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Jesy Nelson starts petition to raise awareness for SMA


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Jesy revealed earlier in the year her twin daughters have SMA and as a result are severely disabled and will never be able to walk.

Her daughters have had the necessary treatment luckily, had they not been diagnosed they would not have survived past the age of 2.

Jesy is campaigning to have SMA part of the newborn screening in the UK.

She has launched her petition today, she has already achieved 10,000 signatures so Parliament will respond. The next step is to reach 100k signatures so the matter is debated in Parliament.

Jesy confirmed in recent interviews she has no current plans to return to music and her sole purpose is to look after her daughters and campaigning.

If you live in the UK please sign and/or share the link. Jesy doing this will save many lives.

SIGN:

https://petition.parliament.uk/petitions/755980?utm_source=ig&utm_medium=social&utm_content=link_in_bio&fbclid=PAZnRzaAP6mxJleHRuA2FlbQIxMQBzcnRjBmFwcF9pZA8xMjQwMjQ1NzQyODc0MTQAAacADkds18GknzQJ0LXf1veJ6uuMVaDp6_IR9_4l4g2ykLR0miAL28nmFAzHNg_aem_9QtJhMFG44yHtNOhVaa8LQ

 

 

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PartySick

You would think something that affects 1/10,000 kids would be screened for already.

I'm not in the UK but I hope they get this through.

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