08/21/2026
Our SVFSA business cards, flyers, and tri-folds are finally here — and we were able to put them to use at a very special event.
Last night at the UC Davis Conference Center was a major milestone for me and for Sacramento Valley Fever Survivors & Awareness (SVFSA).
For the first time, I sat in a room with Valley Fever survivors, physicians, researchers, public health professionals, pharmaceutical representatives, caregivers, nurses, advocates, and others working to better understand and address this disease.
I was there first as a Valley Fever survivor — and also as the Founder & President of Sacramento Valley Fever Survivors & Awareness.
I shared my Valley Fever journey and what this disease looks like from the patient's perspective — not as a statistic or textbook case, but through lived experience.
The response was unforgettable. People came up afterward, shook my hand, gave me thumbs up from across the room, and told me how much my story impacted them. Several individuals from public health and federal agencies personally thanked me for sharing my experience and helping bring the patient voice into the conversation. It reaffirmed exactly why SVFSA exists.
I want to sincerely thank Rob Purdie and the MyCARE Foundation for inviting us to the Valley Fever Patient Forum and making our team feel so welcome. I also want to recognize my physician, Dr. George Thompson, who attended and has played an important role in my care.
We were also able to record the forum, and we're excited to share highlights from this important conversation with our community. Once the footage is reviewed and edited, we'll be sharing approved portions on the SVFSA YouTube channel, Facebook, Instagram, and our other social media platforms.
Stay tuned — there's a lot of valuable Valley Fever information coming.
I was proud to have members of the SVFSA team there with me — our Secretary Zarinah Galovich, Treasurer Gretta Etheridge, and our friend and media support Eric Barnes.
SVFSA is growing, and nights like this show we're moving in the right direction.
Our goal is to work alongside survivors, caregivers, doctors, researchers, public health organizations, nonprofits, and advocates to educate our communities, support survivors, and make sure the patient voice is heard.
If your organization is interested in collaborating with SVFSA, supporting our work, sharing educational resources, or helping expand Valley Fever awareness, we'd love to connect.
🌐 svfsa.org
Survivors have a voice. We're making sure it's heard.
Raising awareness, supporting survivors and families, and promoting early detection of Valley Fever. Advocating for research, prevention, and partnerships to improve outcomes and work toward a cure—built from real experience.SVFSA is a judgment-free zone.