A very significant portion of people leave those exact ailments unchecked specifically because a single doctors visit means bills and groceries are unable to be paid.
I got my Crohn’s diagnosis about 3 years ago. While it has been worth it, the amount I have spent on medication, procedures, doctor’s visits, etc has kept my credit card near its limit for years and is a constant source of anxiety. This is with decent insurance. I have a job that is flexible with hours, but between flare ups and infusions, I have to miss work semifrequently and someone not in my position could be in a very tenuous state with their employer. Not to mention the stress of fighting the insurance for coverage of medications that are thousands of dollars per dose and dealing with systemic incompetence of the people involved in every stage of the process. They all fail (doctor’s office, infusion clinic, insurance, etc) to communicate in anything resembling a timely manner without my constant pestering and prodding. It is torturous, and only marginally better than the symptoms themself, and I understand exactly why people forego treatment if they have deal with any one of these issues individually, let alone with all of them. Just so BCBS/UHC/etc can turn a profit off our suffering.
It sucks and makes dealing ith the illness so much worse. Ironically, stress is a trigger for Crohns/UC and the stress of dealing with this has been responsible for multiple flareups of mine. Luckily, a lifeline might be on the horizon for autoimmune disorders like Crohns, Celiacs, and MS
A new (anti?)vaccine is being tested that can rewrite the immune system to take the body’s normal, healthy cells off its kill list. Fingers crossed that before I turn 35 I can just be done with this horseshit before it causes any lasting damage to my insides
A very significant portion of people leave those exact ailments unchecked specifically because a single doctors visit means bills and groceries are unable to be paid.
I got my Crohn’s diagnosis about 3 years ago. While it has been worth it, the amount I have spent on medication, procedures, doctor’s visits, etc has kept my credit card near its limit for years and is a constant source of anxiety. This is with decent insurance. I have a job that is flexible with hours, but between flare ups and infusions, I have to miss work semifrequently and someone not in my position could be in a very tenuous state with their employer. Not to mention the stress of fighting the insurance for coverage of medications that are thousands of dollars per dose and dealing with systemic incompetence of the people involved in every stage of the process. They all fail (doctor’s office, infusion clinic, insurance, etc) to communicate in anything resembling a timely manner without my constant pestering and prodding. It is torturous, and only marginally better than the symptoms themself, and I understand exactly why people forego treatment if they have deal with any one of these issues individually, let alone with all of them. Just so BCBS/UHC/etc can turn a profit off our suffering.
Man I am so sad to hear that
It sucks and makes dealing ith the illness so much worse. Ironically, stress is a trigger for Crohns/UC and the stress of dealing with this has been responsible for multiple flareups of mine. Luckily, a lifeline might be on the horizon for autoimmune disorders like Crohns, Celiacs, and MS
A new (anti?)vaccine is being tested that can rewrite the immune system to take the body’s normal, healthy cells off its kill list. Fingers crossed that before I turn 35 I can just be done with this horseshit before it causes any lasting damage to my insides
https://scitechdaily.com/new-vaccine-can-completely-reverse-autoimmune-diseases-like-multiple-sclerosis-type-1-diabetes-and-crohns-disease/
I’ll honestly hope for the best for you!