As promised, I am writing this post to share what the Mayo #LongCovid Clinic found on my recent visit. I have high inflammatory markers (CRP, IL-6, and TNF), so the dr wants to focus on lowering inflammation as a first step. She is recommending LDN for that. She believes 1/
that my positive (but short lived) response to HELP apheresis was due to removal of inflammatory molecules. I was also dx with small fiber neuropathy, endothelial damage, and reduced blood flow in my brain. These were the pharmacological recommendations: 2/
Low-dose naltrexone for fatigue/brain fog, POTS/dysautonomia, and MCAS, starting at 1.5mg capsule daily (given vivid dreams already) uptitrating every 2 weeks or as tolerated to 4.5mg; if significant side effects do occur at 1.5mg, can use liquid form to start at 0.1-0.5mg and 3/
uptitrate as tolerated. Fludrocortisone to improve fluid holding for POTS/dysautonomia, 0.1mg (range 0.05-2mg as tolerated), with consideration of midodrine 2.5mg up to 10mg every 4 hours as needed during the day before activity and/or pyridostigmine 30mg up to 60mg 3 times 4/
daily as next steps. Low-dose aripiprazole for fatigue/brain fog and sensory sensitivity, 0.5mg up to 2mg. Dextromethorphan for PEM envelope extension, 15mg available over-the-counter/online. 5/
for #MCAS ketotifen 1-2mg nightlyor cromolyn sodiumfour times daily before meals and bedtime. keep Plasmalogen on board, potentially keep nattokinase on as well.
For endothelial dysfunction: arginine 1.5-2g and vitamin C 500mg twice dailymay be helpful. We also talked 6/
about oxaloacetate 500mg-1g which shows promise for PEM envelope extension but tends to be cost-prohibitive.
Additionally, #CCI/tethered cord is suspected but not confirmed as Mayo does not have anyone who specializes in that area. So that's a medical odyssey for another day. 7/
Finally, Mayo has a "long covid class" that I agreed to participate in. I think it is just going to be how to manage symptoms with lifestyle changes, but I'll update after I do the 12 week program. That is all I know for now. Good luck all! Happy to answer what I can. /END
To be very clear, I am not planning to take every drug listed in the recommendations. These are just potential paths forward. I will trial them as I see fit, under supervision of my PCP.
I fortunately have a Wonderful PCP who is willing to try just about anything. She just hasn't known what to try.
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One last update as I think this will also be helpful for other patients to discuss w their drs. I asked about potential treatments for viral reactivation (I have reactivated EBV, CMV, and an enterovirus perthe Yale LISTEN study). My PCP has no idea what to do for it. 1/
Here was the advice from my Mayo dr (as always, check w your own physician): For viral reactivation, a study of interest right now is the Bateman Horne trial of valacyclovir + celecoxib: Research - Bateman Horne Center . However, with CMV being a potential driver rather than 2/
HSV (which valacyclovir is more geared towards), it may make more sense to go with the "ganciclovir" (CMV-directed antiviral) equivalent, valgancyclovir. There have also been studies in the past with EBV reduction to valgancyclovir. If you trialed this, would substitute in 3/
A lot of ppl have asked in my DMs what blood tests Mayo Clinic did for my #LongCOVID visit, so I'll list them here. I did not ask for any of these and don't know what a lot of them are, so pls speak with your dr if you have questions.
*ACTH
*CBC with Differential (Hemocrit, 1/
Crowd sourcing for a friend: have any ppl w #LongCovid had a deep vein thrombosis that was completely resistant to treatment? Friend is in a very dire situation with a clot (now >3.5 ft long) that has been removed & come back twice in a matter of days. Drs stumped. Femoral artery
Tomrrw I leave my family for a mo to try #helpapheresis for #LongCovid. I know it isn't a cure & results vary & understand my privilege for being able to try it. But I'm going to give an honest, real-time account of it here bc so many are curious. Watch this space #TeamClots
Day 1: up @ 5AM thinking of all the things I shld do today before I leave. Realizing last night was our last fam dinner at home for a mo was tough. Hubs & kids so hopeful this will bring back some of the person I used to be. We all miss her. #LongCovid#HelpApheresis#TeamClots
Two legs of the journey down, one to go. Exhausted but in good spirits. Traveling is hard with #LongCovid & #POTS (understatement of the year). My companion is good company and keeps me smiling.