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Has anyone with AIHA received the COVID vaccine? Reactions?
Has anyone with AIHA received the COVID vaccine? Any autoimmune issues?
Hello @gailiebird and welcome to Mayo Clinic Connect, where members get and give support. I can see that you are interested in connecting with members who may be able to share information on the COVID vaccine and potential reactions due to AIHA. Members such as @gg17 and @whoey have both mentioned associations with AHIA and might be able to share more with you depending if they've received the vaccine.
Are you scheduled to receive the vaccine?
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I'm on covid-19 vaccine waiting list and expect to be scheduled soon. After catching a cold a couple of winters ago my hemoglobin dropped and I required Rituxan transfusions to get it under control. I'm currently able to control AIHA with steroids but concerned how the vaccine may cause my autoimmune system to go in overdrive.
Hi! My rheumatologist said that I will have a huge flare up that will make me feel like I need to go to the ER but “ I must remember that it’s a reaction from the vaccination and the flare will be severe but just remember that you’ll live” wonderful advice! Lol!! But that is what I’m told. I’m on the waitlist…..still.. I have RA, Sjögren syndrome and HEP C ( unaware of how/where that came from. So, as for your question: except pain, inflammation etc. at its worst for 1-2 weeks. ( I can’t wait!!)
@gailiebird I understand your being anxious about your disease and the vaccine. I was nervous, too, but my oncologist and neurologist were thrilled that I had it. No reactions, thank heavens! But, I know we’re all different.
Have you talked with any of your doctors about the vaccine?
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