Hello!

17 Comments

Extensive skin surgery will be conducted on a seven-month-old from Wollongong to remove a large, dark, hairy birthmark which covers the top half of her tiny face.

Ruby Ashby is one in 500,000 children born with Congenital Melanocytic Nevus which covers the right side of her face and head.  She will need seven operations to fully remove the birthmark before she is school age.  

“Ruby is like any normal baby, she has such a happy personality and is just perfect,” Mum Natalie told Daily Mail Australia. “We wouldn’t change her but it is important to have it removed before she starts school – she was born with it but it doesn’t mean she has to live with it.”

Natalie continued, “We just want the best for her. We are hoping by the time she starts school the mark will be gone, it takes time though because we have to give time for the skin to heal between surgeries.”

The first operation will take place on January 12 with a cost of $10,000.  The procedure includes inserting a silicone balloon under her skin on a part of her body not covered by the birthmark. The balloon is then slowly inflated with saline over a number of weeks.  The part of her face covered in the birthmark will then slowly be replaced with the excess skin gained from the first procedure.

Her parents Natalie and Ben have chosen to use one of the top plastic surgeons in Australia, because of the sensitivity of operating on such a young child.  They are hoping to raise $30,000 towards the cost of the operations via the Go Fund Me page that has been set up for the cause.  They will also host a fundraising event night in January.

The Go Fund Me page has already raised $12,000 in the few short days it has been operational.  The young family have been overwhelmed with the support and money they have received so far from friends and total strangers.

“In the first day it was so unexpected, we were overwhelmed,” Natalie explained to Daily Mail Australia. “It has been amazing. It was set up for people who couldn’t attend our fundraising night but still wanted to donate but people have been sharing it on Facebook and we have received donations from people we don’t know and a few anonymous ones too.”

Image Source: GoFundMe\ RubyAshbyFundraiser

 

 

  • She is such a beautiful little girl – I do hope all goes well with the surgery and that you raise the full amount you need for your daughter.

    Reply

  • This is a real reason for plastic surgery. The world can be so cruel to people who look different and this condition can change to a more dangerous condition later. A very hard decision for the parents to make and I wish them the best in the for coming years for a great result.

    Reply

  • I hope it all works out she is such a beautiful baby.

    Reply

  • It looks like a very big surgery. Hopefully it will give excellent results!!

    Reply

  • With or without this condition: such a precious and gorgeous wee girl ! I understand the parents decision as well. Not only because the world can be cruel, but also because the condition may now be benign but there is always the risk it turns malignant.

    Reply

  • Lke us

    Reply

  • What a beautiful bub with such a gorgeous smile. I hope it all goes well for them.

    Reply

  • What a gorgeous little bub. I can understand what her parents are doing. It’s going to be tough process for them and I wish them well

    Reply

  • What a beautiful smile the baby has. I wish the family well on the procedures and hope that it is over with quickly.

    Reply

  • Goodluck to the family, it would be a tough decision to make

    Reply

  • I wish them all the best. She is gorgeous.

    Reply

  • what a beautiful child! when i first saw the pic, i thought that she was a doll! wow!

    Reply

  • Such a gorgeous baby, I totally understand why the parents have chosen this as the world can be so cruel.

    Reply

  • What a gorgeous baby. I can understand her parents’ decision, though.

    Reply

  • I hope it works for them, and that any extra money they are receive goes towards a foundation/hospital to help others with the same condition.

    Reply

Post a comment
Like Facebook page

LIKE MoM on Facebook

Please enter your comment below
Would you like to include a photo?
No picture uploaded yet.
Please wait to see your image preview here before hitting the submit button.
Your MoM account


Lost your password?

Enter your email and a password below to post your comment and join MoM:

You May Like

Loading…

Looks like this may be blocked by you browser or content filtering.

↥ Back to top

Thanks For Your Star Rating!

Would you like to add a written rating or just a star rating?

Write A Rating Just A Star Rating
Join