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Lovely email :)

Today I received a lovely email from a complete stranger and just wanted to share it as it was so lovely: I had to tell you that the video that you made of your daughter is just such a wonderful gift of hope to parents everywhere who can see what a difference SDR can make. I don't have a child with CP but somehow started following one family on Facebook and now follow several. What an amazing difference its made to all their lives but to see your daughter on the video that you made makes me cry every time (I am a wuss!
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Latest News

I haven't added any news on here for sometime now.  Life is so very different from pre SDR days.  In 2015 Megan took her German GCSE's two years early.  Her school work improved greatly after SDR and I am proud to say that Megan achieved an A in German.  She didn't get any extra time/help during the exams (due to her stubborness!) so obviously we are all very proud of this achievement.  We also had our annual appointment with Megan's consultant at Winchester hospital at the end of 2015.

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4 year SDR anniversary!!

Today Megan is 4 years post op - she had SDR on 18 October 2010. In the past I have made a video on every anniversary to celebrate her amazing achievements but last years video kind of topped it all when Megan walked up Snowdon (2,000ft - 4.5 miles) and she didn't even ache the next day! She is still just as strong and active today and I really couldn't ask for anything more. One thing I have noticed in Megan during the past 12 months is that her walking pace has got faster. Since SDR she has been able to walk very long distances but it always had to be at her pace.

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Another lovely message

Dear Stephanie, we exchanged some messages regarding SDR a few months. My son is already accepted and I would like to thank you for the information and support. Actually Megan's videos was one of the first and very important steps to our decision. We will have a fundraising site soon and I would like to ask you for permission to put some of Megan's videos there to illustrate the amazing success that can be achieved after SDR. Thank you very much. Best regards, Anna

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Another Lovely Message!!

I just wanted to share this lovely message which I received this week.  (I have taken the names out).  It really is messages like these which keep me going with keeping Megan's website up to date.

Hello, my name is XXXX and I just have to tell you have much I love the
videos of you beautiful daughter Megan! My son is almost 4, has
hydrocephalus, spastic diplegic cerebral palsy and dystonia.  He will be
having SDR performed by Dr.
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Update

 

 

 

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More Fund Raising to help raise money for Ollie's Garden

Very proud of Megan today as she did a cake sale to help raise money for a lovely local boy called Ollie.  Ollie has cerebral palsy and his mum is raising money to have their garden levelled out so Ollie can use his walker around the garden.  She managed to raise just over £270.  She worked so hard and enjoyed EVERY single minute of it - including a day of baking the day before.

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Update

Just thought I would update Megan’s progress as I haven’t done so for a little while.  Obviously Megan’s progress has been amazing and life changing and she is nearly 4 years post op now.

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Video from the Daventry SDR Party 2014

A lovely guy called Tim put some photo's together at the SDR party in Daventry.  Megan, Grandma and myself are in a couple of the photo's!!  The video clip can be found under 'Video/Links'.

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SDR Party in Daventry made it in the Daily Mirror today (31.3.2014)

The Daily Mirror were at the SDR Party in Daventry 2014.  Megan is in the photo, although she is difficult to spot!  She is just off centre to the right in the back row and is wearing a very pale peach dress with a peach flower in her hair.

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