NTUK Dolphins at the Swim Serpentine 2019
24 September 2019
NTUK Dolphins at the Swim Serpentine 2019
On a beautiful day the Nerve Tumour Dolphins arrived at Hyde Park ready to tackle the chilly waters of Swim Serpentine 2019. Every single one of dolphins managed to complete the race and we at Nerve Tumours UK would like to thank each and every one of them for going the extra mile to support our shared vital cause!
Our amazing swimmers for the day were as follows:
- Barbara Braeunlich
- Jasmine Munyard
- Kurt Braidley
- Nikki Stuart
- Gail Sherrick
- Markus Bell
- Ian Boden
- Jess Lakin
- Rachael Knights
Members of the office their family and friends were also amongst the swimmers and all have highlighted just how incredible the day was!
![](/images/common/Swim-serpentine-3Page-Preview-800-x-500-px-copy-5.png)
![](/images/common/Swim-serpentine-2Page-Preview-800-x-500-px-copy-4.png)
![](/images/common/Swim-serpentine-3Page-Preview-800-x-500-px-copy-4.png)
![](/images/common/Swim-serpentine-2Page-Preview-800-x-500-px-copy-5.png)
Following the race everyone gathered to share a picnic under the sun to cap off what was a truly wonderful day. We hope you all enjoyed it as much as we did, and we can't wait till next year!
![](/images/common/Swim-serpentine-2Page-Preview-800-x-500-px.png)
![](/images/common/Swim-serpentine-2Page-Preview-800-x-500-px-copy-2.png)
![](/images/common/Swim-serpentine-2Page-Preview-800-x-500-px-copy-3.png)
![](/images/common/Swim-serpentine-2Page-Preview-800-x-500-px-copy.png)
If you would like to register your interest or even sign up to next year's race and join the team of NTUK Dolphins, then you can do so by clicking on the link below. Make sure to also check out the video below of this year's event 😊
Filter News
![](https://nervetumours.org.uk/images/made/images/common/ACT_It_Out_logo__taglinepreviewq_800_600_s_c1.png)
Act it Out Prototype App Trial
If you are experiencing difficulties related to NF & 'Visible Difference' - find out how you can take part
Read More![](https://nervetumours.org.uk/images/made/images/common/London_Marathon_Website_Header_370x280_800_600_s_c1.jpg)
The Virgin Money London Marathon Goes Virtual
Sign up for your Virtual London Marathon experience Sunday 04.10.2020
Read More![](https://nervetumours.org.uk/images/made/images/common/FH_portrait_square_Jan_2018370x280_800_600_s_c1.jpg)
Accessible Online Meetings for those with hearing impairment
Frances Harris talks to us about the difficulties faced by those with NF2 & hearing loss communicating online and solutions
Read More![](https://nervetumours.org.uk/images/made/images/common/Mr._Cohen_London_to_Paris_take_offpreview_800_600_s_c1.png)
Pipers to Paris - Ride for Neurofibromatosis
Read all about Mr. Cohen's epic 230 mile bike ride to help support those affected with Neurofibromatosis in the UK
Read More![](https://nervetumours.org.uk/images/made/images/common/AI__employment_Article_image_3-preview_800_600_s_c1.jpg)
Artificial Intelligence & Disability Recruitment
Creating fair processes for people with disabilities by the HR teams that are using artificial intelligence/face recognition
Read More![](https://nervetumours.org.uk/images/made/images/common/Mikes_NF1_Story_370x280_800_600_s_c1.png)
It’s a Kind of Magic
Mike Brennan has had to deal with the stigma as well as the symptoms of NF1, which he has battled since he was a young child.
Read More![](https://nervetumours.org.uk/images/made/images/common/CAR__UWE__VTCT_Logo370x280_800_600_s_c1.jpg)
Centre for Appearance Research (CAR) and The VTCT Foundation Virtual Showcase 28th July 2020
Get the latest updates on the Centre for Appearance Research's work into helping people with Visible Difference
Read More![](https://nervetumours.org.uk/images/made/images/common/Wales_Nurse_Job_Post_banner_edit370x280_800_600_s_c1.jpg)
Specialist Neurofibromatosis Nurse - Wales
Find out more about our latest position available in Wales
Read More![](https://nervetumours.org.uk/images/made/images/common/picsea-EQlTyDZRx7U-unsplash-preview_800_600_s_c1.jpg)
Covid-19 Impact on Wellbeing in Families of Children with Rare Neurogenetic Disorders (CoIN Study)
Find out how you can get involved
Read More