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Hey Sally, I am new to this and not computer savvy.Still learning to get around in here! I appreciate the humor that you guys are providing. That's the only way to deal with life.I have RSD(1st in rt leg)recently, however;had rt hand surgery and it followed suit.That just sucks like a big bucket of ticks as my grandmother would say!:)It is wonderful to be able to 'talk' to others who are having any kind of health issues.I was DX'd 16 years ago so, quiet like you, I have many stories to tell. Anyway, I'll try to stop in more often.(even though w/o my hand it takes a while) Keep smiling and Take care of you!!!
Sunny |
Welcome, Sunny..:) Post, whenever you feel up to it. I hope you've found the RSD Forum, too.
:hug: |
Hi Sunny!
Welcome aboard. I'm sure you'll find whatever are you need here. many choices :) :winky: |
Hello!
Hi. My name is Marion. The first time I heard a doctor utter the words “multiple sclerosis” it was 2002. I was officially diagnosed in early 2007.
I have chosen the Mandell Center for Multiple Sclerosis at Mount Sinai in Hartford, Connecticut for medical care. This is a new center in Hartford, and some of the most talented medical professionals in the field are now working together there. It is kind of fun being involved with the Mandell Center at its very beginning. I have been to the center three times now. They seem to know what they are doing. That having been said, I’ll drop them in a New York minute if they turn out to be the “same old, same old” MS center. <<grin>> Life is short, ya know? RollBob (don’t you just LOVE that screen name?) suggested I check this BB out, so I’ve been lurking for a respectable period of time. I look forward to contributing here. I usually feel that I have very little of value to add, but you all seem so friendly – well lets hope I don’t put my foot in my mouth too much. Hello, all! :):) |
Welcome to NeuroTalk, Marion, so nice to meet you. :)
Is your name the male or female version? And who is Rollbob? I'd love to meet him too.:D Join In anywhere and don't worry about the foot in mouth syndrum. We all do with pizazz..:p |
Hello Marion and welcome to NeuroTalk.
It's great to have you here with us, but it's certainly not a great reason why you came lurking. :( We have a very active MS Forum here as you will have seen by now, and we're a strong group who support each other through trials of every kind. Don't forget to pop in to The Stumble Inn, as that's where we het together for a bit of fun. :D |
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You will be suprised how much your opinions, stories or sense of humor can add to the MS forum and other forums here at NT. If you put your foot in your mouth then you fit right in ;) :p |
This is great...The 2nd introduction...So I should have called this Pete RePete..For real....
Hi my name is Pete And I'm a recovering '..Oops sorry wrong group.. Hi I'm Pete..PJAMES from the other place...And sometimes The Other Place Pub if you live in West Boylston.... OK...sorry about the nonsense....I am still in Limbo.....I was actually starting to think..This MS stuff was maybe overblown....Then came the warm...Then the heat.....Then went my sensation...And as the sun shines..My tremors came back----The fog---the buzzing.. Etc..So little ole me went back looking for you folks.... Well here I am... And yes I am very happy to be here..and glad Twinkletoes gave me the address.... |
Hi Pete.....Welcome to NeuroTalk..So glad you found us. We have quite a few still doing the Limbo, here, so just join in anywhere and enjoy.:hug:
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I am so sorry that you are going through this! The summer heat is when I [I]knew[I] that I had MS before the neuro would give me a definite. Once I cooled my body temp down the symptoms went away. I hope you are seeing a neuro and I am glad that you found us...well that Twink sent you here. You will have to let me know where you are at...no I will not stalk you, promise! There is another MSer that lives in Worcester too. She is on here every now and then. Welcome! |
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