I understand if you go on Facebook the admin who created “multiple myeloma warrior community” actually set this up to help us with different drs., hospitals, information for us he actually has a video on the page explaining all about this project. There’s also a research company doing research on blood plasma I just signed up and I won’t find out for several weeks if I can donate my plasma or not. But they paid me $100 just for drawing my blood 🤷🏼‍♀️🤷🏼‍♀️🤷🏼‍♀️. They’re trying so hard to find a cure for this disease. I know it probably won’t help me but if someone else down the road benefits then it’s well worth trying.

FYI to all in regards to this site for Polygon Health, I put my story on my pin yesterday. I feel the more information that is provided by each of us, the more strides can be made to find a cure, maybe not for me, but for others in the future. The more cures we can find for disease the better for us all.

I’m in that group too! They don’t seem to be as active as Alan’s group and he’s very involved with different organizations that are trying to find a cure for MM. also he’s trying to help us find people who live close to each other for support or just communication.

I forgot the admins name is “Alan Stephenson”. A really nice guy and very knowledgeable.

I did it...hoping it's ok. Merri,I'm sorry that I am ...questioning. Trust is not my best asset these days