ジョージア・メイ・フットさんのインスタグラム写真 - (ジョージア・メイ・フットInstagram)「Happy World Vitiligo Day ✨ I developed little white patches on my skin in 2020. To which was wrongly diagnosed as tinea versicolour. I tried everything the doctors said and none of it worked. This just resulted in me feeling worse every time I saw it spread and get bigger in other places. It took a whole 12 months before I was even seen by a dermatologist. I went in the room, was diagnosed with vitiligo within minutes and sent away being told there was nothing that could be done. The only thing they tried to give me was steroid cream. Which I refuse to use. As I know it will do absolutely nothing for me. And can cause further damage. I have never, to this day, been offered support for what this condition can do to your mental health. Please believe me when I say this has been a huge struggle for me to come to terms with. On the surface I’m ok. Deep down I have never felt so insecure. But I try to push past this every day and see it as something beautiful and unique. I have more patches appear and patches disappear constantly. I was told it was meant to stop after 2 years? I was also told once a patch appears it wouldn’t ever go away? So why have some of mine? It’s spreading on to my face now which is something I’m not sure how to feel about. My hands are the most affected as you can see. There is so little information and support given to people with this condition. How and why did mine develop 3 years ago? Why does it change so often? Can I treat it? Has the Covid jab caused this which I’ve also been told about? I have so many questions and no answers. All I know is this is now me. And this has been a very hard condition to process. I will be the girl who refuses to cover it up so that you can feel more confident with yours. And I promise to always be a voice for those going through the same for as long as my platform means anything. You are beautiful 💜 and you are unique 😍 G x」6月25日 22時23分