Joe Goodlad

Trusts & Grants Lead @M_R_F | Medical research, health & wellbeing, international development.

[Meningitis Research Foundation @M_R_F]

Good luck to just under 200 runners taking on the London Marathon today for Meningitis Research Foundation.🏃‍♂️💜

Your miles are making a life-saving difference. We’re cheering you on every step of the way. 🙌

#LondonMarathon #MeningitisAwareness

[Joe Goodlad @Joe_Goodlad]

"This Is the Vaccine Story RFK Jr. Doesn’t Want You to Hear" https://t.co/65p65sWaWg

[Meningitis Research Foundation @M_R_F]

<1% of meningitis research funding targets lifelong impacts, yet 1 in 5 survivors face disabilities.

✨That’s why we’re offering grants of up to £50k for research in the UK, Ireland & LMICs.

Apply now 👉https://t.co/LoCb7iRGLF

#Meningitis #MeningitisResearch #ECRChat

[Joe Goodlad @Joe_Goodlad]

Today on World Meningitis Day, we remember all those we've lost and the lives that have been forever changed by this devastating disease. By lighting the road ahead, we also see our path towards a world free from meningitis #WorldMeningitisDay

[Meningitis Research Foundation @M_R_F]

🕯️ Wherever you are in the world, join the millions of people who will illuminate something on the 5th October at 20:30 (8.30pm).

Share it online using #WorldMeningitisDay or #DefeatMeningitis

Learn more: https://t.co/RFAh9KfhfU

[Meningitis Research Foundation @M_R_F]

The Meningitis Flag is on the move again 🌍

Where’s it going next? Find out next week... 🏁

💛💜💙 #MeningitisFlag #DefeatMeningitis

[Asthma + Lung UK @asthmalunguk]

⚠🚧 We’ve taken over #ToxicAirPlaygrounds in London, Manchester, and Birmingham 🚧⚠

99% of playgrounds in the UK have dangerous levels of air pollution. Children deserve to breathe clean air while they play 🛝

Join us in the fight for clean air: https://t.co/oJwPx0y7on

[Joe Goodlad @Joe_Goodlad]

We need the new government to push for a 'fit for purpose' NHS. I'd welcome greater public investment in early diagnosis for health conditions that put the biggest strains on the system and we need driven members to push forward changes like these #UKElection2024

[Joe Goodlad @Joe_Goodlad]

A historic win for the Labour Party today. My best wishes to the new wave of MPs that'll be joining parliament at such a fractious time in UK politics, and at a time when the public they serve are truly divided and their faith in the political system was at an all time low.

[Joe Goodlad @Joe_Goodlad]

It is vital that the Party now turns their excitement at this long awaited victory into determination and drive for change, addressing key issues in the economy, public services and the environment.

[Cystic Fibrosis Trust @cftrust]

The Your life and CF survey is back and we want to hear from you!

Last year, 1000 of you told us about your experience of life with CF.
Because of you, we were able to continue to campaign for long-lasting and meaningful change.

➡️ https://t.co/Iu0QyljdLI

[Guardian Environment @guardianeco]

Evidence grows of air pollution link with dementia and stroke risk https://t.co/8l31RVx1Vp

[Cystic Fibrosis Trust @cftrust]

"The challenge of living with #cysticfibrosis is invisible. Except to the ones who live it."

This is Kieron's story. Find out how you can share your own #CFTruths by visiting our website. 💛

➡️ https://t.co/Kkbz7fMx0A

[Joe Goodlad @Joe_Goodlad]

Had a fantastic day at the Marathon yesterday cheering on the #TeamCF runners. Loved this video and all of the emotion crossing the line for one of our runners

[TCS London Marathon @LondonMarathon]

💌 𝙏𝙤 𝙩𝙝𝙚 𝘾𝙡𝙖𝙨𝙨 𝙤𝙛 '23

We, along with thousands of others, will never forget today. It was a privilege to share the streets of this incredible city with you all today.

Already counting the days 'til we get to do this all again ❤️

#LondonMarathon #WeRunTogether

[Cystic Fibrosis Trust @cftrust]

We want to wish all of our London Marathon runners the best of luck for today - you are all superstars ✨

Don't forget to tag us in your photos 📸 and use #TeamCF in your posts.

See you at the finish line!

[Cystic Fibrosis Trust @cftrust]

It's #ThankYouThursday! Today we are absolutely over the moon to announce the support of the @TNLComFund for three years to support our Work Forwards employment programme - thank you to everyone who has made this possible! 💛

[Cystic Fibrosis Trust @cftrust]

In response to PM @trussliz's speech at the #ConservativePartyConference today, David Ramsden, our Chief Executive, said: "It is disappointing that the Prime Minister did not take the opportunity today to offer some reassurance to people with cystic fibrosis..." (1/3)

[Sophie @Sophienjones]

My daugter was born with CF. She didn't choose her condition.
Her medication isn't optional. It keeps her alive. She shouldn't have to pay for these life saving drugs - CF prescriptions need to be made exempt! #reviewthelist @Jeremy_Hunt @CommonsHealth

[Joe Goodlad @Joe_Goodlad]

People in England living with life-long conditions like cystic fibrosis shouldn't be paying prescription charges when their health outcomes are so dependant on their medication #ReviewTheList @Jeremy_Hunt @CommonsHealth

[Cystic Fibrosis Trust @cftrust]

Sir David Amess MP had been a long and valued friend to the CF community, especially championing access to Orkambi and Kaftrio.
We were saddened to hear news of his death and offer our deepest condolences to his family for their loss at this difficult time.