Caring for Connor

Family, friends and supporters who want to help 6 year old Connor and his family raise awareness and ultimately find a cure for Duchenne Muscular Dystrophy

[Caring for Connor @caringforconnor]

@piersmorgan Such a devastating disease that needs huge awareness to save our boys. Hard having one with #duchenne but 3😥

[Caring for Connor @caringforconnor]

💙💙💙

[Join Our Boys Trust @joinourboys]

Hi Everyone, I hate asking, but my three sons have a terminal illness called Duchenne Muscular Dystrophy and are sadly dying. I am trying my best to save their lives.
Is there anyway you could all retweet this and follow us to help with awareness and funds? Thank you.

[Caring for Connor @caringforconnor]

@piersmorgan 💙💙💙

[Piers Morgan @piersmorgan]

Such a heartbreaking situation. Please read up about this wonderful family, retweet the thread below to spread awareness, & donate if you can. They need all the help we can give them. Thanks.

[Masons Muscles @MusclesMasons]

@GMB @piersmorgan @susannareid100 As a Duchenne mum myself, Mason is 7yrs old, this was Inspirational and emotional. Thank you @joinourboys 💚🙏🙏🧡

[Oliver's Army @oliversarmydmd]

@GMB @piersmorgan @susannareid100 This is my son Oliver who is 12 and living with this condition 💙💙 thank you for raising awareness 🙏🏻 xx

[Caring for Connor @caringforconnor]

💙💙💙 @joinourboys

[Good Morning Britain @GMB]

'Your story has really moved us.'

Watch the sweet moment @piersmorgan and @susannareid100 give inspirational teen Archie, who is a fan of GMB, some early Christmas and birthday presents.

💕

Watch the inspirational interview here 👉 https://t.co/yyUUJmzswF

[Caring for Connor @caringforconnor]

@GMB @piersmorgan @susannareid100 An amazing family!! Hard enough with one child but 3 😓 We hope for continued support and awareness for #duchenne 🙏

[Caring for Connor @caringforconnor]

@virginmedia real shocking shocking service so far..... lost count how many hours over the past 3 weeks I've lost on hold to you....do you actually have any engineers??

[Caring for Connor @caringforconnor]

@Mike060890 Weve had exactly the same thing with gas and electric.... shocking!! We don't use that much! And yesterday and today no phone or internet working 😤

[Caring for Connor @caringforconnor]

@SuDempster How many you want? Pop over pls after work 😘

[Ramsgate Town Council @RamsgateTown]

#FF @Kent6aside, @RMaritimeMuseum, @caringforconnor, @HIEXRamsgate

[Caring for Connor @caringforconnor]

2nd day running in the @MetroUK paper 😳💙👊 CONNOR NEEDS A CURE! #duchenne

Thank you Jack for the picture 😁

[Caring for Connor @caringforconnor]

Connor made it into the @MetroUK paper today. Keep a look out if in London today. Massive thank to Mark&Co for making this possible. Helping us raise much needed awareness for #duchenne & all the children suffering from this vile, progressive muscle wasting&life limiting disease

[Caring for Connor @caringforconnor]

@SimonCowell think you should invite #duchenne boys to the show. Raise the profile, help save our kids 💙👊
https://t.co/HGj2ddz1t6

[Caring for Connor @caringforconnor]

Absolutely shocking!! Really concerns me for Connor growing up in this world now and being a vulnerable person. Why are people soooo evil! 🤬 Where's the... https://t.co/poqTYjXZJd

[Caring for Connor @caringforconnor]

Pinched from another #duchenne parent.....

Being a Duchenne parent means telling your child they can’t climb at the playground because in the end they won’t be able to walk.
Being a Duchenne Mum means being... https://t.co/0OLskWay2m

[Caring for Connor @caringforconnor]

Amazing!! https://t.co/GxJMj3e9D0

[Caring for Connor @caringforconnor]

Thank you so much Dreamland Margate, they had a blast on the world's biggest bouncy castle 👍😍

#duchenne is sooo crap but to see the smiles and make special memories is awesome #lifelimiting #photostoremember #musclewasting 💙