At the moment (touch wood) my Multiple Sclerosis does not really stop me getting out and enjoying the outdoors too much. Beyond the additional fatigue that follows a weekend outdoors, some balance issues as I tire during a hike and some interesting nerve buzzing when ascending a hill (and post river swims), the outdoors is still accessible to me. Positivity is really important when you have an degenerative disease, but it is sometimes really hard to shake the pangs of fear that my future MIGHT* involve significant reduced mobility and the impact the resulting loss of outdoor time would have to my physical and mental well-being. Because of this, the accessibility of the outdoors for people with different abilities (both as a place and the activities within it) is increasing a topic I am interested in (albeit with currently zero knowledge or experience).
In 83 days I, as part of Team Social Hiking, will be on a mountain somewhere in the Lake District taking part in the 10in10 challenge to raise money for MS Society. Actually as it is 6:13pm, I should hopefully be off the mountains and in the pub celebrating with the team after a job well done. But honestly? I am scared, very scared in fact, that I am going to struggle and ultimately fail to complete what on face value seems like a fairly straight forward challenge for a hiker.
Earlier in the year, I came across an article in the MS Society magazine about an annual event where a bunch of people climb some mountains to raise money to help support people affected by Multiple Sclerosis. As I have not done much fundraising in a while, I cut the article out and put it in my in-tray for future consideration, then promptly forgot about it…. until a few weeks ago.
As I re-read the article, it occurred to me that I happen to know a bunch of people who like walking, especially mountains- wouldn’t it be brilliant if we could get together, hike some peaks, raise some money, and have some fun?
So why am I supporting the Multiple Sclerosis Society?
About a year ago, after several years of having symptoms, a family member was officially diagnosed with Multiple Sclerosis (MS). Like most people I was ignorant of what MS is, so when I heard the news I did some research.
It seems a very long time ago when I came up with the idea of walking Offa’s Dyke to raise money for Multiple Sclerosis Society. But now, with just two weeks to go, it is probably a good time to remind everyone what we are doing, how and why. Continue reading “What is Offa’s Dyke 4 MS all about?”