fmdchat.blogspot.com
FMD Chat - Fibromuscular Dysplasia SupportFMD Chat is an international nonprofit organization dedicated to supporting those affected by fibromuscular dysplasia.
http://fmdchat.blogspot.com/
FMD Chat is an international nonprofit organization dedicated to supporting those affected by fibromuscular dysplasia.
http://fmdchat.blogspot.com/
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FMD Chat - Fibromuscular Dysplasia Support | fmdchat.blogspot.com Reviews
https://fmdchat.blogspot.com
FMD Chat is an international nonprofit organization dedicated to supporting those affected by fibromuscular dysplasia.
Riander Blog: Learning from ePatient( scholar)s
http://riander.blogspot.com/2013/09/learning-from-epatient-scholars.html
On Experience Design Practice, Management, and Organizational Strategy. Thursday, September 19, 2013. Learning from ePatient( scholar)s. A version of this post has been published as an interactions magazine blog post. Increasingly, patients are making invaluable contributions to the redesign of our broken healthcare system and the patient experience. Designers working in healthcare should be aware of and leverage these contributions. Among the facilitators of this is Medicine X. EPatient scholar: 1. ...
fibromusculardysplasia.blogspot.com
Fibromuscular Dysplasia: Patients Advocate for Rare Disease Research in Washington D.C. for Rare Disease Week
http://fibromusculardysplasia.blogspot.com/2014/02/patients-advocate-for-our-rare-disease.html
An informal place to help support people afflicted with FMD. Monday, February 24, 2014. Patients Advocate for Rare Disease Research in Washington D.C. for Rare Disease Week. Dr Francis S. Collins,. With this petition of over 10,000 signatures. Thank you to FMD Chat. For printing and delivering our petition to Washington D.C. Special thank you to Rare Disease Patients: Sarah Kucharski, Fran Saplis RN, and Judy Brown for delivering our petition! Croatian Alliance for Rare Diseases. The Joe Niekro Foundation.
SCAD Research, Inc Spontaneous Coronary Artery Dissection | Support & Additional Information
http://www.scadresearch.org/about/support-additional-information
Spontaneous Coronary Artery Dissection. The Scientific Advisory Committee. Mayo Clinic SCAD Research Program. Support & Additional Information. Participating in SCAD Research. Be a Part of the Solution. 5k SCADaddle Events Schedule. 2016 West Coast 5k SCADaddle for Research. 2016 Pennsylvania 5K SCADaddle for Research and Cocktail Reception. 2016 New Jersey 5k SCADaddle. 2016 National 5k SCADaddle. 2016 Aussie 5km SCADaddles. 2015 West Coast 5k SCADaddle. 2015 National 5k SCADaddle. Reunions Help Us Heal.
myreallifeunnecessarynightmare.blogspot.com
My Real Life, Unnecessary Nightmare: Learning from ePatient( scholar)s
http://myreallifeunnecessarynightmare.blogspot.com/2013/09/learning-from-epatient-scholars.html
My Real Life, Unnecessary Nightmare. The tale of: a parasite infection of my body and brain; how "friends," family, and medical professionals helped contribute to it largely destroying my life; and (reflections on) what I've done and has happened to me since then. Thursday, September 19, 2013. Learning from ePatient( scholar)s. A version of this post has been published as an interactions. Among the facilitators of this is Medicine X. To fulfill this goal, Medicine X invites select ePatient scholar applic...
myreallifeunnecessarynightmare.blogspot.com
My Real Life, Unnecessary Nightmare: September 2013
http://myreallifeunnecessarynightmare.blogspot.com/2013_09_01_archive.html
My Real Life, Unnecessary Nightmare. The tale of: a parasite infection of my body and brain; how "friends," family, and medical professionals helped contribute to it largely destroying my life; and (reflections on) what I've done and has happened to me since then. Thursday, September 19, 2013. Learning from ePatient( scholar)s. A version of this post has been published as an interactions. Among the facilitators of this is Medicine X. To fulfill this goal, Medicine X invites select ePatient scholar applic...
fibromusculardysplasia.blogspot.com
Fibromuscular Dysplasia: Update from Washington DC Rare Disease Day 2014
http://fibromusculardysplasia.blogspot.com/2014/02/hot-of-press-from-washington-dc-rare.html
An informal place to help support people afflicted with FMD. Friday, February 28, 2014. Update from Washington DC Rare Disease Day 2014. It is with great joy to announce that today Dr. Collins, NIH Director was presented our petition on behalf of Fibromuscular Dysplasia, Ehlers-Danlos Syndrome, Marfans and Sticklers. The petition was hand delivered in Washington DC by Sarah. Kucharski, Patient and Founder of FMD Chat. And Fran Richmond Saplis. Patient and Advisor to FMDChat. View my complete profile.
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Blog de FMDCC - Mon Skyblog (FMDCC) - Skyrock.com
Mot de passe :. J'ai oublié mon mot de passe. Un blog avec pas mal de clip, video,. Et un peu de moi. Mise à jour :. Abonne-toi à mon blog! Sebastien Leger and Chris Lake - Aqualight. Ajouter cette vidéo à mon blog. N'oublie pas que les propos injurieux, racistes, etc. sont interdits par les conditions générales d'utilisation de Skyrock et que tu peux être identifié par ton adresse internet (67.219.144.114) si quelqu'un porte plainte. Ou poster avec :. Posté le lundi 26 février 2007 10:07. Retape dans le...
www.fmdceducation.com coming soon!
This domain is parked free, courtesy of. Is this your domain? Add hosting, email and more. Enter a domain name:. See how Business Registration. Is one of the most affordable advertising investments you can make! Starting at just $2.99/mo. Use of this Site is subject to express Terms of Use. By using this Site, you signify that you agree to be bound by these Terms of Use. Which were last revised on.
FMD Chat - Fibromuscular Dysplasia Support
Fibromuscular dysplasia support, education and advocacy. Traduire / Traducir / Verdolmetschen / Natłumaczyć / Tulkot / переводить / 翻译. Lighting Up The Night For Rare Disease Patients. The North Carolina Rare Disease Advisory Council is calling on state residents to join in celebrating Rare Disease Day at the end of February. Feb 28 as Rare Disease Day in North Carolina. Establishing the Advisory Council on Rare Diseases housed within the School of Medicine at UNC Chapel Hill in 2015. The councilR...
FMD Chat - Fibromuscular Dysplasia Support
Fibromuscular dysplasia support, education and advocacy. Traduire / Traducir / Verdolmetschen / Natłumaczyć / Tulkot / переводить / 翻译. It's Rare Disease Week in Washington! The world marks Rare Disease Day. On Feb. 29, 2016 and fibromuscular dysplasia patients will be in Washington, D.C. to increase awareness of the disease and policies impacting the rare community. Rare Disease Week on Capitol Hill. And the National Institutes of Health (NIH) Clinical Center. Is free, and a live webcast. Connections Be...
FMDchat | We know the famous game together
Angry Birds 2 Reviews: very cool. Since there is no restart highlight, then every stride that you do will be extremely compelling in your life to play. Coming up short on cards will be viewed as the same as surrender that implies you fizzled in finishing these levels and the lives of less one. It sounds really muddled and I must concede, Angry Birds 2 is recognizably multiplied to make ‘his Angry’. Posted in Game reviews. Utilization Boom Beach Diamonds Wisely. Investigate and Build a Radar. When you can...
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