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Severe Allergy to Paxlovid

Post-COVID Recovery & COVID-19 | Last Active: Feb 10 9:20pm | Replies (41)

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@colleenyoung

I understand the frustration and the desperation. It is hard to imagine your exhaustion living with CFS, not being able to sleep and dealing with this persistent allergic reaction.

I know you are looking to talk to others who have made similar experiences. Some members have talked about allergic reactions related to COVID, albeit not necessarily to Paxlovid, in these discussions:
- Newly developed allergies, excema in ears
https://connect.mayoclinic.org/discussion/newly-developed-allergies-excema-in-ears/
- Post COVID skin conditions: What can I do to control the reactions?
https://connect.mayoclinic.org/discussion/post-covid-skin-conditions/
- Post covid itch and hives
https://connect.mayoclinic.org/discussion/post-covid-itch-and-hives/
- Post COVID-19 skin reactions: anyone else?
https://connect.mayoclinic.org/discussion/covid-19-skin-conditions/
Venting and being emotional is a-okay here. You've got a lot going on and finding answers is really hard work.

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Replies to "I understand the frustration and the desperation. It is hard to imagine your exhaustion living with..."

The work of finding answers is NOT only hard work but a FULL TIME JOB.

Contact Joeswfl(@joeswlf On Mayo clinic connect LC support grp. He sent me 3 articles that I found very helpful and interesting. Mast cell activation diseases. Hope they help you. I too am a 46 YR. CFS/ME Survivor and now LC on top of this. Very overwhelming. I agree with you. Hang in there. WE are there for you. Keep us posted.