This is the MOST frustrating challenge I have with living with ADRENAL INSUFFICIENCY. It is the F WORD of Addison's Disease.
Dealing with a STATIC dose of medication in a world that is forever changing and every moment it takes a bit more cortisol leads to a crippling existence of low cortisol symptoms. Living in an illness lacking the tools to measure my critical LIFE SUSTAINING CORTISOL levels I am left to fend for myself based on physical symptoms.
This is my perspective on how it feels living with the F WORD of Addison's Disease.
We are a family and as a family, we can make a difference.
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DISCLAIMER: The information from THE PICKLE JAR represents the experiences of the host Jill Battle and the individual experiences of each guest. No information is intended to provide or replace the medical advice of a medical professional. The host or guests are not liable for any negative consequences from any treatment, action, application or preparation, to any person following the information from the podcast.
15 май 2024