The tiny Tamworth toddler has been diagnosed with a rare genetic disorder which means she has a higher risk of strokes, heart attacks and aneurysms due to the twisting, lengthening and narrowing of her arteries.

Imogen has Arterial Tortuosity Syndrome(ATS) and her parents Teleah and Thomas are now exploring treatment options for their little girl, which could mean months in hospitals for specialist care both in Australia and overseas.

Family friends say not only is it taking a toll on the family emotionally, but the financial cost to get Imogen on the mend is unknown. That’s when friends Hannah Bewley, Aimee Grills and Shelley Frazier stepped in to help.

This week they launched a crowdfunding campaign and have been overwhelmed by the support, raising more than $15,000 in about 48 hours.

According to Miss Bewley, the trio are doing what any good friends would.

“I just really want to help them because with all of this going on,” she said. “And to give her the best chance healthwise – they need money. As ATS is so rare, little research has been carried out and most of her many doctors are still uncertain on the best options moving forward.

“As Imogen is unable to go on living with her arteries in this state, a heart reconstruction surgery in Brisbane and further overseas treatment is being considered to give Imogen a chance at the life she so truly deserves. 

“I have started this fund in the hopes to come together as one and raise money for the Michells so their main focus can be put towards the tough little girl, who has so unfairly been shown how tough life can be.”

Miss Grills said the campaign would help ease the financial burden on the family when away from home and work.

“Thank you so much to those who have donated, it has made everything so much better,” she said.

To find out more, or donate to the cause, head to the Go Fund Me website and search for ‘Hope for Imogen’.