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The Genetics Interest Group (GIG) announces the publication of an exciting new booklet "Research and Rare Genetic Differences" for members of Research Ethics Committees and medical researchers. |
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| Ride in a Ferrari and Help Fight SMA was a resounding success. Read Roy's report on this year's exciting event. |
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Could you offer exchange accommodation this summer for a 17 year old French boy with SMA? |
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| Due to our change in status, we are legally required to ask you to renew your membership to the 'new' registered charity. Please read on! |
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| The JTSMA is delighted to announce further details of its 2005 conference. |
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| Roy Twycross arranged a great birthday day out for friend Lee Richardson, both of whom are great fundraisers for the JTSMA. |
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| The Minister of Health announces an extension to the Moratorium on genetic testing in relation to purchasing insurance products. |
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| Our new easy-to-navigate web site is now live! |
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| SMA family to feature in ITV programme 'Precious Babies'. |
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| We are delighted to announce that the first Drugs Trials for SMA in the UK likely to start within the year! |
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| The Jennifer Trust mails out the very first issue of its JTSMA TEEN MAG. |
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| Don't forget to keep in touch; any ideas for activities? |
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| Karen Yates shares her findings about her study into disability tourism. |
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| If you couldn't make the Scottish Christmas party, Joan lets you know all about it! |
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| Can your family help promote the JTSMA and provide information at local KFA events? |
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You are invited to enter a photographic competition which aims to highlight the wider picture of genetics in our lives. (please note that the competition is now closed) |
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| The Muscular Dystropy Campaign would like to hear of your experiences of this grant, good or bad. |
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| Christmas time is the biggest opportunity for raising our much needed funds - read how you can help. |
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| A Bonn Balloon takes the prize... |
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