In March 2021 my world was literally turned upside down by a diagnosis of an autoimmune condition of Alopecia. In 6 months I found a patch of hair missing and a week before my birthday in March 2021 I lost it all and still don't know the cause.

In the past 4 years I have overcome so many challenges and found my own way with alopecia with support from the NHS, friends and most importantly my family.

Its had its challenges but also its positives (modelling and being in Edinburgh evening News to name a few!!) but now I run a support group in Edinburgh helping other females, do a blog and have even modelled for hair companies whilst campaigning that life can still go on!

Normally I fundraise for Chest, Heart and Stroke but this year I am fundraising for hairloss and alopecia which is a charity very close to my heart.

In September this year I will be abseiling from the Forth Rail Bridge for the 4th time please give what you can (even the price of a coffee can help someone suffering!!)

Also here is to rocking the different looks each day and owning alopecia!

Love to all who suffer x (link below) also for my colleagues at Hymans who have shown love and support along the way!

Please like and share if can too, all proceeds go directly to the charity.

Thanks all!

Here's to hair hope and being the first to trial the JAK inhibitors drug which has been released in Scotland at long last.

Also an even bigger shoutout to the hair companies that help me with integrated hair lace systems to help me feel like me 💙💙💙

💗