Information and Support for MPD's
Our Personal Journey With a Myeloproliferative Disease
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10 Comments
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Mary (Webmaster)
11:30 AM on August 18, 2009
You can find new LINKS on the Links page, and also in the sidebar. Very imformative information there.
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Helena
03:56 AM on May 20, 2008
Hi. it was nice to find your pages with lot of information. I was diagnosed 4 years ago and have used Interferon Alfa (IntronA) 3 years. This was the first site, where I have seen info of Peg interferon. By the way, I live in Finland. Thanks for a nice website.
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lindatunstall
06:28 PM on January 30, 2008
Mary/John, thanks for informing me of this web site. I look forward to sharing info with you and others that are participating in this venture.
Linda
Linda
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Michael
01:17 AM on January 15, 2008
Thank you for the information about your site. We look forward to learning more and hearing from others like us. Diagnosed PV 1/2/08.
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From Mary, Webmaster
10:14 AM on January 13, 2008
You can find lots of links on my Links page. I would love for the forum on my site to be productive, so feel free to start a discussion.
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karen
11:01 PM on January 12, 2008
Hello. I'm recently diagnosed with PV and am located in Australia. I've not been able to locate a support group or chat room here and hope I can participate from "Down Under"
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Janet
02:32 AM on January 12, 2008
Thanks for this website....I was diagnosed in Oct of 2007 and have been looking for support groups for this. I have not been able to find any with people in them that post often. It would be nice to find more people and more information about this disease.
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Brad B
03:07 PM on January 10, 2008
Thanks for putting this site together!! I have MPD unclassified, there are not enough sites about MPD out there!
Reply
Jennifer Bair
03:32 PM on December 03, 2007
Hi Mary~This is a nice website.Thank you for doing this.
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