New: Suffering from MBL2 and Undiagnosed Mental Disorders, What to Do?

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Background: In 2015 I was diagnosed during my second hospitalization for the same infection with Mannose-Binding Lectin Protein Deficiency { MBL2 } and have been in and out of the hospital since then. I'm almost 20 now and have aged out of my parents', and I still live with them because of this, insurance and haven't been able to find a plan that doesn't cost an arm and a leg for them and myself. I also have no job and had to drop out of High School because of said Deficiency and lived in three different states and two of which charge for records I need in order to properly file for SSI/SSDI. I'm feeling super weak and am in need of a specialist in order to make a plan to ensure I don't wind up with Sepsis for a fourth time. What do I do?

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