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Surviving with ME/CFS

Became disabled after contracting Covid-19 in early 2020. 코로나 후유증때문에 장애인이 되버렸네요

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Links for Healthcare Providers are

at the Bottom of this List

아래로 내리면 한국말도 있어요.

This article can show you what my illness ME/CFS is like

Please read and share

You can donate a single dollar to me every month automatically here. Only $1, but it helps, Seriously!
You can also donate your precious time so I don't feel so isolated stuck in bed 😁
Help Make My & my Familys Life a bit Lighter - Amazon Gift List
Help Make My & my Familys Life a bit Lighter - Amazon Gift List
Help Me Have at Least Some Kind of Life as a Human
Help Me Have at Least Some Kind of Life as a Human

Information on long Covid & ME/CFS

근육통성 뇌수막염에 대해 한국어로 된 제대로 된 정보를 찾을수 있는 곳은 딱 한군데 뿐이었다． "바이러스 후 만성피로증후군" 이라는 병을 한국은 아직 연구조차 하지않고 있다． 이 링크는 한의약융합연구정보센터에서 다룬 내용이다．
ME/CFS resources from Workwell Foundation
Patient Education from Bateman Horne Center
About ME/CFS from Massachusetts ME/CFS & FM Association
Library | ME/CFS & Fibromyalgia Self-Help
Resources for People with ME from #MEaction
Resources for People with ME from #MEaction
Patient and Caregiver Resources - Solve ME/CFS Initiative
Patient and Caregiver Resources - Solve ME/CFS Initiative
The Hummingbirds' Foundation for M.E.
Long-COVID Alliance
Post viral Illnesses from National Library of Medicine
RECOVER Research Review (R3) Seminar Series
RECOVER Research Review (R3) Seminar Series
ACTIV Seminar Series: Post-Acute Sequelae of SARS-CoV-2 | The Foundation for the National Institutes of Health

Related Articles

AACN's article on PASC (Long COVID-19) w/ resourceful links
I got a virus, I didn't die, but I never recovered. We are the #MillionsMissing.
I got a virus, I didn't die, but I never recovered. We are the #MillionsMissing.
Killing Me Softly: FM/CFS & Suicide

Informative Patient Social Medias

m.e_and_more
standby.m.e

Worth Checking Out

Spoonie Press
Spoonie Press
Free Depression Peer Support Groups for All
Free Depression Peer Support Groups for All

Journal Articles

Caring for the Patient with Severe or Very Severe Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
Caring for the Patient with Severe or Very Severe Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
Long COVID Now Looks like a Neurological Disease, Helping Doctors to Focus Treatments
Long COVID Now Looks like a Neurological Disease, Helping Doctors to Focus Treatments

Dear Healthcare Providers

U.S. ME/CFS Clinician Coalition
U.S. ME/CFS Clinician Coalition
Resources: For Medical Providers - Solve ME/CFS Initiative
Resources: For Medical Providers - Solve ME/CFS Initiative
About ME/CFS for Health Professionals from Bateman Horne Center
Resources for Healthcare Providers from #MEaction
Resources for Healthcare Providers from #MEaction

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