Should I take monoclonal antibodies during active infection

[alinanmsnrn]

I have found a place that would give me sotrovimab
Considerations:
https://www.nejm.org/doi/10.1056/NEJMc2120219

Remission of severe forms of long COVID following monoclonal antibody (MCA)...

My doctors don’t seem to know what to do with me. I don’t know if I should do it. Any thoughts or help would be appreciated.

[glenn_chan]

This forum has a breakdown of the paper that you are citing. See this thread:

Remission of severe forms of long COVID following monoclonal antibody (MCA) infusions - summary of this 'scientific' paper

Scheppke and colleagues have published a paper on 3 patients who experienced ‘complete’ remission after Regeneron monoclonal antibodies (casirivimab/imdevimab). What we already know about monoclonals against COVID-19 is that a small percentage of patients may experience recovery following treatment. Most do not. (Data is from the Treatment Outcomes Survey. See slide 11. The 3 case reports may add some weight to the idea that a few people will be really helped by monoclonals.) However, I do…

Scheppke and colleagues are painting an overly optimistic portrait of monoclonals. However, the data suggests that they may be worth trying. As with other treatments that people have been trying, response rates are very low.

If you do get this treatment, get it ASAP as they work better the earlier that you get them.

Survey data

There is limited data on monoclonal antibodies in the survey data. See

Has anybody tried ___? Here's how you can get answers to that question fast

[image] I have a data dump of survey data here: Patient Experiences Survey: longhaulwiki.com/pes/ Treatment Outcomes Survey: longhaulwiki.com/treatment-outcomes/ ← While this data set is older, it has more data on IVIG and the demographics are quite different. Use the search feature on the name of the treatment that you want to find data for. Desktops: Hit Crtl + F (⌘+F) in your browser. Mobile: Tap and hold on your web browser app (while in the app). The search function will have a na…

However, I probably should have asked how these treatments affect chronic illness symptoms and not acute COVID symptoms. Surveyees may be answering for either context and I don’t know which context they chose.

PES

TOS

Doctors, what to do

@alinanmsnrn

My doctors don’t seem to know what to do with me.

See the videos that I’ve put up on the Odysee or Youtube channels. There are more videos on Odysee due to YT"s censorship.

• Odysee: What worked for 36 people who recovered (Patient Experiences Survey Jan 2024)
• YT: https://youtu.be/IfeEIWorozg?si=cXkWIKCrq8LaXGRR

The what worked videos give a concise overview on what’s working.

The medicine is full of grifters video / chronic illness taught me video (and the misdiagnosis video) gets into why mainstream medicine is doing a bad job. There are structural issues that get in the way of patient outcomes because politics, social politics, and money are such dominating forces in ‘medicine’. Even if a doctor wants to do the right thing, they risk losing their license.

There are a few safe treatments such as pacing strategies. See the slides or video here: Patient Experiences Protocol (Dec 2022)