Julie's blog - looking on the bright side
Hello all!
My name is Julie, I’m 31 and I have secondary progressive MS. I’ve been in a wheelchair for about a year now. Still haven’t mastered the wheelie yet but there is time.
I was diagnosed on 7 June 2006. The symptoms had been going on for a while before then. The doctor said my tingling hands were a sign of stress and so I was put on tablets which I think triggered off a fully-blown relapse and my right leg started to drag. After a couple of months of tests (thanks goodness for the private healthcare my employers provided – cost them a fortune!!), I was given the official diagnosis. I was actually relieved that my condition now had a name and I knew what I was facing. It was relapsing remitting MS at that point. I went and bought my wedding dress the same day! I’m happy to tell you that I walked down the aisle.
Because at the time the symptoms couldn’t really be seen, people didn’t really think I was ill and I was taking the mick at work. I was angry with people for not understanding or not trying to understand and I lost a few good friends. But when it hits the fan, you know who your friends are. It’s made me a stronger person I think. I still hold grudges though!
I would not be forgiven if I didn’t mention the two most important people in my life. My husband Michael has stuck with me through everything. Couldn’t have asked for more because I was a wreck coming to terms with the frustration of not being able to do a lot of things that are taken for granted. He is now going to university to become a nurse. I am so proud of him. And Alice Rose, my beautiful baby girl, who is the main reason I keep going. The little minx is now 20 months and running around the place, but I can still chase her in my chair!
The MS has changed me as a person, but not necessarily in a bad way. OK so I can’t drive, or walk, or write etc, but I’ve kept looking on the bright side as much as I can. For example, we get great parking and I get great tickets for gigs! I’ve seen more live music than ever and as a rock chick, I love it! I’m doing a home study course in diet and nutrition as I’d like to help people to lose weight after I lost 5 stone myself (so anything’s possible!).
Please feel free to ask me any questions and I will answer them. I’m honest and don’t mince my words!
See ya later
Julie xx

Comments
Hi Julie - Thanks for your blog
I am awaiting dx been 2 years over the last year have been trying with diet and nutrition and would love to exchange views with you.
How can I contact you on ???
Best Regards
Y
Hi Julie,
I'm Natalie 28 with Rrms and a 2 year old daughter so feel Like I can really relate to you, I've just been reading your blog after a rough night with my leg spasms and it has cheered me right up lol, I was feeling very down this Morning but your blog and your amazing positive attitude had made me think there is light at the end of the tunnel and it's not all that bad, like you said the parking is a bonus lol. Thanks for cheering me up Julie and I hope you take care, I'm waiting for your next blog now so get typing lol.
Hopefully speak soon
Natalie x
Hi Julie,
Very interesting to read you blog!
My name is Wendy. I am 53 and have been diagnosed for 20 years in May this year. I have been stuck in my wheelchair for about 2 1/2 years and think I now have secondary progressive MS. My daughter (26) gets married next May and I am really trying to lose weight so can knock 'em dead as mother of the bride. Luckily one of my Carers does the
Slimming World diet and cooks me their meals! Any more ideas?
Regards
Wendy x