Saturday, 6 February 2010


ME/CFS, Fibromyalgia, Arthritis patients would do well to follow what is going on over the politics of Lyme disease.
Recently Lorraine Johnson CALDA posted the following do follow my link and read the full story.

Responding to patient concerns, the President of ILADS, Dr. Robert Bransfield today delivered a letter to the IDSA calling upon the organization to remove barriers to guidelines change.

The controversy over the IDSA guidelines have caused many patients who like me suffered from ME/CFS or Fibromyalgia or Arthiritis to have many years delay before being diagnosed, many more will infact be unaware of what has caused their illness and symptoms and remain in pain without realising that treatment by long term antibiotics can help those of us who find their illness to be caused by Lyme Disease.

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