About The CIRS Group

One of the most common symptoms of CIRS is brain fog and difficulty assimilating new information. So when Jacie and Barbara were first diagnosed with CIRS, they both experienced major overwhelm at the depth of information, science and studies on CIRS they had to dig through.

Not only that, but all of the information currently out about CIRS seemed geared towards practitioners and scientists, not patients.

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What is CIRS?

Community

You don’t have to go through this alone. Join our private group to connect, chat, and show up for each other during twice-a-month calls and Q&As. Healing is better together.

Visit our Membership Page

Coaching

Learn from others who’ve been where you are. Get budgeting tips, protocol guidance, and ideas for what to ask your doctor. Plus, join our live coaching classes — all recorded for you to watch later.

Learn More about Coaching

Resources

Looking for answers? We’ve gathered top podcasts, articles, books, videos, and product tips — all in one spot. Stay current, stay supported.

See our Resources

About the Founders

Jacie Gregory

Jacie is a published author, certified nutrition coach, and carnivore recipe developer determined to share the life changing information of carnivore and CIRS to anyone who will listen. Check out her book, carnivore recipes and other content at LadyCarnivory.com

Barbara Williams

Barbara is a coach, facilitator, speaker, and a big fan of health and freedom. In addition to co-founding TheCIRSGroup.com with Jacie, Barbara is also a Facilitator for The Tom Woods School of Life and offers business coaching for people wanting to make a bigger impact in the world.

I’ve had CIRS for over 40 years and never knew what was making me ill until just a couple of years ago. I thought it was just something I was going to have to live with. I also felt very alone since my symptoms never seemed to fit with the other diagnoses I was given.

Gail I.

[The CIRS Group] has given me a sense of community where I can get feedback, learn more about CIRS, and develop connections that are invaluable to healing.

Colin T.

Access to new knowledge and ideas. It’s great to learn from others at various points along their journey. I appreciate everyone’s vulnerability and willingness to share things that normally have some sort of stigma attached. Being a member allows me to be more educated which improves my ability to spread CIRS awareness with people in other areas of my life.

Allison O.

I've had CIRS for over 40 years and never knew what was making me ill until just a couple of years ago. I thought it was just something I was going to have to live with. I also felt very alone since my symptoms never seemed to fit with the other diagnoses I was given.

Gail I.

[The CIRS Group] has given me a sense of community where I can get feedback, learn more about CIRS, and develop connections that are invaluable to healing.