Multisystem Atrophy

[anita1968]

Hi my name is anita and my aunt has MSA.She was diagnosed 6 months ago and we are not able to find any support groups in Melbourne.My aunt has had cancer of just about every kind for 40 years and has fought it every step of the way.The trouble she is having is she feels she has little knowledge of the disease(only what we can find on the internet)and she is very scared also of the outcome.We seem to be hitting a brick wall regarding infomation and support groups.My question is:does anyone know of a support group in Melbourne or a specialist we may not have seen already? Any help would be much appreciated :)Thankyou for taking the time to read this .

[sh15rose]

I'am only 51 years old and have been diagnosed with MSA. My speciallist is Prof. Drago. He carries out research for MSA and is an expert with stem cells.

All the other neurologists say to ask Dr Drago, when I ask them questions. He has numerous neurological reports on the internet.

Cheeers
Sue