I only just saw this thread today... thanks so much for getting it going because so much is related to awareness, education and sharing. I'm a 4 year ovarian cancer survivor, but am facing a recurrence. Tomorrow I'm having a CT and then possibly a PET. Then we're on to surgery and treatment. Of course, this could all be a lab mistake (wouldn't that be nice... but unrealistic). I'm like "let's get this party started... I have a cruise to go on in November."
Over the years, I've learned that sharing with other survivors is rather important. I'd love to make a plug here for The Wellness Community. As a single mom, this site enabled me to participate in an online support group without taking time from my son or my job.
I ditto the recommendation for the book
Chicken Soup for the Cancer Survivor. I would also recommend
The Wellness Community Guide to Fighting for Recovery from Cancer, written by Harold Benjamin (I knew I couldn't go wrong with that book... my DS' name is Benjamin Harold). The whole concept behind the book is being "patient active." Powerful stuff.
Anyway, re: hair loss and chemo... I lost hair everywhere (nice not having to shave legs and pits) and was down to my last few eyelashes and eyebrow hairs by the time I had my last treatment. Your mileage may vary.
NHAnne... from many former survivors, we feel like a headache is rarely seen as simply a headache; a backache is rarely just a backache. They are but we tend to worry a bit. It's hard to deal with sometimes, but the fact of the matter is that we're here, alive and kicking, to deal with it.
I'm glad to have stumbled across this thread. If anyone happens to have some extra pixie dust, could you please throw some my way?