← Return to Parsonage turner syndrome *
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Brain & Nervous System | Last Active: Aug 4 7:56am | Replies (239)
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Replies to "Would love to connect with people who are suffering from Parsonage Turner Syndrome. Would like to..."
Hi, @smf - just wanted to let you know I did move your post here as @johnbishop suggested to this existing discussion on Parsonage Turner Syndrome so you can connect with others on how they are coping and what progress one can expect. Hoping @kgoodwin9 @jjspokane61 @11b20 @adriennes @elained @richman54660 and others will have some thoughts for you.
When were you diagnosed with Parsonage Turner Syndrome, @smf? What have you found particularly useful in managing your condition thus far?
Hello @smf, welcome to Mayo Clinic Connect. There is already a discussion for Parsonage Turner Syndrome. I'm tagging our moderator @lisalucier to see if we can move your post and combine it with the following discussion where you will meet other members discussing Parsonage Turner Syndrome.
> Groups > Brain & Nervous System > Parsonage turner syndrome *
-- https://connect.mayoclinic.org/discussion/parsonage-turner-syndrome/
May I ask if your doctor shared any suggestions for treatment or therapy with you?