Motor Neurone Disease, fighting it together.

Hello, my name is Lesley Roberts and my husband Christopher, who was a farmer, was diagnosed with MND on May 5th 2014, sadly he lost his courageous fight with this awful disease on September 5th 2015. I wrote this blog to ,share our journey as a family with this disease, the good days and the the bad days and hope to raise awareness of MND in the process. (Follow on Google+ or on Twitter for updates at @soulpunkpixie, or sign up at the bottom of the page for email notification.)

Sunday, 21 June 2015

No. 199. `JumpFest 2015`

We had the most amazing morning at JumpFest 2015 at Perranporth aerodrome in Cornwall. We were so proud of our daughter Tamara who did a tandem sky dive to raise funds for the MND association. She has raised over £650 so far.

Some wonderful friends from the Cornwall MNDA turned up and held a raffle and cake stall. The clouds cleared and even though it was a bit breezy, everyone jumped. I was so relieved when Tam`s shoot opened and then we enjoyed watching her slow descent to the ground, she loved it.

Chris is exhausted and is catching up on some sleep, but neither of us would have missed a second of it.

Memories were made for sure.

Here is a link to some photos. Most are my own, others were taken by the professional photographer there.

https://www.facebook.com/media/set/?set=a.10204943031195702.1073741906.1238559617&type=1&l=0d899db5ed

You can still donate too if you wish at:

https://www.justgiving.com/TamaraBewMND/

The fight never ends.