Newly diagnosed
Hi all,
I was diagnosed with relapsing remitting in December of 2021.
Feeling a bit abandoned after going through so many appointments and tests last winter to checking in once or twice a year going forward. I am on Ocrevus, next infusion is in August.
I am grateful for the appointments and care I was shown at the MS Clinic at Mayo in Rochester, Minnesota but had anyone else felt abandoned after the initial diagnosis?
Thanks,
Keke
Yes totally get what you are saying, that is one reason why I resorted to looking up information online and visiting this forum.
Okay, thank you. Sometimes it can be so isolating so I’m very glad to have found this forum.