Emma Jerred

Cure Duchenne Muscular Dystrophy xx #TeamSam

[Thin Blue Paw Foundation @ThinBluePaw]

Last night three police dogs from Merseyside suffered injuries on duty whilst assisting with the violent disorder that took place in #Southport. PD Zoe & PD Ike sustained leg injuries from bricks thrown at them, and PD Quga who was bitten, strangled and kicked by an offender at the beginning of this month at a separate incident, suffered further injuries yesterday evening, with burns to her back leg. Thank you for your bravery PDs Zoe, Ike and Quga, we're wishing you a speedy recovery. 💙🇬🇧🐶

[Donna Duffy @Donna_d99]

I'm literally begging now I just want to see or hear from my son. Please if any has seen him or knows of his whereabouts please get in touch.
#helpfinddillonduffy #MissingPerson #missing

[Emma Jerred @Em_1978]

@martynsibley @BBC @RightsOnFlights Brilliant stuff 🤩@TheAngelaRippon 🫶

[Rare Disease Day @rarediseaseday]

🚨 IT'S RARE DISEASE DAY GLOBALLY! 🚨 Join us marking #RareDiseaseDay 2024! Spread awareness, share stories, and support those living with rare diseases. Together, we make a lasting impact! #ShareYourColours

[Emma Jerred @Em_1978]

RT @HairyBikers: Hi everyone, I’m afraid I bear some sad news. Most of you will know Dave has been fighting cancer for the past couple of y…

[Emma Jerred @Em_1978]

@vicilou @NewcastleHosps Whoop whoop 🙌 xx

[Emma Jerred @Em_1978]

@SkySportsPL @pumpinghearts ❤️

[Sky Sports Premier League @SkySportsPL]

Luton captain Tom Lockyer explains how his newly-fitted defibrillator will 'give him a shock' if his heart-rate goes outside of the normal parameters 💭

[Emma Jerred @Em_1978]

@GMB What a fantastic interview. @pumpinghearts ❤️❤️

[Pumping Marvellous Foundation @pumpinghearts]

Great interview with Tom Lockyer on @GMB with @susannareid100 & @edballs - important message about raising the awareness of CPR and another important message around ICD’s. This interview will help those people, who experience anxiety whilst being offered an ICD. The way Tom articulated himself was marvellous. As a footnote many of our community name their ICD, what’s yours called. #BeatHF @LutonTown

[Timor O’Seery @seery_o]

I have to show this.
This is Liverpool Lime Street Station.
Have a look and then squint your eyes and look again.

[Meridian Trust @meridiantrustuk]

A huge congratulations to the team at Somersham Primary School.

The school has secured an ‘Outstanding’ Ofsted report – with Outstanding judgements in all areas.

Read more - https://t.co/MyBZSumEeF

#MeridianTrust #AchievementForAll

[Emma Jerred @Em_1978]

@jackwhitehall They are the best! 😂🩷🩵xx

[Krishnan Guru-Murthy @krishgm]

Tomorrow 140 cyclists go from London to Paris to raise money for medical research into fatal Duchenne muscular dystrophy. Its the 10th Duchenne Dash. As chairman of @DuchenneUk if you’d be kind enough to help with a donation we’d be enormously grateful https://t.co/KWKaqP4tMx

[Emma Jerred @Em_1978]

@thelizcarr @OlivierAwards @RoyalAlbertHall @lisahammondwhop @thevjoiners @HouseOfTammam You look absolutely amazing @thelizcarr 🥰🥰🥰

[Emma Jerred @Em_1978]

Grant an inquiry of the Ofsted inspection at Caversham Primary School - Sign the Petition! https://t.co/jEaZ4dapMb via @UKChange

[BBC Breakfast @BBCBreakfast]

Let's get Eli to Glastonbury.

15 year old Eli Crossley is living with Duchenne Muscular Dystrophy and has trialled a new piece of technology he hopes will one day let him play with Sam Fender.

@samfendermusic @glastonbury

https://t.co/6WrVN1nJds

[Duchenne UK @DuchenneUK]

Thank you so much to @SkyNews for welcoming us this morning, and to the people of @PostcodeLottery for supporting the suit - helping people with Duchenne Muscular Dystrophy to restore function to their arms, helping them to chase their dreams 🙌

Now it's time to #GetEliToGlasto

[Duchenne UK @DuchenneUK]

There are 300 million people living with a rare disease worldwide. This includes Duchenne muscular dystrophy, which affects approximately 300,000 people and 1 in 3,500 male births.

Support our work and join our mission to #EndDuchenne
https://t.co/ZDOhzrwnaS

#RareDiseaseDay

[Emma Jerred @Em_1978]

Save AutumnWatch - Sign the Petition! https://t.co/2Em5Mjul0a via @UKChange