Take a look around! We have a ton to share with you! (and please share with us!). Everything here is hopefully something that will help your little girl fight a stronger fight against Rett Syndrome. Check out our product reviews, tips from other families, and even our own little Rett-"bay" where you can find/sell/donate used items.
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Rett Girl! is only a referral site. Proceed with caution before purchasing an item, trying a new therapy or any of the tips recommended by our users on this site. Girl Power 2 Cure, Inc. is not liable for unsatisfactory or harmful outcomes. Especially in referrals involving diet, supplements or therapy, please check with your doctor before proceeding.
Adaptive bibs, hooded capes, and sleep wear by Spatzgear
Spatzgear is the brainchild of Syndi Knowlton, a stay-at-home “Rett mom” living in Utah. Faced with meeting the needs of her three children, two of whom are disabled, she began developing adaptive children’s clothing and accessories to meet those needs. She then realized that other special needs kids could benefit as well. Not just children, but adults also.
Anyone who has ever shopped for special needs products has probably noticed that items labeled as such seem to double in price. Understanding that money is often tight in families with special needs children, Spatzgear is dedicated to offering its products inexpensively; adaptive gear without the adaptive price!
*She will also custom-make just about any piece of adaptive clothing you desire. If you do not see an item that meets your needs, please let her know!