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Neo Nasopharynx after treatment

oneburns
Posts: 4
Joined: Feb 2006

My husband had thirty radiations treatments with around the clock chemo. He finished these in Dec. The scan shows the tumor has shrunk about half and he is due another scan next week. he has a feeding tube and will hardly eat anything as he said it tastes so bad and his mouth is always dry. He also has congestive heart problems. Most of the time he sleeps and stays so tired and weak. Does the body take months to rebuild? After the first week of chemo in the hospital he dehydrated and was readmitted for four weeks and four transfusions. After this was when he had the radiation and chemo. We were told that this is a very rare cancer and treatable. Is there anyone here that has this kind. It had eroded bone before it was found and to the brain. Sorry this is so long and mixed up. Thank you, Jackie

Christmas
Posts: 88
Joined: May 2005

Jackie:
It's a long road, but there' light at the end of the tunnel. There are lots of survivors out here. Hang it there. Take it one day at a time. The body does take time to recover.

rogerbfi
Posts: 16
Joined: Dec 2003

Hi, I'm not sure what is Neo Nasopharnnx. My husband had Nasopharyngeal stage 4. My husband had over 38 radiation, front back both sides, with huge chemo. on each end of and included with rad. Please post update

oneburns
Posts: 4
Joined: Feb 2006

Hi rogerbfi, my husbands tumor was in the back nasal cavity. It had blocked the Eustachian tubes,was around the eye nerves and eroded bone between sinus and had eroded the cranium and was to the brain. We go tomorrow to get results of last weeks scan. In Jan,it had shrunk a little more. The Dr. said this is very rare as he only has maybe one case a year. This type is very common in the Asian country he said. How is your husband now? I think my husbands is just called Nasopharynx. Sometimes I get mixed up.lol Would love to hear from you, thanks for the answer. Jackie

pixysplash
Posts: 2
Joined: Mar 2006

i have been diagnosed with nasalpharynx cancer. i'm 19 and cantonese. there is a lot more experience treating this cancer in china, and somewhat more in San Francisco, where i live. they are giving me IMRT radiation for 7 weeks concurrent with chemo. and then more chemo for several months after. i'm starting on monday.

oneburns
Posts: 4
Joined: Feb 2006