No, not me I have 4000 friends online that I can say anything to. Talk about my darkest fears and tell my most embarrassing moments too. "SO DO YOU". If I may suggest, we are a family. Brought together on a very long journey through a life with ms in all its various forms. I do not know you personally, intimately, or physically but I can relate to what "YOU" are going through. Not better than anybody else, just differently and it is that difference that makes us a family of sorts.
ADuring your ms life journey always, remember "YOU" are never alone. There is always somebody ahead of "YOU" on the path, who has had ms longer, and regrettably, there are those behind us starting to experience this our ms journey. So talk, ask questions give answers. "YOU" are never alone.
I tell "YOU" what, give yourself a hug, say it is from me, do "YOU" feel a little less alone now. I thought so feel free to do it tomorrow and keep your chin up and have a better day.
This can be, and is a very frustrating illness. It seems to do things to our body with no rhyme or reason. The Central Nervous System (CNS) is a large area for ms to attack, so many things can happen to us. That is why "YOU" need to learn all that "YOU" can about ms in general and your ms in particular. Knowledge, my friend, is power, do "YOU" not want a little extra power? Keep yourself physically strong as best "YOU" can and make yourself mentally even stronger. This is a confusing and frustrating condition, but "NEVER" hopeless. The hope is within "YOU", that flame that I talk about gives"YOU" strength for the next five minutes. That is all "YOU" need five minutes, just keep repeating it. Soon enough "YOU" will have had a very long multi 8decade ms life, five minutes at a time. I know that "YOU" can do that, we all are here with "YOU."
five minutes lets do it together