You Are My Sunshine Foundation (YAMS) | Charitable organisation

You Are My Sunshine Foundation (YAMS)

Phone: +61 409 961 904

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23.01.2022 I just saw this on the FB page of a beautiful family who lost their daughter Rylea to neuroblastoma. I don't think many people would realise just how true this is. We watched the impact on Indigo when Lilla was going through treatment and even though she's been gone for 11 years now, that impact is still evident. It's heartening to see many of our little fighters beating the monster that is neuroblastoma but there is more to do. ... ##NBsux

23.01.2022 I know we've shared this before but it is one of my favourites, especially today Jan 26. Kahlilla singing ..We are one, but we many, and from all the land on earth we come.... We miss your voice, we miss your beautiful face, we love you Kahlilla

21.01.2022 The lovely folks at Phillip Island's Lifestyle Grossard Court- a Blue Cross Aged Care Facility had a charity day and raised $247.10 with donations and a raffle. Thank you to Bev the Lifestyle Co-ordinator and everyone for thinking about our little neuroblastoma kids.

19.01.2022 Lachie Kinsella is one of our NB heroes and his kindergarten, Tarralla Kindergarten has been raising funds for YAMS Foundation. They held a Pyjama Day recently and raised $808.45, I'm sure you'll all agree they look pretty good all dressed up in their PJs. They have just held a further fundraiser raising another $286.... Our sincere thanks to everyone involved. Together we will find a cure for Neuroblastoma.

18.01.2022 Lachie's family and friends Trivia Night raised a total of $21,464 for our research program. Thank you to all involved, we couldn't do what we do without your contributions. Together, we can find a cure!!! This is a few pics from the Trivia Night. Once again sincere thanks to everyone involved.

15.01.2022 The lovely CRAFTMYWORLD Retreat Girls chose YAMS Foundation to donate $440 raised at their craft retreat last week. A huge thank you to Kaz, Sheryn, Jen, Faysy, Anne, Heather, Deb, Alison, Giselle, Heidi, Leanda, Amanda & Liz for the generous donation. Thank you for thinking about our little neuroblastoma kids. Together we can find a cure

15.01.2022 Merry Christmas to all our FB friends. May your day be full of fun and laughter. Give your children the biggest hug today and every day. Special thoughts are with those of you who have lost their beautiful child to neuroblastoma. We love this video of Kahlilla, like all kids, she loved the magic of Christmas

14.01.2022 Natalie & her friend Tracey are running a 44km marathon and have chosen to run 1 km for 44 little NB kids impacted by neuroblastoma. Natalie has been fundraising and raising awareness of childhood cancer for the last 5 years after her friend's son relapsed with neuroblastoma. She has followed YAMS Foundation for a number of years and asked if she could run 1 km for Lilla. Of course we are honoured that she is running for our beautiful girl. So, Lilla is #14 of #44. This y...ear they are raising funds for Neuroblastoma Australia. If you would like to support them, please click on the link. Isn't she just adorable. We miss you Kahlilla Blyss Donahoo x

13.01.2022 Our NB angels are always with us .....

11.01.2022 Neuroblastoma Awareness Day Feb 2 ..... #2little

11.01.2022 Yes Neuroblastoma Australia - #2little #2soon. Thank you for all you do.

11.01.2022 I remember so well. 15th November 2005. Our world changed forever.

08.01.2022 For Kahlilla, all the other neuroblastoma angels, and for all the fighters ... working for a cure

07.01.2022 Sending love and positive thoughts to NB fighter Ava and her family. Somes it seems this neuroblastoma journey will never end .... we never know what is around the corner, and we are ever vigilant. Keep fighting little one, your YAMS Foundation family is thinking of you

06.01.2022 A message from our ambassador Matthew Le Nevez for new friends of YAMS Foundation https://donate.everydayhero.com/d/VTIeZTBIUMCZLpmFME/amount

05.01.2022 Wonderful to see Casey (front row on RHS in main pic), another neuroblastoma survivor living life to the full. Congratulations to you and your team.

05.01.2022 It's almost International Neuroblastoma Awareness Week!!!

03.01.2022 An update from Ava's mum .... what an amazing little NB warrior

01.01.2022 It always warms my heart to read about our NB warriors who have fought and won the battle with neuroblastoma. The first time we were introduced to Bodie was around 2011 and he was going through treatment of Stage 4 NB. Look at him now, 2nd from left, pictured with his big brothers and cousin. He might be small in stature but he has the heart of a lion on the footy field and has just been voted 3rd in his teams best and fairest.... Congratulations Bodie Windsor, we are proud of your achievement.

01.01.2022 Some wonderful news from YAMS Lilla's aunty Jess recently had a little girl, and has honoured our precious Lilla in a very special way. Please welcome Frankie Lilla to the family. May Frankie learn to live in the world with the same grace and presence as miss Lilla did.