I had my 2nd just 4 weeks after my initial episode. Dr. Kerr and my neuro don't call it that - my first episode was just a continuation of my initial. But with that much time in-between, I call it my second! If I had a cold, recovered, and got another cold a month later isn't one continutal cold - not to me.
Candy K.
-----Original Message-----
From: "Tim Holder (Work)" <[EMAIL PROTECTED]>
Sent: Jun 11, 2007 1:20 PM
To: tmic-list@eskimo.com
Cc: tmic-list@eskimo.com, [EMAIL PROTECTED]
Subject: RE: [TMIC] otCould you all talk a little bit about the “2nd episodes?” I haven’t had a second episode. I’m wondering how far it was between the first one and second one. I understood from researching TM that 2nd episodes were relatively rare. But, it seems quite a few of you have had more than one. Maybe I should get my house really cleaned up…just in case. You are all so inspirational to me. I know that my symptoms are nothing compared to what many of you experience. So, I’m not going to complain about my minor aches and pains.
Tim
Tim Holder
Worship Leader for
Celebrate Recovery
(501)224-7171 ext. 1454
Fellowship Bible Church
1901 Napa Valley Drive
Little Rock, AR 72212-3913
From: cakalley [mailto:[EMAIL PROTECTED]
Sent: Monday, June 11, 2007 8:28 AM
To: [EMAIL PROTECTED]
Cc: tmic-list@eskimo.com; [EMAIL PROTECTED]
Subject: Re: [TMIC] ot
When I asked my neuro, he said that (I'm paravasing) it depends on how deep the attack on the myeli, the shaft surrounding the spinal cord, and the degree of scar. My C4 - T2 was on my second episode and had already been treated with steriods. All of my leisions were difficult to see on MRI and overlooked on the first couple. Thats why I had 4 MRI's before finding. Maybe that's the difference? Everyone is differant even with other diseases - some people have worst attacks of some disesase, some people react to different meds than others.
God has made each and everyone of us similiar but DIFFERENT - we are like snowflakes - unique and beautiful in our differances.
Candy K.
-----Original Message-----
From: [EMAIL PROTECTED]
Sent: Jun 10, 2007 10:30 PM
To: [EMAIL PROTECTED], [EMAIL PROTECTED]
Cc: tmic-list@eskimo.com
Subject: Re: [TMIC] otIn a message dated 6/10/2007 4:32:37 PM Eastern Daylight Time, [EMAIL PROTECTED] writes:
I have multiple levels. One at C4 to T2 the other at T10 to T12. The T10 - T12 leison made me paralyzed from bra line down. I went thru PT/OT and walked with a walker and was "hell on wheels" in a wheel chair. The C4 - T2 made me a quad. With Plasma Exchange (PLEX) and starting at square one with PT/OT after 6 months I walk with a walker but have no strength for the wheelchair. I can walk 25 - 30 feet but need to stop and rest before going on. I have an electric scooter for those times I need to go out and about. The 2nd episode really zapped me of my strength, stamini and durance. I work in burst of 10 - 15 min. before I need to rest which maybe from 20 min to hours or days depending on what I have been doing. Shopping for groceries is usually a day and half R&R.
I just can't get my mind around the fact that there are paraplegics who are truly paralyzed and those that can walk. There are quadraplegics who are also the same. It seems as though TM ought to stay the same all of the time...meaning I ought to be able to walk a bit like some of you. I don't know if it is better to be one of the "walking wounded" or not. I don't mean it to sound like I think any of you have it easier than those of us in wheelchairs 24/7. I just don't understand the various ways the same disease can affect us.
Is there anyone out there who can explain it better to me?
Love you,
Jude
2 Corinthians 4:17
NLT
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