BLOGGER, CARTOONIST, CYCLIST, BEARD OWNER & NORTHMAN

DESCENDED FROM NORSE KINGS & NORMAN INVADERS
Showing posts with label CFS/ME. Show all posts
Showing posts with label CFS/ME. Show all posts

Friday, 18 November 2011

1111.18 SINGLE FATHER

Sometimes it's advantageous to sent Morticia away to her Mum's for the week. Her ME can take it's toll on her so a short restbite break is in order. This week, following a visit from her Mum, she went down to the little town of St Neots for the week and left me home with the kids.

It probably sounds like I get quite a lot out of this, you know, suddenly being on my own, doing my own thing etc. this couldn't be further from the truth. The kids, even though they're older are still a handful. Add to that the fact that I still go into work (albeit for half days). Rest for me? Not a chance. It's been all go until 22:30 each night when I have myself a chance to catch up with my Sky+ recordings. Come bed time I find that I don't enjoy sleeping alone (I found this out many years ago).

Today, in fact tonight I drive down to be with her. We return home on Sunday.

Sunday, 30 October 2011

1110.30 A DIFFICULT TIME

I've had a very difficult few weeks. I suffered with a nasty chest infection which knocked me off my feet for a while, I had to take a week off work (and anyone who knows me knows that it takes a lot to keep me from work). On top of that we had more difficulties with our teenager. Thankfully we managed to sort out most of the issues, the challenges remain of course, as they do for most parents of teenage girls.

There are changes afoot in our outlook too, Morticia is being a lot more open about her condition with a view to learning to live with it and come to terms with her life. She is now accepting that she is disabled and she has to live to her abilities and not push herself. I find myself accepting the fact that I am officially her primary carer and also the target for many of her frustrations. Juggling work, being a parent and a carer isn't easy, in fact it is sometimes frustrating and feels impossible. The last few weeks I've had all that on top of illness and teenage issues, thankfully I managed to get through. I feel drained at this moment but determined to make Morticia's life more comfortable.


Sunday, 20 February 2011

1102.20 CFS/ME AWARENESS

I'm currently crusading on behalf of my wife who has suffered from ME for several years and has only just started to receive treatment. The only reason for this is lack of knowledge from health care professionals. I am researching online support both via websites and Facebook groups/pages.

So many doctors don't 'believe' in CFS/ME and most sufferers have to battle just to be diagnosed.

Support us on 12th May for 2011 Blue Ribbon ME/CFS Awareness Day.

http://www.gopetition.co.uk/petitions/justice-for-cfs-me-sufferers.html