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cgrammie2 avatar

Pachymeningitis: Anyone else?

Brain & Nervous System | Last Active: Nov 9 9:58am | Replies (122)

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Profile picture for Wendy @wendyaustralia

@77smith77
@gilby53

Dear @77smith77 and @gilby53
Thank you both for sharing more of your personal stories – it sounds like you have each been through such a lot in trying to find solutions.
I am currently waiting to hear from my neurologist regarding my own next steps, as the blood patch does not seem to have alleviated any of my pachymeningitis symptoms.
@gilby53 – I hope that your upcoming audiology and ophthalmology appointments give you some relief.
@77smith77 – you are right that there is a strong bond between Australians and Americans. My husband and I have been to the US multiple times, and have a number of US friends whom we hold dear.
Regards
Wendy

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Replies to "@77smith77 @gilby53 Dear @77smith77 and @gilby53 Thank you both for sharing more of your personal stories..."

@wendyaustralia Thanks so much for your response, Wendy. Just knowing that you and @77smith77 are out there--that there are others with pachymeningitis--brings me comfort. Thank you both for sharing your stories. I wish you both the best. I just celebrated my 72nd birthday on the 4th and am so very grateful that I remain as healthy as I do. God bless.