Guess I didn't get the memo about ALL the posts being moved to the archive. Ouch. Here's hoping everybody catches on pretty quick.
gosh, things have changed.
how do we post a new topic?
just replying to see if this works
talian..just clik on view all topics, then look at the top of the topics, you'll see a spot that says "create new topic'
Testing the anonymous reply.
I don't really like this, although I'll try not to be judgemental yet.
I've been following this website for quite a while, but am just now jumping in because, Charlie S., I 'm glad to see you back. Over the past year, I've been informed, comforted, moved and enlightened by you and many others on this board. So glad you are all here.
Diagnosed 8/08, now at Stage IIC w/ met. to just one lymph node, finished induction phase of interferon in 1/10, but was too sick to continue. NED at this time - just holding on, hoping for the best and grateful to be alive and feeling well today! I'm sticking with you guys because you are smart!
just testing to see if I m doing it right?
Sharon in Reno
To Thy Own Self Be True & Move Fast When You "Know" You Have To!!
Good to hear from you Charlie S. I am still quite confused by the new forum and inching my way through it.
looks like everything is working.
Bill from Illinois
Stage IV Spine Mets, brain mets ans subq mets.
starting whole brain radiation on 11/8 and then compassionate use IPI ASAP.
This does take getting use to - I like that Charlie has a picture makes it more personal, assuming that is a picture of you, charlie? would be interesting if more did that put faces to the names
Yes, that is my true picture, just without eyeglasses. I was sailing when that pic was taken.
Charlie you did your best and didn't get paid a dime(at least I would like to think that, so don't say anything if you did)
Insert Generic Inspirational Motto Here
I was only a small participant in the process and not and principle and no I didn't get even a nickle, let alone a dime; truth be known, I was really only thrown a bone.
I see you know how to read between the lines.......................I DO hold nothing but good wishes though.
Now if we can only turn it around to being a melanoma patients information board rather than a forum on how do you use this site.
Thanks for all your diligent work Charles. I have been learning (other things) on computer all day, so this is just another problem on my list of things that are changing in my life. If an old dog like you can adjust, I should be able to as well....One good thing about getting old is that I can hardly remember what the old board looked like..LOL...now I am going to try to get on chat...
Squeeze Page Designer
Landing Page Designer
Are all the posts for the past 17 years in one archive now? Are is there a second archive been started?
Meet and talk to others about melanoma in our forums:
See also: History of the MPIP Forum
–CURE OM Forum
Questions to Ask Your Doctor
Email the MRF Nurse
Get matched with a Phone Buddy
View the Melanoma Glossary
Get updates on melanoma research, education & advocacy
Raise awareness and funds to fight melanoma by participating in a Miles for Melanoma 5k walk/run this year!
Find a Miles for Melanoma event near you.
Patient Helpline: (877) 673-6460
1411 K Street, NW Suite 800
Washington, DC 20005
(800) 673-1290 Office
(202) 347-9678 Fax
The Melanoma Research Foundation (MRF) is leading the melanoma community to transform melanoma from one of the deadliest cancers to one of the most treatable through research, education and advocacy.
The Melanoma Research Foundation is a 501(c)(3) non-profit organization.