u give urticaria a face
Thanks to all of you who have posted your picture... Urticaria patients in Africa and Asia? Let us know you're out there. You are not alone... Post your pics: http://urticariaday.org/face/
Քրոնիկ եղնջացանը Հայաստանում ևս աճող և միաժամանակ՝ թերագնահատված խնդիր է: Հուսով եմ՝ եղնջացանի օրվան նվիրված միջոցառումները կբարձրացնեն հանրության իրազեկվածության մակարդակը և կստիպեն ավելի լուրջ մոտենալ այս խնդրին: The problem of Chronic urticaria is a raising and underestimated problem in Armenia. I hope, the events organized on Urticaria Day will raise the awareness of population and will help to take urticaria more seriously.
Emma Ivette Rolón de Puerto Rico, estuve sufriendo urticaria cronica desde 2010, estoy en Xolair desde julio 2014 y estoy libre de urticaria y estoy feliz. Pero que pasará cuando mi seguro medico no pueda pagar mi Xolair, regresará la urticaria?
My first Urticária reaction came when I was 7 years old, my parents did'nt know about it and came with fever, at the same time they gave me aspirin as they thought I had ony flu. With the time we found out I had Urticária..since then I never realised how difficult it would be understand and accept I had this until now. By the time I had few reactions, the strongest one during my living time on the UK for almost 3 months I was trying to discover why I had this...but then..just went away...I got back to my normal life..then after while I had another small reactions, until now. It's been almost 2 months that I have to take care of everything...what to eat, where to go, how to dress, and to do..get notes and try to discover all alternatives forms to slip out of this. I can not make plans for travel anymore, since I dont know if I might have and reaction at the place..during my flight, my trip or after...To be honest, anything they said might help, I am trying now...limes on the morning time , camomile tea , water, sport, open air places...I just wanted to understand why we have so much doctors interested at differente deseas..and urticaria still the same thing..every doctor I talk to says : the is no cure for this..you need to get to learn how to live with it... I am talking and sharing a bit more my experiences and now as I found this group of people I can at least see that I not alone!! I dont have friends that understand this , I have people that think is just some drama...could be sometimes ,but is hard to know that you ll need to get to learn how to live with this sometimes!
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