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Team Beat It

Phone: +61 401 093 024



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25.01.2022 Congratulations again Grandad Peter Mayhew Cystic Fibrosis Community Care - NSW Still time to donate ... https://www.65kroses.com/my-fundraising/213/team-beat-it



24.01.2022 Before school everyday the boys have to do their morning treatments. Jacob helps me set everything up and then we sit together and complete the treatments. Liam still has to sit on the exercise ball with me and we bounce and do percussions but he loves it.... Ben and I are so proud of the boys with everything they have to do.

23.01.2022 Congratulations Jacob! Mummy, Daddy and Liam are so proud of you for completing a lap for the walk yesterday! 7klm on your scooter! Well done buddy Cystic Fibrosis Community Care - NSW Ben Mayhew

23.01.2022 What an amazing day that was full of love, laughter, tears and happiness. Ben and I would like to say Thankyou to each and everyone of you that supported us yesterday by either registering for the walk, walking laps with us, volunteering and donating but most importantly your support through the years! Thankyou to Cystic Fibrosis Community Care - NSW and our amazing CF Clinic Team for making this event possible. Without your continued efforts and support this event wouldnt... run year after year and we wouldnt havnt the vital needs that the CF community need. If you would like to donate the page will be open till the end of February https://www.65kroses.com/my-fundraising/213/team-beat-it Congratulations to Jacob - he done a whole lap on his scooter !!! 7klm! Mummy, daddy and Liam are so proud of you!! Congratulations to Peter Mayhew (Jacob and Liams Grandad) 4th year completing the full 65klms plus an extra 2klms to walk with me to the finigh line! And in record time this year- under 12 hours!! Congratulations to Lauren Mayhew 3rd year competing and walking an amazing 44klms!! It was another amazing year! Thankyou to all our family and friends that walked with us this year! Our feet are a little sore today but we are on our way to the beach to soak up some salty air



22.01.2022 Still having fun

19.01.2022 We had a fantastic family day at the snow this weekend. Jacob and Liam rugged up and we couldnt wipe the smiles of their little faces. #cfsucks #snowday #familydayout #fightcf #loveourboys

19.01.2022 Merry Christmas from our family to yours! We are spending the day at the beach soaking up the sun and breathing in the much needed salty air.



19.01.2022 And there off! 65kms to go

19.01.2022 Merry Christmas

18.01.2022 Dancing our sillys out in isolation

17.01.2022 Watching Church Mass on the tv with Jacob. Not the same but at least we have this.

15.01.2022 Enjoying a night with family and friends to raise awareness and funds for Cystic Fibrosis Community Care - NSW



14.01.2022 Not just for the CF community, helpful advise for everyone!

13.01.2022 When it comes to celebration, where there's a will, there's a way! For the past two years you may remember seeing lots of pictures and videos posted on our page from when we have attended the A Night For CF Gala Ball, but due to the coronavirus this year its going virtual! Ben and I are hosting an ungala event this Saturday and most importantly sticking to the restrictions to spread the word about CF. ... You can donate or register to be apart of the live auction that you can bid on or buy some raffle tickets to win an amazing antartica flight! If you want more information click on the link! Most importantly keep an eye out on our page over the weekend for some videos and pictures of our amazing night to help raise awareness and funds for Cystic Fibrosis Community Care - NSW

13.01.2022 Some much needed R&R for our family and we still have the rest of the week to enjoy the beautiful summer sun!

12.01.2022 New faces to keep us walking

12.01.2022 Just over 4 weeks to go! Time to rattle the tin for anyone who can help us raise our goal for CF! Anyone willing to come and complete some laps are also very welcome, we will be there from 2am until 4pm, so come and join us

12.01.2022 Brad is an inspiration for everyone living with Cystic Fibrosis!

12.01.2022 Happy birthday to daddy

11.01.2022 Fun physio - we have two funny cowboys in the house

11.01.2022 Self isolation is something that the CF community know to well. Jacob and Liam spent the weekend inside having a movie weekend and playing games. We know how to self isolate and socially distance ourselves. PLEASE be responsible with these concepts that are potentially new to you. Be aware of the damage you can cause to those who are medically compromised. (Rose Prince)

10.01.2022 Today we celebrated Liams 4th birthday and Mothers Day. It was a day full of fun, laughs and lots of love. We wish all mums a very happy Mother Day

09.01.2022 Clinic day again........ first clinic in a very long time where the boys finally had a clear sputum!!!! No bugs!!!! Liam had to have another sweat test as he medically isnt diagnosed ( the only way is through a positive sweat test- even though he is genetically diagnosed). Jacob didnt show a positive till he was 4.5!! Photos are thanks to the boys! They take great photos :)

09.01.2022 Well done Mummy and Bonnie Belinda Mayhew Cystic Fibrosis Community Care - NSW Theres still time to donate: https://www.65kroses.com/my-fundraising/213/team-beat-it

08.01.2022 Happy Easter from our family to yours. We hope the bunny came and you get to eat lots of yummy chocolate today

08.01.2022 Every dad needs socks and jocks for Christmas, why not buy a pair of red CF socks to raise awareness for Cystic Fibrosis this Christmas https://www.sockit2cf.com.au/

08.01.2022 Ready to go! Tomorrow is the day we walk for Cystic Fibrosis and paint the town red! If you have spare time tomorrow and want to come down and walk a lap with us or even just to come and enjoy the entertainment then get in touch! If you would like to donate then please click the link below and help us raise much needed funds for Cystic Fibrosis Community Care and our CF clinic at Westmead Childrens Hospital.... If you would like to donate and help spread awareness for CF you can click the link below. Every dollar helps! Lastly thanks to everyone for supporting Jacob, Liam, Ben and I, not just tomorrow but throughout our lives We need a cure!! Cystic Fibrosis Community Care - NSW https://www.65kroses.com/my-fundraising/213/team-beat-it

08.01.2022 Home schooling begins as the boys are now in isolation! Ben and I are extremely lucky that we work for such supportive businesses that allows us to be here for the boys.

07.01.2022 Please watch this powerful interview.

07.01.2022 Happy Saturday Everyone

06.01.2022 1 week to go! Come and join us on the day

05.01.2022 First day of Year One!!

03.01.2022 Morning treatments are done and now its time for school!

03.01.2022 Enjoying the sun and eating mummys yummy pancakes extra early today! Because thats how we roll when we wake up at 445am!

03.01.2022 I'm 32, the life expectancy is 37 and that's not okay. I'm not a carton of milk with a use-by date. Diagnosed with cystic fibrosis as a newborn, Emmah Money ...was given up for adoption after doctors believed she wouldn't survive. 2020 SA Local Hero, Emmah Money | Australian of the Year Awards

03.01.2022 School Holidays arent always about LEGO and beyblades at home! Jacob doing a lung function test today at Westmead, trying a new mask this time

02.01.2022 We had a fantastic family day at the snow this weekend. Jacob and Liam rugged up and we couldn’t wipe the smiles of their little faces. #cfsucks #snowday #familydayout #fightcf #loveourboys

02.01.2022 We are so proud of our boys

02.01.2022 With everything happening around us we have not posted in a while but......... May is Cystic Fibrosis awareness Month and we will be sharing posts from Cystic Fibrosis Australia for everyone to read

01.01.2022 Are you going to join us? 22nd February 2020!! https://www.65kroses.com/my-fundraising/212/team-beat-it

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