Nick Warren

@robkitson What a shame the announcement was overshadowed by the news Exe Men is becoming a stage play!

A few Lions squad reflections from the O2 Arena... theguardian.com/sport/2025/may…

Hearing that if a General Election is called today, the Victims & Prisoners Bill which sets up the Infected Blood Compensation Authority will not be included in the wash up. Just appalling. The PM said on Monday: Whatever it takes… #ContaminatedBloodScandal

@mstevo1976 @ExeterChiefs We had some fun back in the day! Best of luck with everything mate

As one chapter finishes, a new one begins. Thanks to everyone for their support, friendship and fun times during my time at @ExeterChiefs

@alexdowsett Thanks for the support for Ella again. We'll be cheering you on from afar!

We’ve helped over 60 families and want to continue supporting them and more, it’s especially important in the cost of living crisis. We’ve got families into things like swimming, tennis, bouldering, archery, dance, cricket, toddler soft play sessions and of course cycling!

The four quarters of the @londonmarathon in pictures 😅 So it’s giveaway(ish) time. As you know Chanel and I are running the marathon on Sunday for @littlebleeders and @HaemoSocUK we’re giving away a pair of custom Little Bleeders @oakley glasses.

We always like to do a challenge to raise money for @HaemoSocUK on World Haemophilia Day, which is tomorrow. This year it was the girls' turn, doing their first junior parkrun (2k) in Exeter this morning and running every step #proud justgiving.com/page/leah-ella…

Day three of #12DaysOfChristmas and we have reached the end of our series of blogs looking at von Willebrands Disease. In the final blog, Carly realises what their new normal has become, and looks to the future to what challenges may lie ahead. Read Now: haemophilia.org.uk/living-with-vo…

The 'this s**t just got real' blog, with gory detail. This explains why we treat our daughter every other day at home now

@HaemoSocUK The link's not working for me, just getting an error message

In part 5 of our ongoing blogs about living with von Willebrand disorder, Ella's mum Carly shares the story of an incident they knew would change all of their lives forever. Warning: some readers may find this latest blog difficult to read. ow.ly/vsQt50LVajP

My youngest did her first dance show in January with a cannula in her hand less than a week after her first major bleed. Three more big bleeds followed in the next two months as things escalated somewhat...

My wife's series of blogs continues about our life with a daughter with a rare bleeding disorder

Part two of my wife's blog about our youngest daughter

My wife's insight into what it's like having a young child with a rare and severe bleeding disorder, with more blogs following over the next few weeks to bring people up to date with how things are now she's started school

My youngest daughter's pre-school @Starcrossschool did a fun run yesterday to raise money to help people with a similar bleeding disorder. Already more than £500 donated. Note the expert drawing on the medal...

DD No.4 chalked up today (32 miles on Dartmoor). Only started training 10 weeks ago after Ella's issues so just making the start line felt like an achievement!

The red cap returned to racing today, second race in 28 months. Did the Haldon 10k on home @tarmacdodgers territory and was 5th (out of 25!) in 57.45. Warming up (literally) for DD next month

More about my little girl, and what she's been through this year

A video about our daughter for #whd2022 Take two as the first video was too long! @HaemoSocUK

And they're done! All for @HaemoSocUK

Nine miles in

With World Haemophilia Day this weekend, my wife is running a half marathon this morning in aid of @HaemoSocUK so if you see a big group of people running in red between Kenton and Dawlish you know why justgiving.com/fundraising/bl…