You can tell him with the actions of loving kindness. Don't worry so much about "telling" him him. Words can often fail, as you know. I love you is fine, but...
bubbina_1999
May 2, 2006 9:05 pm
4509
I found a this good link to look for new info on M.S. There is good news about larger doses of Copaxone. It's worth looking at: http://www.medlineplus.com/ I'm...
My daughter who is 29 and just diagnosed last June has been on Copaxone since Christmas time. She has already had another episode since starting it. Is this...
Hi, this is Sherry. I would say just love him. Did he just get diagnosed? If he did, he probably is dealing with all the issues and symptoms. I started with...
Since your daughter was just diagnosed she doesn't have much history to know if the Copaxone is working or not. It should decrease the frequency of episodes....
Hi everyone! I'm Toni. I'm 39 and was diagnosed with MS 2 weeks ago (I actually started having the attack on my birthday, 3 weeks ago - I just ignored the...
Hi everyone I just wrote this big long post and then accidently erased it so I'll just get straight to it this time. I joined awhile ago but stopped reading...
Hello. My dear husband just had an MRI last week to rule out MS. He is 51. We have two sons, 3 and 7. I am 39. We live in southeast TN. We have been...
I started with blurry vision, fatigue, trigeminal neuralgia, cramps in back, and chronic depression. I was lucky enough to start my treatment with a wonderful...
I took my first shot today! i used the autoject and put the shot in my leg. It didnt hurt at all, until after ... it stung just a little and I have a big red...
And...I'm glad they caught it so quick. There are some wonderful treatments out there that slow down the progression of MS. I've been on the Beta Seron for 5...
Hi, I've been on copaxone for several years now. It's a daily injection just under the skin so a small needle. There are no flu-like symptoms with Copaxone....
Hooray for you. The Copaxone is usually well tolerated. The injections become very routine. I have been using Copaxone for several months now and had one...
Hey Everyone I have a question that I would like to ask. I have been on Copaxone for 2 yrs now. I am thinking about changing over to Avonex. If you are on...
Hi all, I am thankful I found this site. I am currently being tested for MS, and really confused. All my troubles started with an electric type shock...
I don't recommend switching to Avonex -- it's been found to be the least effective MS treatment -- plus the interferon side effects were tough on me, I had...
Hello everyone, Sherry here. I've been on vacation in TN, great time. Just read some of the last posts. I've been on Avonex and Copaxone. Currently on the...
Good evening everyone! I had just typed a long message when I hit the wrong key - oops! I'll try to remember most of it, but I was rambling :-) Thank you for...
Hi everyone - I went to my family reunion this past weekend. It was entertaining, to say the least. I had been trying to figure out how to tell them about my...
Hi! I was diagnosed with MS a year ago ~ my neurologist told me all the options for meds and I chose Copaxone. When I 1st started my shots - I had some...
My husband, who is 52, was just diagnosed with progressive MS. We're not sure about the primary/secondary part. He has balance isssues. We have been going to...
Hi all, I am brand new here, and glad I found this place :) In late March, I was very stressed out with work piling up and very little rest. 10 days later, I...
Hi! I'm new to all this but was so impressed with the message about the family reunion etc. The positive attitude will take you far and not let this disease...
Hi, I'm new with questions too & I'm hoping to get to know you all and interact. So sorry for what you've gone thru. I was told about 20 years ago I might...
Hey people, I am Amy about to take the plunge and move in with my guy who has MS. His symptoms at the moment are: Bi-Polar, depression, fatigue and weak left...
My doctor has started talking about moving me over to Tysabri. I have been on Avonex for about 5 years. Just wanted to see if anyone here is using it and has...
I would definitely get a second opinion not only to ease your mind but because if it is MS you should get on one of the meds that slow it down as soon as...
Hello, my name is Sherry. It doesn't hurt to get a second opinion. Some of my first symptoms were optic neuritis and my leg going numb, especially first...
I have been told I should go on intermittant catheterization. Does anyone have any experience with this. I am told once you start you can't stop. Needless to...
