After 10 years of chronic pain and illness, I was diagnosed with Chronic Lyme Disease and Coinfections in 2019. To be honest, it feels like a lifetime ago. Back then, I had just started this page in an effort to connect with others dealing with similar symptoms and embarked on a journey that I had no idea would entirely change my life. For years, I shared my experience - all my ups and downs, which turned into more of what you see now which is sharing health tips and my education. When I say that I have been where you are I really mean it. I have seen multiple doctors, I have searched for answers. I have taken medications, been gaslit, and have cried in frustration and pain. I tried a million things and spent way too much money (they always say lyme isn’t a poor man’s disease, which is ironic considering anyone can get it). The journey isn’t linear which makes it difficult to share but I promise I will write a book one day. For now - I aim to show the light at the end of the tunnel, even if it is just a glimmer. I aim to empower others to advocate for themselves and to provide hope, because so many times in my journey I needed that hope.
Everyone is different and everyone’s “cocktail of illness” is different. Because of that, what works for some may not work for others. All I can do is share the support that actually helped me along the way. Here are some of the big things below:
I hope you found this helpful, I have a lot more to come! Please comment if you are enjoying the blog and share with anyone who may benefit from it!
5 Comments
Teri
5/26/2023 08:43:41 am
I am beyond proud of how far you have come and all the effort you have put into getting healthy.. Your dark days were MY dark days also. You open yourself up in such a beautiful way to help others get to where you are today. Your empathy to help others is a testimonial to how real you truly are in a world of “all about me”.
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Dana Lewis
5/26/2023 06:24:23 pm
You have helped me in so many new ways. I love the calming methods. I pass your methods on to my childbirth class students. Being able to relax takes practice so I encourage it. Personally I live with joint pain and fatigue. i can add a million more things that resemble auto immune issues. However nothing ever comes up positive for a diagnosis. It’s frustrating. My regular doctor said - you know our infectious disease doctor says there is no Lyme disease here in Missouri because we don’t have those type of ticks. She sort of rolled her eyes. My rheumatologist retired and his replacement was a joke. She kept telling me it was my age. When I told her it has been going on since my thirties she brushed me off and told me still it was my age. So I gave up. Migraines and pain are my life. The silicone cups help with lymphatic flow for me. Thanks for the instruction. Maybe someday I will know but for now I don’t. Bless you and your education which you share.
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Michael Mauldin
5/28/2023 10:01:58 am
You have changed my life as I continue on my journey. This really helps I hope you continue these emails, You would be surprised at the amount of people this information helps.
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5/30/2023 11:43:50 pm
I was just wondering if you had a bullseye 🎯 rash after your tick encounter.
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6/1/2023 11:09:58 am
I did not, I never saw one if I did have one. But I was not aware of what I was looking for so it could have happened at any point throughout my life and was reactivated as an adult. - Amanda
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AuthorAmanda Nova, MS, HHP Archives
December 2023
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