Any one else out there suffer from Chronic Fatigue syndrome?

If so, what treatment do you use to help?? I’m not sure what to do.
Yeah i have low blood pressure. I’ve seen 5 different specialists and they all believe it’s chronic fatigue syndrome.

Yes, I was diagnosed with CFS in March this year after going backwards and forwards to the doctor with the various symptoms for a year. During that time they did all the numerous blood tests etc to rule out any other conditions.
Once the diagnosis has been made it’s usually the GP who will offer medication/treatments to help with the various symptoms, with the specialists help if necessary.
I found the ME Association very helpful. I also find on here a group called MEChat very helpful and you may find a local support group for wherever you are. Personally I try to use Pacing as a technique for the fatigue and use a combination of anti depressants and muscle relaxants to help with my sleep pattern and the chronic muscle pain but anyone with CFS knows the symptoms vary so much from person to person that there’s no set answer and it’s often ongoing communication with the right GP that gets you the right help.

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3 Responses to “Any one else out there suffer from Chronic Fatigue syndrome?”

  1. Terry L Says:

    Do you have other illnesses that attribute to this fatigue? Have you had your white blood cell count checked? How about your blood pressure? You can go to just about any pharmacy these days and they usually have a free blood pressure check. I would do this.
    References :

  2. Christopher S Says:

    Any doctor that diagnoses this is just trying to avoid saying "I don’t know" by coming up with a condition that describes your SYMPTOMS. Ask him to come up with something that describes the CAUSE, or get another doctor.
    References :

  3. Karen Says:

    Yes, I was diagnosed with CFS in March this year after going backwards and forwards to the doctor with the various symptoms for a year. During that time they did all the numerous blood tests etc to rule out any other conditions.
    Once the diagnosis has been made it’s usually the GP who will offer medication/treatments to help with the various symptoms, with the specialists help if necessary.
    I found the ME Association very helpful. I also find on here a group called MEChat very helpful and you may find a local support group for wherever you are. Personally I try to use Pacing as a technique for the fatigue and use a combination of anti depressants and muscle relaxants to help with my sleep pattern and the chronic muscle pain but anyone with CFS knows the symptoms vary so much from person to person that there’s no set answer and it’s often ongoing communication with the right GP that gets you the right help.
    References :

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