my-ms-and-me.blogspot.com my-ms-and-me.blogspot.com

my-ms-and-me.blogspot.com

My MS and Me

How does MS feel? Sunday, 13 September 2015. Every September the MS Society in the UK has a fundraising campaign to raise money for research. This is an important and worthy undertaking - there is no cure for MS and a slowly expanding roster of disease modifying drugs. You can read about my #ChallengeMS on my JustGiving page; if you can spare a small donation then it would be much appreciated by the MS Society and people with MS. Tuesday, 10 February 2015. What feels like trapped wind or a vague bladder ...

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My MS and Me | my-ms-and-me.blogspot.com Reviews
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How does MS feel? Sunday, 13 September 2015. Every September the MS Society in the UK has a fundraising campaign to raise money for research. This is an important and worthy undertaking - there is no cure for MS and a slowly expanding roster of disease modifying drugs. You can read about my #ChallengeMS on my JustGiving page; if you can spare a small donation then it would be much appreciated by the MS Society and people with MS. Tuesday, 10 February 2015. What feels like trapped wind or a vague bladder ...
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My MS and Me | my-ms-and-me.blogspot.com Reviews

https://my-ms-and-me.blogspot.com

How does MS feel? Sunday, 13 September 2015. Every September the MS Society in the UK has a fundraising campaign to raise money for research. This is an important and worthy undertaking - there is no cure for MS and a slowly expanding roster of disease modifying drugs. You can read about my #ChallengeMS on my JustGiving page; if you can spare a small donation then it would be much appreciated by the MS Society and people with MS. Tuesday, 10 February 2015. What feels like trapped wind or a vague bladder ...

INTERNAL PAGES

my-ms-and-me.blogspot.com my-ms-and-me.blogspot.com
1

My MS and Me: Another relapse

http://my-ms-and-me.blogspot.com/2012/11/another-relapse.html

How does MS feel? Tuesday, 27 November 2012. The net effect of this is, I certainly get enough rest (I vie with the cat for who sleeps the most). The less useful side effect is that I slowly stultify with boredom. Staying positive, the drug they gave me for the vertigo works (first choice lucky) and I am feeling better than I did two and a half weeks ago. Subscribe to: Post Comments (Atom). Access denied-living with multiple sclerosis. Blindbeard's Multiple Sclerosis Blog. Carnival of MS Bloggers. Everyo...

2

My MS and Me: Cooking with gas!

http://my-ms-and-me.blogspot.com/2012/09/cooking-with-gas.html

How does MS feel? Sunday, 23 September 2012. Last week I bought a 'perching stool' for the kitchen. This is why disabled people need the Disabled Living Allowance. These things aren't cheap. What it means though is that I can cook again. Can cats use it too, eggs up there! Folds away for small kitchens. Just the right solution. Me - cooking again. Subscribe to: Post Comments (Atom). Access denied-living with multiple sclerosis. Blindbeard's Multiple Sclerosis Blog. Carnival of MS Bloggers. On Friday I ta...

3

My MS and Me: June 2012

http://my-ms-and-me.blogspot.com/2012_06_01_archive.html

How does MS feel? Saturday, 9 June 2012. On Friday I take my Avonex shot. It usually goes something like this; eat dinner, take shot, have cup of tea and biscuit, go to bed, take paracetamol, go to sleep. This means that I very rarely experience any real side effects. What with an unscheduled afternoon nap and all the football the day of the week kept slipping my mind yesterday. I took the shot late, and due to the nap in the afternoon stayed up watching TV. Big mistake, huge. Subscribe to: Posts (Atom).

4

My MS and Me: Sleep and MS

http://my-ms-and-me.blogspot.com/2014/02/sleep-and-ms.html

How does MS feel? Tuesday, 4 February 2014. I have a lot of problems with sleep. I never used to. It has all been since MS and I became acquainted. First problem is that all my night time tablets are supposed to make me sleepy. They do about 90% of the time. I think I'm developing tolerance as that 10% I can't sleep at all. When I do fall into a chemical sleep it happens within about ten to twenty minutes. but it does not often last until dawn. Subscribe to: Post Comments (Atom). Carnival of MS Bloggers.

5

My MS and Me: November 2012

http://my-ms-and-me.blogspot.com/2012_11_01_archive.html

How does MS feel? Tuesday, 27 November 2012. The net effect of this is, I certainly get enough rest (I vie with the cat for who sleeps the most). The less useful side effect is that I slowly stultify with boredom. Staying positive, the drug they gave me for the vertigo works (first choice lucky) and I am feeling better than I did two and a half weeks ago. Subscribe to: Posts (Atom). Access denied-living with multiple sclerosis. Blindbeard's Multiple Sclerosis Blog. Carnival of MS Bloggers. Everyones expe...

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My MS and Me

How does MS feel? Sunday, 13 September 2015. Every September the MS Society in the UK has a fundraising campaign to raise money for research. This is an important and worthy undertaking - there is no cure for MS and a slowly expanding roster of disease modifying drugs. You can read about my #ChallengeMS on my JustGiving page; if you can spare a small donation then it would be much appreciated by the MS Society and people with MS. Tuesday, 10 February 2015. What feels like trapped wind or a vague bladder ...

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