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Can anyone please give me advice to how to handle this?
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Myalgic Encephalomyelitis
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655d
Pacing has been the most effective tool for me after 20+ years with CFS but it isn’t always easy or possible to do
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666d
Oops … support community
Forums.phoenixrising.me is a chat forum that has been around for years and is a very active CFS/ME support for every aspect of the illness You will find a ton of information there
Pacing is paramount to living with CFS/ME. Know your limits and practice self care ☺️
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Just relax don’t stress out and go with the flow…
☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision
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