Main image

Help Malachi Fight his pain and do his Bucket List

Closed Cause page created in the Health category by judy dewar for "Malachi Agnew"


$2,655 of $30,000 goal

Given by 65 generous donors in 5 weeks

Share   Closed

Help Malachi in his fight to be pain free and keep mobile, with medical expenses, and help Malachi achieve all his bucket list dreams.

Main image
  Bay of Plenty

An update as been added in Updates.

Malachi is 12 years old and has fought his whole life with numerous medical conditions. Malachi has been dealt a really tough journey in life but he fights daily trying to be positive. On his good days he is busy encouraging everyone he can, he is a true blooded champion.

Malachi had his first hospital admission at only 6 weeks old and his journey in and out of hospitals has grown over the years, hospitals are common ground to him and his Mum and brothers. He developed seizures, drop attacks( his legs would paralyse underneath him) and horrific head pain. By 4 years old he had his first major brain surgery for Chiari Malformation which was paralysing him and leaving him in continuous pain. He has had numerous operations for Intracranial Pressure monitoring and had shunts inserted in his head to drain fluid from pressing around his brain.

Malachi has Chiari Malformation, Intracranial Pressure, Migraines, Scoliosis, Epilepsy, ADHD, Asthma, Eczema, his spine has fused some vertebrae which now pinch nerves and discs and he has battled with Failure to Thrive resulting in him having nasogastric tubes in his nose to be fed through and eventually a Mic-Key port in his tummy to be fed through and he can no longer grow with normal food. Mum feeds him every 3 hours for an hour and all night long via a feeding pump, she has had to give up her career to be his fulltime carer. She is raising her 4 sons on her own.

Malachi is in pain daily, does physiotherapy 3 times a day resulting in some powerful pain medications. His pain is lessened if he does hydrotherapy during and after physiotherapy. He has little muscle as they have degenerated, genetic testing has been sent overseas to find the cause of his muscles degenerating. Meanwhile with the help of Neurosurgeons, Neurologists, Paediatricains, Dieticians, Physiotherapists, Occupational Therapists and Mum he fights to save muscle, keep the painful swelling in his joints down, doing it all through a haze of at times excruciating pain caused by his medical conditions. He lives on pain meds 24 hours a day.

Malachi woke up in Starship in the High Dependency Unit and looked at all the machines he was hooked to and how he felt and made a bucket list as there were things he wanted to experience in life and didn't want to miss out on. He has been working through these. Malachi is NOT terminally ill but his conditions are life threatening.

Malachi is so delightful, he is so positive and fights so hard but I have seen him so often on his knees in pain struggling to get through physio or a bout of pain, his Mum on the floor with him every step of the way. This affects her whole family and I really want to help them.

If anyone knows Jacinda Arden, can you let us know as one of his huge wishes is to meet her and "have a chat"

There is a link below to his FB page, and there is the bucket list being added to that.

https://www.facebook.com/julie.major.908

There is a video attached of some of his journey.

https://www.youtube.com/watch?v=D80rHRd2GFA&t=

Please share this page.

judy dewar's involvement (page creator)

I'm Malachi's aunty and I want to help my nephew and his Mum with his medical expenses and to help him get the equipment he needs in his medical fight and fulfil his Bucket List.

Use of funds

The money will be spent on medical and gym equipment for Malachi to do his physiotherapy 3 times a day, to help with ongoing medical expenses and clear old medical expenses and help Malachi to do his bucket list dreams.

Other page links


Latest update

More news  12 February 2018

Malachi's genetic tests come back. He does have 2 genes that have mutations in them. It is the ssme gene as Muscular dysyrophy but IS NOT Muscular dystrophy, a different mutation. He is the 3rd of 3 people in the world with this condition. There is little information about it but it is in fact a degenerative muscle condition. As there is little information about his conditions he has volunteered himself to genetic testers to have all his symptoms, medical information recorded accurately to help people in the future. Unfortubately there is no cure. He has taken this with a positive fighting spirit and is battling on despite his tired painful body.

Malachi also had a positive MRSA results which leaves him vulnerable to infections. It is resistant already to some antibiotics so that's pretty scary.

Malachi's bucket list has been almost filled with offers and he will tick through these as he is able. Any help with his Givealittle to receive medical equipment, assistance, help with medical bills and ongoing costs will be truly appreciated. Please share and help this little guy fight.

View and comment


Latest donations

  • Louise

    Louise on 23 Feb 2018

    $10

    Hope this helps do something you like

    $10

  • Guest Donor

    Guest Donor on 23 Feb 2018

    $25

    $25

  • WWL

    WWL on 21 Feb 2018

    Private

    Private

  • Antony Douglas

    Antony Douglas on 21 Feb 2018

    Private

    Best of luck with your bucket list buddy!

    Private

  • Rob Henson

    Rob Henson on 21 Feb 2018

    $50

    $50


Who's involved?

judy dewar's avatar
Created by judy dewar
Julie Agnew's avatar
Paying to a verified bank account of Julie Agnew on behalf of Malachi Agnew

Page Moderated The page has been checked by our team to make sure it complies with our terms and conditions.

Gallery


Got a question for the page owner?

3 questions have been asked already. Check them out and ask yours here.

Any concerns?

Report this page
This page was created on 18 Jan 2018 and closed on 28 Feb 2018.
$2,655 of $30,000 goal

Given by 65 generous donors in 5 weeks

  Closed Share
Share
Share a link to this page to help spread the word

  Facebook

  Twitter

  Email

  Copy Link

  Embed

×