DLS

[Giselle - Adult Social Care Warriors @Giselle_ASCWs]

@LeicsCountyHall is this really how you treat older disabled people needing social care?

Unaffordable charges, repeated assessments & threats to remove DPs if they don’t “play ball”

They’re exhausted & distressed, yet the badgering continues!

This isn’t care. It’s coercion!

[DLS @HalcyonDays_Rye]

@BentleysKent Hi Matt. Having trouble getting hold of you. Can you give me a ring please? Many thanks Dawn

[Ricky Gervais @rickygervais]

Watch the award-winning,
record-breaking stand up special #SuperNature. Streaming on @Netflix around the world 🌎

[Chris Pearson @Chris_G_Pearson]

This summer is going to be tough for a lot of families, please #RT it may help someone

[NAA10 Families Together @naa10gene]

Only 2 Days to go until Rare Disease Day! Learn what live is like having a child with NAA10/ Ogden Syndrome ❤️ Meet our Anika and family: https://t.co/OBW7OZ5Lzc. #RareisMany #RareisStrong #RareisProud #RareReach2021 #RareReality #naa10 #ogdensyndrome

[NAA10 Families Together @naa10gene]

Rare Disease Day 2021 is 5 days away! The chance of having a child with NAA10 Ogden syndrome is 1 in 11 million!! About the same chance as meeting a superhero 💕Please Share #rareadiseaseday #rarediseaseday2021 #naa10gene #ogdensyndrome #RAREfact #RAREtruth

[CamRARE (Cambridge Rare Disease Network) @camraredisease]

Rare diseases are not uncommon.
There are over 6000 known #RareConditions & the number continues to increase as knowledge grows. Yet diagnosis is often a long process and treatment options for many #RareDiseases are few.
#RAREfact #RareDiseaseDay #RareAware
@rarediseaseuk

[NAA10 Families Together @naa10gene]

“We are rare, we are many, we are strong, we are proud" We are NAA10 Ogden Syndrome parents! help us spread the word and teach the world https://t.co/79lS78fGzZ
Thanks @eurordis for raising awareness of rare. New video for all patients with a rare disease #RareDiseaseDay2021

[NAA10 Families Together @naa10gene]

We are excited to be taking part in this years #Rarefest20 Check out our poster in the gallery! Raising awareness for NAA10 Ogden syndrome! Thanks @camraredisease for having us! Enjoying the event so far

[Nikki Fox - BBC News & Watchdog Presenter @FoxNikkiFox]

Azaria has an ultra-rare genetic condition called NAA10 syndrome. It's SO incredibly rare only a handful of people in the world have it and as a result, very little is known, so wonderful Carolyn's set up a support group. For more info go to @naa10gene and https://t.co/i1v4Cn8NbU

[DLS @HalcyonDays_Rye]

https://t.co/v9CQO7gF3p

[DLS @HalcyonDays_Rye]

https://t.co/LBhfiXIyzo

[DLS @HalcyonDays_Rye]

Stuart Austin gave Enterprise 1 star. Check out the full review... https://t.co/xUxYtZKVfb

[DLS @HalcyonDays_Rye]

Andy Waters gave Enterprise 1 star. Check out the full review... https://t.co/exvPFkvSk5

[DLS @HalcyonDays_Rye]

Darren Upton gave Enterprise 1 star. Check out the full review... https://t.co/IxWYdnlAhp

[DLS @HalcyonDays_Rye]

Dawn Stanley gave Enterprise 1 star. Check out the full review... https://t.co/FNNlrSCzZ0

[DLS @HalcyonDays_Rye]

https://t.co/sRlhr54AlJ

[DLS @HalcyonDays_Rye]

https://t.co/1y4UqktuHE

[DLS @HalcyonDays_Rye]

Beautiful pictures and great understanding of children and their needs

[DLS @HalcyonDays_Rye]

Pay carers more than Aldi and Lidl shelf stackers - says care boss https://t.co/9TxcPwcqJj