When someone says they’re having a 2020. Immediately I have to be respectful and resourceful due to the situations that are happening in this world. My patience has become minimal because my resources have depleted💔 everyone is going through their own battles in their own ways. Here’s to the next giant leap in my life, not to mention all the other bad energy bubbles orbiting around my body. Let’s go baby!!!!! I can deflect, I’m Detroit super star 💫 lol.
I can push that shit off. Roll it off my shoulders. My caseworkers have not promise what they could deliver. Go figure right? We are on our “sixth extension” meaning the process started over a year ago in last July. I’ve been really chill and calm about the whole process but when your caseworker has switched 4 times & the supervisor has switched 2 times & each person has their own excuse. I am wondering if it would have been easier, for me to go door-to-door & ask for $5 to fund all the resources myself because insurance won’t cover them.
The small business plan was to be approved and distributed for funds, —->August 24 where I received A nice little “fukkk you” letter from the office to say we’re going to push your plan another three months. i’ve met with the orthopedic therapist for an evaluation on the type of scooter that I need. I spent four weeks of research that my caseworker asked me to develop because their level of laziness is 100! I found perfect one that fits my size and lifestyle to fold it up + travel.I have let these Individuals take me so far low into the ground and yet; I continuously smile. I’m tired of crying, all I can do is smile. I miss half days of work to sit in the hospital for written letters to show my physical stature ! even though it’s clearly, mo fo present. 🥵I am physically disabled + permanent! Hello, look at my body ; crutches to walk. Im 4’4” With 14 surgeries & limitless obstacles 😶💔
I am so dumbfounded by how crazy the system makes me feel because they can’t get it together. wake up! This is a systematic problem, this has nothing to do with me. If I was a rich person, I will be going out there helping people like myself. The best I can do is smile and chill out. #lifeofmissydi
Breaking Barriers & Defining The Odds
Using forearm crutches to move around is a way of life that I have come to know all too well. As a person with a disability, I am constantly dealing with the challenge of balancing my energy and resources while adapting to the limitations that come with my condition. I’ve grown from full body braces […]
My Disability Is Called Sacral Agenesis
My Disability Is Called Sacral Agenesis I don’t know what to say half the time when I’m speaking about a subject that I haven’t talked about in so long. So bare with me 🤘🏻 #disabled #disabilityawareness View this post on Instagram A post shared by Missydi Fanpage (@missydi.jpeg)
I Am My Own Advocate
I am my own advocate #disabilityawareness View this post on Instagram A post shared by Missydi Fanpage (@missydi.jpeg)
Preparing My Camera Angle For Filming My Full Body Shot
Preparing my camera angle for my first full body shot video. Trying to walk better into my disability suit as a leader that’s inspired and motivational. It’s really hard to wear a smile all the time. I am so tired just from my muscles and the pain in my shoulders. I don’t like to talk […]
Doing My Best 😍
Doing my best 😍 #disabilityawareness View this post on Instagram A post shared by MissyDi (@missydi)
