Chronic Fatigue Syndrome Support Group
Chronic Fatigue Syndrome (ME/CFS) describes a sense of exhaustion and post-exertion malaise, even when you have gotten enough rest and sleep. The disease is characterized by six months of incapacitating fatigue experienced as profound exhaustion and extremely poor stamina, and problems with concentration and short-term memory. The cause is unknown, but it is a...

Are you being seen or being treated for depression.
I no longer feel exhausted, or lethargic. I have energy to do the things I need to do. They helped me feel normal again. I dropped the SSRI I was given.
I also got my other hormones (estrogen, progesterone, testosterone) checked and discovered those were severely low so you might want to have yours checked. I had to INSIST for the Endo to check mine, he didn't want to at first. He told me, I think those will come back normal and when they didn't I was sent to get the results from the other physician in the office, I guess he was too embarrassed to give me the results! I hope this information is helpful.
Today I'm in bed again, have cried my heart out because I'm too weak to walk. Now I'm surrendering to my condition once again rather than fighting it, and doing my best to find some self love.
So please be kind to yourself and forgiving to yourself and know that others acknowledge your suffering and feel for you and genuinely care..Try not to lose hope despite your continual suffering. Let us both practice positive affirmations to gain resilience. Love and healing to you.
Tonight's not a good night. I feel bad all over, inside out.
I'm able to function a bit. But not enough. And I don't have family to help. I'm 63, and fortunately I have some money coming in and a place to live. My sadness is that I watch my living space deteriorating around me because I'm not able to keep up with cleaning or home repair. And I can't drive the 8 hours to visit my son and his wife. And I can't drive the 14 hours it takes to visit my brother. And I accidentally dropped my poor dog today because I lost my balance. Fortunately she didn't get hurt at all. But it made me sad inside.
I spend my time reading and playing ToonBlast, ToyBlast, Grand Harvest Solitaire, and Word Crossy. I listen to the news. I don't have a TV, but that's OK. I've got a computer. I'm sad and sometimes frustrated. But I can be thankful because for awhile there I thought I was going to be homeless.
I have a strong feeling that you are not able to do as much as I am able to do. I'm sorry. If it helps, just know that there are many who can relate to how sad and frustrating this disease is.
Oh, for some GOOD NEWS. A scientist whose son has CFS is researching cause and cure. In spring of 2019 his team found a biomarker for CFS that was consistent in the 20 sufferers of CFS - and didn't appear in the control group of 20. Research is continuing. Now that they've found a biomarker, they can start looking for cures. His son is extremely debilitated. So the father is very motivated.
Stay strong, Lilly23.