This is a blog about Lyme Disease, Alpha-Gal Syndrome, MCAS (mast cell activation syndrome) & Fibromyalgia . . . living with them, getting diagnosed & finally going through treatment. It's also a blog about Celiac disease . . . being diagnosed and living as an HLA DQ8 lactose intolerant Celiac . . . as well as being a blog about fitness . . . running helped me physically and mentally survive all that I went through. Last, it's a blog about how to work around doctors . . . doctors who are dismissive at dealing with complicated medical labs and are so controlled by insurance, law suits, medical malpractice fears and big pharma that they can't think out of the box to help their patients anymore.
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My brother was diagnosed with a rare blood disorder when he was in elementary school. My mom learned young how vital the role of nutrition was going to be in his life if he was to stay healthy. As such she was voracious in reading about dietary changes she could make to help him out, supplements and vitamins that would help as well, etc. While I'm younger than my brother I was my mom's sous-chef and became very interested in all of her research. Thankfully that love of taking charge of health later on became important in me taking care of my own health issues decades later. While I'm not medically trained and no one in their own right mind should take anything I say and suggest to heart without at least doing their own research first (seeking their own medical advice, etc.), I'd like to think I've learned much over the years and would like to share my experiences and knowledge that has helped me reclaim my health in the off chance there's at least one person out there who can relate to me and who's tired of feeling frustrated, belittled and powerless when it comes to becoming and staying healthy again.
The goal of this site is to inform others of how to do research and find things out. To open peoples' eyes as to new ways to do things, etc. Empowerment and being your own vigilant advocate would be a nice word to sum up my goal.
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In my blog entry https://itsokaytosecondguessdoctors.info/f/h3-histamine-receptors I discuss H3 histamine receptors and what can get affected if these receptors are activated. I also discuss H3 histamine antagonists, one of which is Conessine. In my blog entry https://itsokaytosecondguessdoctors.info/f/i-found-funtamia-elastica-aka-yamoa-powder-online I discuss natural products from which Conessine is derived, one of which is the bark of a rubber tree in Africa called Funtumia elastica.
Yamoa powder is made from Funtumia elastica. The Yamoa Powder website https://yamoapowder.com/?ref=0AvCFzDaUtfrWP sells two forms of this product, powder and capsule. Due to my having Alpha-Gal Syndrome I use the powder form as it is free of magnesium stearate, and I miss it into my daily tea or coffee.
This website also sells other products such as Toxin Buster https://yamoapowder.com/?ref=0AvCFzDaUtfrWP (natural Charcoal for digestion and detoxing) as well as Arthromend https://yamoapowder.com/products/arthromend-food-supplement-to-support-healthy-joints for joint support.
Use the coupon code YAMOAWORKS at checkout to receive a 15% discount!
This is the type of product the majority of doctors will not tell you about either because they don't know about it/haven't done any research on it or because it's not produced by one of the large pharmaceutical companies.
*This product is not sold nor intended to cure, treat or diagnose any disease, illness, etc and is not FDA approved, but it is written about extensively in pubmed.gov
I was starting the quest to find out what was wrong with my liver at the same time my business was forced to be closed for 52 days. To help me remain positive and productive I started a website featuring my favourite travel and nature photos. Please feel free to check out my photos and maybe be inspired to order one or two 📷
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