Surviving with ME/CFS

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

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 Me Have at Least Some Kind of Life as a Human

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

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

ACTIV Seminar Series: Post-Acute Sequelae of SARS-CoV-2 | The Foundation for the National Institutes of Health

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.

Killing Me Softly: FM/CFS & Suicide

m.e_and_more

standby.m.e

Spoonie Press

Free Depression Peer Support Groups for All

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

U.S. ME/CFS Clinician Coalition

Resources: For Medical Providers - Solve ME/CFS Initiative

About ME/CFS for Health Professionals from Bateman Horne Center

Resources for Healthcare Providers from #MEaction