ME/ Chronic Fatigue Syndrome and Fibromyalgia deals a different hand to every sufferer. No one sufferer is dealt the same symptoms, with the same severity, in the same order, over the same length of time…
What’s more, your environment and the people around you, can all play a part…
Has your doctor been understanding and supportive? Did you fight to get a diagnosis? Did they help you explore your options when it came to treatments and therapies for ME/ Chronic Fatigue Syndrome and/or Fibromyalgia? Do your family and friends offer the love and support you need? Or do you feel largely misunderstood and isolated from the world?
There’s nothing like reading first-hand experience of other sufferers, who have ‘been there’. New sufferers and those who have been disconnected from the ME/CFS and FMS communities can take comfort in reading other sufferers’ experiences. Knowing that they are not the only ones going through this.
I’ve spent time adding as much of my experiences about living with, recovering from, and/or learning about Post Viral Fatigue Syndrome, Chronic Fatigue Syndrome, M.E., and Fibromyalgia. And now I’m turning it over to you. What’s your story?
And would you be willing to share it?
You can share your experiences of ME/ Chronic Fatigue Syndrome and/or Fibromyalgia here…
You never know. Maybe your story will speak to someone out there too.
