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Check In Time For All MIAs.

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Old 07-17-2010, 01:22 PM #1
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Default Check In Time For All MIAs.
OK, I know we're a little boooooring, this Summer and not too entertaining....even when we're here....but, we still miss you and wonder if you're okie dokie

DM, Jappy, AMN, Cheryl, Chris, Bill, Moose, Pete, Larry, Frank ....to name just a few. The rest of you know who you are and so do I. Your names are in the windmills of my MS brain, but I miss you all, very much.

Come on you guys, don't forget us, we still love you and need you.
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Old 07-17-2010, 09:36 PM #2
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Here I am Sally dear!!
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RRMS DX 01/28/03 Started Copaxone again on 12/09/09
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Old 07-18-2010, 11:41 AM #3
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Thanks, Sally. I've been hanging around, but mostly just posting on the welcome pages. I did post today in the Tysabri forum, and will make a conscious effort to start posting again.
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Old 07-18-2010, 03:20 PM #4
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We've chased many of the guys away...what gives?
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Old 07-18-2010, 05:45 PM #5
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I'm here, just a little under the ms fatigue thing and not doing much of anything. I thought I would check in today, so hi to everyone!
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Old 07-18-2010, 07:26 PM #6
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Hi Wizzy, Maryann, Debbie and SW...I love you guys.
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Old 07-18-2010, 11:00 PM #7
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Default chemo drugs and MS?
sorry, I was wanting to start a new thread and posted on this one!
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Old 07-19-2010, 07:17 AM #8
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Ah Sal,
We're not boring. We're fassscinating, aren't we?I think you are.
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Old 07-19-2010, 09:21 AM #9
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Hi everyone! I'm here! Nothing new with me.....same old boring same old......but I like consistency!
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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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Old 07-25-2010, 12:21 PM #10
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I'm back to working full time myself, so I find time to sit down and read the boards is getting more and more difficult. I'm usually out and about walking/enjoying the summer and doing chores.

Besides that, I think after my initial diagnosis, I just wanted to go about living my life. I find my best defense is to sometimes forget I have this disease. Which I'm truly thankful that, other than my head pains and occasional sensory symptoms, I can.

Distance is good, but this is still the best place to come and connect, vent, etc with others who understand us
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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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