I have PV and don't look sick but I fight to do everything I do.
on 5 May, 2018
NCCN is hosting two different MPN Patient webinars at the beginning of may. Dont miss it.
on 28 April, 2018
Other MPN Resources.
Denial, Anger. Bargaining, Sadness and Acceptance, My stages of grief realized.
Today marked my monthly visit with oncology, Today we start a new journey in this fight.
Found this NCCN Guideline for MPNs today. I think it is a pretty good resource.
It has been a while since my last post thanks to a very busy holiday season. So here is some news, updates and information on my MPN.
My reflection and take on the Voices of MPN live event in Charlotte, NC
Our mission here at MPNjourney.com is to provide a place for people to share their journey with myeloproliferative neoplasms, while at the same time helping to educate about this orphaned blood cancer.
Read along and share with our family and friends. We welcome you and hope to see you more often.
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