intake.There was complete hair loss after 1st chemo sessions,however they reappeared as curls within four months of end session. After 2nd line chemo sessions hair reappeared straightened! neuropathy of hands has increased. Still unable to drive car, or run, or walk fast.
07/20/2017 - Extremely tired, some nausea, fidgety legs, no energy for a week.
Chemo consisted of 6 total treatments - 1 treatment every 21 days of a variety of steroids, anti-nausia meds and anti allergy meds along with 300mg of Taxal & 580mg of Carboplatin. Treatments started on Oct 2, 2014 and then every 21 days from there with the exception of late Dec. which was 25 days because the 21st day fell on Christmas day. Last Treatment was Jan. 20, 2015.
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?
taxol/carbo dec 2008-april2009 topotecan sept 2009/present
1st. Chemo July - August 2009 2nd. Chemo February 2010 ip.chemo 3rd. Chemo January 2011 ip.chemo
Paclitaxel (Taxol)/Carboplatin (Paraplatin)combination. 6 treatments. 21 days apart.

Thyroid Cancer Chemotherapies

What Thyroid Cancer Survivors said about their Chemotherapies.

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

Stomach Cancer Chemotherapies

What Stomach Cancer Survivors said about their Chemotherapies.

Original Chemo was Epirubicin, Cisplatin and 5-FU April-September 2nd Irinotecan and Taxane Current Fol Fox 4 + Avastin
4 months...not helping
Folfox, nausea/vomiting
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.
Cisplatin, Epirubicin, Capecitabine (Xeloda) #1 June 12, 2017, #2 July 4, 2017 Nausea, Dry mouth, Tingly fingers, blood clot in spleen, hair loss
No help says' the doctor.

Brain Cancer Chemotherapies

What Brain Cancer Survivors said about their Chemotherapies.

Avastin drip. 12/2009 - 2/2010. Nausea. Sidenote - everyday I'd go to a juice cafe where they had wheat grass juice. When I went for my last treatment, nurse told me my blood counts throughout treatment were spot on... It's worth researching as has many benefits. Please check with your doc as told it may not be appropriate for some during their treatment.
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.
Radiation & Temodar daily for 42 days then cycles of 5 days on 23 days off
Scheduled for first time chemo (Temodar) in July 2011
No chemo
temador nightly before bed. also on a target therapy trial of avastin which was researched at duke hosptiol
Timodar Started in March 2006 and still ongoing. Side Effects: NAUSEA!
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.
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.
February-continued weakness, tiredness, fatigue, sores in mouth
Taking a Temodar pill for 2 months.more fatigue, and sickness.
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 !!!
What more can I say other than YUCK! It has been very difficult thus far. Upon my first treatment I left the hospital, only to return a few hours later vomiting non-stop. Zofran hasn't helped. The only thing that does anything at all to combat the nausea is to drink plain green tea. I know it sounds weird, but it sometimes works.
started 9/13/2010-7 days a week, temedar. nausea and vomiting forst two nights. was ok last night so we'll see.
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
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.
3 Cycles of Chemo - Cyclophosphamide, Vincristine, Cisplatin - Dec to Feb. (3 weeks apart) - Foot Drops and trips and falls 3 Cycles of Intensive Chemo with Autologous Stem Cell Transplant - Carboplatin & Thiotepa - Feb to May (4 weeks apart) - Hearing Damage
temodar 42 straight days
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.
Temodal - started Aug 15, 2011
Hair loss, fatigue, loss of appetite, bruising from all of the blood work, achy muscles and joints, off balance, loss of concentration.
1/12/12 - begin taking daily chemo pill Temador (not sure how to spell that) for up to 12 months.
Began 150mg Temodar on 1/3/2011 2nd Dose of Chemo to begin 3/17/2011
CLV- Cisplatin, Lomustine, and Vincristine Started in June of 2012 and stopped early at the end of December 2012, was supposed to have it till March 2013. Side effects were very bad and the tumour was not responding. Also used Steroids, anti-nausea meds and a daily antibiotic

Multiple Myeloma Cancer Chemotherapies

What Multiple Myeloma Cancer Survivors said about their Chemotherapies.

began 12/1/14 - 4/30/15 (Velcade, dexamethasone and cytoxin), Cytoxin priming 6/5/15, Stem cell transplant6/16/15 and Malthalon 6/25/15 , also neuropathy (mild) in parts of hand and feet.
8/13/15 Cyclo,dexamethasone, velcaide, huge stomach, very nauseous,no life. After5 1/2 months fired oncologist and went to natural treating dr.
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
Revlamid - daily - ongoing
4 monthly rounds of VAD prior to allogenous bone marrow transplant.
Velcade, dexamethazone, since transplant just added revlamid
18 series VRDD and VRD so far
Thalomid: Fatigue. Red spots that eventually covered my entire body. Neuropathy in feet and hands. Revlimid: rash, upper body.

Colon and Rectal Cancer Chemotherapies

What Colon and Rectal Cancer Survivors said about their Chemotherapies.

My mum went through a number of drugs to treat the cancer which kept on returning almost every single year from 2008-2011: Avasatin, Xeloda, Folfox, Folfiri, Erbitux. The side-effects are almost always similar: nausea, tiredness, vomiting, loss of appetite, mouth and throat sores. The first day after chemo she never manages to sleep well.
Folfox and Avastin. Very debilitating, very fatigued and nauseated. Thinning hair.
Started October 28, 2009 5FU 24/7
12/23/13-02/03/14- fatigue
I had 2 chemotherapy drugs. Eloxatin (oxaliplatin) which was given through my port at my Oncologist's office. I also took Xeloda which is a chemotherapy drug (pills) taken at home. I also had a wonderful Oncologist who worked well with my surgeon.
Oxilioplatin for 5 weekly sessions along with Xeloda twice a day during radiation days. Felt alright for the first two days after the IV of oxilioplatin (probably because of the steroid and anti-nausea meds) but then hit a wall the rest of the week and was pretty run down. Felt almost back to normal by Monday, but then had to do the whole thing over again.
During my 6 month treatment fatigue and nausea were the most consistent chemo side effects. Exercise helped with the fatigue and taking compazine helped with the nausea.
November 1, 2006, Started with 5-FU, missing DPD enzyme causing life threatening toxicity issues and discontinuing the 5-FU. No additional chemo available to me for any treatment of this condition. Now in wait and see mode.
May 2009 - Sept 2009 FolFox, peripheral nerve damage to hands and feet (used to unload dishwasher with ski gloves on cause touching plates etc felt like pickiing up glass!) All good now with help of Vit E and Alpha-lipoic acid suppliments. Xeloda - long term chemo. March 2010 til now and according to onologist, forever!! damages skin on my fingers and feet.
Started Chemotherapy on July 18,2016
Started chemo 1/4/2016
Folfox with avastin. for 6 months. with lots of side effects (the worst was vomiting and neuropathy). After liver resection Folfuri(nausea, lethargy,confusion ect.) after the second recurrence and percutaneous ablation I had Cetuximab with Irenotecan with a horrible acne type rash
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?
Xeloda- oral chemo, twice a day for 7 weeks, June 22-August 7, headaches, tightness in chest after physical activity, leukopenia Intravenous- 4 months of chemo after surgery, details have yet to be determined
5FU Begining 1-18-11, 5 days on, weekends off...
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.
folofox: 3/14-9/14, starting again 1/15
Body would only take 1 day session.
No chemotherapy
Alt Folfiri/Folfox 2010/Feb through 2010/June Folfiri/Erbitux started 2011/March Changed to Folfox/Avastin 2011/Oct Clinical trials 2012/Sept
FOLFOX first cycle June 11 (infusion) and then the pump 46 hrs; some odd effects on swallowing, a little constipation, a little diarrhea, no food problems :)
FOLFIRI w/ Avastin 4/2009 - 11/2009, FOLFOX 12/2009-2/2010 Nausea and fatique
First visit to oncologist 29th March.
Pre-Surgery April 19-May 26 Five FU for 6 weeks continuous with take home pump Post Surgery started Sept 22 Full Fox
12 so far, 5Fu, Avastin, Oxiplatin, Leucovorin

Liver Cancer Chemotherapies

What Liver Cancer Survivors said about their Chemotherapies.

11-19 chemo pellets not sure of the name, nausea,
On going chemo regiment and had one chemoembolization.
TACEdeb procedure begining of June....side effects... all haha vomitting, nausea, fever, pain, pancreatitis.
Nexavar 8/22/12 - forever, side effects all listed
Nexavar - Current (8 months)
First treatment was June 8th 7 hours between the other meds olus the chemo..Cisplatin and Gemzar.. Felt ok the day after but then started feeling very sick, achy, headache, ringing in ears, coulnt eat, weak, dizzy,tired,shaky all over I only felt well enough to go to the doctor on the 7th to have my blood drawn..saw dr and he said he would up my steroids next time and that should help second treatment was on the 8th, Just the gemzar.. Really tired and achy. Dizzy and weak. Had my shot of Lewnasta on Monday. Still fell tired and bone pain
Nexavar for 6 months. Infusion therapy started 2 weeks ago and ongoing bi-weekly.
every kind, all the time for the last 5 years
No chemo as no primary cancer found and chemo will only add a few months to life, yet these extra few months will be with the side-effects of chemo
7-2008 to present. Lethargic, no appetite, not able to focus for too long on anything, weight loss, strange thoughts, sleep seems to be all REM, dreams and or nightmares about Nam seem to pop up while I'm awake,anger, especially at the VA for not stepping up and admitting and approving my claims.
Tried Nexavar for one day, but decided against it; bad side effects--felt cloudy, nauseated like when I was on Interferon/Ribaviron and had rectal bleeding from the Nexavar; not worth it to buy a few more months of life; discontinued
i will tell you

Cervical Cancer Chemotherapies

What Cervical Cancer Survivors said about their Chemotherapies.

Intravenous Ferritin + Cisplatin: 04/16/2019 and 04/25/2019 Cisplatin every Thursday: 05/02, 05/09, 05/16 (Low WBC count, rescheduled), 05/23, 05/30, 06/06/2019 Side effects: Skin staining from ferritin on left forearm, anemia, loss of appetite, weight loss, nausea, vomiting, IV infiltration, fatigue, headache
Metallic taste heart burn mild nausea ringing in ears
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!
Had cisplatin for 6 weeks during radiation, now am on my 5th of 6 treatments every three weeks (taxol and cisplatin)
First chemo was on Friday 9/15/17. 3 chemo infusions over 8 hours. To be done every 3 weeks. Next scheduled 10/6/17. Have had no nausea or vomiting. Saturday night, severe pressure in rectum, vaginal area and lower pelvic region. Contacted physician due to pain and that no amount of medicine was subsiding pain. Was advised that it seems as if the chemo is working. The pressure could be due to the necrotic tissue from the cancer itself is moving, liquid retention, or inflammation from the chemo. He reassured me that pain and pressure should go away within a few days. Was instructed to take higher dose of percocet. The higher dose of pain meds has done its due diligence, but knocks me out too. It is now three days later and pain and pressure has become more bearable, and treatable with 800mg motrin. Feeling extremely tired, which is very odd being that I am very active. Powering through, I will win this battle.
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!
Chemotherapy is bi weekly on fridays! Side effects include Nausea, fatigue, and weakness, hair thinning
Cisplatin started 7/8/08
Done and it sucked
Chemist Monday's only decadron steroids potassium
Cisplatin once a week In conjunction with the radiation. Then Five series with Etoposide.
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.
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.
Nausea and fatigue, Extreme Vomiting, Neuropathy
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!!
5 chemotherapy sessions with cisplatin over 5 weeks
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
Extreme nausea, vomiting, some tingling in my toes.
Pain, itchiness , Burning , insomnia
methotrexate injections every other day via injection
Sept 6-Nov 6 2008: every three weeks for 6 hours. Side effects: hair loss, tired, and sore from the Nuesta shot, but overall not as bad as it could have been.
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).
Loss of hair and nausea
Cisplatin 2009 six weekly treatments
That also starts withen the next 3 weeks.

Larynx Cancer Chemotherapies

What Larynx Cancer Survivors said about their Chemotherapies.

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

Acute Myeloid Leukemia Cancer Chemotherapies

What Acute Myeloid Leukemia Cancer Survivors said about their Chemotherapies.

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.
On April 19th 2018, I also received my first dose of chemotherapy. I don't remember much of what happened during this time except I broke out in a red rash from head to toe and ran a fever for 5 days straight. The red drug, daunorubicin, makes me extremely sick. I'm a wreck when they give it to me.
Induction round 12/22/14-1/19-15: nausea, vomiting, diarrhea, fatigue Consolidation February '15, Consolidation March '15, Consolidation April '15
hydrea - 02/2009 little/to no side effects
Started daunorubicin and cytarabine 7+3 therapy on January 10, 2015. I stayed in the hospital approximately thirty days. A bone marrow biopsy at the end of this stay confirmed remission. My nausea was not too bad, except for a time that they served some green beans from the cafeteria. I dry heaved several times, and then ate only food from home. I suffered diarrhea, hair loss, a neutropenia fever, an acute kidney injury, fatigue, and weight loss. I started my first round of consolidation chemotherapy in February, second round in March, and third round in April. I have been very fortunate to this point to avoid a bone marrow transplant.
Since June 2012 - july induction, August consolidation, Sept. consolidation, december 2012 induction. Stem cell transplant now on hold.
1st round-12/09/2011Atromycin for 3 days nd Cytosar. for 7 days.
All through out until transplant
April 9 - 15th 2017 & April 27th - May 1st 2017.Finished 2nd round of Chemo May 1st. Experiencing hair loss, fatigue & weakness, SOB, Colitis, Diverticulitis, diarrhea, loss of appetite, confusion, hallucination, Acute Renal failure, low BP, and neutripinic sepsis.
Induction Theraphy Cytarabine and Doxorubicin for 8 days. I just start my Consolidation theraphy last March 30. Which is Doxorubicin for 1hour and vincristine(push) and cytarabine IT(so painful)
chronic vommiting ,hair loss tiredness
High dose chemotherapy, March-June 2012. Side effects: Nausea, vomiting, weight loss, fatigue.
Oct 14th- 7 days Vidaza Nov 23rd- 7 plus 3 Dec 25th- fludarabine and busulfan
Had two induction rounds and two consolidation rounds.
i had three induction therapies spaced about 6 months apart. and just completed two consolidation therapies. i am preparing for a bone marrow transplant.
Achieved remission October 2017 with 2 IV drugs — few side effects aside of minor peripheral neuropathy in feet. Out of remission in January 2018. On cytsribinevsubce Feb 2018; Also on oral chemo since March 2018: Venetoclax. Peripheral neuropathy (feet); anal fissures w/bleeds; mucocitis of throat (hard to eat or drink ANYthing); dyspepsia (nausea); fatigue; 15% wt loss (BMI=18.4)
11/2009. 1/2010. Neuro side effects. Vision compromised. Weakness. Nausea.
the only side affect she has had is toxemia, and neuropothy.
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.
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.
Multiple protocols for ALL & AML.
7 + 3 , tired, weight loss, neuropathy
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.
Seven days straight starting on Monday August 15th.
I have been through my first month of Chemotherapy. I am now going to the Mayo Clinic daily as an outpatient taking doses of arsenic. No Fun!!!

Chronic Lymphocytic Leukemia Cancer Chemotherapies

What Chronic Lymphocytic Leukemia Cancer Survivors said about their Chemotherapies.

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

Testicular Cancer Chemotherapies

What Testicular Cancer Survivors said about their Chemotherapies.

VIPx4. Etoposide, ifosfomide, cisplatin- four cycles, five days in a row each, every three weeks.
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
Initial diagnosis required 1 round chemo -Carboplatin - minimal side effects Return of cancer - 4 rounds of chemo ( EP) 21 day cycles includes five continuous days of infusion then rest. No nausea but gastric reflux with vomiting, scalp pain, metallic taste in mouth, tiredness, neutropenia
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

GIST (Gastro-Intestinal Stromal Tumors) Cancer Chemotherapies

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

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

Chronic Myeloid Leukemia Cancer Chemotherapies

What Chronic Myeloid Leukemia Cancer Survivors said about their Chemotherapies.

An unpleasant mix of fatigue, diarrhea, headaches, water retention, muscle and bone pain.
Daily 400mg Gleevec. Daily fatigue. Slow morning wake up. Memory problems they call Gleevec brain. Polyneuropathy: pain and weakness in body. I use a cane when walking outside. Diarrhea. I did just find out that I am now in remission but must stay on the Gleevec for 2 years. I am totally grateful that Gleevec exists for me and for all CML patients. Good luck to all of us!
Gleevec
I've been on Gleevec for 3 weeks. the first week was no different than the previous ones, lots of fatigue, but that is from the leukemia. In the second week, I started having more pain and some diahrrea. The diahrrea cleared up in a few days but the pains got worse. By week three, I have a lot of bone pain. I can get around and i can work, but it hurts quite a bit to move and my legs (thighs) are the worst. I often wake up with pain and my fatigue is not improving.

Acute Lymphocytic Leukemia Cancer Chemotherapies

What Acute Lymphocytic Leukemia Cancer Survivors said about their Chemotherapies.

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

Anal Cancer Chemotherapies

What Anal Cancer Survivors said about their Chemotherapies.

two 96-hour stretches of chemo with mytomycin and 5 FU (guess what my nickname for "FU" is...) Horrible side effects, bleeding and cracking at corners of lips, raw inside mouth, chronic nausea (nausea meds helped), weakness, depression, sleep problems, etc.
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
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
Two cycles Week one Mitomycin C & 5FU(Flouracil) Week Five 5FU
june 15-August 6, 2015
Sores in mouth, loss of appetite
5 FU and mitomycin
scheduled for Jan 4, 2010
1/23/2012 had IV mitomyacin then 96 hrs of 5 FU via pump. Extremely fatigued all week, not sure if it was the 5 FU or mito. Started Neupogen injections following Monday for 7 days. No nausea at all. Appetite great. Mouth sores began with a vengeance following sat and lasted 7 days. Could only swallow liquids so I mostly lived on instant breakfasts. Two weeks later my finger tips began peeling and hair loss began.
January 2010- January 2011- Cisplatinin and 5 FU February 2011-May 2011- Oxaliplatinin and 5 FU June 2011-present - pclitaxol
Some nausea, kept most of my hair.
Chemo week 1 & 5 of the 6 week treatment. Mytomycin only 60% of normal dose because of high creatinine levels and 5 FU 96 hours All chemo done in patient at hospital for 5 days. Not really nausea...Zofran works wonders, BAD diareaha and painful stomach cramps...Lomotil helped with that, terrible bone pain in my arms sternun and lower back and legs from the Nuprogen to raise my white counts, headaches,one huge mouth sore on the roof of my mouth and gums were out of wack and bleeding...was given Valtrex and that did the trick
2 rounds. constipation and not too much else
First round...mouth sores, nausea, weight loss, chemo rash on face and on upper torso, hair loss (about 80%).
Nausea and fatigue. Hair thinning and loss due to mytomycin.
not yet determined
No problems with chemo. Lots of itching from radiation
F5U 2 runs of 96 hours, Side effects included some nausea and tiredness.
XELODA 500mgs x2 twice a day for two weeks during radiation. Recommenced 14.10.15 to stop on 28.10.15...Having this treatment as insertion of PICC line failed and ceases during radiation due to platelets dropping to 108.
Cisplatin infusion weekly for 7 weeks, 5FU 5 days a week through a picc line.
2- 5 day rounds of Mitomycin infusion followed by Flouracil pump- Severe mouth sores & tongue swelling 1st round. Had Neupogen shots x4. NeulAsta shot after 2nd round - no sores.
1st round 23-27 March 2015 - minimal physical side effects, more pyscologial with PICC line fear and awareness of carrying chemo bottle around for a week. 2nd round 20th -24th April - felt more at ease with the bottle and had no real side effects until the end of the week, then developed terrible mouth sores around back teeth - which I didn't first time round.
Chemo started 3/14 - 3/19. Nausea lingered under surface the whole time. If I missed the anti nausea pill by 1/2 hour it’d take all day to catch back up. Mouth sores started on day 4. I caught a cold that stared on day 2 with a sore throat, full sinuses, lungs etc. the mouth sores progressed quickly and caused the sore throat to become excruciating. I’m still struggling to eat and get enough fluids. I was given iv fluids 2 days after the pump was taken off. And I’m currently trying to not have to go there again. Mouth sores finally abated after 2+ weeks. Unfortunately food still sounds awful, nothing tastes good and I start feeling bad after every time I eat. The blister in my bum apparently is from the chemo not the radiation. Great news is my doc is cutting the dose for 2nd round by 25% because I’m a slow metabolizer. Great. I hope it helps!with round 2 (which starts in 10 days -ugh) I’ve also started experiencing hypersensitivity on my upper left leg, and occasionally on my feet and hands. Started taking B6 to help. Hair started falling out 2 weeks after chemo- getting it cut short end of week 3.
10/2011-12/2011 2 rounds of 5FU through picline., 6/2012-2/2013 Several rounds of Cisplatin
Mitomycin C and 5FU infused for 96 hours (4 days) during week one and week 5 of radiation

Vulva Cancer Chemotherapies

What Vulva Cancer Survivors said about their Chemotherapies.

1/4/17-2/15/18
I didn’t lose my hair.

Gallbladder Cancer Chemotherapies

What Gallbladder Cancer Survivors said about their Chemotherapies.

4 rounds (8 sessions) as of 7/13/19; serious weight loss and fatigue

Pleura, Malignant Mesothelioma Cancer Chemotherapies

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

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

Bone Cancer Chemotherapies

What Bone Cancer Survivors said about their Chemotherapies.

Carboplatin, Doxorubicin, Cyclophosphamide, Tamoxifen, Toceranib, Piroxicam. No significant side effects to start with but after so many months of home chemo/meds I get diarrhoea and occasional nausea (am on meds to combat). My fur is very slow growing now - months later, surgery sites are still sparsely covered in fur, and I now have bald patches (my paws, muzzle, bottom).
i cannot sleep..i cannot eat..i do vomiting

Nose, Nasal Cavity and Middle Ear Cancer Chemotherapies

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

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

Nasopharyngeal Cancer Chemotherapies

What Nasopharyngeal Cancer Survivors said about their Chemotherapies.

Protocol #1: First of 3-21 day cycles of 5-FU, Cisplatin and Docetaxel started 10/7/13 - around the 2 or 3 week started losing hair and experiencing nausea, fatigue, weight loss, etc; Protocol #2: Eribtux and concurrent radiation for 6 weeks started ~12/10/13 - neuropathy in feetbegan a few months after treatment stopped and is still ongoing.
chemotherapy given from January to September Side effects: dehydration, vomiting, blood transfusions
Tinnitus weakness nausea
3 x cycles of Cisplatin 80mg/m^2 over 9 weeks prior to Radiotherapy 3 x cycles of Xeloda (14 tablets) over 9 weeks prior to Radiotherapy Once weekly 40mg2 Cisplatin during Radiotherapy
Every 3 weeks during radiation then once a month x 3 for cisplatin. 5FU home infusion will start in Sept for five days then again in October and November. Nausea, vomiting, fatigue for cisplatin have not had 5FU yet
3- 8 hr chemos mostly nausea.
Jan 2009-june 2009: lung nodules shrunk a bit and last CT scan end of june showed no growth: little nausea, tired all that stuff
Started weekly induction chemo on 9/5/13 with carboplatin and paclitaxel- soreness in mouth, slight nausea, dry skin (severe itching), acid reflux. Started chemo-radiation on 11/4/13 using cisplatin. Received 5 weekly cisplatin treatments until wbc count was too low.

Peritoneum, Omentum and Mesentery Cancer Chemotherapies

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

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

Gastrointestinal Carcinoid Tumors Cancer Chemotherapies

What Gastrointestinal Carcinoid Tumors Cancer Survivors said about their Chemotherapies.

chemo side effects hair loss some weight loss vomitting sweats shakes hot cold pain emotional skin tone looked unhealthy

Esophagus Cancer Chemotherapies

What Esophagus Cancer Survivors said about their Chemotherapies.

Chemo is rough.
every 3 weeks, side effects: tinnitus and stomatitis after the last one
Oxaliplatin infusion; Leucovorin infusion; Fluorouracil continuous infusion pump.
2 low dose chemo sessions. Became immuno suppressed
5FU and cisplatin 12/2016 for 4 days. Hospitalized due to toxic overdose of 5FU. Oncologist did no give me the DFD test because he didnt believe in th test, hi negligence nearly killed me.
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
Ended in Nov 2013. Chemo: Memory loss Radiation Side effects: Loss of bone density resulting in back pain.
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.
chemo from 2/98 through 9/98
Carbo-taxol once a week for 5 weeks

Tonsil Cancer Chemotherapies

What Tonsil Cancer Survivors said about their Chemotherapies.

Starting march 12 2009
Cisplatin gave my husband ringing in ears but much better now. Had complications each time after a chemo. Was hospitalized twice for them.
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.)
Hyporexia, nausea, tinntitus
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.
Begin weekly Erbitux 9/10/13, Cisplatin/5FU 5/14, CarboTaxol 7/15
1 chemo treatment so far have to have 7
10 weeks of 2 chemo drugs per week
Taxol and carboplatin. 6 weekly infusions.
6 low-dose cisplatin treatments, one every Monday for 6 weeks. Felt great; actually took away the joint pain I experience from Lupus!
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!!!
11 treatments ended about 11/07/2011
6 treatments of Cisplatin, every Monday for 6 weeks, ending on November 13, 2012. Improved symptoms of systemic lupus, but caused further hearing loss.
Cisplatin, 5-FU, Docetaxel
Begin Erbitux treatments February 13 2012 and finished on May 2nd.
The first chemo treatment of Cisplatin was on 8/31 with another scheduled for 9/21 and 10/12.
2 six hour Cisplatin courses. Some hearing loss. Some nausea. Actually felt better after Chemo treatments
Chemotherapy Cisplatin. Vomiting started the first day of chemo and stopped two weeks after treatment complete (9 weeks of vomiting & vomiting).
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.
April 9, 2012 (Only made it through 4 treatments as it made me incredibly sick.)
Carboplatin - 6 Weekly infusions completed February 27
Chemo coming up
Chemo start date 10/5/09, three sessions, one every three weeks (cisplatin)
fatigue, nauseous, loss of hair, very very weak.
Chem with Cisplatin, taxotere and 5-FU in pump.

Mesothelioma Cancer Chemotherapies

What Mesothelioma Cancer Survivors said about their Chemotherapies.

carboplatin, alimta 8-27-09

Endometrial-Uterine Cancer Chemotherapies

What Endometrial-Uterine Cancer Survivors said about their Chemotherapies.

Carbo/Taxol every 3 weeks, 6 cycles
recommended to start after radiation
currently doing carbo/taxol every three weeks. Extreme fatigue, muscle aches, taste changes
I have had two rounds of chemo, and the next will take place on Jan 31, 2012. After that, three more rounds!
5/2010-tired, nausea 10/2014-tired, nausea,low blood countsand turned into mds 12/9/2015 start cgeno with doxil after mds in remission
Starting chemo (carboplatin and taxol) on 4/27/11. Will have 6 sessions, one every 3 weeks.
6 chemotherpay treatments. Cisplatin for 2 and Taxol/Carbo for 4. Stomach nausea,bone pain after Neulasta shot, constant dehydration, tired all the time & neuropathy in feet.
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
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
Haven't started yet. Need advice.
CarboPlatin & taxol w/ neuplasta at 3 wk intervals from Aug to Oct Severe constant leg pains, neuropathy in feet and hands, high heart rate. Unable to stand for more than 10 minutes, stumbling, dropping things regularly Treatment changing to CarboPlatin & doxil w/ neuplasta.
Lost hair not much else
None required
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.
Start in mid October.
4/17/15 Allergic reaction to Emend and Taxol
See Surgery Description> apparently I cannot follow directions
Every week on Day 1 & 2 and Day 8.
TBD but they definitely want to do it.
Cyclophosphamid Carpoplatin Taxol
Chemotherapy November 2014-April 2015. Hair loss, neuropathy in feet, achy joints.
felt sick all the time, metal icky taste, neuropathy, ruined joints >:( bone pain
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.
My symptoms became SO much worse after chemo: Pain, nausea, vomiting, mouth sores, chemical taste in mouth, fatigue, weight loss
Chemo came after radiation the first time, chemo only the second time, radiation only the 3rd time. Allergic reactions to almost all the drugs tried, but that was the second time. The ones that I didn't react to made me very sick, so I'd go in to be hydrated the day after chemo since I was unable to do that at home. It's hard to eat and drink when you're asleep. Another side effect of the drugs and certainly the pain killers for me.

Sarcoma Cancer Chemotherapies

What Sarcoma Cancer Survivors said about their Chemotherapies.

Temodar and potentially IV Chemotherapy
Doxorubicin Cisplation Methotrexate Ifosfomide Etoposide
AIM Chemotherapy, 3 cycles, inpatient in hospital for 5 days each cycle, started on 16th May finished on 1st July. Side effects, hair loss, chronic diarrhea, piles, sore mouth, tiredness.
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.
Chemo not a proven treatment for my type of cancer
Chemotherapy lasted from July 2010 - August 2011 His chemotherapy consisted of Vincristine, Doxorubicin, Cyclophosphamide, Ifosfamide, and Etoposide. Some vomiting and lots of nausea.
Adriamycin Dec 14/15 on going
Multiple regimens
Currently going through chemo... some of the side effects that I am experiencing are mouth sores, and sore GI tract. Definite tiredness, lunula turning black, of course hair falling out, complete loss of taste buds and smell during chemo but fine after.
Gleevec, vomiting, diarra, swollen eyes and ankles, cramping in hands feet arms legs, fatique, from 10/19/07 till 5/2013. Didn't work for me after awhile.
Cisplatin usual side effect after two months still have mouth spares, hard to swallow, tennitis, loss of hearing.
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.
Had only 4 appointments for chemo. Hair falling out. Nausa.
I have Chemo once a month. The Chemo caused the whites of my eyes to turn Fire Engine Red. It was a reaction that none of the nurses had ever seen. I was given IV Benedryl. The dose of the medicine knocked my butt out. That was my first treatment on May 21, 2012. I was set for 3 treatments. My Oncologist was not sure if the Chemo would work to begin with. Within the first treatment I could tell a difference. I was amazed. I could actually feel the mass and it was smaller. So, Dr. M ordered another 3 treatments for a total of six. I lost all my hair, eyebrows and eyelashes. Hey, they will grow back one day. I don't mind. I love all the scarves and hats I have bought and been given.
Chemotherapy to start in 2016
Chemotherapy started in September 2011 and continued every three weeks either daily for a week, or a single day dose of VAC - crappy crappy side effects, where do I start......numb finger tips, constipation, hair loss, loss of taste buds, thrush in mouth, lack of concentration, sooooo exhausted after each dose and weeks later. It is very true that the chemo is so much harder than the cancer to deal with.
On year of chemo. Chemo brain. Short term memory issues

Parotid Cancer Chemotherapies

What Parotid Cancer Survivors said about their Chemotherapies.

Adriamycin and cytoxin. 11/03 so sick with vomiting till meds were figured out. Lost 50 lbs. Taxol 1/04. Sick Rituxan 5/13 no effects used for platelet issues Taxol 5/16 with experimental drug

Skin Cancer Chemotherapies

What Skin Cancer Survivors said about their Chemotherapies.

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

Throat Cancer Chemotherapies

What Throat Cancer Survivors said about their Chemotherapies.

Dry Mouth. Lost body hair, Sick at stomach, weight loss.
1997- Cisplatin/5FU - I wanted to die (permanent hearing loss & temporary vein loss) 2003 - Cisplatin/5FU - Extreme discomfort; bloating, burning, nausea, etc. I refused further treatment. 2005 - Taxol, 5FU, Carboplatin, Leucovorin - side effects so bad I quit 12 course regimen after 4th course 2007 - Taxol, 5FU, Carboplatin, Erbitux, Leucovorin - I wished I were dead! after 9th course I was not recognizable; the erbitux had caused my face and neck to break out with puss filled sores that burst and bled. I quit after 11th course.
May 7, May 14, May 24. (Now scheduled for June 1, 8 and 15). Side effects are fatigue and nausea. Taking anti-nausea meds. Worst part is we can't keep enough fluids in him to flush out the toxins due to chemo. We're told this is more common in throat cancer where food and fluids are taken through a feeding tube. Starting to lose patches of hair.
Ringing in ears
It seems that my side effects (nausea, tiredness) start a couple days after treatment. Emend and Zofran seem to be helping.
Chemotherapy due to start 6 weeks after surgery, September 2016
Start November 29, 2010. The drug was erbitux. No side effects with the weekly treatments except for after weeks four and five. After treatment I immediately had chronic chills and shakes in which I was given an injection of demorol and had to lie down for an additional hour until the effects subsided.
3 during 6 week radiation treatment (beginning middle & end.
Feb 14, 2011, Cisplatin, slightly tired immediately following treatment. March 7, 2011, same as treatement number 1. March 28th, 2011 - TBD
Erbitux. Loss of hair, lesions on my hands, scab around my neck, vomiting, etc.
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.
Erbitux (Cetuximab) taken, due to success with HPV-16 related cancers. 7 infusion sessions, starting one week before radiation commencement. First session gave me the worst headache of my life, terrible chills, fever, nausea (but only brief vomiting) and profound weakness. Started about 7 hours after treatment. Subsequent sessions have had less impact; primary complaint being weakness and fatigue. Blistering rash encompassing head, neck, shoulders, chest and back. Very itchy and painful. Appeared by second week of treatment. Now in 4th week, the pustules have subsided somewhat, but lotions are essential to keep the skin peeling controlled.
February - June 2009 Taxotere Cisplaten 5FU
Three rounds of Cisplatin - nausea, metallic taste and tired

Tongue Cancer Chemotherapies

What Tongue Cancer Survivors said about their Chemotherapies.

Three Cisplatin chemo doses, Jan 4, Jan 26, Feb 16. Never got the Feb 16 dose as I was too sick from throwing up.
second form of chemo 3 more weeks, no side effects
A 2 chemical soup every 3rd Monday and then a 24/5 fanny pack pump the same week as above. I have 1 week on and 2 weeks off treatment
For me Chemo was much easier than Radiation. Cisplatin and 5-FU 24/7 for which I was hospitalized. I refused my last chemo treatment because I was too sick, and honestly I thought it would take a lot more than chemo to save me from this beast called cancer. Yet I survived and have for the last 20 years.
Set for July 6 and July 21
No chemotherapy.
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.
Only 5 of 6 Cisplain treatments given because of so much nausea. Hospitalized for nausea and given extra intravenous fluids bags 2-3 weeks separate days from the chemo infusions.
3 bags of cisplatin
Do not know yet if I will have to go through Chemotherapy.
Cisplatin 2007. I was one that had the carotid do it's number, so have permanent heartbeat in my ear. Sometimes loud and intrusive, very loud and intrusive when I am lying down trying to sleep. This too conversation, Chemo and Radiation were simultaneous. It was a dark night of the soul. Burnt skin, inside the mouth and outside. I lost over 60 lbs in less than 9 weeks. Dehydrated, diarrhea, high irregular heartbeats, constipation, impacted, and the list there too goes on.

Hodgkins Lymphoma Cancer Chemotherapies

What Hodgkins Lymphoma Cancer Survivors said about their Chemotherapies.

ABVD, hair loss, night sweats, depression, low white blood count, prone to bacterial infections.
started ABVD March 2011
12 rounds of ABVD. Side effects: hair loss, weight gain, nausea and fatigue
I am having ABVD. Side effects: nausea, fatigue, hair loss, constipation, bone pain, fever, infection...
4 cycles of chemotherapy ending in late August, radiation to follow depending on how the cancer responds.
ABVD Six months
Started Chemotherapy (ABVD) on 30th March 2010. Found that the side effects of consist of bad heartburn & indigestion for a few days after chemo. My hair started to fall out about two weeks later and has slowly been falling out ever since, but not bald yet! Have had to give up fizzy drinks and spicy food, two thinks I enjoy. Unfortunately they cause uncomfortable consequences, like bloating, passing a lot of gas, nausea, heartburn, the list goes on.
7/13/2012~ABVD
hair loss... weight gain... nerve tingling... bad taste... feet pain... but no vomiting... so not all bad...
ABVD for 6 cycles (12 treatments). Was quite well tolerated, tired for a few days after, hair loss, mild nausea but no vomiting, changes in bowel motions, mild rash on feet and arms, aching veins. MADEC (methotrexate, cytosine, dex, etoposide, cyclophosphamide) for 2 cycles, one week of chemo in hospital, 2 weeks to recover then repeat. Fatigue, mild nausea, hair loss. BEAM (carmustine, etoposide, cytosine, melphalan) prior to stem cell transplant. Have only just started this today, had carmustine and so far all good but I know this will change.
ABVD 12 rounds, 6 months
I had chemotherapy for the first part of 2014 and now I am back on ice and chemotherapy with a test drug for 2015
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.
8/23/12 - Hot-flash (minor) and a little fatigue 8/26/12 - Mouth sores.
ABVD chemotherapy, treatment every two weeks for six months (6 cycles). Extreme nausea and vomiting (eventually brought under control by drugs), fatigue and breathlessness, stomach pain and bloating, complete loss of hair, tooth pain, mouth sores, extreme salivary gland pain, loss of some finger and toe nails, mild nose bleeds, mild constipation.
ABVD- October 22, 2010-
Yes, My chemotherapy treatment was ABVD.
ABVD- nausea, fatigue, wooziness, thinning hair ICE- nausea, fatigue, wooziness, total hair loss, bleeding gums and mouth sores GND- some fatigue, mouth sores
ABVD, started Feb. 13, 2009.
(A)driamycin, (B)leomycin, (V)inblastine, (D)acarbazine
ABVD: 8 Cycles (16 total treatments). My side effects were severe bone pain, fatigue, nausea, burning in my stomach, constipation, ileus, thinning hair
Delayed until I deliver my baby.
ABVD May 2008-October 2008 ICE January 2009-March 2009 BEAM April 2009
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)
Chemotherapy from August 2006 - September 2007. Some of the chemotherapies were ABVD, ARA-C and carboplat. Side effects experienced were hair fell out, constipation, low white blood and platelet counts, nausea, vomiting, pain in joints.

Acute Lymphoblastic Leukemia Cancer Chemotherapies

What Acute Lymphoblastic Leukemia Cancer Survivors said about their Chemotherapies.

Although I am 23, I am receiving the pediatric regimen for ALL. This involves 2 and a half years of chemotherapy. The first 8 months are pretty intensive and then I enter the maintenance phase. Side effects of the chemo have widely ranged throughout different cycles. Extreme fatigue, nausea, headache, joint pain, intestinal issues, mouth sores, and the infamous hair loss.
I'm getting three chemo a dont know what they're called but they all make me feel like crap. But whatever makes me better I guess. Fatigue, sick, swollen ankles, sensitive skin, pins and needles in finger tips. Bowel movements slow down. But speed up after a while
Started induction chemo within the first week of November. Integrating it with holistic therapies
started Feb. 26, 2010 I was admitted to hospital every 3 weeks for a total of 6 rounds of treatment - Cycles A and B.
Hyper CVAD Protocol 6/1/2015-2/7/2016 including spinal chemo X 4
currently undergoing HYPER C-VAD
Started chemo once my pneumonia was under control which took 3 days after I was at the hospital(4/4/10 was start date). While in the hospital for a month getting very strong drugs I didn't have any sick-feeling side effects and ate like a horse. I did however lose a lot of muscle mass and after a bit I was barely able to walk and there were occasions where I passed out for various reasons and wasn't able to get myself back up. But I was on 150mg of prednisone at 7am and 7pm each and every day and the side effects from it were awful and probably the worst part about my hospital experience as it made me feel very strung out, nervous, antsy, you name it. Towards the end I started to feel as if I was starting to lose my mind which was more than likely just a chemo brain effect. However after my primary induction was over at the hospital, side effects became more prevalent doing chemo 5 days a week from May-July of 2010 where I passed out, god very sick, could barely eat, had no energy, was extremely depressed but that put me out of my second phase and into the long part, maintenance. I got to come home for maintenance which wasn't possible for the other treatments due to not having any blood cancer specialists where I live, but my doctor personally knew many of my doctors out of state and was who sent me to the group of doctors that he did. I was almost constantly vomiting, Intense chronic pain in my lower back, legs, shoulders, hands, feet, and various other parts of my body. Now I'm chemo free for two years from 2/26/13 but I still have very bad physical issues as well as PTSD, Depression, General Anxiety and other mental health related issues.
finished with induction therapy, now gonna begin with consolidation.
October 2010 - current; Unfortunately, I've had nearly every side effect from chemotherapy.

Bile Duct Cancer Chemotherapies

What Bile Duct Cancer Survivors said about their Chemotherapies.

HAIC 24/7 for two consecutive weeks of constant flow chemo delivered directly to the liver. Every two week chem, alt two weeks pump is filled with Saline. NO Side Effects
begin chemo 11/30/16
iam a nice girl loking for man
On my second round of 2 sessions each which are a week apart

Leukemia Cancer Chemotherapies

What Leukemia Cancer Survivors said about their Chemotherapies.

January 6 2014 and February 15 2014

Myelodysplastic Syndrome Cancer Chemotherapies

What Myelodysplastic Syndrome Cancer Survivors said about their Chemotherapies.

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

Appendiceal Cancer Chemotherapies

What Appendiceal Cancer Survivors said about their Chemotherapies.

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