Welcome to the story of My Meniere’s Diagnosis
June 6, 2008 6:31 pm General Site InfoI don’t expect this site to JUST be about my being diagnosed with Meniere’s Disease. I do expect to provide resources that may be of use if you have, or suspect you have Meniere’s disease. I also want to explore some of the things that I’ve learned through all of this. Thanks for visiting, please come back soon!
May 2nd, 2011 at 1:20 am
My husband may have this….has been on Prednisone for a week, has one more week to go until he sees the Dr again. He doesn’t think it’s working, but i wonder if it’s even been long enough. When/If did you notice a difference after taking it?
Thanks, Erica
May 2nd, 2011 at 11:18 am
It seems every time I’ve been on prednasone it’s been a
slightly different experience. The first time I had a clear
improvement from taking prednasone it was a 25mg dose shortly after
onset of symptoms (then stepping down to 20, 15, 10, 5 consecutive
days if I recall correctly.)
These days I’m on prednasone low dose (5mg daily) for rheumatoid
arthritis and have not been having too many vertigo issues. I’ve also
been getting allergy shots which seemed to have helped my trigger.
One of the keys to being able to manage it is to try to figure out
what triggers attacks for you. Allergies/diet/etc….
Good luck to you and your husband, I know it can be difficult finding
answers and will keep you in my thoughts and prayers…
Avery