[Blossom25]

Originally Posted by Old Gal

Hello everyone! I was diagnosed with MS in '97 and have been on Betaserone ever since. My MRI's haven't changed much but I have gotten more and worse symptoms. Have any of ya'll ever heard of pudendal nerve entrapment? MS is rotten enough without having the ignominy of this !!!!! I won't even talk about the pain cause I bet every one of you has thier own little "Shop of Horrors" when it comes to pain talks. It is nice to find a place where like minded folks can talk about things. I hope to talk to each of you soon......Happy Trails!!

I do not have MS, but my Grandson has just been diagnosed with it. He's 27 and just got married, bought a new house, has a great job after going to college and then boooooom Life changing disease hits him. He just fell on a ramp and broke his ankle and had surgery today. He has a lot of trouble with his eyes. So far they are not getting any better but gradually getting worse. He can't drive. His place of employment are very empathetic and love Justin so they bought him bigger screens for his computer so he could continue to work. Bless his heart, he still always has a smile. Does anyone have any suggestion on how they made their eye sight better??? Thank you. Blossom25