This has been a low week on the training front. With having Abigail here for a few days and the dreadful weather as well, there has been a forced break in the time available. So maybe I can just comment on a couple of things that have struck me over the week.
I am amazed at how positive people are with MND. I have mentioned Maria Foreman before. Her facebook page Motor Neurone Together We Stand is always full positive thoughts and it is only occasionally that there is a glimpse of the difficulties that are obviously there.
Then I have recently come across a blog maintained by Pauline Hardy. This is a very honest look at the problems faced and overcome by another sufferer and her family. But, again, she has a very positive attitude towards her condition. Perhaps you could take a look. It makes me appreciate even more how good it is to have good health. We forget how well blessed we are. Pauline has also recently put together this site which explains the condition and how it can affect those with it. MND Laid Bare
And I most not forget Mike Hardy, living at the top of my road. I have never seen him without a smile on his face. He illustrates so well what it is like to have MND. The brain functions as it always has done but the body can't keep up.
In thinking of those with MND, we must remember those who care for them. It quickly becomes a full time job. My father retired early (mid fifties) because my mother needed full time support. Afterwards he said that he had just got to the stage where he felt he couldn't cope any longer. God took her at the right moment. Mike's wife is always cheerful despite the burden that falls on her - even more so with Mike's father's recent health problems.
It must be so frustrating and there seems to be so little support for them and their needs. So although the mountain climbs to Geneva will be tough, I do, at least, know that they are soon over. My hope is that I can raise just a bit more to help someone whose mountain climbs are rather longer than mine.Please help out.
I am amazed at how positive people are with MND. I have mentioned Maria Foreman before. Her facebook page Motor Neurone Together We Stand is always full positive thoughts and it is only occasionally that there is a glimpse of the difficulties that are obviously there.
Then I have recently come across a blog maintained by Pauline Hardy. This is a very honest look at the problems faced and overcome by another sufferer and her family. But, again, she has a very positive attitude towards her condition. Perhaps you could take a look. It makes me appreciate even more how good it is to have good health. We forget how well blessed we are. Pauline has also recently put together this site which explains the condition and how it can affect those with it. MND Laid Bare
And I most not forget Mike Hardy, living at the top of my road. I have never seen him without a smile on his face. He illustrates so well what it is like to have MND. The brain functions as it always has done but the body can't keep up.
In thinking of those with MND, we must remember those who care for them. It quickly becomes a full time job. My father retired early (mid fifties) because my mother needed full time support. Afterwards he said that he had just got to the stage where he felt he couldn't cope any longer. God took her at the right moment. Mike's wife is always cheerful despite the burden that falls on her - even more so with Mike's father's recent health problems.
It must be so frustrating and there seems to be so little support for them and their needs. So although the mountain climbs to Geneva will be tough, I do, at least, know that they are soon over. My hope is that I can raise just a bit more to help someone whose mountain climbs are rather longer than mine.Please help out.