Surviving with ME/CFS

Surviving with ME/CFS has been a member of Linktree for 3 years and joined in September 2022. The social media accounts linked to from Surviving with ME/CFS are: • Instagram • Amazon • Payment Besides social media accounts, 032020 has populated their site with: • 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