Let’s Get Started

Are you a patient or family caregiver with something to say? Make your voice heard by participating in paid surveys, interviews and online communities! Start talking to the right people. It's free! We accept rare and non-rare diagnoses! In celebration of our 10th Anniversary our studies now pay at a rate of $120 an hour! Sign up today!

About Our Referral Partner:

Dreamsickle Kids Foundation, Inc SCDAA Nevada Chapter is a Sickle Cell Disease (SCD) and Rare Disease nonprofit with focus on supporting patients and caregivers impacted by SCD and other Rare Diseases. They have made tremendous legislative progress in Nevada to #MakeSickleCellPopular addressing health disparities and promoting health equity for those impacted by SCD and are working tirelessly to do the same for all Rare Diseases.

“There isn’t a more gratifying experience that I can think of that helps my own health and the health of others.”

— Indira, patient

“I like voicing my opinion and getting paid for it is a needed bonus.”

— Michelle, patient

“It was empowering to help inform people so that my learnings from this dreaded disease could help contribute to a greater good.”

— Nancy, patient

“I loved doing the survey – it was interesting and informative.”

— Karen, patient

“It is satisfying to know I can do my part to help get feedback to companies about our rare disease.”

— Angela, patient

“I appreciate that you allow us to participate in these studies. The money helps to pay my co-pays and I am grateful.”

— Jane, patient

“I love the way this organization treats me.”

— Marian, patient

“I enjoyed being the “expert” and being able to share some of my son’s story and our experience.”

— Abbie, patient

Let’s Get Started

Rare Patient Voice

For Patients

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Rare Patient Voice

For Patients

For Related Groups

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