Long COVID: What bloodwork and vitamin/supplement recommendations?
My daughter has debilitating fatigue as well as other symptoms (including but not limited to brain fog, cognitive issues, sudden onset nerve pain in feet, cough, shortness of breath). She's looking for non-western medical advice in addition to traditional. Any info you can provide would be greatly appreciated?
Two part question:
1) What blood tests do you recommend requesting for LC?
In addition to CBC, my thought was vitamin panel, ferritin bloodwork, CRP. Any others?
2) What supplements / herbs, etc. have been helpful?
All B vitamins, Vitamin D, Turmeric, Quercetin, NAC (not sure that that is, but read it in a posting), Magnesium, Zinc.
Thank you!
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Well that is extremely helpful to know!
Months ago her GP said she had one of the lowest levels of vit D she’s seen but only recommended her to take 500 IU. She was to go back to get follow up bloodwork but that’s when she fell and tore her labrum in hip and 4 bulging discs so that has put other things on hold.
I don’t know if she had the type of blood test you mentioned so that is another thing I’ll list on notes for when she sees this new GP. I just pray that this new Dr is more willing to spend time and effort on helping her.
Thank you SO much for this information. Thank you.
Excellent info! Can totally relate to your au natural approach! Doctors are still in left field…
Here’s my take..
Unfortunately, too many doctors cannot even think of adding long hauler to their concerns regarding patients. I am a long hauler for 3 years now…and functioning as if cured…but not.! Had to take it upon myself to save my own life after seeing way too many doctors who were, frankly, useless. I am fully aware of their lack of knowledge as understanding of Covid and subsequent treatments develop, BUT the profiteering in long Covid treatment centers and encouragement regarding same by major medical institutions is blatant.
So, I’ve spent the last 3 years requesting testing to confirm that my symptoms weren’t (aren’t) going to kill me…, once able to resume exercising slowly building up to pre-covid modified routine, tolerating the horrible fatigue with determination not to completely atrophy, read any and all literature I could find on the internet, incorporating every supplement that showed any influence on mitigating symptoms ( now at 41 supplements…with my recent
( and final) Cleveland Clinic PCP annual visit, via her body language and haughtiness…unaccepting of my approach that is “working”). Covid fatigue, pins and needles in lower legs and bottom of feet remaining as primary symptoms. I take no medications. ALL of my bloodwork is within range. The doctors have very typically disregarded the printed research findings I have handed them the last three years, handing it back to me with a distrust and since “ all of my testing is “normal.”
I exercise everyday and have built back up to 10 and 15lb weights, treadmill speed walking, resistance bands. AND I have totally healthy eating habits for many years because of my dedicated exercising habits for many many years.
Punchline: I am a 76 year old female. ( Covid at 73) AND I HAVE NEVER BEEN IN PUBLIC WITHOUT A MASK SINCE COVID.
My next focus is on the very recent validation of mitochondria involvement in Covid fatigue. I will Google and gather as much info as possible in order to address possible tests and treatments…
Kudos for you for sharing important details.
You mention that you contracted LC from your first booster. I find that interesting because the symptoms I had after each of my 4 Covid shots continued for more than a year. I do feel that it was from the shots. My blood type is A which is supposed to have a low level of immunity. I am wondering if blood type A's and AB's are more vulnerable to this occurence. Could I ask if you know your blood type and what it is? It would be interesting to know the blood types of all the longhaulers on the blog.
AB negative
Interesting, thank you. I have started on each of these except the natto….in addition to vit C, vit D, magnesium, L-carnetine and co-Q10 - all as a result of my own research since I’ve been left feeling like I’m on my own with all this after a number of specialists over the course of 18 mos. and no success at eliminating my symptoms. In fact it seems to be progressing. So then my primary said stop everything except prescribed meds, vit-D and magnesium. That was 4 mos ago. After reading your story I’m going to try the B-12, berberine and zinc (during the night-thanks, that was real interesting as I always took it in the morning) and ginger. My question to you is what are the dosages for each of the supplements you’ve mentioned?
Hi @rmca. I'm entering year 4. Your approach to managing with LC sounds like mine. I research all I can, often sharing findings and studies with various providers. I've found they don't have the time to research and this is a very fluid field. And traditional medicine doesn't inform treatment.
I've made some great improvement especially in my 3rd year, and am now focusing on rebuilding mitochondria. My LC clinic doc prescribes Mitocore by Orthomolecular Products. The important thing is to pair L Acetyl-Carnitine (LACAR) with Alpha Lipoic Acid (ALA). ALCAR alone can actually deplete mitochondria - it needs an antioxidant to counter balance the oxidation it created.
Dr. Bruce Ames has done extensive research in this area and found that a ratio of 500 ALCAR to 200 ALA is best. Mitocore fits this ratio as does Juvenon's Cellular Health product. I've used both, most recently Cellular Health.
A+
O+
I’m seeing there are a number of us that got the message early on that we have save ourselves…I’m grateful for your info! Alcar is part of my 41 supplement routine along with R-Lipoic Acid which supposedly better. But the ratio you provided is very helpful. I like being able to put a star next my supplements when someone validates them. Thank you.
All I know is that things are working . I can’t tell which ones, all if it’s all of the above…but the holistic approach has very obviously got me to this point.
The mitochondria is my focus now also. That is THEE most recent revelation in the research with NAD+ appearing to play a major role.
Keep in touch, uget1shot!
Again, thank you!
wow, 41 supplements! would love to see your list if you're willing to share? I probably take close to that many individual pills a day so I get it. I like your idea to 'star' validations.
You mentioned NAD+. I had forgotten about this. My doc had me taking NAD+ Gold by Quicksilver Scientific earlier in my journey. Are you taking anything for this now?