Life Changing Surgery for Macy

£122,221 of £150k goal

Raised by 1,374 people in 3 months

Our daughter Macy has just had her 10th birthday. To say she is active is an understatement. She likes gymnastics, trampolining & hip-hop. She likes riding her bike & swinging from trees. She is daring, adventurous & has no fear. Flexibility & mobility are very important to her, but for the last three years, Macy’s activities have been severely restricted.

Macy was diagnosed with scoliosis at six years old, with three curves in her spine, each measuring from 40 to 48 degrees. For three years, she wore a brace 20 hours a day, to prevent her condition from becoming worse. While Macy coped well with this to start with, by year three she lost her ability to cope. Bracing is widely acknowledged to produce immense psychological stress and in common with many other brace wearers, at times she felt ashamed, scared, angry and stressed. It made her feel different from her friends at a sensitive age, was restrictive and often uncomfortable. We sought a second opinion in August 2016 and were advised that given the negative impacts on Macy’s emotional well-being, she should discontinue brace treatment. Her condition has since deteriorated rapidly & she needs surgery now, before she has another growth spurt. In such cases, the NHS perform a spinal fusion.

Spinal fusion will be life changing for Macy. It will involve inserting metal rods into her spine & fusing the vertebrae, so that her spine becomes one solid bone structure. She will not grow any more in height, although her limbs will continue to grow. It will severely limit her flexibility & movement, which is so important to her. While the NHS only offer spinal fusion, as Macy’s parents, we have always been unwilling to accept that this is the only option for her. After countless sleepless nights & weeks of research to find an alternative treatment, we found our miracle - vertebral body tethering or VBT.

Unlike fusion, it allows for continued growth & mobility of the whole spine. It is the only procedure which will straighten Macy’s spine while allowing her to grow & remain flexible. Surgeons place screws in the affected vertebrae & attach the screws to a flexible cord to pull the spine in a straighter position. This realigns the spine so it can continue to straighten with growth & maintain flexibility. The surgery is less invasive than fusion, involving a five-inch scar as opposed to a full spine incision down the middle of the back. While this is desirable cosmetically, it also means less blood loss, less risk of infection & faster recovery time, as there is less muscle, bone & tissue damage.

We met with a private consultant in England in the summer & planned to take Macy there for this surgery, when an operation was necessary. However, recent red tape around medical re-classification of VBT means private consultants are unable to offer this treatment in the UK for 6-12 months from October 2016.

This decision could not have come at a worse time for us. Macy’s condition has deteriorated significantly in recent weeks & she is often in pain. Her consultant states he must operate now. But as Macy’s parents, we cannot let her have the fusion. It may save her physically, but it will destroy her in other ways, having major consequences for the rest of her life. As fusion is now the only option in the UK, our only hope is to go to America for anterior scoliosis correction, but time is running out.

We are committed to having this life changing surgery done for Macy & will do whatever it takes. The operation is likley to cost in the region of £130k plus expenses and in view of this, we are hoping to raise £150k by February 2017. It would mean the world to us if you could donate, however small; share this page with others or assist with fundraising in some other way. This would help to give our daughter the quality of life she deserves.

Thankyou so much for your support
Macy's parents - Nicky and Mark
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Update 3
Posted by Nicola Robertson
2 months ago
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Update 11 January - Thanks to the kindness & generosity of everyone who has contributed to Macy's fund, we have managed to raise enough money to set a provisional date for her surgery, which is fantastic!! Thanks so much to everyone who has helped us get this far, it really has been an incredible journey & you have all been amazing. The operation will only go ahead however, if we are able to pay the full costs in advance, so we still really need your continued support, to ensure we can get Macy this life changing surgery.

If all continues to go well with fundraising, we will leave for America during the last week of January and the surgery will take place on 2 February at St Peters University Children's Hospital in New Jersey, carried out by the wonderful Drs A, B & C (Antonacci, Betz & Cuddihy) of the Institute for Spine & Scoliosis.

A number of events are taking place during January and February to boost funds. To find out more or to receive more regular progress updates please see our facebook page Life Changing Op Macy.

Thank you so much to everyone who has helped us get this far xxxx
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Update 2
Posted by Nicola Robertson
3 months ago
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Hi everyone. I just want to say that I am still completely overwhelmed by the support we have received. People have been so kind and generous, I really can't believe it. I am feeling a bit emotional just now to say the least and have cried on quite a few occasions at people's generosity. Some ladies who have a craft group at Dunbar library intend to make a large donation to Macy's fund, contributing money they have raised for charity. Dunbar swimming club intend to donate the proceeds from sponsored swims in 2016 and 2017. Macy's Uncle is having a Christmas Jumper fundraiser at his work... There are so many things going on to help us reach our target and so many people getting involved, it is unbelievable. I don't know how I can ever begin to repay people for their kindness.

Last week I felt completely alone in my battle to get Macy the treatment I want for her to grow and be flexible and lead a normal life and now I feel like everyone is behind me. The local community in Dunbar has been amazing, we have had support from friends and relatives across the country and even donations from America, Ireland and Norway. Thank you all so much.

Macy has been quite poorly this week, she has been in a lot of pain and on morphine, which has made her even worse, but she has definitely perked up this morning. We are flying to America on Sunday to speak to a specialist so I will keep you posted re progress. Today my challenge is to learn how to use facebook so I can start providing you all with proper updates on our progress. (Bear with me for now, I am known for being useless with social media). Fingers crossed Dr Betz and Dr Antonacci at the Institute of Spine and Scoliosis can fix my girl xx
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Update 1
Posted by Nicola Robertson
3 months ago
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To everyone who donated or shared this page yesterday I can't thank you enough. I was completely overwhelmed by how much people care and still can't believe how many people donated. Thank you from the bottom of my heart.

Please, please keep donating, keep sharing and help us, time is running out for Macy and I cannot fail her. I am appealing to you all as parents to please help us. Thank you xxxxx
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Read a Previous Update
Becca Pringle
3 months ago
1
1

There is nothing more refreshing than a winter run, so why not join us on Saturday 7th January and take part in the Great Edinburgh Winter Run 5k. Join our event here or come along to cheer the runners along! https://www.facebook.com/events/721773924642235/

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Becca Pringle
3 months ago

We've created a Facebook page to help spread the word and get this page further. Please like us and share! - https://www.facebook.com/LifeChangingOpMacy/?ref_type=aymt_megaphone

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Tim Sangster
1 month ago

My 10 year old twins are running a Talent Show for Children at the Strawberrybarn Dunbar on the 25th Feb - https://www.facebook.com/TalentShowforMacy/ Looking for School aged children for Stage, Science and Baking talent shows - entries close 21st Feb. Tickets at Knox's Newsagent or The Store, Dunbar - or get in touch through Facebook.

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£122,221 of £150k goal

Raised by 1,374 people in 3 months
Created December 6, 2016
TS
£1,000
Tracey Stevenson
7 days ago
1
1
RR
£10
Robert Russel
11 days ago
1
1
RS
£180
RBS tuck shop - Gerry Sheridan's son
12 days ago(Offline Donation)
1
1
LG
£20
Lorna Gray
13 days ago
MT
£10
Michael Trueman
13 days ago

Well done Tina, such a worthwhile cause,

MS
£20
Michael Smith
14 days ago
1
1

Well done Tina

CM
£10
catriona manson
14 days ago
1
1
KC
£25
Kenka Judo - Davy Cleary
15 days ago(Offline Donation)
1
1
AD
£20
Anita Davidson
16 days ago
1
1
SF
£120
Sandra Frey
17 days ago
1
1
Becca Pringle
3 months ago
1
1

There is nothing more refreshing than a winter run, so why not join us on Saturday 7th January and take part in the Great Edinburgh Winter Run 5k. Join our event here or come along to cheer the runners along! https://www.facebook.com/events/721773924642235/

+ Read More
Becca Pringle
3 months ago

We've created a Facebook page to help spread the word and get this page further. Please like us and share! - https://www.facebook.com/LifeChangingOpMacy/?ref_type=aymt_megaphone

+ Read More
Tim Sangster
1 month ago

My 10 year old twins are running a Talent Show for Children at the Strawberrybarn Dunbar on the 25th Feb - https://www.facebook.com/TalentShowforMacy/ Looking for School aged children for Stage, Science and Baking talent shows - entries close 21st Feb. Tickets at Knox's Newsagent or The Store, Dunbar - or get in touch through Facebook.

+ Read More
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