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I just read about you, Rivka, and you are amazing doing what you do as a person with ME.

I live in R.I. where there is no support groups or an organization for CFIDS/ME. I have lived with CFS for 26 years.  I was actually doing fairly well for some years(with not getting any help from any health care professional)and this fall had a bad relapse with a multitude of symptoms besides fatigue.  This has been very depressing for me.  Especially since  I can't find anyone I can go to for help.  At my recent visit to my MD for an annual check-up, she told me there is no cure and I will just have to live this.

My prayers and wellness wishes to all of you out there trying to live your life and coping with this little understood and researched disease.

 

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