Newest and best long covid recovery treatments?
Has anyone had any substantial or helpful treatment for severe long covid?
Interested to hear any novel therapies being explored. At this point, I am so tired and now have pots and ME with significant symptoms for 2 years.
Looking for some hopeful ideas.
Interested in more discussions like this? Go to the Post-COVID Recovery & COVID-19 Support Group.
I do get a burst of energy from the LDN after about two hours...I try to time it to keep my energy up for a few extra hours a day. So, yes, it does help with my fatigue.
I just saw this new research published in Nature. This may give doctors new pathway to help patients.
A Nature study published in June 2025 by Australian scientists revealed that in patients with severe COVID-19, the delicate lining of blood vessels, called endothelial cells, starts to break down when oxygen-rich blood cannot reach tissues. This breakdown of endothelial cells, potentially triggered by COVID-19 infection, causes immune signals that lead to red blood cells bursting and releasing sticky contents into the bloodstream. This “glue-like” material can clog the smallest blood vessels (capillaries), blocking circulation and causing tissue damage in organs like the kidneys, liver, and heart.
Interestingly, the researchers were surprised to find no widespread fibrin and clotting in analyzing patient samples, which was initially expected. Instead, they found that the microcirculation issues were primarily due to the debris from broken red blood cells. This suggested a novel mechanism of vascular damage in COVID-19 through the death of endothelial cells, which had not been previously considered. The study highlights that this microvascular damage and broken red blood cell issue were significant problems in the microcirculation of COVID-19 patients.
This research suggests that targeting the death of these vessel-lining cells could be a potential strategy to combat COVID-19 symptoms and long COVID, potentially requiring a combination of treatments. These findings may also impact our understanding of other conditions like stroke and heart attack where standard treatments are not effective.
To bmekdeci —
Thank you for your clear, detailed, and articulate summary of the new research published in Nature.
I had read before about endothelial damage as a potential cause of LC symptoms.
But I hadn’t read before about the related problem of microvascular malfunction caused by red blood cell debris.
Thank you for bringing this new evidence to our attention!
~ friedrich
I have documented endothelial dysfunction and microvascular spasms as a result of the J&J Covid vaccine, worsened by several additional Covid infections. Unfortunately they don't have good solutions for endothelial dysfunction, but there is a tremendous amount of research, so hopefully there will be answers eventually.
Thanks for sharing. Can you please paste the specific Nature URL/website link for said study, for reference?
Thank you in advance!
No heart issues but I recently had pneumonia and going to a pulmonologist Monday. I have weird lack of feeling real. Like nothing looks or feels real. Anyone else have this?
Please look up Dr Jordan Vaughn on the internet. He has done wonderful things with long term COVID and does a lot thru mailings. He's even testified before Congress on issues relating to long term COVID.
Here is the citation in Nature which you can find in PubMed (the National Library of Medicine).
https://pubmed.ncbi.nlm.nih.gov/40468079/
Although some studies can be accessed at no cost, this one is behind a pay wall.
I’m in the Uk but had already come across Dr Vaughn’s pages and various advice sheets….unfortunately if you are the one who has suffered all the Long Covid problems for 5 years they are rather ‘teaching a grandma to suck eggs’ ( if you understand this English expression!
Hello Wilson, I have never heard that about grandma but it gave me a chuckle. Have you tried three different blood thinners at the same time to try to get rid of the amyloid fibrin blood clots? If that doesn't work what a bummer. I see a hemotologist in August and I sure.hope he can do something but I'm not terribly optimistic because we have all been thru so much. Good luck to you my friend.