Is ME Infectious?

[frozenborderline]

Have you heard 'Origin Story Pt. 3' by Headless Youth Podcast on SoundCloud? https://soundcloud.com/headlessyouthpodcast%2Forigins-pt-3
We talk about Tahoe outbreak and nanoparticles theory

 

[frozenborderline]

https://soundcloud.com/headlessyouthpodcast%2Ftribulations-25-ft-allegedlyzo Also in the second half of this episode we really get into Tahoe in detail

I highly recommend it

 

[frozenborderline]

https://twitter.com/i/web/status/1386438286147657729

Here is a preview of one of the episodes

 

[Pyrrhus]

Related discussions:

Prevalence of Chronic Fatigue Syndrome and Chronic Fatigue Within Families of CFS Patients
https://forums.phoenixrising.me/thr...atigue-within-families-of-cfs-patients.46305/

Significant differences were seen between the prevalence of CFS in all groups of family members relative to the published community prevalence of 0.422% (spouses/partners: 3.2%, p < 0.001; offspring: 5.1%, p < .001; parents and siblings: 1.1%, p < 0.02; second and third degree blood relatives 0.8%, p < 0.02). The prevalence of CFS was higher in genetically unrelated household contacts and in nonresident genetic relatives than in the community, indicating that both household contact and genetic relationship are risk factors for CFS.

I have had CFS for 6 years and my wife just developed it too
https://forums.phoenixrising.me/thr...ears-and-my-wife-just-developed-it-too.81560/

This feels surreal to type. And I have actually been in denial for a while. But I can no longer deny that my wife now also has CFS. Her illness mirrors mine to a T. We have seen every doc in every specialty, virtually all the tests come back normal, as they did for me. We share so many little specific symptoms. It’s obvious to me that we are suffering from the same disease.

 

[frozenborderline]

Related discussions:

Prevalence of Chronic Fatigue Syndrome and Chronic Fatigue Within Families of CFS Patients
https://forums.phoenixrising.me/thr...atigue-within-families-of-cfs-patients.46305/



I have had CFS for 6 years and my wife just developed it too
https://forums.phoenixrising.me/thr...ears-and-my-wife-just-developed-it-too.81560/

I think it may come down to shared environment and shared slight genetic predisposition. My sister has mcas and probably has the hereditary alpha tryptasemia gene like me, but also the fact we grew up in a literally toxic environment probably explains both of us being sick. she doesnt have PEM, but she has a lot of similar mcas symptoms, there's a venn diagram overlap

 

[unto]

hi, for me surely ME is of infectious origin, before the epidemic on Lake Tahoe there were that of Los Angeles and then those of London and others, I exclude that in all of them there was a concomitance between viruses and molds, yet the disease is the same ....; then what to say about today's diffusion in all countries of the world (apart from those whose inhabitants cannot afford to notice that they are sick ...)

 

[unto]

also genetics for the same reasons is to be excluded, it should be noted that very often the spouses both get sick and rarely have similar genes ..... In my 36-year experience of ME, I have seen family and relatives manifesting clear symptoms of ME but also friends, colleagues and acquaintances who although some had never been to my home (therefore without genetic or environmental link) over time they developed ME