This is our brave little girl who has always been full of joy and laughter. Alopecia took this away for a short period but now Charlotte has a newfound happiness inside her which makes us realise that hair or no hair she is still our little Charlotte, Alopecia is just a part of who she is.
As parents we couldn’t be more proud of our daughter, as we know this condition changes lives, but yet after Charlotte having alopecia for 2 years now we are starting to see great signs of strength within her and our family.
We need to thank you all, as we know that meeting others with alopecia has helped give Charlotte her confidence back and also helped her in learning to accept alopecia as just a part of her life, we hope it’s done the same for you.
We feel the foundation has been a wonderful success in bringing children and families together, thankyou all for your support throughout the last year. We feel that we have raised the profile of alopecia greatly but yet have a long way to go. The foundation has helped pay for a number of wigs for various individuals which is just fantastic. While Trish continues tirelessly to lobby the government in removing GST from wigs which we consider to be medical prosthesis not a cosmetic appliance.
Unfortunately, we will not be holding a gala ball this year but will start planning for the next ball hopefully to be held in 2010.
We encourage all to help in any way you can and please continue to support the foundation. We welcome any fundraising ideas!
Matthew and Rebecca Adamson
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