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Don't copy me. |
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Isn't it your bedtime Sal! :Zzzz: :D:D:D:D |
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Look who crashed the party!
Hello all, I've also got a case of Mass Exodusitis (oh yeah, and MS). this place is kinda huge so I'm feeling a little overwhelmed at the moment. Anywho, I'm glad to see some familiar people and am looking forward to getting to know those whom I don't already. Take care. |
*Stands* I am an MSW apostate. *sits back down*
I'd love to post cute animated pics like y'all, but I don't even know how to get my VCR off 12:00. Lol. My creditials: RRMS dxd April 2006. On Copaxone. Is it okay if I hang out here? (Do I have to go thru hazing or anything like that to belong?) *wanders off to look for red carpet* |
I hope there isn't a hazing! LOL
Sassy, you didn't mention a hazing. |
:mfr_wha: A HAZING?!?!?!?!?!?!?! Wha'????? Say it ain't so!!!!! :Scratch-Head:
<----newbie who obviously likes the fun smilies :Grin-Nod: no, where's the diet coke smilie? |
As long as the hazing doesn't involve stickiness and feathers!
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Newbie
Hello to all and hugs to you for being survivors of your illness'. :hug:My name is Kim and I have probably the same things as everyone else!! :D DDD, Scoliosis, Tremors, RLS, Severe Spinal Stenosis, & oh Bi-polar! Some days it doesn't pay to get out of bed, but then if I don't, the pain is just as great as getting up. Can't sit, lie, or stand for very long periods of time. I am glad I have you all to converse with and laugh with. If we can't keep our humor about us in our conditions, we may as well not get up at all. :)
Maybe someone can enlighten me about docs. My neuro said he could not do anything for me. Hell, I guess I am looking forward to a chair, NOT! :mad: My mind refuses but my body keeps saying, guess what? So there you have it. I am 55 single and happy. Feel free to stop by sometime, up for conversation. See ya! :cool: |
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Hi everyone! I said this on another thread, but want to make sure everyone notices me (since humbleness is my best virtue). I am also a part of the MSW mass move. Funny, I never got my engraved invitation to come here. Thanks to Putter I found all y'all.
I am a 39 y/o Swamp Yankee now living VA. Been with my DH Michael for 18 years and we care for my DSister Sara. I have a goofy dog (golden ret/irish setter) and a very vocal cat. I am "highly probable" on 2nd neuro. Have the asociated issues to make life interesting. Cuff crutches and AFOs for most of the day and a chair for field trips. I dont drive due to seizures so watch out I might ask for a ride on the next road trip. Feel like I have found the secret clubhouse:grouphug: jane |
We have to go thru hazing?!? Oh no, and me without a party dress!
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Newbie here although feel at home with several familiar faces.:) Glad to see them.
I did an intro on the New Member board but it's been a few hours and it hasn't posted. Don't know where that went. LOL. Fumbling through how this new board works. LOL I really don't feel like going through the hazing process. Besides, how would I be hazed with MS? Walking 50 ft without an assistive device? Stepping in and out of the bathtub more than twice? Or maybe a neuropsych test? LOL |
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here it is: http://neurotalk.psychcentral.com/sh...637#post190637 i think it got bumped to page 2...or 50...since we have been rather busy today. :hug: |
LOL, Thrik.:D WELCOME!!! Nice to meet you. :)
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ROTFL! :D |
Hey everyone! I also posted on the new thread and I think I am there, but I thought I would say hi here also. so HI!
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Welcome, Barb. I hope to get to know you..:)
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I am another member of the aforementioned exodus. I hope I have found a new home. I was feeling lost and sad before and now I have hope!
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Nice to see you Holly and Welcome..:)
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Hi!
I am Janie and my dh and I are retired (I took early retirement because of MS-CIS problems) and living in Arizona. I am so happy to find a warm welcome and so many familiar names and faces here! :D We are leaving in the mornin' for a weeks vacation in a rainy California. We will be on a bus trip to Reagan library, tour of Air Force One, Cal Poly Arabian horse training, and some other places including Lawreys Prime Rib in Beverly Hills where we have to dress fancy! :cool: Us desert rats arent used to getting all gussied up!! I was really going to miss you all so glad we can all be a family again and not just talk shop!! :grouphug: Azjanie formerly known as AZmomma |
Hi everyone. I'm a newbie and I posted on the other thread but thought I'd sign in here too! :)
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I'm Faith.
Have had MS for 6 years. Been dx for 4.
Tend to have big flares, about a year apart. 2-week hospitalizations, etc. Big variety of symtoms -- stroke-like -- cognitive, manic, vision, etc. Most recent flare was finally less severe. Just lots of fatigue. I attribute that to double dose of /betaseron, and sleepng pill at night during steroids to help me get adequate rest. Good to meet you all. ~ Faith |
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ANOTHER PERSON FROM GA.!!!!! Where do you live? I'm Chris and we've just been here less than a year. I believe you are the first person I've met on here from GA. :Wave-Hello: Welcome to the rest of you who joined us today as well. We're a wonderful family if I say so myself.:grouphug: |
Welcome to you Faith....So nice to have you here at home.:)
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Hi Everyone!:)
I am from Oklahoma City and just found this site today.:grouphug: |
Just found this site an hour ago.... and very grateful.
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Welcome Moose! I'm glad you found your way here! :)
Becky - welcome, again :) |
:Wave-Hello: Hey Kitty Janie, Moose and Becky....Welcome!!:)
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I'm new, too
Just found y'all an hour or so ago.
Intro - Karen, from Buffalo. Dx RRMS 6/05. Doing pretty well since starting Tysabri 2/07. I think I'm going to like it here :) |
I see Janie, Moose, Becky21, Krohe . . .
Welcome everyone. Glad you found us. |
Hi eveyone! I found my way over, sad and glad in the same breath. Hope I can bring something to this forum. Thanks for having me!
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Hi Pawndude. Welcome to the "other" side. lol. Glad you found your way here.
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A community that has something for everyone....I LIKE IT. :D
Hi....I'm sooo glad I found my way here. Just hope I can continue to find my way back. I get lost alot. :wink: I'm a 54 yr. old Wife (married 30 yrs in June), Mom of 3, Grandma of 4. I live in Illinois and Wisconsin, mostly Wisconsin. I was dx'd chronic progressive MS in Feb. 2002, and that was just the beginning. In Aug. 2002 had back surgery, and have numerous spinal problems. Arthritis, mild scoliosis, osteoporosis, and dx'd last fall with Degenerative Disk Disease. In 2004 I was dx'd with Autonomic Dysfunction w/vasovagal episodes and syncope. And just recently severe hypertension which has been impossible to get under control. I was forced into early retirement in July 2002 because the MS took total control of my body. The first hit was to the short term memory, then the eyes (double vision and oscillopsia), drop foot, trigeminal neuralgia, optic neuritis, tingling and numbness. Walked and talked like I'd been on a 3 day drinking binge....spent 1 year in bed, fairly incoherant. To be honest, right now I am angry, depressed, hurt and really don't find life much worth waking up to. I guess that's why I came in search, but I'm not sure what I'm searching for.:( |
Hi everyone.
Gad to see you! Happy to meet you!! Purrrrrrrrrrrrr |
Oh, wow. This is a little confusing. Introduced myself I guess in the BIG main section. Going to take a while to get used to the different navigation!
Dxed with MS very quickly after a bout of ON last March. Hello to everyone I don't know and to those I do, good to see you!! :grouphug: |
Just a Bit About....
Hi everyone, I'm John from Louisville, KY. I'm retired from the Army as a Senior Law Enforcement officer. I'm now a Political Editorialist for a regional newspaper here and a veteran activist along with my work with the American Legion. I was diagnosed with MS just a couple of months ago at the ripe young age of 56 so it's been a learning experience for me, but not an experience that I'm planning on letting get me down. I don't have time for it to get me down. Looking forward to getting to know you better.
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:Wave-Hello: Hello Pawndude, Bearygood, Guyskitten, pepper and JoHnKy and :welcome_sign: to NeuroTalk.
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Take a look around, as there are alot of forums to navigate. Glad to see you. :trampoline: |
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