News Archive

Listing Articles 81 to 100 of 151

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Get your brochure now for our fantastic personalised company Christmas cards. Also ideal for individuals!
Congratulations to the Jennifer Trust team who took part in the London 10k on Sunday 1st August.
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
Six areas in England are to receive a share of £18m to upgrade genetic laboratories and help patients get genetic test results quicker.
Read an event report of our epic Birmingham to Oxford Bike ride, by brave participant Marion Main!
Can you spare 15 minutes to take part in this on-line survey?
The balloons are off!
Your names, stories, pictures are wanted to help our friends in the US petition Oprah for a programme about SMA.
Ride in a Ferrari and Help Fight SMA was a resounding success. Read Roy's report on this year's exciting event.
Would you like to have some input into a series of TV programmes featuring bereavement?
Are you currently undergoing or about to start PGD and interested in making a contribution to a documentary series on the subject of IVF treatment?
Help the superheroes with your stories, suggestions and articles about SMA.
Real life 'Superheroes' will be taking a 56 hour stand against Spinal Muscular Atrophy (SMA) high above Times Square, New York.
We are delighted to announce that England and Manchester City goal keeper, David James, donated an astounding £10,000 to the Jennifer Trust as a result of the 'Johnny Charity Challenge'.
An article from Therapy Weekly discussing the needs of Disabled People and the regulations that apply to their carers.
Your help is needed now to help save European research using clinical trials to find the cure for rare disorders such as SMA.
Want to make those resolutions stick?
Please consider helping researchers by taking part in this research.
The Keep Fit Association choose the JTSMA to benefit from their charity appeal in 2004-5.
Read Anita's review of the Helen Baldwin's new book about looking after Jeffrey, her baby with Type I SMA.
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