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April 17, 2010
1 person found this review helpful

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April 17, 2010
1 person found this review helpful

The MPD Foundation reached out to me after I found its website. I was newly-diagnosed with Polycythemia Vera and had many questions and fears. It maintains a resource-rich website with links to the latest in research and education. The Board chair and staff have provided me wonderful guidance and support. MPD Foundation financially supports research for these rare MPDs as well as patient advocacy. We are fortunate to have this organization and I will continue to support its mission.

The Great!

I've personally experienced the results of this organization in...

its funding of important research for cures that otherwise would not occur.

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What I've enjoyed the most about my experience with this nonprofit is...

it is my first stop for information on the latest MPD research. Through the website, I've connected with internet support groups comprised of patients around the world. This offers shared learning, support, and encouragement.

The kinds of staff and volunteers that I met were...

knowledgeable, supportive, and kind. They understand the challenges of living with an MPD and are great advocates for further research for cures.

How frequently have you been involved with the organization?

About every six months

When was your last experience with this nonprofit?

2010

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