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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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| Get your brochure now for our fantastic personalised company Christmas cards. Also ideal for individuals! |
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| Congratulations to the Jennifer Trust team who took part in the London 10k on Sunday 1st August. |
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| The JTSMA have learnt that the Muscular Dystrophy Campaign (MDC) are consulting about plans to axe their entire Family Care Officer Team with effect from 31 December 2004 |
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| Six areas in England are to receive a share of £18m to upgrade genetic laboratories and help patients get genetic test results quicker. |
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| Read an event report of our epic Birmingham to Oxford Bike ride, by brave participant Marion Main! |
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| Can you spare 15 minutes to take part in this on-line survey? |
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| Your names, stories, pictures are wanted to help our friends in the US petition Oprah for a programme about SMA. |
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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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