The Cancer Survivors Network (CSN) is a peer support community for cancer patients, survivors, caregivers, families, and friends! CSN is a safe place to connect with others who share your interests and experiences.
Thank you for being a part of the Cancer Survivor Network community. Survivors and caregivers like you have played a unique role in fostering an online environment that encourages connection among those needing support, community, and education. On May 28, the Network will be discontinued. More details are available here . If you have any questions, contact CSNSupportTeam@cancer.org. Thanks again for the support you’ve provided each other over the years. We remain committed to supporting you in other ways throughout your cancer journey.
terrified of recurrence
inkognita
CSN Member Posts: 9
My initial melanoma was diagnosed approx. 4 years ago. A wide excision was performed with clear margins, and I was told there was a 95% chance it would never recur. However, about 9 months later, a lymph node popped up and was positive for melanoma. A radical lymph node dissection was performed with an additional positive node. I began Interferon therapy but was only able to take about 1/4 of the full year course due to impending liver failure (not a typical reaction). I was told there was about a 70% chance of recurrence. At my checkup last week, my liver enzymes were very abnormal and I am scheduled to undergo an abdominal CT on Friday to rule out recurrence, this time in the liver area. Does the terror ever get any better? I am so paranoid about recurrence and the very limited treatment options available to me. I have many other health problems which also complicate the situation. Can anyone help me with this feeling of panic?
Comments
-
It is frightening but it does get better...slowly but surely. Knowledge and laughter I think are key. I went to comedy shops and things of that nature to "force" laughter and to force the thoughts of cancer from my head. I also joined a melanoma support group and over time became a senior member of the group and felt great comfort in knowing that I could help the newly diagnosed find information, show them a living example of someone who has had stage 3 melanoma since July '99. If you ever want to chat via e-mail, messenger programs or the phone I am more than happy to do so. My e-mail address is gnail@sky.net.
-
Hello, I realize you posted this months ago, but I haven't been on the message board. If you would like to write me at hpydncr@earthlink.net, I can give you a support group of hundreds of melanoma patients who communicate daily by email. It is a group of people unlike any I have ever known and the information is up to date. Good luck. Linda Talbott
-
Discussion Boards
- All Discussion Boards
- 7 Cancer Survivors Network Information
- 6 Welcome to CSN
- 1 CSN Update
- 122.7K Cancer specific
- 2.8K Anal Cancer
- 457 Bladder Cancer
- 311 Bone Cancers
- 1.7K Brain Cancer
- 28.6K Breast Cancer
- 410 Childhood Cancers
- 28K Colorectal Cancer
- 4.6K Esophageal Cancer
- 1.2K Gynecological Cancers (other than ovarian and uterine)
- 13.1K Head and Neck Cancer
- 6.4K Kidney Cancer
- 682 Leukemia
- 805 Liver Cancer
- 4.2K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 243 Multiple Myeloma
- 7.2K Ovarian Cancer
- 71 Pancreatic Cancer
- 493 Peritoneal Cancer
- 5.7K Prostate Cancer
- 1.2K Rare and Other Cancers
- 544 Sarcoma
- 745 Skin Cancer
- 662 Stomach Cancer
- 194 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.9K Uterine/Endometrial Cancer
- 6.5K Lifestyle Discussion Boards

