my-ms-and-me.blogspot.com
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).
my-ms-and-me.blogspot.com
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...
my-ms-and-me.blogspot.com
My MS and Me: February 2014
http://my-ms-and-me.blogspot.com/2014_02_01_archive.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: Posts (Atom). Carnival of MS Bloggers. Relapse...
my-ms-and-me.blogspot.com
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.
my-ms-and-me.blogspot.com
My MS and Me: February 2015
http://my-ms-and-me.blogspot.com/2015_02_01_archive.html
How does MS feel? Tuesday, 10 February 2015. Let's face it. Nobody really feels comfortable talking about their bladder or bowels. It's something that you have to get use to when you have MS. A routine question at the end of an appointment with the Neuro or MS Nurse is "bladder, bowels? I nearly reached the ladies in time. Really nearly. Ever changed a nappy? You get the picture. I cleaned up with the cheap nasty toilet roll our building supplies, and then again and some more. Knickers went in th...And t...
my-ms-and-me.blogspot.com
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...
tejascubbie.blogspot.com
The Gimp Chronicles: Shade-Stealing Crips
http://tejascubbie.blogspot.com/2013/11/what-hell-is-aetnaother-insurances.html
The Gimp Chronicles: Shade-Stealing Crips. An exasperated and probably often angry look at life in general and with multiple sclerosis in particular, because, "It's not Lupus! Wednesday, November 06, 2013. What the hell is AETNA/other insurances thinking with this "Step Treatment"? Check this out, few readers and NSA types:. A documented diagnosis of relapsing remitting multiple sclerosis AND. Documentation of all of the following:. Recent (within 6 months) complete blood count (CBC). EVERY one of the fi...
tejascubbie.blogspot.com
The Gimp Chronicles: Shade-Stealing Crips: February 2013
http://tejascubbie.blogspot.com/2013_02_01_archive.html
The Gimp Chronicles: Shade-Stealing Crips. An exasperated and probably often angry look at life in general and with multiple sclerosis in particular, because, "It's not Lupus! Wednesday, February 06, 2013. So it's clearly been too long, during which time I've gotten a temporary title and money raise, and for the most part my MS has been manageable except for recent muscle weakness issues. Subscribe to: Posts (Atom). House's cranky diagnostician granddad. House- happy as ever. John and Lionel Barrymore.
