It’s been a while!!

So, it has been a few weeks since I last wrote about anything. There has been alot happening in the world of Lexi! Where do I start? Lets start on a high note. The NHS have finally conceeded that I need an active wheelchair. So I am eagerly awaiting the arrival of my Quickie Argon. Im so excited. They said it could take uo to 12 weeks for it to arrive, and I saw them about 3 weeks ago….so hopefully it wont be much longer. The chair that I have is still causing quite bad injuries, so I have had to cut my training down to a minimum. What does this mean for my event? Well, if the chair comes soon and there is no lasting damage to my shoulders, then fundraising depending, I can still go ahead with June next year as planned. If however I need any treatment on my shoulders, ie Surgery, then it will have to be postponed to later in the year, or worst case scenario, the following year. But I will be doing it still. It would have to be a major incident to stop me. Im more determined than ever now. Just need to get on with some more fundraising when my chair arrives. With thanks to the lovely lot at Invictus active, I have been able to do some training on the indoor wheelchair trainer, which they have leant me. It is amazing. Its set up in my living room, behind my sofa at the moment. So I can hop on and off (so to speak!) Whenever I want.

As I think Ive mentioned before, im also an artist, and have an exhibition on at the moment at the Custom House in Exeter, Devon. I have 2 days left! Ive managed to sell some pieces, which Im so happy about. The weather hasnt been that great, so I havnt had tons of bodies through the door, bu there have been a few. U fortunately none of my friends have come in as yet. One of them is currently in hospital after having babies, so she is forgiven! As for any others, ‘sham on you’. Just kidding! People are busy. I understand that.

So what else has kept me from here….

Well, I have enroled back in college. Im redoing some of my gcse’s. I diddnt get bad grades. Just not the A and B which I need in a couple of subjects, to hopefully go back to university in a couple of years. I wont say too much about that, as I dont want to tempt fate with telling anyone (other than the wife of course) about what Id like to study, until I get accepted (hopefully!). I am also doing 3 other gcse’s on line, thanks to BLESMA, who have funded me. They have also paid for me to do my driving lessons. I passed my theory the other day (which was quite a shock!). They recommend that you take it whilst driving, and I havnt even started yet! I start my weeks course in November. So watch out roads! It will be fantastic though. With the new chair and driving, I will finally be independant. Which will be absolutely amazing. You take for granted simple things like, getting out of your own home to pop to the local shop for a pint of milk. Little things like this, I just cant do. I rely on my wife to take my wheelchair down stairs, and put it in the car and drive me places. I cant go far in my current chair because of the damage it has caused to my shoulders, and so she now has to push me alot. I find this impossable to take. I hate being reliant on anyone, let alone the person who is my world, my wife. I dont want her to become my carer too. (Not very sexy!). But that is wha has heppend. She is just amazing. One in a million. I am so lucky. She loves ‘stumpey’. She thinks its amazing. My ‘floopy boobie’ she says it looks like!! She likes to draw on it and turn it into a vast array of animals (as you can see below!).

Im still fighting with ‘flo’ and my wonderful prosthetist. My leg is quite baggy now. Its been filled out twice so far, after I was wearin 5-7 thick socks with it. Imagine wearing 5-7 thick sports socks on your foot in this summer heat!! Not much fun. On top of that the pain of the crps being back in my stump, is not very condusive to prosthetic leg wearing. So im awaiting an appointment at the end of September where we hopefully agree that it is time for me to have a new smaller socket. I may be able to wear some of my old clother again. Yippee….i have 3 pairs of trousers out of the, well estimated twenty pairs which I have. Its a nightmare. None of them are smart either. So ive gone from wearing chinos, shirt, belt, nice shoes and often a blazer, to wearing tracksuit bottoms or shorts everywhere! Not fun for me. I love my clothes! So I cannot wait to get a new socket. Hopefully one which fits and is smaller. I can only wear it for short periods of time. Its very much dependant on the day, and how much pain I can cope with. As with the nature of crps. The pain is always there. The flare ups are the worst. But im forever hopeful that I will be one of those who sends it into remission. I seem to spend alot of time waiting for things. Im waiting to hear from the OT who saw me over a month ago, who was supposed to ring me the very next day, who diddnt. Im waiting to see my prosthetist, im waiting for my chair, im waiting to see my consultant. Thats the funniest one. My GP put in a request for an URGENT appointment with him over 3 months ago!

Anyway. Here we are. Im waiting for alot. When it is all here. My life will be much better. Alot easier. But until then…..

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