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Vital Info


Peggy (peggyjean)


May 12, 2011


walstonburg, North Carolina 27888


July 17, 1955


Cancer Fighter

Cancer Info


Esophagus Cancer


May 6, 2011


Stage 4


Yes


Re-excision Surgery, Lymph Node Removal


Radiation Therapy


Taxol (Paclitaxel), Carboplatin (Paraplatin)


none


not being in control of my life


keep the encouragement up


prayers


take your mind off them


do something anything. don't think




Stats


Posts: 18
Photos: 0
Events: 0
My Supporters: 12
I Support: 5
Comments: 37
Views: 12864


Peggy's Profile Page

Cancer Symptoms

trouble swallowing

Surgery Description, Dates & Side Effects

9/23/11 took out esophgus and strech stomach to top of throat

Chemotherapy Description, Dates & Side Effects

june 13 2011. no side effects yet




Comments:

went through the surgery just find. only 2 scars instead of normal 3. one down my chest and one on my back. really big one. stayed in hospital 10 days. i am still having problems learning how to eat. just found out today that all the symtoms i am having now are normal and expected

Hi Peggy! I’m about to go through that same surgery (if they feel they can operate) ..how are you making out since surgery?
Wally Silvia
Thanks Peggy..

dont know what didn’t work just that it didn’t.

Peggy, what part didn’t work? Were you able to find the RSS feed? or was it the link that didn’t take the feed? I will try and find a better way. Thanks so much for letting me know.

Not only are you my little sister, but you are also my best friend, and I’m going to be with you all of the way. We have too many festivals and road trips in our future—have to get you well. I know I don’t say this often enough—I love you. Juanita

I had tonsil cancer. The mask was to hold my head and neck in place for radiation. The radiologist pin points the places for the radiation. I have cancer at several places. They did not want an accidental cough moving my position. It is a mesh material that is heated just enough to be pliable to form the face. Mine had larger holes cut into it for my eyes, nose and mouth. Each side of the mask is attached to a bar that fastened to the table that I laid on for the radiation treatments. The idea of it was weird at first but I was glad for the mask because I have allergies. I did not want to move if I had to cough or sneeze!
The PEG tube was a life saver for me. My radiologist wanted me to have it before treatment started. He said if I don’t need it, wonderful, but he’d rather not have me need the surgery when I was already feeling bad from radiation or chemo. I started using it within a week because my throat already hurt when I ate and I was loosing weight. I always used the gravety feed. It was the only way I was taught. I have to use 5 cans of a nutritional drink to maintain my weight (118 lbs). A friend gave me a juicer so sometimes I also juiced fruit and veges. This added more calories when I lost weight during the last 2 weeks of radiation and it also gave my body more nutrition and fresh veges.
Try to keep your neck moving several times a day-front and back and side to side. Also your mouth-open it as far as you can even if you loose you voice-I did loose mine but not everyone does. When all was done, I could only open my mouth 1/4 inch. I do not know if trying to force it open between treatments would have helped or not. I do think trying to keep it open would be easier then having to get it to open more after treatments are compelted.
If I can help you with anything else, I will sure try. Just let me know.
Take care, hugs and prays for you, Sandyjo

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