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10-11-2008, 12:03 AM
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Junior Member
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Thanks all for acknowlaging me and my entrance to a comunity of fellow why me'ers. Well i know all of us have thought that at one time or thousands. Here we i can talk to a bunch of friends that actually and truely understand why i have the handicaps that i do. You know exactly, EXACTLY what i am saying. Let me tell you about myself but i don't know if in the threads is where i'm suppose to do that. Maybe all could give me advice.
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| "Thanks for this!" says: | dmplaura (10-11-2008), FinLady (10-12-2008), Jappy (10-12-2008), JessieSue (10-12-2008), Koala77 (10-12-2008), NurseNancy (10-11-2008), TwoKidsTwoCats (10-11-2008), weegot5kiz (10-11-2008) |
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10-11-2008, 01:53 AM
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Legendary
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I think you're right! We all understand because we've all been there ourselves.
MS seems to be such an individual disease that we can each have symptoms that are way different to those that other people have, but the common diagnosis draws us together and enables us to share. I've made some wonderful friends since joining this site. Not a good way to make friends I'll admit, but knowing that everyone here understands what I'm going through and will reach out to me when I'm suffering, makes it all worthwhile. Welcome to NeuroTalk. I hope that you too will feel like I do. 
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Eastern Australian Daylight Savings Time and my temperature . |
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10-11-2008, 07:16 AM
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Wisest Elder Ever
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You're in exactly the right place! Post away! We'd love to hear all about you and your journey with MS. It is nice to be able to speak about our condition and know that others understand what we mean. So glad you decided to join the group!
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These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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10-11-2008, 08:22 AM
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Magnate
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Welcome drb!
this is a wonderful place to ask questions, vent, laugh, scream or even cry. You will be amazed at the support you will find here, at least I was! I too have met some wonderful friends here - two have already posted - and I am sure you will too. Post away!
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Tough Times Don't Last ~ Tough People Do Courage is doing what you're afraid to do. There can be NO courage unless you're scared.
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| "Thanks for this!" says: | drb1264 (10-12-2008), Jappy (10-12-2008), JessieSue (10-12-2008), Koala77 (10-12-2008), weegot5kiz (10-11-2008) |
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10-11-2008, 09:02 AM
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I have to 2nd this and say I have gotten GREAT info and support from people here, I really don't know what i would have done sometimes if I didn't have this place to ask questions, vent and sometimes cry on someones shoulder.....this place is great.
Enjoy what ya can Dan, we ALL understand in one way or another and even SOMETIME we understand in ALL ways.......this disease sucks!!! Joe Quote:
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Dxd RRMS 12/23,06, Copaxone 2/07 to 9/07 - Rebif 10/07 to 7/08, BAD flare with Transverse Myelitis & Pancreatitis.....,9/08 Pseudo Cyst!!!! and another TM attack. Started Tysabri 9/22/08 - 10/21 Allergic reaction to Tysabri, SSDI Approved 11/14!! Continued Ty 11/17 with a Pre-medicate. Solumedral 12/11-12/13 Ty #5 Jan 12th! |
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10-11-2008, 09:09 AM
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Junior Member
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Welcome aboard, take your shoes off and stay awhile. You joined just in time rumor has it that some of us R havin a naaaaaaaaaaaaaaked party down at the swimmin hole....
 and naaaaaaaaaaaaaaaked scooter races for pink slips.
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10-12-2008, 06:49 AM
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Member
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Wait a minute. Waitaminutewait A MINUTE!
*gets confused look on face, flips through paperwork on clipboard... You slipped past me.  Well, one big, warm, tight, hug, hanshake and howdy, moose-size official type welcome to the site. This place is amazing! I got the MS too. I'm kinda like a WalMart greeter here... but younger, bigger, louder and much more aggressive.  As you've already seen; You are not alone.  You are one of us.  And we are here to help. Eerie, PA? I got a set of ex in-laws in Eerie. Well, it's Guys Mills actually. Sorry.  They say I'm kinda long winded. Kinda. 
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You can't have everything. Where would you put it? -Steven Wright Once you change your mind, you can change your life. -Della Reese . Always outnumbered... Never outgunned . *I* am the MonSter that MS fears |
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10-12-2008, 10:32 AM
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Magnate
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Hai there!
We're a crazy bunch around these parts, but from my experience, crazy = laughs = the best medicine
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2004 to present - Trigeminal Neuralgia 2007 to present - Burning Mouth Syndrome March 2008 - Multiple Sclerosis DX 05/2008 - Relapse 05/2008 to 02/2009 - Copaxone 10/2011 - Relapse - Optic Neuritis developed 9/2012 - Relapse - Balance issues 1 sided 8/2012 - Erythema Nodosum - diagnosed 10/2012, reaction to Topiramate (Topamax) April 7/14 - Raynaud's Syndrome DX |
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10-12-2008, 11:33 AM
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Junior Member
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I'm starting to think i'm on the wrong talk line. None the less, when does the race start ? You know Charlie i think you and i will be crossing paths often. Plus i have the new BIMFORD 9000 scooter with turbo. So watch out !
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| "Thanks for this!" says: | JessieSue (10-12-2008) |
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10-13-2008, 09:35 AM
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Junior Member
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thanks
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