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My MS Story | The ups and downs of life with MSThe ups and downs of life with MS
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The ups and downs of life with MS
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My MS Story | The ups and downs of life with MS | mymsstory.wordpress.com Reviews
https://mymsstory.wordpress.com
The ups and downs of life with MS
mymsstory.wordpress.com
June Neuro Appt | My MS Story
https://mymsstory.wordpress.com/2012/06/27/june-neuro-appt
The ups and downs of life with MS. June 27, 2012. I had my June appointment with Dr. Rossman yesterday. I got my results from the MRI in May and was happy to find I have NO NEW LESIONS! The Tysabri must be doing it’s job. As far as the MRI and my symptoms show, the disease is not progressing. My monthly infusion went normally. Just gotta keep putting one foot in front of the other and hoping everything stays stable! Leave a Reply Cancel reply. Enter your comment here. Address never made public).
Walk MS 2014 | My MS Story
https://mymsstory.wordpress.com/2014/05/02/walk-ms-2014
The ups and downs of life with MS. May 2, 2014. Is gearing up for our fourth annual Walk MS. We are raising money for MS research. We are excited that we have already raised over $6,000 for the cause. I am on a treatment right now that is keeping me relatively stable, but I still need a cure. I struggle daily with the effects of MS. Fatigue, tingling, numbness, headaches, impaired vision. I go to bed every night praying that I don’t wake up in the morning with any new symptoms. Visit my donation page.
Walk MS 2013 | My MS Story
https://mymsstory.wordpress.com/2013/04/17/walk-ms-2013
The ups and downs of life with MS. April 17, 2013. For the third year in a row, a growing group of my friends and family are getting together to fundraise and walk toward a cure for MS! I am in the relapsing/remitting stage of the disease, and I’m currently in remission. I go to Farmington Hills once a month and have a 2 hour IV infusion. The medication I’m currently on is Tysabri and it is working very well at keeping me stable. However, it is NOT a cure. Donate to Team Tonya. Leave a Reply Cancel reply.
How Am I? | My MS Story
https://mymsstory.wordpress.com/2012/04/24/how-am-i
The ups and downs of life with MS. April 24, 2012. It has been a while since I posted how my MS is doing. As they say, no news is good news! I am officially off my Zoloft. I had a busy week early in April where I forgot to take it and when I realized I forgot, I decided to see how things went without it. I’m happy to report things went just fine! How amazing is that? We had a great time without incident. I’m still in vacation hangover mode this week, but I feel my energy level coming back. You are commen...
May | 2014 | My MS Story
https://mymsstory.wordpress.com/2014/05
The ups and downs of life with MS. Archive for May, 2014. Is gearing up for our fourth annual Walk MS. We are raising money for MS research. We are excited that we have already raised over $6,000 for the cause. I am on a treatment right now that is keeping me relatively stable, but I still need a cure. I struggle daily with the effects of MS. Fatigue, tingling, numbness, headaches, impaired vision. I go to bed every night praying that I don’t wake up in the morning with any new symptoms. And mail it to me.
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MyMSSpeech.com
You have no items in your shopping cart. We specialize in software for WSR (Windows Speech Recognition). Our WSRToolkit. Adds many features to WSR. These include easy to create macro shortcuts without programming, and accuracy features among others. Click the link to read about all. The WSRToolkit works with Windows 10, Windows 8, Windows 7 and Vista computers. Use our Chat Forum. For support and to get your questions answered. Getting Started with Windows Speech Recognition. WSRMacros: The Users Guide.
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my story: one womans journey with ms (75%, $2850
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My Story - One Woman's Journey With Multiple Sclerosis (MS)
My Story by Val Moffat:. E-book containing methods of controlling the symptoms of Multiple Sclerosis. In 1981, Val Moffat. Was diagnosed with Multiple Sclerosis. By 1983 she was completely housebound. Valerie Moffat walks, drives, showers and cooks for herself and no longer suffers constant shaking, trembling, chronic fatigue, double vision or slurred speech. My Story: One Woman's Journey With MS". Is the story of Valerie Moffat and how she learnt to control and overcome the symptoms of MS. Found it incr...
My MS Story | The ups and downs of life with MS
The ups and downs of life with MS. The Incredible Shrinking PML Risk! March 7, 2018. In August of 2015 we decided I would get my Tysabri every 8 weeks instead of every 4 weeks in hopes of lowering my PML risk while maintaining effectiveness [see this post. For more info]. There were no studies done and no definite info about whether this change would make a difference, but today we found out this:. EID – Extended Interval Dosing ( 15 doses in 18 mo). July 30, 2017. I live with acquired monocular vision&#...
MS Blog | The greatest WordPress.com site in all the land!
The greatest WordPress.com site in all the land! A New Day, an Old Dog. It’s been a couple of days since I last posted an update. What the hay, I’ll post another! Thump, thump….Nope. Either I’m just so dazzlingly gorgeous they can’t take their eyes off me, or they know something’s up. 🙂 Dogs are weird that way. It just makes me all the more curious what’s going to be on that MRI tomorrow. The fatigue, I think is probably the worst part. I wish I could train these dogs to do all of the necessary thin...
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