The job of Patient Advocate came upon me uninvited. I did not apply for this job, nor did I have any qualifications for it. I am a sculptor, not a doctor or a researcher. LOOKING AT LYME DISEASE - MSIDS. BREAKTHROUGH IN FRANCE FOR TREATING CHRONIC LYME PATIENTS.

Sunday, January 29, 2017. I love to travel and experience new things. I am restless and, in my healthy days, I thrived on change. I am somewhat claustrophobic and hate being in small, confined spaces .

Decorative artwork and illustrations designed for children. The Simmaron Research Foundation for Nuero-Immune Diseseases. I have trained in many painting mediums but now work primarily in acrylic, watercolor, and tempera for health and and environmental reasons. My cat and I would love to hear from you.

Es sind vor allem junge Menschen, die durch einen Infekt aus dem Leben gerissen werden. Für Menschen mit ME wird der Alltag zur Qual. Sie verfügen nur noch über einen Bruchteil ihres früheren Leistungsvermögens. Dadurch sind sie nicht mehr in der Lage, ihr bisheriges Leben im Beruf, Familie und Freize.

FOLLOW US ON FACEBOOK AND TWITTER. 7, 11630 Kingsway Avenue. Edmonton, AB T5G 0X5.

Was established to address the issues of recognition and definition,. And to raise awareness of this devastating neuroimmune disease. That has afflicted nearly 1 million people in the U. , and 17 million worldwide. ME is more debilitating than most diseases.

Friday, March 13, 2015. I was 11 years old and Fred Meyer. Not that I got to wear them often as I was perpetually spraining my right ankle thanks to my genetically-defective collagen. I quickly zeroed in on a choice between my Anne of Green Gables. Both have a lot of det.