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Kimbauet -
Could you tell all of us more about your experience with Dr. K at NMH?
1. Meds recommended or
administered?
2. If so, which one(s)?
3. If not, why not?

The ONLY med I’ve heard that Dr.K uses for LC is Amantadine, but that med has a long list of very un-
pleasant side effects - maybe worse than LC symptoms.
You say your symptoms have gotten better! How much? Which ones? Any idea about why. Please tell us what you can about your improvement. So many write tif-bits about their experience with LC but leave us in the dark about how and why they got better.
Some say low dose Naltrexone helps but it also has brutal side effects. Those who have reported using it say nothing about the side effects, if any. We need to hear all, not just rid-bits, if you are willing to take the time and make the effort.
Thanks, and best wishes, Kim.
Stuart

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Replies to "Kimbauet - Could you tell all of us more about your experience with Dr. K at..."

stuartkjones4,
My lengthy reply above was addressed to you, as the originator of this entire thread.
Additionally, I don't know about "brutal side effects" from LDN, as it is, as described, quite low in dosage, but I did give that a try and it did nothing for me, not really any side effects a ssuch.
The search function on this system is quite useful, incidentally, so do make use of that.

Kim, I saw Dr. Igor Koralnik at the Northwestern Covid Clinic in the city of Chicago. He did not mention medication to me, but after a cognitive test and after he looked at my brain MRI’s from 2 and 3 years ago, told me that I will not be getting my taste or smell back if I have lost it for over a year. It’s going on 3! He didn’t say why and I was in such a state when he told me that I didn’t ask why and neither did my husband. He also said the olfactory nerves don’t regenerate and I’ve read where others say that it does. I was more confused after my visit than before. He never mentioned any treatment plan or anything for me. I walked out of his office angry and depressed. I did have over these past almost 3 years, 7 Stellate Ganglion Block injections and they helped diminish my anxiety/PTSD and body tremors. I’m not leaving anyone in the dark here, I’m just finding that “TIME” is what has made a difference for me and doing what I can for myself to feel better. I guess you have to figure out what that is for you. Good luck!