I am Megan, the creator behind Flowercrowns and Treatment. I started this blog when I was going through a very difficult time in my life, and I really wanted to find the good in every day. I have a rare disease, Myasthenia Gravis, and underwent a stem cell transplant in January 2019. The “Treatment” aspect of my blog is to create awareness around rare diseases and health issues in general. The “Flowercrowns” side is to remind me to always look for the good, choose kindness, support local businesses and share all of these with you. I look forward to having you along for the ride, and hope that you enjoy my blog and all the colours it contains!
You can follow my personal journey on social media to see more behind-the-scenes, as well as adorable pics of my four fur-kids and the occasional pic of husband (when he allows me to!). I also share information about campaigns I am working on, places to visit, and an honest authentic snapshot into my life and those around me.
If you have a local business that you would like me to feature on my blog, please visit here or feel free to pop me an email with more information. I look forward to hearing from you, and have you join me on my journey through living my second chance at life.
I am also the owner of The Rare Bear Project, and a manager at Rare Diseases South Africa NPO 120-991. I would so appreciate your support of both the charity, and community upliftment program, where you can also learn more about me and my passions.