Fabry Support (@fabrydisease2) 's Twitter Profile
Fabry Support

@fabrydisease2

An account made for anyone with an interest in Fabry Disease. To share information and experiences, ask questions and raise awareness!!

ID: 1095133046

calendar_today16-01-2013 12:56:09

1,1K Tweet

1,1K Followers

1,1K Following

Fabry, Australia (@fabryaustralia) 's Twitter Profile Photo

While this article is not specifically about Fabry Disease, but if you've ever felt you've been judged for your... fb.me/6cd4SfQDM

Sabina Kineen (@sabkin12) 's Twitter Profile Photo

Thank you FSIG & other Patient Advocacy groups for working hard on our behalf! #FabryDisease #PatientAdvocacy #Medicare #Medicaid x.com/fabryorg/statu…

Raremark (@raremarkhealth) 's Twitter Profile Photo

A 41-year-old shares his story of how his signs of #FabryDisease were missed by doctors in several countries. raremark.com/fabry-disease/…

A 41-year-old shares his story of how his signs of #FabryDisease were missed by doctors in several countries. raremark.com/fabry-disease/…
Fabry, Australia (@fabryaustralia) 's Twitter Profile Photo

Have you been diagnosed with Fabry Disease? Researchers at The Royal Melbourne Hospital are investigating several... fb.me/2gJjWzmAa

Fabry, Australia (@fabryaustralia) 's Twitter Profile Photo

Shire has developed a series of short films about a family from Argentina who are living with Fabry disease. This... fb.me/v7Sg4mEU

Rare Diseases (@checkorphan) 's Twitter Profile Photo

#Fabry #disease #symptoms? clusters of small, dark red spots on the skin called angiokeratomas; a decreased ability to sweat (hypohidrosis) and more here bit.ly/2y4Rk42 #researched by @SanofiGenzyme Sanofi Sanofi US Fabry Support Nat Fabry Diseas Fdn RareConnect Rare

Bernard Dan (@profbernarddan) 's Twitter Profile Photo

Very clear update on new treatments for #lysosomal diseases, including enzyme replacement, small molecules, and #GeneTherapy - and perspectives for the near future #mucopolysaccharidosis Gaucher's Disease Fabry Support #niemannpick National Organization for Rare Disorders (NORD) onlinelibrary.wiley.com/doi/10.1111/dm…

Very clear update on new treatments for #lysosomal diseases, including enzyme replacement, small molecules, and #GeneTherapy - and perspectives for the near future #mucopolysaccharidosis <a href="/GaucherDisease/">Gaucher's Disease</a> <a href="/FabryDisease2/">Fabry Support</a> #niemannpick <a href="/RareDiseases/">National Organization for Rare Disorders (NORD)</a> onlinelibrary.wiley.com/doi/10.1111/dm…
Rare Diseases (@checkorphan) 's Twitter Profile Photo

#Fabry #disease #fact - All #male and #female #children of an #affected #female have a 50% chance of #inheriting the #defective #gene from their #mother. Click here for more info - bit.ly/2y4Rk42 #researched by @SanofiGenzyme Fabry Support Nat Fabry Diseas Fdn National Organization for Rare Disorders (NORD)

Patient Worthy (@patientworthy) 's Twitter Profile Photo

The FDA Just Approved the New Drug Application for Migalastat, a Treatment For Fabry Disease bit.ly/2GwapNM #FabryDisease #LysosomalStorageDisease Fabry Support

Nat Fabry Diseas Fdn (@fabrydisease1) 's Twitter Profile Photo

Fabry Disease Awareness Month Day #5 - According to the Human Genetic Mutation Database there are over 900 known Fabry disease mutations so far. About 70% are missense and nonsense mutations. See facebook.com/FabryDisease.