My MS Story.

It was a Friday in the end of March 2007 and I was about 4 months pregnant with the little man. I woke up that morning with pins and needles from the chest and down. Thought I'd call the maternity ward and ask if there were any reason to worry. As we were off on Easter holiday to Denmark the next day, they wanted me to have a scan just to make sure everything was fine. It was and I was told the pins and needles probably were from the baby pressing on some nerves. Well then, no need to think more about that.

A couple of days later a little black spot appeared in front of my right eye. Annoying but I drew no connection between that and the pins and needles. A week and a half later we were back home in London. The pins and needles had gone but the black spot in front of my eye was still there. What to do...? I should really get it checked out shouldn't I? My friend and I were out shopping on my day off and passed an optician, I thought let's ask if they can see anything before ringing the doctor. The optician was very nice and helpful bit he said he would strongly advise me to go to the eye hospital in Queens Square straight away. Puzzled, we left. My friend said she'll come with me so she could look after the princess (who was 20 months old at the time) so off we went and waited for hours when we got there. I was finally seen by a doctor and told it's inflamation on the optic nerve. It would go away by itself but would I kindly come back in 1 or 2 weeks time to see their neurologist. Thought it was a bit strange but got an appointment the following Friday.

I arranged for the princess to be looked after, turn down my husbands offer to come with me. I don't really see the need and won't have him using a holiday to come with me. That Friday afternoon, I wished I'd said "Yes, you can come".

I saw the neurologist. He's very nice (he had even been to the little town in Denmark I'm from) but he was also very sorry to inform me that I had MS. He couldn't say 100% before I had a MRI scan but he was 99% sure. I left, called my husband to tell him and cried my eyes out. I put on my sunglasses and with a knot in my tummy and tears running down my cheeks I then took the underground home to my little princess, her daddy (my soulmate) with a message that changed our lives.

We  moved to my home town in Denmark in the end of November that year 2007 and have lived a fantastic and happy life since. No it's not always easy and MS sucks but we do try and get the best out life despite me having MS. Yes, I'm disabled (handicapable as I like to call it) but first of all, I am a mummy with a fantastic family!

14 comments:

  1. Mette du slår mig simpelthen som værende en fantastisk og livsglad kvinde! Jeg nærer stor respekt for din åbenhed og dit livssyn! Tak fordi du gider dele det med os læsere! :)

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    1. Tusind tak Katharina og i lige måde. Jeg nyder at læse med på din blog:)

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  2. Wow! You actually sent chills down my spine with this post. I hope you can keep MS at bay and stay healthy. I don't know what to say, beside sending you virtual hugs. Good luck and thanks for sharing your story, it is always good to remind ourselves to not undermine aches, pains and what not. x

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    1. Thanks for your lovely comment and your virtual hugs. I love the picture on your blog of your little girl sleeping on her back:)

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  3. Bless your heart! I don't know too much about MS and thanks to you, will start learning more. You have a beautiful family!

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  4. im so glad you shared your story. my uncle has ms and also walks with a cane. i wish he had the same upbeat attitude you have because i think it makes a difference but i understand its hard to manage as well. its so nice to *meet* you here and look forward to getting to know you all the way over there in denmark. i was an "olsen" before marriage and my great grandparents came to the united states from denmark and some day i hope to visit.

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    1. Thank you:) Sorry to hear your uncle has MS too. How funny you have Danish ancestors. There's a new program on Danish channel 5 tonight about americans coming to Denmark to find their roots. I'm watching it:) Thanks for reading.

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  5. Just read this. Took me back 10 years. And even though I don´t wish this on anyone, it´s still nice to know that I´m not alone. So nice to know you, let´s not give up!!!

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    1. Thanks Sanna. Giving up is not an option:) And yes it's nice to know you're not alone. Have a lovely Sunday:)

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  6. Thank you for this post, I have some symptoms I must get checked out. Hayley x

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    1. I'm glad this post can help but very sad to hear you have symptoms. Hope it's nothing. X

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  7. Hi Mette, I just read this and it made me cry. You write so beautifully, so simply and with such dignity and courage. And yet I know that this doesn't begin to tell the depths of your story. I'm not sure whether you have elsewhere but I know it would touch - and help- so many people. I salute you. Rachel (weber/allen). Xx

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