I was diagnosed with MS about 2 months ago. First I was diagnosed with
hypothyroidism, I have Hashimotos disease. Then I was diagnosed with
Fibromyalgia and now I have had several MRIs done in the last few
months and there are lesions on my upper spine and in my brain. I am
going for the VEP test the 21st of this month. I also have
degenerative joint disease, the worst places are my knees, hips and my
right shoulder. I am currently under no medications for the MS. I am
40 years old and a stay at home mom. I don't post alot, maybe I am a
semi-lurker, LOL! I am a dedicated reader though and try to check in
at least once every two weeks.
Hi everyone: I'm Lisa and 39 yrs old. Have recently been diagnosed with MS. My brain MRI shows all kinds of lesions. MY back, neck MRI is clear. I am lucky...
Hello All, I was diagnosed with MS about 2 months ago. First I was diagnosed with hypothyroidism, I have Hashimotos disease. Then I was diagnosed with ...
Hi, I am new to the group and I am hoping for some support and information. First a little about myself...ok, a lot. I am 21 years old and have been having...
I know that this info has been discussed before, but fatigue is one MS problem that I don't have and I haven't kept track of what was posted. However, a good...
My mom was diagnosed with MS about 9 years ago. She is still doing good (walking with a cane) but has her "bad" days. I am only able to talk to her each week...
For all of you, I am telling this to all of you to give you all hope that there Is "love after MS"! I was diagnosed with ms "October 27, 1997". I was in the...
My name is Valary, I was dx'ed in '03 with r/r ms, although I've had symptoms since '99, I had a previous nuerologic disorder that kind've hid it, & at the...
I was diagnosed at age 39 - and am now 57. Sounds like you have familiar early symptoms, Lisa - but there are a variety of tests that will better confirm....
Hello, Thank you for letting me join your group. My name is Linda Angela Hoecker. I do not have MS but I am here to learn and understand. I'm a second-degree...
Hello everybody Sorry I haven't posted since joining it's just been some busy months. I have had R&R MS since 1989. I am 45 yr old widower and I enjoy cooking...
Ginseng sometimes helps fatigue. It helped me almost as much as caffiene for awhile. I still take ginseng even though it does not seem to help my fatigue...
Every single symptom Jen has, I have. I still don't have an official diagnosis because all my tests are "clean" too. My Dr finally gave me something that's...
Hi, I have been diagnosed with multiple scloresis in 1986. I was pretty young and scared. it affected my eyes first and eventually I lost the vision on one of...
What suggestion do you have for losing weight? I should weigh 115, but weight abit over 143. I am doing 'gentle yoga' two times a week, and I don't think you...
Hello group, I have been lurking around for a while and reading some of your postings. Ever since my mom was diagnosed with MS 9 years ago, I have been afraid...
Wow, that's a great love story from Happy in Kentucky Derby Land. I also met my man on the net, about 7 years after being diagnosed (and about 4-5 years ago)....
Hi everyone, is there a place that you go to purchase things that you need, like special chairs, home improvement items, or anything that would help in your...
I had a weight issue before I started taking this medicine (El Dopa) which luckily has something in it that made me lose weight. Have you asked your doctor for...
I don't think weight has anything to do with it. My left leg doesn't work that well, and it doesn't matter that I wasn't overweight when it started, and it...
Just wanted to say Hi to everyone. Just joined this morning. I need a place that has a good view and attitude toward life with this MonSter. Actually, what I...
I don't think weight has anything to do with it all, was just providing an example of ignorant things people say. El Dopa is the nickname of a Parkinson's...
Hi all, I have hashimotos thyroid disease along with the MS. Since I was just recently diagnosed with the MS I haven't started treatment yet. I am trying to...
Sherry is right! Sometimes we shouldn't take all of our symptoms too seriously, although we need to be cognizant that we can share with our Doctors that...
Has anyone else had this awful pulling down feeling that can last for hours. Even my tongue feels like it is being pulled down. Every part of my body, while...
I am concerned that your doctor says you shouldn't be on MS meds because you aren't "bad enough." The MS Society has recommended that people go on one of the...
Having problems with message search?
Fill out this form to ensure your group is one of the first to be migrated to the new message search system.
Offline 
Send Email