Michael Harvey (@harvoose) header
Michael Harvey (@harvoose) profile picture

All views are my own.

Glasgow
Joined December 2011
Photo by Michael Harvey (@harvoose)Photo by Michael Harvey (@harvoose)Photo by Michael Harvey (@harvoose)Photo by Michael Harvey (@harvoose)Photo by Michael Harvey (@harvoose)Photo by Michael Harvey (@harvoose)Photo by Michael Harvey (@harvoose)Photo by Michael Harvey (@harvoose)Photo by Michael Harvey (@harvoose)
Michael Harvey retweeted
We are proud to support #WDAD2025 this evening on World Duchenne Awareness Day
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Young boys in Scotland will now receive life saving drug Givinostat, after we fought a 2month campaign - their families are grateful to Health Sec. @neilcgray for cutting thro red tape & @Sunday_Mail for backing their fight ❤️🏴󠁧󠁢󠁳󠁣󠁴󠁿#DuchenneMuscularDystrophy dailyrecord.co.uk/news/scott…
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Michael Harvey retweeted
Replying to @JohnSwinney
Enjoy John as these kids are certainly not having a fun time .
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“The right to life is enshrined in law. We cannot allow the NHS to continue delaying this treatment. These children have a right to receive the medication that could save their lives, you need to act now” 🏴󠁧󠁢󠁳󠁣󠁴󠁿@neilcgray @ScotGovFM dailyrecord.co.uk/news/scott…
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Replying to @DuchenneUK
@DuchenneUK is WSHA's 2023 corporate charity and we're going to be working to raise funds for this amazing cause for the rest of the year. More info soon! In the meantime, you can donate to support @DuchenneUK here: duchenneuk.org/donate/.
The @OVOHydro in Glasgow was lit up in red last night for World Duchenne Awareness Day. What a beautiful show of support for the Duchenne community! Thank you to everyone who made it happen! @DuchenneDay @worldduchenne #WDAD2023
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Michael Harvey retweeted
The @OVOHydro in Glasgow was lit up in red last night for World Duchenne Awareness Day. What a beautiful show of support for the Duchenne community! Thank you to everyone who made it happen! @DuchenneDay @worldduchenne #WDAD2023
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#IsItOk that I went to hand deliver a letter to the Prime Minister today & the ramp only deals with one step & doesn’t leave enough turning space to use it safely… If #accessibility isn’t right at @10DowningStreet what hope do we have on public transport? #DisabledByTheRailway
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Michael Harvey retweeted
🙌 Fundraiser Friday 🙌 14 year old Scottish girl, Kitty Reilly, will be partaking in a sponsored run in Bangkok this Sunday. She will be running for her best friend's brother, Michael, who has Duchenne. Donate here: justgiving.com/fundraising/k…
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Michael Harvey retweeted
Thank you Paula & Padraic for sharing brave Archie's story @joinourboys💙 DMD has a devastating impact on families, but with groundbreaking research and better care, we CAN change this. Please support, donate, and join our fight in anyway you can. Together, we will #EndDuchenne
In 2020, Archie Naughton joined us alongside his parents, Paula & Padraic, to speak about his terminal 'muscle wasting' condition, Duchenne Muscular Dystrophy. Sadly, Archie passed away in July. Paula & Padraic pay tribute to their son as they continue to raise awareness.
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Thank you @GMB, @susannareid100, @edballs for this Interview and giving us the opportunity to fulfil Archie’s Dying Wish; to find a cure for his brothers George and Isaac. Let’s all End Duchenne together 🙏🏼🧡 joinourboys.org/donate OR gofund.me/e65371d5
In 2020, Archie Naughton joined us alongside his parents, Paula & Padraic, to speak about his terminal 'muscle wasting' condition, Duchenne Muscular Dystrophy. Sadly, Archie passed away in July. Paula & Padraic pay tribute to their son as they continue to raise awareness.
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Michael Harvey retweeted
In 2020, Archie Naughton joined us alongside his parents, Paula & Padraic, to speak about his terminal 'muscle wasting' condition, Duchenne Muscular Dystrophy. Sadly, Archie passed away in July. Paula & Padraic pay tribute to their son as they continue to raise awareness.
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“I will not leave my fate to chance” This was Emery’s gr 8 grad quote. Today, he posed philosophically for his 1st day of gr 10. A day that happens to be World Duchenne Awareness Day. #Duchenneawarenessday More…
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This is my Nephew 💙 2 years ago he was diagnosed with Duchenne Muscular Dystrophy. A cruel disease effecting body muscle. Average life expectancy is only 26yrs. There is no treatment, no cure. Today is #Duchenneawarenessday Help raise awareness & help find cure @DuchenneUK
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This is how it feels to be Celtic 🍀 @josephharvey06 @celticdsa @CelticFC @NCCeltic @CelticFCSLO #CELHEA #CelticFC
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Wordle 243 6/6 What's aw the fuss aboot? #First #Wordle ⬜⬜⬜⬜⬜ ⬜🟨🟩⬜🟨 🟩🟩🟩⬜🟩 🟩🟩🟩⬜🟩 🟩🟩🟩⬜🟩 🟩🟩🟩🟩🟩
Michael Harvey retweeted
Did you spot Duchenne UK in @thetimes today? #Duchennemsuculardystrophy #TheTimes #DMD
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Two days after my sister was buried in the ground and before many other of the children had been laid to rest, Boris Johnson said that the calls for tighter gun controls were a “knee-jerk reaction” and a case of “something-must-be-doneism“. He is not our ally.
The brutal murder of 16 primary school children and their teacher in Dunblane 25 years ago shocked the world. We must never forget all those who lost their lives on that terrible day. Today my thoughts are with the bereaved, the survivors, and the whole Dunblane community.
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Michael Harvey retweeted
No, thank YOU. What a wonderfully brave & inspiring family. 👏👏👏
Thank you so much @piersmorgan and @susannareid100 for the interview on Good Morning Britain. We are so so grateful.🧡🧡🧡
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Nice one Mike! Live from Scotland, he ain't welcome here either 🏴󠁧󠁢󠁳󠁣󠁴󠁿🏴󠁧󠁢󠁳󠁣󠁴󠁿🏴󠁧󠁢󠁳󠁣󠁴󠁿
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