Hi there fellow Creatrix! I’m Georgie, founder of the enchanted living blog 'Georgie xoxo', 'The Art Of Blogging' and 'Art Of Pinterest' E-Courses and creator of an art and history online school called 'Academy Of The Enchanted Arts.'
After creating my handmade hair accessory company, Beauxoxo, when I was just a teenager feeling creatively unfulfilled and depressed at University, I learned a lot about how to balance a business that both nourishes the needs of a soulful, creative entrepreneur alongside managing 6 chronic illnesses.
I realised I too struggled with spreading myself too thin across a million social platforms, spinning all the plates in my business, and getting swept up in the toxic 24/7 hustle culture that has led me on my current path of reclaiming Sacred Simplicity.
Fast forward to today, I'm now on a deeply personal mission to inspire highly-sensitive, creative soulful entrepreneurs just like you to build a business and creative content strategy that brings you an abundance of ease, flow and simplicity so that you spend the majority of your time drenched in the richness of the relationship with your Creative Muse.
If you have even resonated with 5% of the above, I know we’ve not met by accident, and that we were destined to meet and I can't wait to connect through my E-Course, Workshop or bespoke mentoring offerings.
Scleroderma & Raynaud's UK (SRUK) is the only UK charity dedicated to improving the lives of people with Scleroderma and Raynaud's phenomenon. SRUK aims to improve awareness and understanding of these conditions, to support those affected, fund groundbreaking research and ultimately to find a cure.
I was diagnosed with Scleroderma in 2018, and my work has since been dedicated to spreading awareness of this condition alongside helping you to bring your cherished creatives gifts into the world through Blogging and Pinterest.
By supporting my work through any of my E-Courses, 1-1 Mentoring or Live Workshops, a portion of your purchase goes towards SRUK so that they can continue to support me and others who live with this debilitating auto-immune disease.