Hi @coni, I moved your thread to this discussion as I think it may help better connect you with some great people to talk to who have gone through similar situations. I'm also tagging @lorimar89 and @annieg in the hopes that they may share some of their experiences with you.
I also wanted to welcome you to Connect, @mdmendel81! Have you also experienced facial paralysis?
Hello @elreid, Sorry that you haven't had any responses to your posts in this older discussion on Ramsay Hunt Syndrome. I thought I would share the following resources in case you haven't already seen them.
Hello @elreid, Sorry that you haven't had any responses to your posts in this older discussion on Ramsay Hunt Syndrome. I thought I would share the following resources in case you haven't already seen them.
Their experiences and treatment experiences.
Slight swelling. I do facial exercises and suck on a spoon to reduce the swelling.
Hello @elreid, Sorry that you haven't had any responses to your posts in this older discussion on Ramsay Hunt Syndrome. I thought I would share the following resources in case you haven't already seen them.
-- Ramsay Hunt Syndrome Foundation: https://www.ramsayhuntfoundation.org/
-- National Organization for Rare Disorders - Ramsay Hunt Syndrome:
https://rarediseases.org/rare-diseases/ramsay-hunt-syndrome/
I believe @mattey741 is still active in this discussion and hopefully will see your posts and respond.
Thank you John, very much appreciated.
Rgds, Matt.
Thanks John,
The information you have provided has been helpful. I definitely will follow up.
Thanks again
Larry
Yes I've been diagnosed with RHS. Any treatment information would be greatly appreciated.
Larry