Been a long road of painful misdiagnosis one after another and I'm finally here. Embracing the future and open to a supportive community.
Hello I'm a newbe on this. Hi! - My MSAA Community
Hello I'm a newbe on this. Hi!
Welcome to the group that no one wants to join! You'll find a great bunch of people here with fantastic senses of humor and personal experiences in pretty much anything you want to talk about. I think politics is the only thing actually banned, so feel free to tell us about your quintuplet pot-bellied pigs, your hobby of pole dancing, or your skyclad neighborhood watch group. 🤪
You'll find amazing support in this group. Don't hesitate to ask questions, you'll get input from thousands of folks who have lived well with ms for years.
Welcome to the group! Your story of a long and painful road to finally getting diagnosed is a very familiar story to us. I spent almost five years going to lots of doctors before my official diagnosis. You have found a great place for resources, for support, to ask any questions, to vent, and to share all the ups and downs of life with M.S. And, of course, the jokes. We love to share a good laugh! All the best!
Thank you so much. I’m still trying to get my head around it!
Welcome!
Welcome to the group!
Welcome! This is a get place to get a laugh when you feel like crying, get support when you need a boost, information when you need perspective, or when you just need to vent, as MS can be very frustrating at times. Remember that everyone's MS is different & keep positive as everyday can be a new adventure!
Welcome - glad you found us!
Welcome to the forum, Lifeisfab . Glad that you found us! You can look at mymsaa.org for more information about ‘ms’. I look forward to hearing more from you but in the meantime, Keep Smiling!
Welcome
Took me 10 years to get diagnosed so understand you completely.Hope you can be comforted by the people on this group
Welcome to our family. One I wish you never had to join but nevertheless now that you're here you couldn't find a better community and family to support you. We'll make you laugh when you need a lift. We'll give you a shoulder to cry on when you go through hard times. And we'll share our common experiences to help you gain perspective for this ever-changing disease. Always remember together we are stronger! Fancy59.
Welcome! It is nice to know there are others out there struggling with this **** disease besides us, right? I am rural and do not know anyone else (in person) who has MS. We hope to see you around. Sorry for the delayed reply, but I still work full time, and life's been .... rough lately. 👍