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Myasthenia Gravis Society
Helping patients with myasthenia gravis. Myasthenia Gravis Society has made great strides in the fight against myasthenia. When the diagnosis is made, patients are often filled with fear, anxiety, limitations, frustration, depression, and anger, but when myasthenics gather to seek information, they hear the collective voice of the MG community offering advice, sharing experiences and providing emotional support. It is our aim to assist patients in this journey. Current Research in MG.
Myasthenia Gravis WA Friends and Support Group - Myasthenia Gravis- Western Australia
If you can see this you browser does not support iframes. Please upgrade your web browser. FEEDBACK: submit your comments/experiences related to. Drugs and Myasthenia Gravis here. 2005-2009 Myasthenia Gravis Friends and Support Group WA.
Myaware Kids – UK & Ireland
Committee & AGM. 8216;myaware kids’. Myaware, the Charity. Committee & AGM – Archived. Paris to Florence – Tom’s Epic Bike Ride. Radio Newcastle – Raising Awareness. Physiotherapy for childhood myasthenia. Speech & Language, and Feeding Therapy. Toby, Acetylcholine Receptor Deficiency. Ellen, unknown gene fault. Charlie, unknown gene fault. Living without a diagnosed condition…. Naomi’s Story – On the inside of a Myasthenic Crisis. Bringing families with myasthenia together. Paris to Florence - June 2013.
MGCC | Strengthening our connections
The Myasthenia Gravis Coalition of Canada. MGCC) is a non-profit organization comprised of Canadian associations, support groups and healthcare professionals dedicated to providing support and assistance to those living with myasthenia gravis, and is committed to increasing knowledge and awareness of MG in both public and professional communities. Together we are creating a strong national voice for myasthenia gravis in Canada. MGCC – Strengthening Our Connections. We invite you to contact us:.
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myasthenie-und-seele.de
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Myasthenie.com - Portail
Association francophone dédiée aux malades de la Myasthénie et à leurs familles. Page Facebook de l'Association. Informations sur la maladie. Centres de compétence MNM. Centres de compétence MNM. Centres de compétence MNM. Site de discussion et d'entre-aide de l'association AMIS. Bienvenue sur le site de. L’Association des Myasthéniques Isolés et Solidaires. 40;les amI.S.)! Nous sommes un groupe de personnes malades et leurs proches regroupant plus de 2000 inscrits dans l’espace francophone. Ce nouveau f...
Myasthenie.fr
Site d'information sur la myasthénie édité par l'Association des Myasthéniques Isolés et Solidaires (les amI.S.). Qu’est ce que la Myasthénie? Stress et maladies neuromusculaires. Signes et symptômes cliniques. Classification de la Myasthénie. La cure d’Immunoglobuline Humaine. Le rituximab (MabThéra ou Rituxan ). L’Automédication et ses risques. Médicaments par familles thérapeutiques. Médicaments par dénomination commune internationale. La MG en 30 questions. Vivre avec la MG. La mise en invalidité.
myasthenie.miacuisine.over-blog.com
Ma vie avec la myasthénie - La myasthénie est une maladie neurologique rare. Ce blog parle de ma vie au quotidien avec cette maladie.
Ma vie avec la myasthénie. La myasthénie est une maladie neurologique rare. Ce blog parle de ma vie au quotidien avec cette maladie. Journée internationale des maladies rares 2013. La sixième édition de la journée internationale des maladies rares a lieu le 28 février 2013 dans 60 pays. Une maladie est considérée comme rare si elle touche moins de 1 personne sur 2000. A ce jour, plus de 6000 maladies rares sont connues et 5 nouvelles. 29/02 Journée Mondiale des maladies rares. Ensemble contre le cancer!
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