|

My name is Amy Ironmonger. I turned 18 in August and I was diagnosed in September last year. It all started when had a fall in the bath, I banged my head etc, I then got out of the bath and fell down the stairs. I was sitting at work the next day, I work on computers, and noticed that my eyesight wasn't quite right, I thought I needed glasses so went to my optician, she checked my eyes and recommended that I go to my doctor. I did this and he could tell that something was wrong, but didn't know what, so referred me to an eye specialist. He discovered that I was partially sighted and could not see out of the side of both my eyes. I was then sent for a CT Scan which revealed that I had inflammation in my brain. This was probably the scariest part as I was told there were 1 in 50 possibilities of what it was, I had so much running through my head, everything from loss of memory to brain operations to dying! My doctor and eye specialist were brilliant with me, they were there in a flash whenever I needed them and I couldn't ask for anything better. I then had to wait on a MRI scan, this took a few months but when I had it done the results came back and showed that I had a lot of scar tissue in my brain. From this I was diagnosed with MS and told they thought I had had it for a while, just never been to my doctor complaining about anything. It took a lot of sinking in, when I was first diagnosed I didn't have a clue what MS was, I just knew it was an incurable disease. My family and friends were there for me all the time and really really good. I couldn't have asked for anything better from them either. Since I was diagnosed last September I have got the attitude now that, yes I have MS but it is not going to beat me. Instead of moping around I decided to fight it and start raising as much money as possible for it! I am now on the daily injection of Copaxone which is working really well with me. Since the relapse in my eyes passed I had a spell of numbness in my face but that quickly passed. I have been doing good since - and fingers crossed I will be able to stay good for a long time. 
Amy © Multiple Sclerosis Resource Centre (MSRC)
|