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ChewyhasMS

699d

Reaching out to say hello to my fellow MS Warriors. It may be a long journey but we do it one day at a time. I’m a bit of an out of the box type, using alternatives to the protocols with SPMS. I live in Orlando Florida where the heat is high and the magic is back after a few long years of the pandemic’s effects. The high heat is definitely not my friend right now. I experienced the unforgiving condition of C-pneumonia, once on 2020 and in Dec 2021. When I say it’s a journey to wellness, I mean a long haul with it has the ability to mimic MS symptoms. This is s great opportunity to share experiences. My shocking diagnosis of MS came was I was 48!!! I had been dismissed many times by several physicians as what my ongoing condition of excessive fatigue, multiple chemical sensitivity and unknown urticaria / rashes along with falling and extreme brain fog. One spinal tap and a few scans and an MRI actually gave me relief finally knowing that my symptoms had a name. It’s never something you are ready to hear however, it’s helped me adjust my lifestyle and positive outlook to care for my future

☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision

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