My MCTD story

This is my story of the road to my diagnoses of Mixed Connective Tissue Disease. It had been a long time coming but I could not give you on myself. Remember to seek a second opinion if you need to it is your right.

[@barbaralane9146]

THANK YOU, THIS IS 2024,I HAVE BEEN NEWLY DIAGNOSED 2DAY ! EVERYONE THOUGHT IN THE MEDICAL PROFESSION THAT I WAS CRAZY AS WELL, ACHES AND PAIN, BODY SORE AS HELL MCTD IS REAL AND IT AIN'T NO JOKE!! BLESSINGS TO YOU MAM.❤❤🎉🎉

[@brethatsme3175]

I love you mommy! You’re soo amazing 🥰😍❤️

[@salii702]

Love you thanks for the transparency, it will your transportation to higher heights

[@lifewithyomichelle8932]

Thank you so much. ❤️

[@ItsMimiBaaaby]

❤️

[@tt2524]

Thank you. Informative but the music is slightly loud and makes it difficult to hear you.

[@lifewithyomichelle8932]

Thank you for your feedback. I will be doing another video on my diagnosis. This was one on my earlier videos I was just learning everything.

[@alexandralowder4680]

How are you doing now?

[@lifewithyomichelle8932]

I am doing well. I was sick for about a week with covid. I am always sick with MCTD but i live day to day.