I’m a neuroscience and nutrition nerd who has spent the last ten years deep diving into research and topics related to Lyme disease, dysautonomia (POTS), chronic fatigue, mold illness, and brain health, including the vagus nerve. Why? Because they were directly impacting me and keeping me from participating in life. I was mostly couchbound/housebound for about 5 years.
All I could really do during that time was make it through the day, watch tv, and obsessively research. (I should note here that this level of fixation can be both a help and a hindrance to healing. Same with online support groups. There needs to be a balance here. It took me a while to find it.) Educating myself so I could work as a partner with my doctors was a key change that started to turn the tide.
Now I want to share what I’ve learned by working with people who are still in the thick of it, supporting and holding space for very valid and difficult experiences, and helping to connect people with resources and specialists that can help you move forward and feel more hope. I can share strategies to make day to day life more bearable, and even enjoyable.