21Hour Sponsored Cycle
On Saturday the 30th January 2021 we will be holding our first ever 21 hour sponsored cycle challenge to raise funds to support young adults living with epilepsy and in recognition of the 21 epilepsy related deaths each week in the UK.
You can cycle indoors in the comfort of your home, at FIT 26 Gym or take in the great oudoors by going on a cycle ride. All you need to do is make sure that you and members of your team take turns to cycle continuosly for 21 hours!
You can cycle for as little or as long as you wish in a team, in a relay or register just your lovely self and we can find a slot for you.
There will be lots of fun, a chance to meet new people and get fit whilst supporting such a worthy cause.
If you would like to get involved please register your team via email: firstname.lastname@example.org or call Joanne (coordinator) on 07865 629626.
You can download our sponsorship form here:
Donate on our just giving page https:/www.justgiving.com/crowdfunding/andre-doody
Donate via paypal https://www.paypal.com/gb/fundraiser/charity/3882213
*If donating electronically please make sure you mention “21hour cycle event” in the donation message. Thank you!
Let’s talk epilepsy
Molly’s interview (partner of person living with epilepsy)
Fran’s interview (pregnancy and living with epilepsy) –
A tribute to Peter
Two of the three accompanying songs in the video are Peters own and the third is a remix of his. Proud beyond words… I love and miss you sweetheart. Eternal love Mum xxxx
A letter to the NHS
On the 19th of July 2019 our local MP Judith Cummins wrote to Simon Stevens the Chief Executive Officer of NHS England on our behalf.
The reason? To address our concerns with regard to the lack of information available/provided by NHS England with regard to Sudden Unexpected Death in Epilepsy (SUDEP).
This morning we have received a reply from Professor Stephen Powiss, National Medical Director, NHS England on Mr Stevens behalf. The letter reads encouragingly with regard to epilepsy care going forward, making reference to one of many examples of several clinical leader network events hosted by the NNAG (National Neurology Advisory Group).
Also the NHS RightCare programme that has ‘developed and published intelligence tools and resources to support reduction in unwarranted variation in neurology services. This includes the upcoming publication of an Epilepsy toolkit which provides support to Clinical Commissioning Groups and Sustainability and Transformation partnerships and aims to address the main challenges facing people living with epilepsy in England Today. These include;
- High rates of misdiagnosis
- Increased mortality attributed to epilepsy, including SUDEP
- Inaccurate understanding of the true epilepsy population in England
- Lack of education and self management strategies for people with epilepsy and their families and carers in orders to reduce unnecessary/inappropriate A&E attendance’.
So this does indeed sound positive in theory albeit a ‘wordy’ letter with the phrase ‘all smoke and mirrors’ coming to mind. Since the clinical guidelines that were brought into practice in 2004 and 2014 there is still continued inconsistencies in epilepsy care plans and the current statistics in relation to Sudden Unexpected Death in Epilepsy show that something must be done now, not another several years later.
Sometimes I wonder how things become over complicated or am I being naive? Surely when it comes to SUDEP it’s as simple as the NHS making a clear directive (not a guideline), that health professionals must make patients aware of SUDEP to give people choice and autonomy where sadly for our family this was denied us. It is too late and I will never ever see or hold my beautiful son again.
I wish with everything I have that the proposed ‘positive’ intentions referred to in Mr Powiss letter are not still theoretical but immediate when it comes to practice.
A big thank you to Nick and Sue Johnson for organising a sponsored cycle ride around Rutland Water and well done to all for completing this challenge today! Thank you to all those involved for your time, support and the generous donations you gave.
Thank you to everyone who supported Doodfest 2019!!
What an amazing day!
Our very first epilepsy friendly music festival was a huge success and supported by so many! The event raised not only awareness around epilepsy but also money to help support young adults living with epilepsy.
If you are between the ages of 19 and 30 and you would like some support or to have a chat about how we may be able to help please do get in touch. We really do want to support you in any way we can.
Check out the official Doodfest video below!!!
Epilepsy Facts & Figures
. There are 3 epilepsy deaths each day in the UK (approximately 1200 each year)
. Epilepsy is in the TOP 10 causes of death in the young (under 35)
. Half of all epilepsy deaths are SUDEP (Sudden Unexplained Death in Epilepsy)
. Sudden death is 24 times more likely in people with epilepsy
. Under 20% of clinicians openly discuss SUDEP & epilepsy risks with patients
. 42% of epilepsy deaths are potentially avoidable
(copyright SUDEP Action 2019)
Countdown to our Masked Classical Ball!
Hi, we hope you will like to join us for an amazing fun filled evening to support our aim in supporting young adults with epilepsy, (please see our facts and figures page).
Don your finest and channel your Downton Abbey, Jane Austen or Mr Darcy persona! Fine food, wine, classical music, charity auction in the company of your friends and those you have yet to meet!
Look forward to seeing you there and thank you……
£343 raised by Olivia Dennison!
“My Mum, Ellie and I hosted a charity bake sale / coffee morning yesterday to raise awareness and money for The Peter Doody Foundation. We raised an amazing £343, more than we ever expected 💜 We want to say the biggest thank you ever to all our family, friends and neighbours that came and donated, supported and baked for us! 💜 #doitforpete”
We want to say a huge thank you to everyone involved in this fundraiser, your time and generosity will help more and more young adults with epilepsy.