Monday 27 July 2009

I am still alive...!

Yes, I'm still here, I've just been very naughty and not updated this in a while. It is getting harder and harder to find a spare few mins to update this as Ava doesn't sleep very much in the day and wants constant attention when she is awake! At this very minute she is kicking our sofa to get my attention as I am ignoring her!

We had a great holiday in France...it seems so long ago. Ava was a very good girl on the plane, and everyone was so great getting me on the plane too. I got to drive my scooter pretty much up to the door of the plane and then they took it off me and loaded it straight away. It was a great service (thank you Easyjet)! So if any of you are worrying about going away on a plane, DON'T WORRY! Just pre-warn your travel company and you will be treated like royalty. We had some mixed weather out there but we still managed to get a nice colour. The picture below is of me and Ava on my scooter.
I can't believe it is only 5 weeks until I go back to work. I am only going back for an afternoon and a full day but I haven't taught for over a year...what if I've forgotten how to teach?! I have been lucky enough to get money from Access to Work to pay for a support worker for the whole time I am teaching and they are buying a very expensive lightweight wheelchair for me to use at school. I am really looking forward to going back, although I've been warned, I have a naughty class this year! School have been fantastic about helping me get back to work. I just want to get stuck in now!
For those of you who knew I had a car on the Motability Scheme, I have finally driven it. I got it a few months back and it has been sat on the drive as I was a little nervous to go out in it. Using your hands to drive is so strange and needs a bit of practice. I found the hardest bit was knowing how far to turn the wheel, with just your left hand, to get the turn you wanted to! But once I get a little bit more confidence, I know it is going to be great.

I have now had 4 infusions of Tysabri and think I am feeling the benefits already. There are little things such as typing, lifting my toes up and sometimes my walking that seem to have improved. I am still writing about Tysabri on the MSRC website so if you want to check it out, the link is on a post below
I am sure that someone will tell me if I have missed anything out on this post!
Emma
P.S Just had to put another pic of my beautiful daughter on!

An insight to my life with MS