05
Aug
It still baffles my mind on the different things people go through and how much resilience and fortitude it builds in them. Our guest in the Issues segment of this episode is one woman I admire so much.
What is Sturge Weber syndrome? Sturge Weber syndrome (SWS) is a neurological disorder marked by a distinctive port-wine stain on the forehead, scalp, or around the eye. This stain is a birthmark caused by an overabundance of capillaries near the surface of the skin. Blood vessels on the same side of the brain as the stain may also be affected.
In this episode, our guest, Chelsey shared how living with this affected her mental health growing up as she was constantly bullied and stigmatized. Please take a listen to educate yourself on this. Also, I’ll be linking stories of more people around the world living with this syndrome towards the end of this post.
About Chelsey Peat
Chelsey was born with a rare neurological condition called Sturge Weber in 1985. Growing up with the condition brought many challenges like extreme surgeries to living in the hospital as a young child.
She didn’t let her struggles stop her and she accomplished everything she set her mind to. From graduating, going to college, getting married and even becoming a mother. She now lives happily with her husband and two daughters in Alberta, Canada. She is an ambassador for the birthmark community and also advocates for individuals born with physical disabilities and facial differences.
The Reality Check segment was inspired by Chelsey which is a reminder not to allow your circumstance or situation define who you are or your value.
In the Common Sense Rule segment, I shared things you should never do or say to someone living with Sturge Weber syndrome.
If you love this podcast, please subscribe, rate and review on any podcast listening app/platform you use in listening to this podcast. I’ll so much appreciate that. It will also aid in visibility and growth of this podcast.
If you would love to support by becoming a patron, that would be great! As a patron, you will get access to so many benefits. Click HERE to become one and choose a membership level Or you can just tip me any amount to support by clicking HERE.
Your support will be so much appreciated to enable the expansion of this podcast.
Articles On Stories Of People With Sturge Weber Syndrome
Social Media Platforms
Instagram @the_calm_down_podcast
Facebook Page @Calm Down Podcast
Twitter @PodcastCalm
To get updates on new episodes and collaborations so you don’t miss out on anything, Click HERE to sign up for my podcast community newsletter. You’ll also get a story prompt once you sign up if you’d love to share your story on this podcast.
Previous Episodes You Should Listen To
What People With Albinism Go Through
This Is Why You Have A Bad Breath And Hole In Your Tooth
Shalom!
