Victorian Clinical Genetics Services (VCGS)(@TeamVCGS) 's Twitter Profile Photo

In 2017, Mackenzie Casella died at seven months of age from a condition for which her parents were unknowingly carriers. The Government would soon fund a large national research study named after Mackenzie.
Read more: mdpi.com/2075-4426/12/1…

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APPG on Surrogacy(@APPGsurrogacy) 's Twitter Profile Photo

Watch Kathryn Chapman speaking at our meeting last month.

She has a , & used / to conceive embryos free of the condition, but could only carry one pregnancy herself & needed to have a 2nd child.

Full video of meeting - andrewpercy.org/appg-surrogacy…

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Katy Munro(@KatyMunro1) 's Twitter Profile Photo

So our little podcast was beaten by the BBC COVID19 podcast but hey! we had a wonderful evening at . So proud to have been there.Also 1:7 of those journalists probably get so just by turning up we may have raised awareness!

So our little podcast was beaten by the BBC COVID19 podcast but hey! we had a wonderful evening at #MJAawards. So proud to have been there.Also 1:7 of those journalists probably get #migraine so just by turning up we may have raised awareness! #geneticcondition #notjustaheadache
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Asianet News(@AsianetNewsML) 's Twitter Profile Photo

ജനിതക രോഗത്തിന് മുന്നിൽ തളരാതെ ജീവിതം പോരാട്ടമാക്കി സേബ സലാം

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Vortan Iskalegar Ex-Labour member #RejoinEU #FBPE(@iskalegar) 's Twitter Profile Photo

To anyone with a who gets this virus can I urge you . Govt want us gone so they can close our benefit claims, dont give them the satisfaction. You know, as I do that they hate us. Use your hate of the Tories to power your recovery! FIGHT!

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TIF(@thalassaemiaTIF) 's Twitter Profile Photo

Living with alpha- doesn't have to be a journey taken alone.

Check out the first-ever from @TIF_thalassaemia for managing this and find comprehensive support and information.
👉 bit.ly/48mY1Ms

📚

Living with alpha-#thalassemia doesn't have to be a journey taken alone. 

Check out the first-ever #guidelines from @TIF_thalassaemia for managing this #geneticcondition and find comprehensive support and information. 
👉 bit.ly/48mY1Ms

#Thalassemia #KnowledgeIsPower📚
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DermNet(@dermnetnz) 's Twitter Profile Photo

Photographed here are blisters and erosions on the dorsal hand and fingers in hereditary coproporphyria. Learn more on our updated DermNet page here: dermnetnz.org/topics/heredit…

Photographed here are blisters and erosions on the dorsal hand and fingers in hereditary coproporphyria. Learn more on our updated DermNet page here: dermnetnz.org/topics/heredit… #geneticcondition #dermatology
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Vortan Iskalegar Ex-Labour member #RejoinEU #FBPE(@iskalegar) 's Twitter Profile Photo

I often find myself apologising to strangers in conversation for costing the too much because of my poor & my . I've been made to feel guilty for inheriting a , like I had a choice in it. I shouldnt have to feel that way!

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Sight Scotland(@SightScotland) 's Twitter Profile Photo

What is Stargardt Disease? It is expected to impact over 8,000 people in the UK. And Macular Society are researching into the already licensed drugs for Stardargt Disease. ow.ly/8hrv50Qtub3

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Jeans for Genes UK(@jeansforgenes) 's Twitter Profile Photo

In 2020 Jeans for Genes was proud to help fund Down Syndrome Training and Support Service's early development groups. Here Yousef shows us what he has learnt at the group which he attends regularly with his mum.

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