• Donate
  • About Us
    • Our Purpose
    • What We Do
    • Our Impact
    • Our Team
    • Work For Us
    • Volunteer
    • The DMD Registry
    • Action Duchenne Policies
  • Get Support
    • Support Calendar – What’s On
    • Register for Support
      • Time Out – A Space for Mums
      • Dads Against Duchenne
      • Grandparents Together
      • Online Group Counselling Programme
    • Recently diagnosed
    • Children and Young People
    • In-Person Support Events
    • Schools
    • End of Life and Bereavement
  • Annual Conference
    • Save the Date for the Action Duchenne Community Summit 2026 (Previously known as Annual International Conference)
    • Highlights from the Action Duchenne Conference 2025
  • News, Webinars and Blogs
    • News
    • Webinar Series 2026
    • Webinar recordings
    • Bite-Sized Duchenne Science Live
      • Facts about Duchenne muscular dystrophy
      • Signs and Symptoms of Duchenne Muscular Dystrophy
      • Diagnosis of Duchenne Muscular Dystrophy
      • Crucial Genetic Terminology
      • Genetics – Blueprint of Duchenne Muscular Dystrophy
      • How is Duchenne Muscular Dystrophy Inherited?
    • Hear From Our Community
  • Support Us
    • Friends of Action Duchenne
    • Upcoming Events and Challenges
    • Give in memory and help us support every family, every time.
    • Organise your own event
    • Fundraising at school
    • Donate by cheque and post
    • Welcome to our Runner Hub
  •  0 items - £0.00
  • Menu
  • Skip to right header navigation
  • Skip to main content
  • Skip to secondary navigation
  • Skip to primary sidebar
  • Skip to footer

Before Header

  • My account
  •  0 items - £0.00

Action Duchenne

Header Right

  • Donate
  • About Us
    • Our Purpose
    • What We Do
    • Our Impact
    • Our Team
    • Work For Us
    • Volunteer
    • The DMD Registry
    • Action Duchenne Policies
  • Get Support
    • Support Calendar – What’s On
    • Register for Support
      • Time Out – A Space for Mums
      • Dads Against Duchenne
      • Grandparents Together
      • Online Group Counselling Programme
    • Recently diagnosed
    • Children and Young People
    • In-Person Support Events
    • Schools
    • End of Life and Bereavement
  • Annual Conference
    • Save the Date for the Action Duchenne Community Summit 2026 (Previously known as Annual International Conference)
    • Highlights from the Action Duchenne Conference 2025
  • News, Webinars and Blogs
    • News
    • Webinar Series 2026
    • Webinar recordings
    • Bite-Sized Duchenne Science Live
      • Facts about Duchenne muscular dystrophy
      • Signs and Symptoms of Duchenne Muscular Dystrophy
      • Diagnosis of Duchenne Muscular Dystrophy
      • Crucial Genetic Terminology
      • Genetics – Blueprint of Duchenne Muscular Dystrophy
      • How is Duchenne Muscular Dystrophy Inherited?
    • Hear From Our Community
  • Support Us
    • Friends of Action Duchenne
    • Upcoming Events and Challenges
    • Give in memory and help us support every family, every time.
    • Organise your own event
    • Fundraising at school
    • Donate by cheque and post
    • Welcome to our Runner Hub

Awesome Abseil 2019 was incredible

You are here: Home / News / Awesome Abseil 2019 was incredible
Gemma Eadie Duchenne Mum
Awesome Abseil 2019 was incredible

10 June 2019 by Lynnette

On Saturday 8 June 2019, 14 brave, amazing people descended the breathtakingly high Northampton Lift Tower.

They were cheered on by their families, friends and Lynnette and Shelley of Action Duchenne. As the weather was too extreme to abseil the 418 feet outside the tower, the descent took place inside. The abseil was broken down into 3 different sections, with the final option of going face-down, meaning that the overall descent was closer to 450 feet!

Well I did it! The weather was not safe enough for abseiling outside today so inside it was. It was an amazing experience. I even did the forward facing abseil.

Lynnette has been amazing, always checking in and being such a friendly person to speak to. She has lots of ideas of how to raise money and awareness. I felt amazing raising money for Action Duchenne. It feels really good to give something back and hopefully raise awareness of the condition.

Sarah Hodgson

The 14 went up to the first stage in small groups where the instructors kitted them up and they got ready for the abseil. Once they were ready, each group went up to the first drop together. The Extreme Abseil team were so professional, encouraging and patient. They reassured each of the abseilers and really made the whole process so smooth and enjoyable.

Amazing, so lovely to take part in something for such a worthwhile cause and the total we have all raised is something to be really proud of.

Lauren Spagnol

While the Awesome Abseilers completed their challenge, their dedicated supporters chatted and met other families outside. The children all played together and people shared stories and experiences. It was a really lovely time for people from the Duchenne community to come together.

Yesterday was amazing, to see everyone’s bravery, hear everyone’s stories of why they were doing it and to meet the inspirational families who live with DMD.

Sarah Read

Although you don’t need to do any official training for the Abseil at the Northampton Lift Tower, it is strenuous as there is lots of physical exertion and you certainly put your arms through a good workout!

I’ve never done anything like this in my life, it was completely out of my comfort zone. On the day it self I was a bag of nerves but Lynnette completely put me at ease. If a scaredy-cat like me can do it anyone can!

Jenny Cocks

Inspired? Will you take one of the 30 places in the Awesome Abseil 2020?

Sign up today

Thank you to each and every one of our amazing team of Awesome Abseilers. It has been a privilege to work with them over the past few months and I was in awe of how they all tackled the challenge this weekend.

Lynnette – Community Fundraising & Marketing Officer
Share this:

Category: News

Previous Post: « Awesome Abseil tomorrow!
Next Post: Stoke by Nayland charity golf day Stoke by Nayland Golf Club»

Primary Sidebar

From our community

Turning Challenges into Change – Our Story with Action Duchenne

I was introduced to Action Duchenne by the Muscle Team in Newcastle shortly after Oliver’s diagnosis in 2017. In those early, overwhelming days, their support meant everything. Members of the Support Team would call just to let me talk, vent, cry — whatever I needed. They were simply there, and that’s why I choose to support them every …

Louise’s London Marathon Story

Louise’s London Marathon Story Written by Louise Ruddick “My relationship with Action Duchenne came about very spontaneously at the beginning of January this year. My brother, George, was diagnosed with Duchenne back in 1992, just before his third birthday. He was obviously too young to be aware however the impact that it had on our …

Parent Story: Scott and Vicki share their story of their son’s diagnosis of Duchenne and their family’s journey.

Parent Story: Scott and Vicki share their story of their son’s diagnosis of Duchenne and their family’s journey. “I was just sitting in the room and the doctor’s mouth was moving but I couldn’t hear anything that was coming out of it”  Parents Scott and Vicki have two children, Josh and Layla. When Josh was just …

Footer

Action Duchenne
5th Floor, Mariner House
62 Prince Street
Bristol
BS1 4QD

07535 498 506
info@actionduchenne.org 

 

 

 

 

 

 

 

 

Subscribe to our mailing list

Do you consent to receiving regular email updates? *
Email Format
  • Accessibility
  • Privacy Policy
  • Terms & Conditions

© Action Duchenne - Registered Charity No 1101971 - Scottish Charity No SC043852