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Welcome to the life of me.

About 5 years ago I started having random tingling in my arms and legs. It was very concerning and bothersome. I've had every lab test and imaging studies under the sun. Nothing was found. Throughout the years I've had increasing joint pain. First it was just my hips now it's literally every single joint in my body. The pain and fatigue are debilitating. It was finally determined by my rheumatologist that I have Fibromyalgia.  I've been on a host of medications and the only relief is when I take opioids. Well with the "opioid crisis" this is no longer an option. And let's be honest, who wants to live forever on these medications. I've been doing some research on low dose naltrexone (LDN). And the results are promising. I have a consultation on Tuesday and I couldn't be more excited. Follow me on my journey of LDN and let's work through this together. Whether you're a fellow sufferer or a supporter, you're welcome here.