Setting herself a mammoth challenge, Rhona Kingett completed her own accessible marathon
As I looked through my emails one day, I came across one about of doing a virtual marathon for MS-UK. It suggested taking a challenge for 26 days, or 26 times, or anything relating to the 26 miles of a marathon, due to the postponement of the Virgin Money London Marathon.,
When young I was a bit of a long distance runner. Never to the extent of running marathons though! I actually put my energies into dancing rather than running, and I became a professional actor, dancer and musician. Unfortunately as my career progressed taking me upwards, the multiple sclerosis (MS) progressed and took me downwards. The MS won and it overtook the work.
I tried to think of how I could get the virtual marathon idea to work for an MS-UK fundraiser. My MS has moved onto secondary progressive about three years ago. I was diagnosed with relapsing remitting MS in 1994. My legs no longer support me and I get hoisted between the bed and my wheelchair. I have bad spasms and I’m supposed to do all sorts of physio exercises but there are so many and my body doesn't do what I tell it to do.
Somehow I let these exercises slip. Then it suddenly struck me how I could do a virtual marathon that would help both me and the charity. I would ask people to sponsor me to do my physio exercises on each of the 26 consecutive days. My husband (my full-time carer) would be making sure that I really do them. The hope being that, once I’d fitted the exercises into my daily routine, I would continue with them.
I sent the link for the sponsorship out on Facebook and Twitter. When money started being pledged by people I realised that I had to do what I had said I would do. But after a number of days, I found that there were certain movements that became easier to do – indeed I increased the number of repetitions of some. That was another encouragement. It made things easier for me and also for my husband. More encouragement.
I sent updates to my social media contacts. Some of these shared them, either electronically or just verbally, which led to further sponsorship donations.
I was pleased to see the money coming in, and therefore the amount available for MS-UK to use, going up. Not just because it showed what supportive friends I have (I knew that) but because I knew it meant MS-UK could give more support and information to people and families who have had the news that ‘the MS monster’ has come into their lives.
To contribute to Rhona’s fundraiser, click here