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The MPD Foundation Blog: August 2010
http://mpdfoundation.blogspot.com/2010_08_01_archive.html
Wednesday, August 18, 2010. MPD patients connect through social media. With increased access to and understanding of technology, people are finding their way online, searching out interests like cooking, basketball and even myelofibrosis. Once assumed to be the domain of the young and frivolous, a new group has turned to the internet as a means of learning about and connecting to what is important to them. This is. Especially true for patients with orphan diseases. Subscribe to: Posts (Atom). 23andMe MPN...
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The MPD Foundation Blog: April 2011
http://mpdfoundation.blogspot.com/2011_04_01_archive.html
Friday, April 15, 2011. Changing a name to fit the science. The MPD Foundation has changed its name to MPN Research Foundation. But don't worry; you'll still be able to reach us at our current web address and email addresses, at least for the foreseeable future. And consider giving the fact that this research is funded primarily by MPN patients around the world. They will be responsible for the next advancement in treatments. Subscribe to: Posts (Atom). This blog has moved! Promote Your Page Too. Septemb...
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The MPD Foundation Blog: Can Environmental Causes Be Behind Some Cases of Polycythemia Vera?
http://mpdfoundation.blogspot.com/2010/10/can-environmental-causes-be-behind-some.html
Friday, October 15, 2010. Can Environmental Causes Be Behind Some Cases of Polycythemia Vera? In August 2008, ATSDR and PADOH organized a. Meeting with a panel of experts in Philadelphia. Medical researchers, environmental scientists, and. Public health professionals met to review the findings. And recommend future studies. Four major. Research areas were identified: epidemiology,. Genetics/biomarkers, toxicology, and environmental. The PV cluster in Carbon, Luzerne and Schuylkill. This article appeared ...
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The MPD Foundation Blog: February 2011
http://mpdfoundation.blogspot.com/2011_02_01_archive.html
Wednesday, February 23, 2011. Spotlight on New Investigators. MPD Foundation's staff and board are constantly revisiting what it means to fund research that produces results. We look at the various ways the work we fund affects patients - from available treatments to increasing their understanding of the scientific underpinnings of their disorder. On that note we'd like to introduce some of our newest grant recipients:. Wei Tong, PhD, Children's Hospital of Pennsylvania. Dr Kawakami's project is titled "...
mpdfoundation.blogspot.com
The MPD Foundation Blog: Spotlight on New Investigators
http://mpdfoundation.blogspot.com/2011/02/spotlight-on-new-investigators.html
Wednesday, February 23, 2011. Spotlight on New Investigators. MPD Foundation's staff and board are constantly revisiting what it means to fund research that produces results. We look at the various ways the work we fund affects patients - from available treatments to increasing their understanding of the scientific underpinnings of their disorder. On that note we'd like to introduce some of our newest grant recipients:. Wei Tong, PhD, Children's Hospital of Pennsylvania. Dr Kawakami's project is titled "...
mpdfoundation.blogspot.com
The MPD Foundation Blog: Changing a name to fit the science
http://mpdfoundation.blogspot.com/2011/04/changing-name-to-fit-science.html
Friday, April 15, 2011. Changing a name to fit the science. The MPD Foundation has changed its name to MPN Research Foundation. But don't worry; you'll still be able to reach us at our current web address and email addresses, at least for the foreseeable future. And consider giving the fact that this research is funded primarily by MPN patients around the world. They will be responsible for the next advancement in treatments. Subscribe to: Post Comments (Atom). This blog has moved! Promote Your Page Too.
mpdfoundation.blogspot.com
The MPD Foundation Blog: July 2010
http://mpdfoundation.blogspot.com/2010_07_01_archive.html
Thursday, July 22, 2010. Meeting of the minds for MPD researchers. MPD Foundation grantees meet at ASH. Tuesday, July 13, 2010. MPD Foundation distributes brochures through NORD's Medical Meetings initiative. A benefit of membership in NORD is participation in their Medical Meetings initiative. As part of this program NORD collects and distributes brochures of member organizations to pertinent meetings. The MPD Foundation utilized this service by forwarding the MPD patient brochure. Friday, July 2, 2010.
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The MPD Foundation Blog: June 2010
http://mpdfoundation.blogspot.com/2010_06_01_archive.html
Monday, June 28, 2010. MPD Patient Symposia Educate and Empower. This fall, the MPD Foundation will host a symposium in San Diego, California. Please continue to check our Events page. For updates on the next MPD symposium. Wednesday, June 23, 2010. Our hope is that as research advances and more treatments are approved insurers and Medicare develop the flexibility to address orphan diseases like myeloproliferative disorders in a manner that works for patients. Friday, June 18, 2010. The MPD Foundation is...
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The MPD Foundation Blog: We have moved! Come join us at our new blog.
http://mpdfoundation.blogspot.com/2011/05/we-have-moved-come-join-us-at-our-new.html
Tuesday, May 10, 2011. Come join us at our new blog. Subscribe to: Post Comments (Atom). This blog has moved! MPD Foundation has changed its name to MPN Research Foundation. Continue reading about the world of MPN at mpnrf.blogspot.com. Promote Your Page Too. There was an error in this gadget. Come join us at our new blog. I'm Here for the Glamour. September is the month for Blood Cancer Awareness. Iron Jak: Bad Blood x 2. Life with Essential Thrombocytosis. 12/28/12 As time goes by. Trek for a Cure.
