My husband has just been diagnosed with MSA after over a year of uncertainty whether it was Parkinson's or not because he went down so quickly. By chance, today I found this site so may need some getting used to finding my way around it. Many thanks as it is such a stunner for us.
New to this Forum: My husband has just... - Multiple System A...
New to this Forum
Hi and welcome to the group. I'm a 52 year old msa sufferer. Still learning to manage the condition
Are we allowed to swear on here because it's a bit of a flooker! He now has a permanent catheter and now needs some antibiotics today as he has an infection again. I'm a retired Scientist in Histopathology so am cognizant with some medical tech info which, on reading, strangely helps me as it did when I had invasive breast cancer many years ago. Phil is 67 and I'm 75 so are hoping to avoid any sudden slow falls which sandwich me between him and the door frame. If you don't laugh you'd cry! 😆
Hi. Welcome. I'm a 52 year old msa sufferer still getting used to this condition
Welcome to this wonderful forum. Sorry you have to be here. I’m 53 and have MSA-C. X
My husband is 67 and was initially diagnosed with Parkinson's but, as he came down so quickly, his Geriatrist has just informed him that he has MSA. Your post says MSA-C which I haven't heard of. Would you mind letting me know what it is about. Many thanks.
No age. The only benefit is extra fitness
I’m an ex-runner and have climbed the Inca Trail but this B****** doesn’t care xx
I ran 42 marathons I had msa undiagnosed with the early stages and just got to the 10km in Amsterdam
I'm hoping the training will buy time. I'm 15 months in now