Simon H Parson

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Simon H Parson

Simon H Parson

@NEAnatomist

Regius Professor of Anatomy, Aberdeen University: interests in education and spinal muscular atrophy. All views my own.

Aberdeen, Scotland Katılım Temmuz 2016
75 Takip Edilen1.2K Takipçiler
Simon H Parson
Simon H Parson@NEAnatomist·
@SMA_UK_ It is fantastic news, that we've finally got this over the line in Scotland
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Spinal Muscular Atrophy UK
Today marks a monumental milestone, one we are proud to celebrate, as Scotland introduces newborn screening for Spinal Muscular Atrophy (SMA) 📣 Read the full blog here 👉 bit.ly/4rKoKvV
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Simon H Parson retweetledi
Spinal Muscular Atrophy UK
Here at SMA UK, We are so proud to support Jesy’s petition, calling for SMA to be added to the UK newborn screening heel-prick test 📣 Please take a moment to read, share and sign 👉 bit.ly/4tvlBlM 🔗 #ScreenTodayForSMA
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LKCMedicine Research
LKCMedicine Research@lkcmedresearch·
3 February – Lee Kuan Yew Distinguished Visitor and 2021 Wolf Prize in Medicine Laureate Professor Adrian Krainer reflected on his research journey, scientific motivation and postdoctoral career pathways at a fireside chat organised by the Neuroscience & Mental Health programme. LKCMedicine faculty, researchers and PhD students engaged in active discussion with Prof Krainer, followed by a lab tour hosted by Assistant Professor Aditya Nair.
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Simon H Parson retweetledi
Spinal Muscular Atrophy UK
SMA UK CEO, Giles Lomax, spoke alongside Jesy Nelson with Health Secretary, Wes Streeting, yesterday on the importance of newborn screening, and to share a clear roadmap for making this a reality.
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Simon H Parson retweetledi
Lindsay Bruce
Lindsay Bruce@LindsayBru60963·
An INCREDIBLE tale of a mother's instincts leading to a life-changing diagnosis. Little Lawson Laidler from Aberdeenshire is poss the youngest child in the UK to be treated for SMA-1, the same condition shared by the beautiful girls of singer Jesy Nelson.pressandjournal.co.uk/fp/lifestyle/h…
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Simon H Parson
Simon H Parson@NEAnatomist·
I contributed to a piece in our local paper @PressandJournal today about a local family with a type 1 SMA child, and the difference their advocacy made to his diagnosis and treatment tinyurl.com/y8c6e34a
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Simon H Parson retweetledi
Spinal Muscular Atrophy UK
With SMA recently receiving wider attention, we wanted to share with you a brief overview of what SMA is, and why early diagnosis is so important, as some people may be learning about it for the first time💡 You can read more on our website here 👉 smauk.org.uk/baww
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Muscular Dystrophy UK
Muscular Dystrophy UK@MDUK_News·
Jesy Nelson has just given a very powerful and emotional interview on @ITV's @thismorning sharing what life is now like with her eight-month-old daughters who have been diagnosed with SMA.
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Simon H Parson
Simon H Parson@NEAnatomist·
Jesy is talking about the importance of new born screening for @SMA. NBS could have picked this up early and given her daughters so much more hope. NBS is not available in England and Wales, but Scotland has just instigated NBS this month. @SMA_NBSalliance @SMA_UK_
Spinal Muscular Atrophy UK@SMA_UK_

We’re deeply moved and saddened by Jesy Nelson’s news that her twin daughters have been diagnosed with Type 1 SMA. SMA UK is here for everyone affected by SMA, No family should face the heartbreak of a preventable delay in diagnosis. Full statement here: smauk.org.uk/jnsma

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Simon H Parson retweetledi
Spinal Muscular Atrophy UK
We’re deeply moved and saddened by Jesy Nelson’s news that her twin daughters have been diagnosed with Type 1 SMA. SMA UK is here for everyone affected by SMA, No family should face the heartbreak of a preventable delay in diagnosis. Full statement here: smauk.org.uk/jnsma
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Simon H Parson retweetledi
Muscular Dystrophy UK
Muscular Dystrophy UK@MDUK_News·
This is a significant and positive step, and we need the rest of the UK to follow at the earliest opportunity, to ensure newborn screening for SMA is available everywhere.  8/8
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Simon H Parson retweetledi
Muscular Dystrophy UK
Muscular Dystrophy UK@MDUK_News·
A major milestone was reached last year, the Scottish Government announced that Scotland will become the first country in the UK to begin national screening for SMA. 7/8
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Muscular Dystrophy UK
Muscular Dystrophy UK@MDUK_News·
Many of you will have seen Jesy Nelson’s video about her twin girls being diagnosed with SMA type 1. She speaks passionately about making the video to raise awareness of the signs of the condition and the importance of newborn screening. 1/8
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