Autoimmune Polyglandular Syndrome Type 1 (APS-1) - IDF Reel Stories, Karissa Schultz 

I'm up, well I never went to bed, searching for what is wrong with me. I remember talking with my sister when she was diagnosed with Addison's about Polyglandular Syndrome so I thought I would just see what I could find on RU-vid and your story was first up. I appreciate so much for posting your story. It is very frustrating when I feel like doctors are not hearing me.

Thank you so much for your very encouraging advice and amazing life experiences! No doubt this will be very helpful to many out there!!! 👍🙂

Thank you so much dear for sharing your story. Felt upset about the fact that the doctors did not believe a 9 yr old because she was young.

Karissa is one of the best people i ever met in my life. and her having these health issues get me not liking the world much. she along with many others with health issues like this dont even remotely come close to deserving this. with how smart and sweet Karissa is. she shares that love with anyone and everyone she comes across.

Awesome Lady!

thank you very much for the informative history appreciated it all the best and kudos for being robust

Thanks so much for sharing your story, can't imagine how much you have had to endure, be well keep smiling😊

Hi I am from India my sister is 6 years old and she got autoimmune polyglandular syndrome type 1 and I am also diagnosed with this disease.

👌👌👌

Thank you soooo much for sharing your story Please i want to contact with you because my daughter 12 years old diagnosis Aps1 also before 5 years and i want to talk about your experience

My son age 6 is diagnosed with APS type I and I don't know what to do