HDSA flowerpetal.com

Flowerpetal.com is pleased to offer a wide variety of fresh flower arrangements and gift baskets, all professionally arranged and delivered by a local florist. Flowers are the perfect way to express your sentiments for any occasion, whether that be romance, congratulations, thank you, sympathy, or just because.

FlowerPetal agrees to pay HDSA 12% of gross sales, net of any local, state, federal taxes & other applicable fees for any flower and gift orders generated by the HDSA and fulfilled by FlowerPetal.

You and your friends can visit any time of the year and send flowers and gifts for birthdays, graduations, anniversaries, and holidays; with every purchase you make, you will be helping us improve the lives of those affected by Huntington’s disease and their families.

Shop hdsa.flowerpetal.com now

FTD.com / HDSA

Purchase flowers online or call 1-800 SEND FTD and use code #3015 and 15% of your total purchase will benefit HDSA.

SHOP FTD.COM/HDSA NOW

iGive.com

Like to help HDSA in a big way? Buy something for yourself. Better yet, buy a lot of somethings for yourself! But first join www.igive.com/hdsa

Because whenever you purchase everyday items at the Mall at iGive, up to 30% (actual amount of donation varies on a day to day basis and from store to store, for an up to date listing on actual donation by store please click here) of every purchase is donated to HDSA, at no cost to you!

Wait, there’s more. At iGive.com you get free membership… access to the over 600 brand-name merchants like Barnes & Noble, Eddie Bauer, Lands’ End and PETsMART… super savings and deals every day … and of course, free donations to HDSA!

Join www.igive.com/hdsa  and then shop till you drop. We’ll appreciate it!

AmazonSmile

Shop at AmazonSmile and Amazon will make a donation to the Huntington’s Disease Society of America (HDSA). Up up 0.5% of your purchase will benefit HDSA.

GET STARTED TODAY!

Kathy Gibson Prints

Kathy Gibson understands Huntington’s disease and the challenges it poses for both the affected individual and their caregiver. She has used her experience as a caregiver to her sister to create a series of signed, limited archival edition gicleé prints that capture the essence of a person with HD. Her wish, in creating these works, is to validate and remind all caregivers that your journey has meaning as well as to stimulate conversation and understanding among those affected by HD and the caregiving community.

Each gicleé image is 11” x 14” (though a few are larger at 14” x 14”). Each costs $125 including tax, shipping and handling. Shown at left are a representative sample of her works. You can view all of these limited edition prints in the Gallery by going to kgibsonart.com. As part of our partnership with Kathy, 15% of your purchase will be donated back to HDSA. To purchase one of these extraordinary prints, contact Kathy at kgibsonart@mediacombb.net.

Kathy Gibson is a distinguished multiple media artist living on Maryland’s Eastern Shore. You may have met Kathy when she exhibited a select number of her original works at the 2016 HDSA Annual Convention in Baltimore this past June.

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EMAIL KATHY GIBSON

I’m Still Me Activity Cards

I’m Still Me Activity Cards

Designed by HD community member Brian Schrag, these light hearted activity cards help persons with HD to engage with those not familiar with HD.  As symptoms progress, many times individuals affected by HD find it difficult and at times embarrassing to talk about what is happening to them. I’m still me cards provide a way to connect with the community at large.

A set of 50 cards costs $12.00. You can read more about the cards and purchase a set by going to www.etsy.com/shop/SchragCreations. You’ll also find the HD Blues t-shirts he designed.

FADE INTO THE BRIGHT

ABOUT THE BOOK

Five Feet Apart meets Tell Me Three Things in this YA contemporary novel about two sisters, one summer, and a diagnosis that changes everything.

Abby needs to escape a life that she no longer recognizes as her own. Her old life–the one where she was a high school volleyball star with a textbook-perfect future–has been ripped away. Abby and her sister, Brooke, have received a letter from their estranged dad informing them he has Huntington’s disease, a fatal, degenerative disorder that you wouldn’t wish on your worst enemy. And when the sisters agree to genetic testing, one of them tests positive.

Fleeing to Catalina Island for the summer, Abby is relieved to be in a place where no one knows her tragic history. But when she meets aspiring documentary filmmaker Ben–tall, outdoorsy, easygoing, with eyes that don’t miss a thing–she’s thrown off her game. Ben’s the kind of guy who loves to figure out people’s stories. What if he learns hers?

ABOUT THE AUTHORS

Jessica Koosed Etting and Alyssa Embree Schwartz met the first day of freshman year of college and have essentially shared a brain ever since. They’ve co-authored the YA thriller The Lost Causes and the contemporary YA series Georgetown Academy. The duo also work as screenwriters in both film and television. They were prompted to write this book by a Huntington’s disease diagnosis within Jessica’s extended family.

Please click here to purchase the book