

Hey yall. I like to use this free page to let you all in a bit on my real life like an uncensored IG as well as to promote. Well this month its Ehlers-Danlos Awareness Month and I wanna let you all know that I have EDS and bring a little awarness to it. Its technically a laxity in my connective tissue. Which can cause my joints to be a little loose goosey sometimes. Here is a pic taken just before my most recent set of incredible experimental treatments that involve getting monthly injections in every major joint and my entire spine 100 injections total every month. Which make me much more stable and strong. I actually started my fetish modeling journey to help cover the expenses of these treatments so every tip and purchase goes to making me that much stronger, stable and comfortable. Having EDS is why I am slow to post at times. And have to take these random hiatus's but when you do get to see me it's a special treat so enjoy. Fyi I use this rainbow zebra pillow under my legs since I'm too tall for even the drs table with my crazy long legs. And Zebras are the mascot for rare conditions of which EDS is considered.
I'm coming out of recoup mode from this last procedure this week and im looking forward to enjoying the spring and my newly regained strength.