With the lack of awareness and education about fibromyalgia, many of us go through years of chronic health issues without finding answers. You might even find that the medications, supplements, and treatments that are supposed to help you to get better are making you worse.

Today’s guest, Gisèle McDiarmid, went through all of that, and today she’s sharing what she uncovered that made all the difference. While her health deteriorated over 20 years, Gisèle received multiple diagnoses and treatment options, but nothing worked. So what do you do when everything makes you feel worse?

In this conversation, Gisèle and Tami talk about Gisèle’s life as a nurse, mother, and caregiver, managing her Hashimoto’s diagnosis, her deteriorating health and experience with injuries, chronic infections and allergic reactions, severe reactions to flu shots and what she learned about her ability to tolerate vaccines, why fibromyalgia awareness and education are so important, Gisèle’s health crash which turned out to be a massive fibro flare, the long journey to receiving her fibromyalgia diagnosis, her struggles with conventional medications and natural treatments, unlearning her disconnected body mindset, the power of tuning in and recognizing that you and your body are on the same side, learning about multiple chemical and environmental sensitivity, common triggers of multiple chemical sensitivity (MCS), why we need to become aware of our individual body burdens and all the things we’re exposed to, the increase in MCS diagnosis worldwide, why green initiatives matter, resources you can use if you think you may have MCS, Gisèle’s message for you, and more.

If it feels like nothing is working for you, Gisèle and Tami hope that her story gives you some new ideas of things to try. Always remember that it doesn’t matter if other people don’t believe you as long as you know what you’re going through is real. Even when we have a chronic illness, our life isn’t over. Gisèle went from a crisis to living a full life again, and you can do it too.

Everyone with fibromyalgia understands how challenging it can be to explain the invisible pain and fatigue that comes with it. Despite affecting millions of people, there’s still a lack of understanding and awareness about fibromyalgia. That’s where the documentary “Invisible” comes in.

Through personal stories and expert interviews, “Invisible” explores the impact of fibromyalgia on people’s lives and the challenges caused by the lack of understanding and research. For today’s episode, filmmaker Nick Demos joins Tami to discuss his feature documentary on fibromyalgia, Invisible. Nick and Tami have been waiting to do this interview ever since they began working on the film eight years ago. Not wanting to give away the ending before people could watch, a lot had to be kept secret during the production process. Now, they finally get to talk about it publicly.

In this conversation, Nick and Tami talk about how Nick became involved with the making of Invisible, its evolution into a documentary about the fibromyalgia community, challenges with finding men when casting the film, how the perception of fibro as a woman’s disease has contributed to the lack of research and understanding, the difficulty balancing creating a piece of art with making a film that would educate and inspire action, Nick’s on-camera life-changing diagnosis, the unfairness of being discriminated against for something outside your control, why this film is vital to the fibro community, Tami’s experience being a part of the film, why it was especially tricky to visually explore stories about an invisible illness, why community is essential, why Tami and Nick consider some aspects of fibromyalgia as a gift, what most surprised Nick while making the film, the truth behind the lack of research on fibromyalgia, upcoming premiere events, how Nick manages his fibromyalgia, Nick’s message for you, and more.

Invisible is the film that the fibro community has wanted and needed, and we know you’ll love it.