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ME/CFS and loss appetite

Just Want to Talk | Last Active: Mar 20, 2022 | Replies (12)

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@colleenyoung

Hi @dan1940, welcome. Let me introduce you to a few other ME/CFS members like @petuniamom567 @karina77 @rarelybees2889 @chaun2947 @clutch @sita @elik @jmmb @susangs @canadagal @sundance6 and others.

Dan, you might also be interested in reviewing the posts in this discussion:
- Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) treatments https://connect.mayoclinic.org/discussion/myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments/

Being active can be helpful. People with chronic fatigue syndrome who experience a worsening of their symptoms after physical, mental or emotional effort may have post-exertional malaise and it can last for days or weeks after the exertion.

Have you experienced post-exertional malaise? What helps you find a good balance between activity and rest, to remain active without overdoing it?

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Replies to "Hi @dan1940, welcome. Let me introduce you to a few other ME/CFS members like @petuniamom567 @karina77..."

I definitely have postexertional malaise. Recently spent about 2 months sitting sleeping in chair due to sciatica pain. I have hurt shoulder and hip because of overall weakness so still recovering from that. I thought lyme/mold infections cured after 2 years good treatment. So I can’t tell if I get lyme/mold flares, or still weak from sciatica or in fact it’s CFS. Thank you for response.