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What's The Most Important Thing You Learned About Living With AIHA This Past Year?
I was diagnosed in September 2022 with Cold Agglutinin Disease and AIHI. Rheumatoid Arthritis diagnosis a few years ago.
I can relate to making choices of what I am able to do based on how I feel. I feel like I'm letting my friends and family down when I cannot attend pre-planned events etc from my Husband's Christmas party to meeting a friend for coffee.
I have to make decisions /choices each day about the activities I can participate in. It often depends on how well I slept the night before.
My Question For The Team: Has Anyone Here Had Any Actual Experience As A Recipient Of Rituximab Intravenous Infusion?
I Was Diagnosed With Warm Aiha Earlier This Year. Do You Find That Hot Weather Makes Your Feel Worse?
What Experience Have Members Here Had With The Use Of Oral Prednisolone?
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