Husband to Katie & father to Felix, comms manager in London, sport lover with CF - author, podcaster & speaker about my survival experiences to help others
"This has to be for everyone"
#Trikafta4all
At 51 and still playing hockey (in a team with his son!) @timwotton is living proof of how effective #Kaftrio/#Trikafta really is
All people with #cysticfibrosis in every country should have the chance to access CF modulators #hope
It's not always been easy to share my hidden disability in the workplace. I hope this is changing with increased diversity, inclusion & belonging. Here's my testimony via my blog post '(In)visible in the workplace'... timwotton.wordpress.com/2022…
“I have a strong urge to write something that will change people... to give them a way of seeing something they didn’t even realize they weren’t seeing.” - Mallory Smith
✨ So she did.
🎬 And now the documentary based on her secret journals comes out January 25th.
ALT A young woman is leaning against a tree trunk, looking contemplative, on a sunny day with palm trees and sand in the background. She is using a nasal cannula.
Have you read Tim's blog yet? When @timwotton was diagnosed with cystic fibrosis in 1971, his parents were told he would only live to his teenage years. Instead, he celebrated his 50th birthday earlier this year. ow.ly/Y6ey50EvN1D
Check out some of the reasons I feel optimistic, despite all the gloom of the pandemic, via my latest blog post 'Optimistic'... wordpress.com/view/timwotton…
Shout out to all my friends taking delivery of the best present they could ever wish for this weekend and over the coming weeks.
Enjoy it, celebrate it, share it!
#kaftrio#Trikafta#ThanksKaftrio
During lockdown, there was little prospect of returning home or starting a great new medication... but hope came with this trick, which you can read about on my blog - 'Seeing is believing'... timwotton.wordpress.com/
24 weeks ago to the day, I started #kaftrio#trikafta.
At the time, my ability to run was pretty much non-existent, managing just 1min on flat treadmill.
With a bit of help from @NHSC25K, I’ve just ran for 20 minutes without stopping. I couldn’t be happier!
#ThanksTrikafta
Only 19 days (maximum) till we get that all important .@EU_Commission rubber stamp
Please hurry up
Don’t make us wait another 19 days
Do it now We are desperately waiting🙏🏻
I’d like Jess to get this before she goes off to university
#kaftrio
.@KingsCollegeNHS
.@hah_insights
Good on you Marc! There are thousands of us in the UK desperately waiting to start this drug ASAP! I should know as I was up all night coughing (for my 49th year!)
After 20 years of rising to uncontrollable coughing, waking up relaxed, calm, rested and taking a long deep breath is something I’ll never take for granted.
It’s hard to explain to others who’ve always had that luxury.
#thankskaftrio
As a community I think we'd all like an update on Hailey Mann's situation as soon as possible @cftrust@NHSGrampian@NicolaSturgeon
From previous experience, it seems entirely possible that Hailey could have #Kaftrio by the end of this week if the right people make that happen.
Miss Mann, said: "We still don't have the European licence, so until that comes through we don't have the drug.
"It could be weeks or months & I don't have the time.
"I need it now and I do not believe there's not a way to do that."
bbc.co.uk/news/uk-scotland-5…