Hi Anna, Thanks for sharing your story. I’m glad you had a compassionate neurologist to explain it to you. How do we get the word out about #FND so others understand it better? I also have a blog about FND- http://FNDRecovery.com
Best wishes-Max
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Hi I think the way to get the word out about FND is for more people to talk about their experiences and to educate medical professionals, because they don't have all the answers. Let's face it, we are the ones with the condition so who better to teach and help others learn?


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Thank you so much for sharing

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You're most welcome x
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Yes I can very much relate to you post thanks for being an fnd voice


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I know! I live with fnd. J can't walk because of it. It's si difficult to explain to people. Thank you for this!
Hvala. Twitter će to iskoristiti za poboljšanje vaše vremenske crte. PoništiPoništi
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Tweet je nedostupan.
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Tweet je nedostupan.
Čini se da učitavanje traje već neko vrijeme.
Twitter je možda preopterećen ili ima kratkotrajnih poteškoća u radu. Pokušajte ponovno ili potražite dodatne informacije u odjeljku Status Twittera.
Living life with
Outspoken more than I should be..maybe..
I love to write about important topics, from my perspective 

