Megan’s Skyfall
03 September 2019
Megan's Skyfall
EDIT:
Megan has now completed her Skydive (see photo below). Continue reading however to see Megan's full story detailing her travels with NF.
Having NF is a constant struggle; whether it be dealing with pain, worrying what people think of the skin tags that are all over my torso or overthinking what the future holds for me.
Since the 15th March 2019 I have been back packing the West Coast, Northern and Central Australia sleeping in a tent for the majority of time and have had the most wonderful time, even with the back, knee and hand pain I struggle with some days.
I have been telling everyone I meet about this condition and how it affects me and others, how I have changed my diet to be a more natural, plant based diet in order to try to stem the growths and how Nerve Tumours UK help us all through information days, research, support centres and raising money to allow for more NF nurses across the country.
I have received nothing but love, support and curiosity from these wonderful people I have met and each person wondering why they have never heard of it before.
![](/images/common/megan-skydive-2Page-Preview-800-x-500-px.png)
![](/images/common/megan-skydive-2Mobile-600-x-800-px.png)
I'm now on the East coast where I have the opportunity to finally tick sky diving off my bucket list and in the most beautiful setting of Airlie beach
Having already written articles for The Sun and The Mirror newspaper and with my cousin running the Birmingham 10k it's now time to do something to myself to raise more money and awareness for our wonderful charity.
15,000 ft isn't that high right?
Megan having after completed her Skydive!
![](/images/common/megans-skydive-completeArtboard-1.png)
![](/images/made/images/common/megan-skydive-2Desktop-1600-x-900-px_800_600_s_c1.png)
Filter News
![](https://nervetumours.org.uk/images/made/images/common/The_Faces_of_NF_At_Xmas_3.70X280_800_600_s_c1.jpg)
2020 A Review
2020 was hard for everyone but our NF community is stronger & more resilient than ever. Read our reflections on 2020
Read More![](https://nervetumours.org.uk/images/made/images/common/Genna_NF_Story_370x280_800_600_s_c1.jpg)
Geena’s Story
James Harkness talks about his late mother Geena Andrews & what Nerve Tumours UK meant to her.
Read More![](https://nervetumours.org.uk/images/made/images/common/Xmas-Party-Heroes-Web-5_Donation370x280_800_600_s_c1.jpg)
Xmas Party Superheroes
Had your Xmas party cancelled? Find out how you can save the day & become instant #XmasPartyHeroes
Read More![](https://nervetumours.org.uk/images/made/images/common/lee_Paterson_Virtual_Santa_Dash_for_NF_370x280_800_600_s_c1.jpg)
Lee’s Santa Dash
Check out Lee's Festive Santa Dash for NF and see how you can get involved
Read More![](https://nervetumours.org.uk/images/made/images/common/Karen__NF_Community_370x280_800_600_s_c1.jpg)
Thinking Forward to 2021 - A Message from our Charity Director
A message from Karen our Charity Director on looking forward to the year ahead
Read More![](https://nervetumours.org.uk/images/made/images/common/RAREfest20-eventbrite-email-image-2_370x280_800_600_s_c1.jpg)
Rarefest 2020
RAREfest20: a free virtual, interactive science, technology, advocacy & arts exhibition with a rare twist. Visit exhibition
Read More![](https://nervetumours.org.uk/images/made/images/common/derek_370x280_800_600_s_c1.jpg)
Kebabathon for Nerve Tumours UK
Find out why Des is taking on this Mammoth Meat Mission for Nerve Tumours UK
Read More