supersonic-chronic.blogspot.com

Supersonic Chronic

My life with ME/CFS. Thursday, 12 May 2011. Blimey, didn't realise it's been a year since I last updated! As today is ME/CFS awareness day I thought I would spread the word again and have linked last years post. For today I thought I would update a year on. Thankfully I have lots of postive things to add to the list! In a short and sweet nutshell:. I was awarded DLA at appeal. High Rate Mobility and Low Rate Care for 2 years. My ESA was renewed with no problems and no medical for 18 months. There have be...

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Supersonic Chronic | supersonic-chronic.blogspot.com Reviews

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My life with ME/CFS. Thursday, 12 May 2011. Blimey, didn't realise it's been a year since I last updated! As today is ME/CFS awareness day I thought I would spread the word again and have linked last years post. For today I thought I would update a year on. Thankfully I have lots of postive things to add to the list! In a short and sweet nutshell:. I was awarded DLA at appeal. High Rate Mobility and Low Rate Care for 2 years. My ESA was renewed with no problems and no medical for 18 months. There have be...

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Supersonic Chronic | supersonic-chronic.blogspot.com Reviews

https://supersonic-chronic.blogspot.com

My life with ME/CFS. Thursday, 12 May 2011. Blimey, didn't realise it's been a year since I last updated! As today is ME/CFS awareness day I thought I would spread the word again and have linked last years post. For today I thought I would update a year on. Thankfully I have lots of postive things to add to the list! In a short and sweet nutshell:. I was awarded DLA at appeal. High Rate Mobility and Low Rate Care for 2 years. My ESA was renewed with no problems and no medical for 18 months. There have be...

INTERNAL PAGES

supersonic-chronic.blogspot.com

1

Supersonic Chronic: Quelle Surprise.

http://supersonic-chronic.blogspot.com/2010/04/quelle-surprise.html

My life with ME/CFS. Wednesday, 28 April 2010. Got my DLA decision today. Turned down flat, no mobility component, no care component. According to them, without even seeing me. Walk up to 50 meters - WRONG. Wash, bathe, shower or dry myself - WRONG. Dress and undress - WRONG. Get up and down stairs - WRONG. Not at risk of falling - WRONG. I do not need help to:. Use a cooker - WRONG. Carry and lift safely - WRONG. Get in and out of a chair - WRONG. I'll see them at the tribunal then.

2

Supersonic Chronic: Weekend update

http://supersonic-chronic.blogspot.com/2010/03/weekend-update.html

My life with ME/CFS. Monday, 29 March 2010. I had a lovely weekend, got out of the house and enjoyed some sunshine! We went off to see Alice which was great, I really enjoyed it and then we went for a meal at the Brewers Fayre afterwards which was delicious! It did wipe me out though and I spent the rest of the Saturday dozing on and off on the sofa all evening, I think I spent more of it asleep than awake. Don't like the idea of him doing it. I'm at the stage now where I know if it will tire me out too ...

3

Supersonic Chronic: "There's no such word as can't!" ...wanna bet?

http://supersonic-chronic.blogspot.com/2010/04/theres-no-such-word-as-cant-wanna-bet.html

My life with ME/CFS. Thursday, 8 April 2010. There's no such word as can't! It's taken me all afternoon to fill in (what I can) the ESA50. Form and I could only complete about 20% of it the rest I have to wait to fill in when Jeanine comes over tomorrow. The coping mechanism is the brave face, the 'don't worry about me! Do The list gets longer and longer as you go through the form and the 'Can't's' woefully outnumber the 'Can's' by 20 to 1. Food for thought? Subscribe to: Post Comments (Atom).

4

Supersonic Chronic: ME/CFS Awareness Day

http://supersonic-chronic.blogspot.com/2010/05/mecfs-awareness-day.html

My life with ME/CFS. Wednesday, 12 May 2010. I'm not the most skilled blog writer in the world, I'm one of those that blogs by saying I did X,Y and Z today, there you go! But today I want to make a difference, even if I just make ONE more person aware of this disorder then I will be grateful. This invisible disorder has slowly turned me invisible. I've never had a massive circle of friends but I had a good social circle at work which has withered down to 2 or 3 that still keep in touch with me. I have to...

5

Supersonic Chronic: April 2010

http://supersonic-chronic.blogspot.com/2010_04_01_archive.html

My life with ME/CFS. Friday, 30 April 2010. This week is proving to be quite eventful. Wednesday was the day I got my DLA decision after waiting 2 months. As much I was expecting the result I think it angered me even more because they haven't even given me a medical. Needless to say I'm appealing and will take it as far as I can go. I also had to go with Charlotte to the hospital as she was called for another 24hr ECG to see how her heart is doing. I also got my letter through from Physiotherapy, there i...

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Supersonic Chronic

My life with ME/CFS. Thursday, 12 May 2011. Blimey, didn't realise it's been a year since I last updated! As today is ME/CFS awareness day I thought I would spread the word again and have linked last years post. For today I thought I would update a year on. Thankfully I have lots of postive things to add to the list! In a short and sweet nutshell:. I was awarded DLA at appeal. High Rate Mobility and Low Rate Care for 2 years. My ESA was renewed with no problems and no medical for 18 months. There have be...

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