Thanks for the posts by you and all the others. We are all the same, suffering from seeing our loved one suffering from MSA. My sister is only 40 and she has just been diagnosed with MSA after many years of weird appearance. She has frequent urination, hypotension and sleep apenea. I am very very sad and really want to know what can be the best way of helping her. She lives in Adelaide but I live close to Melbourne. Do you know any places or doctors that we should go for consultation? Her blood pressure remains very low. People have also talked about the stemcell treatment. What’s your idea about all these things? We are just starting the journey and I will be alongside my sister traveling on it and really appreciate you and many others to be around us. Let’s share the experience and all win the battles.