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#1 | |||
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Senior Member
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Welcome back Sunflour, it's good to "see" you. Please join in here on the board too -- quite a few of us can't "chat" anymore.
![]() Welcome Clark! Nice to meet you, but sorry it's here on the MS board. It sounds like you're having a flare (relapse) and is probably why you were diagnosed. I'm not sure if anyone can prescribe IVSM (steroid infusion -- solumedrol) until your appointment with the neuro, but that's the usual course of action. Sometimes Prednisone is given also. These usually help to end the relapse and send your MS back into remission. Did you have many symptoms before this exacerbation? Hope you get some help soon and find what course works best for you. Take care! ![]()
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_____________________________________________ .....Judy SPMS -- FIBROMYALGIA -- Ouch! and Ouch! . |
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#2 | |||
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In Remembrance
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Welcome to NeuroTalk, Clark.
![]() Please come join us. ![]()
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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"Thanks for this!" says: |
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#3 | |||
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Elder
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Hiya Clark. Pull up a chair and squat a while. We would love to hear your story.
hugs to all the new wee ones, come on in! ![]()
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RRMS 3/26/07 . Betaseron 5/18/07 . Elevated LFTs Beta DC 7/07 Copaxone 8/7/07 . . |
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"Thanks for this!" says: | clarkstar (10-05-2010) |
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#4 | |||
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Senior Member
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Hi sunflour and welcome back. I wasn't on here ten years ago but I wish to welcome you back to our friendly neighborhood.
![]() Hi Clark, Welcome! I'm glad you found us. Yes you do sound like you are in a relapse. Call you Neuro and see what he thinks. Maybe you need to start with IVSM (IV steroids) before going on Avonex or one of the other DMD's. The DMD's won't help you to get out of a relapse, just considered long term therapy. Good luck and I hope you feel better. I get bad and then good again, it's the nature of the beast. (MS). Nice to meet you.
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LADY May happiness be at your door. May it knock early, stay late, and leave the gift of good health behind. "Life is what it is". We can only focus on controlling those things we can control, we must let go of the things we can't. |
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#5 | ||
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New Member
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Hi everyone,
I am just seeing this site for the first time today. It seems like there are heaps of information and support to be found here. Maire DX probable MS because of my abnormal MRI and negative LP. |
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"Thanks for this!" says: | barb02 (10-07-2010), Blessings2You (10-07-2010), Debbie D (10-05-2010), Dejibo (10-11-2010), Lady (10-05-2010), SallyC (10-05-2010), Twinkletoes (10-13-2010) |
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#6 | |||
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In Remembrance
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Welcome to NeuroTalk, Maire. Nice to meet you. Come on in and join your new family..
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ Last edited by SallyC; 10-05-2010 at 11:17 PM. |
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"Thanks for this!" says: | Lady (10-05-2010) |
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#7 | |||
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Elder
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Welcome Sunflower, Clark, and Maire!! loads of info and support here!!
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Instant Karma's gonna get you-gonna knock you right in the head...John Lennon |
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"Thanks for this!" says: | SallyC (10-05-2010) |
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#8 | ||
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New Member
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Hi, I was diagnosed with MS in January 1998. I didn't start medication until after my second child was born. Started Avonex in 1999. Took that for about 6 years until I had a big attack and my neuro switched me to Rebif. I have been on that for the past 5 years. I have to admit that I wasn't the best at taking the shots three times a week. I recently had a bad MRI and now my neuro wants me to swith to either copaxone, Tysabri, or gilenia. I know I can't do copaxone. If I was not good about 3 times a week I'm sure I would be a nightmare if I had to take a shot every day. I am so torn between the T and G. I would like to take the G but am worried because it just came out and because of risk of infection. Have been trying to research my options and came across this board. If anyone has any input I would really appreciate it.
Thanks, Lisa ![]() |
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#9 | |||
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In Remembrance
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Hi Lisa and welcome to NeuroTalk.
![]() I'm sorry that the MS Meds arent working for you so far.. ![]() ![]() I don't have any suggestions, other than LDN, because It has help me to stay stable, when the DMDs did not. I hadn't tried Tusabri and for some, it works and seems to be a good thing, but for some, it does not work at all and then of course, there is that looming risk of contracting PML. I hope you stay right here and work it out with us. There are plenty of people here on one DMD or the other, who will tell you of their experience. We will support you, whatever method of treatment you choose. ![]()
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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"Thanks for this!" says: | Lady (11-06-2010) |
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#10 | |||
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Elder
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Quote:
Welcome to the club house!
__________________
RRMS 3/26/07 . Betaseron 5/18/07 . Elevated LFTs Beta DC 7/07 Copaxone 8/7/07 . . |
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Closed Thread |
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