Bronchiectasis and Covid
I was just diagnosed with Covid/coronavirus and wondering about peoples experiences taking Paxlovid while on the Big 3.
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
I was just diagnosed with Covid/coronavirus and wondering about peoples experiences taking Paxlovid while on the Big 3.
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
I have mac and be. I got covid last year
I did not take paxlovid even though my pulmonologist highly recommended it.. my only symptom was chest pain that moved from front to side to back. Lasted about 12 days . I'm so glad I didn't take it.
I had COVID for the first time this past September and didn’t take paxlovid. My doctor just recommended vitamin c , Zinc flonase and mucinex. I did fine and recovered within a week. I had been really worried about getting COVID so was relieved it wasn’t too bad.
They gave me Lagevrio for Covid
Thanks. A lesson I just learned.
Go onto Mayo Clinic Connect and ask questions, review others experiences and thoughts before taking new medications to understand how others have dealt with matters
their outcomes etc. etc. to give one more 'food for thought' and therefore having given it more thought before starting. Before having Covid I asked the very special pulmonary BE doctor what I should do if I get Covid.....her answer.....take Paxlovid. I wish in a way I had waited for the fourth or fifth day to decide about taking the Paxlovid, after the first two days of symptoms, before starting the Paxlovid.
My first was in October, immediately started paxlovid but still deteriorated and wound up in the ER and got remdesivir and quickly recovered.