Nasopharyngeal
Comments
-
I had nasopharyngeal cancer, finished chemo in December, and finished radiation in March so I can relate, but I hate to hear someone 15 years out is still bothered by the effects of treatment (I was hoping the effects would be lessening in me any month now). Other than the dry mouth, what effects are still tough 15 years down the road?
John0 -
Hi! Can I ever relate to your message. Was diagnosed in Dec of 2001 with stage III nasopharangeal cancer. Began chemo and radiation in Feb 2002 and treatments stopped in June 2002.
I am nowhere near your fifteen year survival, but my last two pet scans have shown no trace of cancer! My longest lasting effects are peripheral neuropathy(pronounced tingling and numbness in both feet), and having to drink a lot more liquid to help swallowing when eating. Chemo doc said the neuropathy may or may not go away, but guess I should nnot gripe too much since I am still here.
Messages from long term survivors llike yourself are reassuring to the rest of us. Glad to see you are doing so well, and I hope and pray you continue to improve.0 -
Keep the faith. It's not easy and it certainly isn't fair, but it can be beaten. I was diagnosed with lymphoepithelioma in Apr 1986 after being misdiagnosed for more than two years. The sinus cancer was so progressed that I was not expected to survive, but here I am, 18 years later. At 34 years old, I'm cancer free. The agressive treatment needed to eradicate the cancer has left me with some issues, but I'm here to **** about them. I certainly don't understand life, but I subscribe to the theory that everything must happen for a reason. Of course that doesn't keep the random chaos of life from pissing me off. But alas...I'm here. If anyone wants to chat, feel free to send me an email.tomalexander said:Hi! Can I ever relate to your message. Was diagnosed in Dec of 2001 with stage III nasopharangeal cancer. Began chemo and radiation in Feb 2002 and treatments stopped in June 2002.
I am nowhere near your fifteen year survival, but my last two pet scans have shown no trace of cancer! My longest lasting effects are peripheral neuropathy(pronounced tingling and numbness in both feet), and having to drink a lot more liquid to help swallowing when eating. Chemo doc said the neuropathy may or may not go away, but guess I should nnot gripe too much since I am still here.
Messages from long term survivors llike yourself are reassuring to the rest of us. Glad to see you are doing so well, and I hope and pray you continue to improve.
We're all in this together.0 -
AFTER READING YOUR BRIEF HISTORY, I WANTED TO SHARE MINE. I HAD A RARE NASOPHRYNGEAL CANCER 24 YEARS AGO. SIX WEEKS OF INTENSE RADIATION "CURED" IT,BUT WHAT HAS FOLLOWED HAS BEEN INTENSE: TINNITUS, NO SALIVA AFFECTING MY DENTITION AND STARTING 5 YEARS AGO NEUROPATHY IN BOTH FEET WHICH HAS AFFECTED MY MOBILITY. AM CURIOUS HOW THE MD KNEW OF CONNECTION BETWEEN TREATMENT AND NEUROPATHY.tomalexander said:Hi! Can I ever relate to your message. Was diagnosed in Dec of 2001 with stage III nasopharangeal cancer. Began chemo and radiation in Feb 2002 and treatments stopped in June 2002.
I am nowhere near your fifteen year survival, but my last two pet scans have shown no trace of cancer! My longest lasting effects are peripheral neuropathy(pronounced tingling and numbness in both feet), and having to drink a lot more liquid to help swallowing when eating. Chemo doc said the neuropathy may or may not go away, but guess I should nnot gripe too much since I am still here.
Messages from long term survivors llike yourself are reassuring to the rest of us. Glad to see you are doing so well, and I hope and pray you continue to improve.0 -
ARE YOU A BETTER OR WORSE PERSON FOR HAVING GONE TO HELL AND BACK? DO YOU APPRECIATE YOUR LIFE AND THOSE AROUND YOU MORE OR LESS THAN BEFORE? NOW THAT YOU KNOW THAT YOU ARE VULNERABLE TO "C", HAVE YOU CHANGED YOUR LIFESTYLE?mercedes280sl said:Keep the faith. It's not easy and it certainly isn't fair, but it can be beaten. I was diagnosed with lymphoepithelioma in Apr 1986 after being misdiagnosed for more than two years. The sinus cancer was so progressed that I was not expected to survive, but here I am, 18 years later. At 34 years old, I'm cancer free. The agressive treatment needed to eradicate the cancer has left me with some issues, but I'm here to **** about them. I certainly don't understand life, but I subscribe to the theory that everything must happen for a reason. Of course that doesn't keep the random chaos of life from pissing me off. But alas...I'm here. If anyone wants to chat, feel free to send me an email.
We're all in this together.0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 121.8K Cancer specific
- 2.8K Anal Cancer
- 446 Bladder Cancer
- 309 Bone Cancers
- 1.6K Brain Cancer
- 28.5K Breast Cancer
- 397 Childhood Cancers
- 27.9K Colorectal Cancer
- 4.6K Esophageal Cancer
- 1.2K Gynecological Cancers (other than ovarian and uterine)
- 13K Head and Neck Cancer
- 6.4K Kidney Cancer
- 671 Leukemia
- 792 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 237 Multiple Myeloma
- 7.1K Ovarian Cancer
- 61 Pancreatic Cancer
- 487 Peritoneal Cancer
- 5.5K Prostate Cancer
- 1.2K Rare and Other Cancers
- 539 Sarcoma
- 730 Skin Cancer
- 653 Stomach Cancer
- 191 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.8K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards