This Is MS Multiple Sclerosis Community: Knowledge & Support

I started a new one since my other one is probaby back on page six there's so many new posts! So I was too lazy to bump it and just started this one to let people know that I did update my blog today.

I tried to put the link in my signature line like it used to be. It shows that it's in there when I pull up my profile, but it's not showing on my posts! I just don't understand, nor do I want to, all this BBC code and HTML shit. So here's a link http://myhopefuljourneyintoactualmsreco ... gspot.com/

I used to have it on there and it just disappeared one day when I tried to add a quote to it. Arrrgghh..

Thanks for the heads up Lew, always look forward to reading your blog...
Mark

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RRMS Dx'd 2007, first episode 2004. Bilateral stent placement, 3 on left, 1 stent on right, at Stanford August 2009. Watch my operation video: http://www.youtube.com/watch?v=cwc6QlLVtko, Virtually symptom free since, no relap

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Lew, That was a good blog post. Especially about the MRI's with Dr Haacke to see if the iron in your brain changes for the better (or worse) over time. You will be continuing to help all of us with this important research. Maybe someday I'll finally get to Detroit. If you read my thread about Detroit then you know my scans were postponed due to "MRI software problems" (???). But Paula said that I WOULD be rescheduled. Have a great holiday !!

ozarkcanoer

I appreciate your post too, Lew. It gives me a glimpse into what my husband (46, ppms) may be feeling at times, but is too tired to tell me at the end of the work day and after dealing with our two active kids!
Thanks!
Theresa

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Good to hear you upbeat Lew!

Be patient with the shoulder -- I know, that is not what you wanted to hear. My shoulder is at 100% and it took close to six months to repair. I think you have more healing to do than I did, so maybe another month of two for you. Good idea on the stretches to keep the range of motion.

Good luck to you in Detroit -- can't wait to hear what you find out.

Sharon

Your signature is not showing up - as you are aware. I noticed that mine was not, then noticed that you need to click a box just down below the text box that says Attach signature

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My name is not really Johnson. MSed up since 1993

I don't get it?

Hey Loobie,

Thanks for sharing the blog, it's looking good buddy!

Ref the signature, this should help: Clicky I think it boils down to the link that you use to edit your profile. One works properly, one doesn't

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Mutley goes to Poland 1st symptom was Optic Neuritis in 1998, DX RRMS Jan 2001, DX SPMS 2007. Last EDSS by doctor 7.5

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bumping to see if my signature line works yet

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http://myhopefuljourneyintoactualmsreco ... ogspot.com

I believe the back story is here:

http://www.thisisms.com/ftopict-9157.html

And in case that post gets edited, in a nutshell:




I'm off to check out your new blog post. Thanks for the heads up.