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Old 02-05-2008, 09:01 PM #311
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Just jump in anywhere and enjoy yourself..

So so sorry about your loss..

Quote:
Originally Posted by Cat_In_The_Hat_ View Post
thanks everyone for the welcome.

Yep Sally it's been a long time, but as I emailed U, I'm trying to get back to the living. After my dad died it was very hard to do anything. I miss him so much.

Anyways, I am here, and I hope to get to meet ya'll.
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Old 02-06-2008, 03:47 PM #312
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Originally Posted by Cat_In_The_Hat_ View Post
Hey everyone. I recognize some of you, so I will say a special Howdie to y'all.

Yep I have SPMS and now have developed RSD. Fun and games.

I live in southern ontario, female, married with children and 2 cats and one dog.

Live in constant pain, use wheel chair in home, and scooter outside.

Hate neuros, but then again who does not?

Don't know what else to say except: I'm heeeeeeeeere !
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Yeaaaaa, My Friend CITH is here....So happy you made it. She and I started out long ago at BT and then to Plaintalk and then notta, for awhile., so, I am glad you came.

I hope you like it here.
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Originally Posted by Cat_In_The_Hat_ View Post
thanks everyone for the welcome.

Yep Sally it's been a long time, but as I emailed U, I'm trying to get back to the living. After my dad died it was very hard to do anything. I miss him so much.

Anyways, I am here, and I hope to get to meet ya'll.
Is that Lime Kitty???

So nice to see you here! Welcome welcome welcome!!

I am sorry to hear about your dad. I lost mine a few years ago and still miss him a lot.
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“When everything seems to be going against you, remember that the airplane takes off against the wind, not with it.” - Henry Ford
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Old 02-06-2008, 03:56 PM #313
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Hiya Limekitty - I remember you from PT. I was bird there! Welcome!
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Old 02-07-2008, 02:24 AM #314
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wow lots of people here that I know. This is gonna be fun

I haven't changed, still have a warped sense of humour.
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Old 02-07-2008, 08:02 AM #315
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Hello everyone! I'm new here too. I haven't read this whole thread, but from what I've seen, it looks as though I'll know plenty of people here (and hope to meet some new ones too).

I'm currently living in limbo. It's been about four years now. I have many positive tests (neurogenic bladder, four brain lesions, documented cognitive problems, a history of many attacks, etc), but not quite enough for a dx.

I do know that I have a copper deficiency, so I'm eating pennies (sorry, couldn't resist ). They haven't found out why I have the copper deficiency, and aren't sure if it's causing all of my problems, or just some of them.

Well, I better go. I'm looking forward to getting to know you all.

Sharon
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Old 02-07-2008, 10:47 AM #316
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Quote:
Originally Posted by shalynn View Post
Hello everyone! I'm new here too. I haven't read this whole thread, but from what I've seen, it looks as though I'll know plenty of people here (and hope to meet some new ones too).

I'm currently living in limbo. It's been about four years now. I have many positive tests (neurogenic bladder, four brain lesions, documented cognitive problems, a history of many attacks, etc), but not quite enough for a dx.

I do know that I have a copper deficiency, so I'm eating pennies (sorry, couldn't resist ). They haven't found out why I have the copper deficiency, and aren't sure if it's causing all of my problems, or just some of them.

Well, I better go. I'm looking forward to getting to know you all.

Sharon

Welcome Sharon, There's a few of us in Limbo Land here, I'm been there about 4 years also (I've had problems for about 10 years but was DX with fibromyalgia so I thought that was it until it got real bad 4 years ago).
Glad you found us and can't wait to see you post more.
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Hi, I'm Julie and mommy to 7 little kids (ages 4 to 11).
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DX with Fibromyalgia, 1998
DX with MCS (Multiple Chemical Sensitivity), June 2008
DX with Food Allergies, wheat, sesame, fresh pineapple


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Old 02-07-2008, 12:27 PM #317
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Welcome to NeuroTalk, Sharon.. Nice to meet you.

Just jump in anywhere and enjoy,

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~Love, Sally
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Old 02-07-2008, 10:02 PM #318
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I can't remember if I have interduced myself here on the MS board. I joined the board a few years ago and just lurked but came over with all the others in January...I am my hubbies fulltime caregiver. He was diagnosed in 1986. He has SPMS. Our biggest challenge is beside the fact that he can't walk and a lot of other things is memory problems. He had a real problem with short term mem. He is also challenged with Cog. problems. His name is Craig or the Olhipie as some refer to him. We have been together for seven years and I love him more everyday!!!
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“Being my sweethearts full-time care partner, I have to remind myself, when some well-meaning friend or relative questions my methods or motives, that I know more than they do because I Live this life 24/7, and they only come for short visits.” Tamiloo

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Gotta love my Olhipie! Dx'd RRMS 1986, SPMS 2004

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Watch my Olhipie Skiing....

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Old 02-08-2008, 05:04 PM #319
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HI I'm Jen (Debbie Downer to some ),

New to this, Have fibro, upper thorasic scoliosis, chronic pain. Take Topamaxx 100mg, Cymbalta 160 mg, and Lyrica 150mg, per day. No side effects but still in pain. What the hell is wrong with me? My back hurts every minute of the day even when I breath in and out. MRIs show nothing ... although I do have a slight pinched nerve in the C5 and a bulging disc in the lower back along with TMJ and carpal tunnel running thru both arms. Help me!!:confu sed:
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Old 02-09-2008, 12:10 AM #320
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Woo-hoo! Shalynn's found us too. Glad to see you here
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