You Deserve More
(Womens Wellness Retreat)
We understand you. We know first-hand how much you have given to your child or loved one. We know the toll being a caregiver to a patient with a rare disease can place on your mind and body. We know because we’ve been there too.
Raregivers offers a wellness experience guided by professionals, clinicians and self-care experts specializing in working with rare families. You will gain experience, education and empowerment to reconnect you with the women you were before you became a Raregivers. Many of our mothers tell us they felt “invisible” before coming to the retreat and after they left empowered, excited and most of all connected to a community of women who truly listen without judgement.
EVENT DETAILS
Raregivers - Women’s Wellness Retreat
$799.00 (Guarantee Your Spot for a future retreat)
We strive to be inclusive. If cost is a barrier to your attendance, please apply for a sponsorship.
If you are interested in participating and/or receiving sponsorship for the next retreat, please fill out the form below. NOTE: Purchasing participation will hold your spot.
Date:
2025 Dates - Coming Soon
Location:
Orange, CA @ Barrett Family Ranch, CA - In Person Event
Information:
Join us for our in-person Women's Wellness Retreat, designed especially for mothers and caregivers of patients with rare diseases. We understand the toll caregiving can take on your mind and body because we've been there too.
Guided by professional wellness gurus, clinicians, and self-care experts, this retreat offers a unique opportunity to gain experience, education, and empowerment. Reconnect with the woman you were before you became a mother and find solace and strength in the women around you.
Rest and Recharge:
BBQs, Libations & Fireside Conversations
Healing with Horses Equine Experience
Strategies for Embracing Change
Tips & Tools for Sustainable Self Care
Luxurious Sensory Gifts. Gourmet Meals.
Don't miss this chance for rejuvenation and connection!
Interested about future retreats? Fill out the form below.
Lynn Hopkins
As a parent of a child with a rare disease, Lynn Hopkins describes why it is going to take more than just investment in research to cure rare diseases. By exploring what all rare diseases have in common, her conversation demonstrates how a cure starts with awareness and how each of us is part of the solution. Lynn Hopkins is the parent of a child with a rare, incurable genetic disease. She is a board member of the National MPS Society and an advocate for the rare disease community. Lynn is also a finance executive who creates the time to build awareness and promote meaningful conversations about curing rare diseases through her advocacy.
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