| Joined: May 2010 Posts: 638 "OCF Down Under" "Above & Beyond" Member (500+ posts) | "OCF Down Under" "Above & Beyond" Member (500+ posts) Joined: May 2010 Posts: 638 | Hi Sue
Alex had the same regimen (see signature). He began to suffer around day 5 with thick saliva, inability to cough it up and nausea. He could not get out of bed. The good news is that after a week of wishing he was dead, he improved to "almost normal". By the time the next cycle was due, he was good to go and almost welcomed the experience as he felt he was doing something active against the tumour.
I cringe when I hear about the health care professionals who make comments as yours did saying your husbands reaction is extreme because this can be unsettling for both the partner and the patient who may interpret this as some sort of failure or weakness. I would disagree with the nurse and say that there are enough people who suffer as your husband has to make it "not unusual" rather than "extreme". The nurse would have been better off looking for practical solutions rather than passing judgement. I think, like others, that the state of one's nutrition has a large impact, and if your husband was underweight or ill from the cancer at diagnosis, he may well be starting behind the eight ball in the first place, putting him towards the higher end of the misery scale. Remember too, that cisplatin is a nasty drug that causes all of manner of grief - adding Taxotere and 5FU just takes it to a whole new level. BUT it also improves your husband's chances of survival AND you will get through it - most do and Alex is just one testament to that.
In Alex's case, he was underweight (60kg or 132lbs) at diagnosis and it was much more than sore throat! It was nausea (and vomiting if he forced himself), loss of appetite, bad taste and pain. Eventually, he was hospitalised when his weight dropped to 48kgs (105lbs) after the second round and the doctors threatened to discontinue treatment if he couldn't gain weight.
The best thing that happened to Alex was a pump. When he was hospitalised they put him on a pump and taught him how to use it. This was a slow drip feed that gave him 2000 calories overnight via a pump and is attached to a PEG. This got around the nausea and vomiting which happened every time he tried to either eat and swallow or use a syringe to deliver liquid nutrition through his PEG.
We also found that changing brands of liquid formula made a difference. When Alex went onto the pump, he was changed to Nutrison and never looked back. Unfortunately, in Australia, this formulation is more expensive than the stuff they originally started him on (TwoCal) so when an offer was made by one of my work colleagues to supply TwoCal that could be administered by pump we jumped at the chance. Alex's vomiting returned.
We learned that it wasn't only slowing down the feeds that made a difference, but the brand as well.
By now, you will have experienced a second round of chemo? And hopefully will have received assistance with your husbands nutrition? A PEG maybe? Please let us know how you are faring.
Karen PS Alex is now two and a half years beyond the end of treatment, is back at work and doing very well. He is still underweight and relies on liquid nutrition (not TwoCal which still makes him sick) Goal is 75kgs (165lbs) which on his frame of 6'1" is still "bean pole" territory.
Karen Love of Life to Alex T4N2M0 SCC Tonsil, BOT, R lymph nodes Dx March 2010 51yrs. Unresectable. HPV+ve Tx Chemo x 3+1 cycles(cisplatin,docetaxel,5FU)- complete May 31 Chemoradiation (IMRTx35 + weekly cisplatin) Finish Aug 27 Return to work 2 years on 3 years out Aug 27 2013 NED Still underweight
| | | | Joined: Dec 2010 Posts: 5,260 Likes: 3 "OCF Canuck" Patient Advocate (old timer, 2000 posts) | "OCF Canuck" Patient Advocate (old timer, 2000 posts) Joined: Dec 2010 Posts: 5,260 Likes: 3 | Did they not give an anti nauseant for breakthrough ? you can use it any time.
Cheryl : Irritation - 2004 BX: 6/2008 : Inflam. BX: 12/10, DX: 12/10 : SCC - LS tongue well dif. T2N1M0. 2/11 hemigloss + recon. : PND - 40 nodes - 39 clear. 3/11 - 5/11 IMRT 33 + cis x2, PEG 3/28/11 - 5/19/11 3 head, 2 chest scans - clear(fingers crossed) HPV-, No smoke, drink, or drugs, Vegan
| | | | Joined: Sep 2012 Posts: 51 Supporting Member (50+ posts) | Supporting Member (50+ posts) Joined: Sep 2012 Posts: 51 | Sue, my husband just finished his 3rd round of the same treatment. The 1st round was the worst with fatigue, nausea and a very sore mouth. We discovered if he took a nausea pill then ate or drank calories about 20 minutes later, the nausea was minimized. Pain meds helped with the sore mouth. For nutrition I bought frozen yogurt, fresh fruit, milk and powdered protein and mixed it in my Magic Bullet. Quick and nutritious.
The 2nd & 3rd chemo had the same side effect but not nearly as much as the 1st. He generally feels pretty good in spite of the chemo. I also advanced from my Magic Bullet to the NutriBullet. See the website. It's perfect for nutrition even if he ends up with a feeding tube. I use the entire vegetable/fruit in this one. I much prefer to use the fresh stuff if possible while trying to keep the protein and calories at a max.
I also do serving-size sugar free jello and puddings with protein powder. Easy to grab and soothing on the mouth.
Hope this helps.
Diane-wife to Paul, age 55 DX 9/17/12 HPV/SCC/BOT Stage 4a Non-smoker/casual drinker Otherwise healthy 9/24/12 Cisplatin, Taxotere,5-FU - 3x 12/3/12 Rad x 35/Carboplatin x 3 1/15/13 DVT upper thigh Passed away 1/23/13
| | | | Joined: Jul 2012 Posts: 3,267 Likes: 4 Patient Advocate (old timer, 2000 posts) | Patient Advocate (old timer, 2000 posts) Joined: Jul 2012 Posts: 3,267 Likes: 4 | I had TPF..Taxotete, Cisplatin and 5-FU in 2009 as induction chemo, which is 5 days continuous infusion. It nearly killed me. In ICU for 2 months, hospital 6 months, lost 110 pounds in one month, paralyzed, blinded me and had every type side effect... Induction chemo is controversial, since it can delay the real trestment cure, and that is radiation, surgery, radiation may be concurrent with chemo too.
10/09 T1N2bM0 Tonsil 11/09 Taxo Cisp 5-FU, 6 Months Hosp 01/11 35 IMRT 70Gy 7 Wks 06/11 30 HBO 08/11 RND PNI 06/12 SND PNI LVI 08/12 RND Pec Flap IORT 12 Gy 10/12 25 IMRT 50Gy 6 Wks Taxo Erbitux 10/13 SND 10/13 TBO/Angiograph 10/13 RND Carotid Remove IORT 10Gy PNI 12/13 25 Protons 50Gy 6 Wks Carbo 11/14 All Teeth Extract 30 HBO 03/15 Sequestromy Buccal Flap ORN 09/16 Mandibulectomy Fib Flap Sternotomy 04/17 Regraft hypergranulation Donor Site 06/17 Heart Attack Stent 02/19 Finally Cancer Free Took 10 yrs
| | | | Joined: Sep 2012 Posts: 64 Supporting Member (50+ posts) | Supporting Member (50+ posts) Joined: Sep 2012 Posts: 64 | I had induction chemo, 3 one week stays in the hospital getting all three chemos by drip 24/7, each week followed by a 2 week recovery period. They included anti-nausea drugs in the drip so I never felt nauseous but did have mouth sores. They also kept me hydrated. Rinsing with a salt or salt and baking soda solution helped the mouth sores some but I was also given a liquid Xylocaine solution to rinse with. I had little appetite and subsisted on Ensure, mostly, but Boost HVC is better. There is also Scandishake which tastes more like a real vanilla milk shake.
During the two week recovery period I drank lots of water and Gatorade. I followed that up with 7 weeks of radiation with one 45 min chemo session per week. Over the course of the entire treatment I lost 20+ pounds. Pre-radiation I had a PEG food tube installed and used it exclusively after a week or two of radiation. I have since regained 5+ pounds. I did feel more and more exhausted as the treatment continued and spent most of my later recovery time sleeping.
Everyone will tell you how important hydration is and it is TRUE. One should drink about 64 oz a day and supplement the liquid diet with water/juice/Gatorade. I could not tolerate most juice with my mouth sores or any later with my radiation burnt throat.
Sounds like your H needs more ant-nausea drugs.
Stage 3-4 Squamous BOT diagnosed 3/19/12 Molars removed 3/29/12 (Cisplatin) inpatient: 4/11/12-4/16/12; 5/2/12-5/9/12; 5/29/12-6/4/12 Feeding tube: 8/9/12-11/21/12 Radiation 8/10/12-8/29/12 Chemo 1X/week 8/10/12-8/22/12 Last PET/CT clear: 9/17/13
| | | | Joined: Apr 2012 Posts: 111 "OCF across the pond" Senior Member (100+ posts) | "OCF across the pond" Senior Member (100+ posts) Joined: Apr 2012 Posts: 111 | Hi Diane, Can you tell me what the difference is between the Magic Bullet and the NutriBullet, they look very similar. I do a lot of jucing but also use a Magic Bullet, which I have had some problems with the plastic gaskets getting chopped up. Sally
Dx 10/11 51yrs LBOT Stage 4 2nodes HPV16+. Non-smoker mod alcohol. 10/11 Induction chemox2 (Docetaxel, 5-Flu, Cisplatin) then Cisplatinx2 IMRTx30. Ended 01/13/12. 12/07/11 RIG. RIG removed 05/05/12. 4/12 CT scan clear. Visual scope checks clear as of 10/13. Learning to live with eating challenges.
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