Renstar Foundation

Renstar Foundation Renstar Foundation in partnership with Mater Foundation Renee was tragically taken from us in a bike training session on the 28th February 2010.

The Renstar Foundation was set up in honour of our beautiful daughter and sister Renee Anne Nicholls memory. In her very short life she achieved so many goals competing in endurance sports since the age of 15, a very motivated and talented young lady. Renee enlisted into the Australian Defence Force 10 years ago, initially working in the area of transport and then as a Physical Training Instructor

. While still in the Defence Force Renee burst on to the Triathlon scene and instantly made a name for herself. From the very first Ironman event she achieved a podium finish and continued on with podium finishes all around Australia which qualified her to represent Australia in the World Championships in Kona, Hawaii which she won in her age group. It was always Renee’s dream to set up a foundation to support all the children in Australia who have a very rare genetic disorder called Angelman Syndrome, after experiencing firsthand the struggles her own sister Jess went through financially when trying to get her son Rhys Diagnosed. For those of you that have never heard of Angelman Syndrome it is a neuro-genetic disorder characterized by intellectual and developmental delay, sleep disturbance, seizures, absence of speech, frequent laughter and usually happy demeanour, but will require full time care their entire life and in Australia there is no government funding. In keeping Renee’s dream alive the Renstar Foundation will be working in partnership with Mater Foundation and families to cover the costs of the UBE3A Mutation testing for all of the children that are suspected but not yet diagnosed with Angelman Syndrome. This page has been set up to spread the word and raise money. If you are interested in donating no matter how small, please send us a private message or contact us via phone and details will be forwarded through to you. Updates will be made on amounts raised, due to privacy reasons we cannot list those who have been helped out by our fundraising efforts. The Nicholls Family thanks you all for your support in helping keep Renee’s dream alive. Diana Nicholls: 07 5543 6551
Jess Nicholls: 0410 798 385
Angie Kruger: 0403 534 335

18/02/2018

Once again, a huge thank you to everyone who helped, attended & donated at the 2018 Run for Renstar event. We are very grateful for the continued support we receive. Having the group of Angels attend and watching them interact was wondrous. They really are little miracles and the Renstar Foundation is proud to honour Renee along with raising money to help fund the genetic testing for those not yet diagnosed. Very worthy cause indeed. Donations are still welcome for those who missed the event, please contact us to obtain details. We will update everyone on the tally raised in a month or two once all donations have been received and accounted for. Thanks again🖤

18/02/2018
20/01/2018

Please note that the Run for Renstar event date is actually Sunday 18th February 2018. Sorry for the date mix up - my mind was in holiday mode!

13/02/2017

Due to declining numbers over the last few years, the Renstar Foundation has come to the decision to hold the 'Run for Renstar' biennially. We are a not-for-profit fundraising group with no current sponsors. It becomes very hard to outlay money to hold the event while trying to increase the size & quality of the event.

We are still extremely passionate about raising funds for Angelman Syndrome (in particular helping fund the UBE3A mutation testing required by families suspected but not yet diagnosed).

Hopefully next year we will be able to gain a higher attendance number & raise the much needed funds.

Until next year, we thank all of our supporters along this journey so far. Without you we wouldn't have gotten to where we are today 💙

07/03/2016
07/03/2016

Once again we had perfect weather for the Run for Renstar! A very big thank you to our continued supporters, new faces & old...also to those who weren't able to make it but have ever so kindly donated to our fundraiser. We will update the total funds raised once all monies have been received & updated with the Mater Foundation. Thank you all again, we really appreciate your time & effort!

05/03/2016

Rain, hail or shine....the Run for Renstar will be on tomorrow morning. 7:30am arrival for 8:00am start. Look forward to seeing you all there!

Last year at the Run for Renstar we decided to make our winners official. Matthew Brand & Stacey Ogilvie were our fastes...
04/02/2016

Last year at the Run for Renstar we decided to make our winners official. Matthew Brand & Stacey Ogilvie were our fastest (on foot) participants & have now been engraved onto our Renstar plaque. Each year we will honor our winners by doing the same......just to add a little encouragement for our event participants 😎🏃🏻

03/08/2015

Our 2015 Run for Renstar event raised $2859 towards the UBE3A mutation testing for families suspected but not yet diagnosed with Anglican Syndrome. In the five years we've been running the foundation our total funds raised are $24,352.00. We are very proud of this figure and look forward to increasing this amount in years to come.

03/03/2015

Another sucessful year with some amazing support from friends and family for the 2015 Run for Renstar! We want to thank all those who took the time to attend, donate & purchase shirts, from the bottom of our hearts. We couldn't have done it without you all

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Watersport Ln.
Gold Coast, QLD
4210

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