Multiple Sclerosis

Hi I am Caroline. I live with my partner Dave and number one son Ben I have secondary progressive Multiple Sclerosis. I struggle with the heat but living here in the UK it isn’t so hot. Recently because of foot drop I have got a FES. I am designing and making ways of carrying the FES, I don’t think that you should have this attachment as an aid but rather as a fashion accessory. I feel that if you have any ideas please get in touch with me by telephone 07969929803 or email lunecushions@gmail.com and we can talk through your ideas, because everyone is different. Attached these are the ways of carrying the FES I have made to date. I am running this website with the help of my daughter Karena. I have lots of friends who help me because I know you always need someone. I have had the MS since 2000 but I still work and keep going to the best of my ability.

We have just had another holiday on Jersey, the weather was absolutely great rather too hot for me but I just lounge on the beautiful beaches under the parasol. We stayed at the guest house http://www.stmagloireguesthouse.com/ David Plowright is the nicest person and all his staff are lovely.