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#84120 11-13-2008 08:31 PM
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Today I had chemo for the 5th treatment and my white blood cell count has dropped to 1.7. The nurse talked to my Dr. and he said to go ahead with the chemo today even though my WBC was so low. Has anyone else had that side effect and should it be treated? I have been very sick and unable to eat hardly anything for over a week. I am going to work very hard to get something down. The good thing about chemo is they give me 1 bag of fluids before chemo, and another bag after. I sure did need those fluids today. I feel better some, but still have nausea. Sores on my neck haven't cleared up and my Dr. gave me a highly strong cortiocosteriod cream today so I am using that. But I am worried about the WBC. Thanks, Angel


SCC left tonsil, tonsillectomy with additional tissue removed 06/10/08, a few teeth on top left side removed 09/05/08,recurrence before treatment started at BOT and tonsil area, 35 IMRT treatments began 10/15/08, and Cisplatin IV (began10/16/08) weekly for duration of radiation.
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Also, when I read the lines on my computer I am seeing 2 lines or like 1 1/2 of the line I am reading overlapping and I have to blink my eyes to clear it up and it just goes back to being 2 lines and I blink again and it clears up aging. Weird huh? Could the low WBC be causing that or would that be something else? Thanks, Angel


SCC left tonsil, tonsillectomy with additional tissue removed 06/10/08, a few teeth on top left side removed 09/05/08,recurrence before treatment started at BOT and tonsil area, 35 IMRT treatments began 10/15/08, and Cisplatin IV (began10/16/08) weekly for duration of radiation.
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The WBC being low is normal for going thru chemo. I know mine werent in the normal range for well over a year from when I was first diagnosed. I dont know at what level is too low, sorry. There are shots of something called procreate and also some others out there that will help with your blood counts. Sorry that Im not more help with this.

I hope you have told your doc everything you said here. Do you have a PEG tube? Do you have anti-nausea meds? How about magic mouthwash to soothe your mouth? No matter what, just make sure you drink everyday. You dont want to lose your swallowing ability or get dehydrated. You must get minimum 2500 calories per day in. I ended up in the hospital twice for dehydration/ malnutrition and that was with a PEG.

I hate to sound harsh here, but if you dont listen to the hydration/nutrition advice you are only hurting yourself. It will make your treatments much harder and probably put you in the hospital. You will feel like crap if you dont get these things right. Easy way to get there is my 3000 calorie choc peanut butter milkshake. You still should have boost /ensure /carnation VHC or prescription formula if you have a peg.

I know how hard this is, Ive done it twice. I also know the more you avoid eating and drinking, the worse you will feel.

Im hoping you feel better tomorrow.


Christine
SCC 6/15/07 L chk & by L molar both Stag I, age44
2x cispltn-35 IMRT end 9/27/07
-65 lbs in 2 mo, no caregvr
Clear PET 1/08
4/4/08 recur L chk Stag I
surg 4/16/08 clr marg
215 HBO dives
3/09 teeth out, trismus
7/2/09 recur, Stg IV
8/24/09 trach, ND, mandiblctmy
3wks medicly inducd coma
2 mo xtended hospital stay, ICU & burn unit
PICC line IV antibx 8 mo
10/4/10, 2/14/11 reconst surg
OC 3x in 3 years
very happy to be alive smile
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Christine Yes, I told both my Dr's. that I have not been eating/drinking like I should. I definately wanted them to know. I also ask for something to increase my appetite and he ordered me something, I just have to pick it up tomorrow. I did get an Ensure doen today and ate a few bites of soup for lunch and ate 3 bites of eggs for supper and I drank sips of water on and off all day and night, No peg tube, I only have 2 more weeks of treatment so I dout they will put one in.

What is the recipe for your 3,000 drink?

Thanks, Angel



SCC left tonsil, tonsillectomy with additional tissue removed 06/10/08, a few teeth on top left side removed 09/05/08,recurrence before treatment started at BOT and tonsil area, 35 IMRT treatments began 10/15/08, and Cisplatin IV (began10/16/08) weekly for duration of radiation.
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If you wanna try the shake its made of all very aproximately measured ingredients....

3 or 4 cups choc ice cream
1 cup peanut butter (I cut it back to 1/2 cup, 1 cup is like 1600 calories alone)
2 cups milk
1/3 cup choc syrup

Its a big, thick shake. You might want to cut back on some of the ice cream and add more milk to make it thinner and easier for you to drink.

Unfortunately the last week and first 2 weeks after it ends are the worst of this whole thing. Hang in there, it will be over soon. Just please make sure to get your calories and water in every day so you dont feel so awful.



Christine
SCC 6/15/07 L chk & by L molar both Stag I, age44
2x cispltn-35 IMRT end 9/27/07
-65 lbs in 2 mo, no caregvr
Clear PET 1/08
4/4/08 recur L chk Stag I
surg 4/16/08 clr marg
215 HBO dives
3/09 teeth out, trismus
7/2/09 recur, Stg IV
8/24/09 trach, ND, mandiblctmy
3wks medicly inducd coma
2 mo xtended hospital stay, ICU & burn unit
PICC line IV antibx 8 mo
10/4/10, 2/14/11 reconst surg
OC 3x in 3 years
very happy to be alive smile
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Thank you Christine. That sounds wonderful. It would be great if I could taste it as well. lol So if I mix that and drink it I would get enough calories for 1 day huh. That is wonderful, so I will try it and hope I can get it down. Thank you so much. Angel


SCC left tonsil, tonsillectomy with additional tissue removed 06/10/08, a few teeth on top left side removed 09/05/08,recurrence before treatment started at BOT and tonsil area, 35 IMRT treatments began 10/15/08, and Cisplatin IV (began10/16/08) weekly for duration of radiation.
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Its the calories you need, but not all the nutrition you need. Thats why you still should get a couple cans of boost ensure or carnation vhc in. Balanced nutrition is always best. Going over on calories right now wont hurt you. I had at one point been getting 5000-6000 per day cuz of those shakes. I didnt gain an ounce even with doing it for a few weeks. If you get at least 2 cans in and a shake and do that for a few days, I know you will start to feel better. It wont be back to how you felt before the big C but it will be better than you feel now.

Dont forget the minimum 48 oz water too. Of course, more is always better with that too.




Christine
SCC 6/15/07 L chk & by L molar both Stag I, age44
2x cispltn-35 IMRT end 9/27/07
-65 lbs in 2 mo, no caregvr
Clear PET 1/08
4/4/08 recur L chk Stag I
surg 4/16/08 clr marg
215 HBO dives
3/09 teeth out, trismus
7/2/09 recur, Stg IV
8/24/09 trach, ND, mandiblctmy
3wks medicly inducd coma
2 mo xtended hospital stay, ICU & burn unit
PICC line IV antibx 8 mo
10/4/10, 2/14/11 reconst surg
OC 3x in 3 years
very happy to be alive smile
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Posts: 756
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Angel,

I also made a lot of shakes during my treatment, got some recipes from the hospital. I don't recall the exact ingredients but did include milk, ice cream, yogart, and ice (the cold sure felt good). I would also add Carnation Breakfast mix, whey protein powder, instant non fat milk, and various fruits for the added nutritional value.

My kids even enjoyed them, so I had to make extra each time!

Also, make sure you mention your vision problems to your doctor.


Susan

SCC R-Lateral tongue, T1N0M0
Age 47 at Dx, non-smoker, casual drinker, HPV-
Surgery: June 2005
RT: Feb-Apr 2006
HBOT: 45 in 2008; 30 in 2013; 30 in 2022 -> Total 105!
Recurrence/Surgeries: Jan & Apr 2010
Biopsy 2/2011: Moderate dysplasia
Surgery 4/2011: Mild dysplasia
Dental issues: 2013-2022 (ORN)
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Angel,

Cut to the bottom line and just drink 6 cans of VHC every day and you won't have to do anything else about calories. I didn't have any appetite or desire to do much and you are entering the worst part of your Tx now. For the next month at least it will not be pleasant and most likely much much worse than anything so far, especially the couple weeks post Tx so you really need to just get those calories down and to me the faster and more convenient, the better.


David

Age 58 at Dx, HPV16+ SCC, Stage IV BOT+2 nodes, non smoker, casual drinker, exercise nut, Cisplatin x 3 & concurrent IMRT x 35,(70 Gy), no surgery, no Peg, Tx at Moffitt over Aug 06. Jun 07, back to riding my bike 100 miles a wk. Now doing 12 Spin classes and 60 outdoor miles per wk. Nov 13 completed Hilly Century ride for Cancer, 104 miles, 1st Place in my age group. Apr 2014 & 15, Spun for 9 straight hrs to raise $$ for YMCA's Livestrong Program. Certified Spin Instructor Jun 2014.
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David, I know you are right about the VHC. The problem is I can't affored it. The company that makes Ensure has a Ross patient assistant program and are providing me with the Ensure at no cost to me. When my Dr. ordered it I didn't need the Ensure Plus which has more calories as my weight was holding up pretty good. But since then, they sent me 9 more cases 2 weeks ago and I can hardly eat or drink anything due to the nausea. Some times just the thought of putting anything in my mouth to swallow makes me want to just up chuck, which makes it harder for me to get anything down. I am definately getting the water down because the dry mouth and throat makes me. But I am going to try to get all I can down to avoid the peg tube. I only have 2 more weeks of treatment. One thing I have found is after I get the fluids, I feel a lot better so I had them yesterday with chemo and I feel pretty good today so I am going to try and keep all the fluids down I can and the jello and yougart and if I can do that they said I might could make it. I sure do hope so.

Did you have any problems with your white blood cell count going low during your treatments and if so what did they do for you?
Thanks, Angel


SCC left tonsil, tonsillectomy with additional tissue removed 06/10/08, a few teeth on top left side removed 09/05/08,recurrence before treatment started at BOT and tonsil area, 35 IMRT treatments began 10/15/08, and Cisplatin IV (began10/16/08) weekly for duration of radiation.
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