via Hughes Syndrome Foundation/Facebook Page: clyp.it/1zolckte
Well done.
MaryF
Thoroughly recommended. Put an hour and ten minutes aside and listen to all that Yvonne Wren has to say.
Keep a note of the URL too, and pass it to anyone wanting to know more about Hughes/APS.
Hi Mary,
I agree with Tim! Thank you!
I have just listened here. Exstremely good intervue about this syndrome!
Kerstin in Stockholm
Well done Yvonne - fantastic interview.
I hope many people/general public and health care workers heard it as well as patients.
I too am a physio and have had some similar experiences to you and self test/medicate and I endorse all you said about this and self-management - this is very much what I teach and encourage my patients to do.
Hope to meet you some day - I live in Wales so may not be so easy
Best wishes
Kerry