Hi my name is Michelle and my MIL Pamela of New Hampshire was on BCMEts. She passed aways last Feb with complications.
Anyway I have started a non profit in her name and would like some feedback if I may.
I donate new/used wigs to people going through treatments that have no insurance of funds. And have or will be opening an account for the donations I wanted to originally pay for treatments for people with no insurance or money but I don't have any money yet and treatments as you know can cost thousands of dollars so I wanted to do something else for them maybe manicure,facial certificates or maybe a gift basket what do you think? What should I put in them. I already have a selection of hats to choose from aswell and am trying to get really soft cotton shirts for after radiation my MIL has chest wall mets and I remember how painful it was for her so thought it may be a good idea. Any  suggestions would be so wonderful.

I am a bc mets cancer patient. I was diagnosed with bc almost 18 years ago at the age of 35. Two years ago this month I was diagnosed with bc mets to the bone.  I had radiation and began Femara and monthly Aredia treatments. After about 4 months on Femara I was classified by my Onc. as being in complete remission. Although I don't look at "remission" as a permanent situation, I have not felt comfortable in participating in many online groups because this disease has hit many other women so hard.  However, I too need support sometimes and I would like to offer my friendship with my sisters.

zip

I am Susan Andrews. 42yrs old. Triple Neg Stage4 in Jan 04. I found my lump in Oct 03. I'm currently NED since May of 2004, yay. Hope this gives someone encouragement.