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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.
As part of our fund-raising initiative, when you purchase fresh flowers, gourmet gift sets and spa baskets online from our flower and gift site 12% of the proceeds are sent directly to the Huntington’s Disease Society of America.
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.
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.
Vita care Medical Products
For over 25 years, Vitacare Medical Products has been manufacturing high quality Comfort and Care products that are used in Hospitals, Long Term Care Facilities, Nursing Homes and Home Care Environments.
Our Huntington’s In-Bed Patient Protection System is a high quality product that provides a safe and comfortable patient environment.
At Vitacare Medical Products we take great pride in our quality, workmanship, service and reliability.
For more information contact:
905 660 2433
Mention HDSA when you call to place your order and a percentage of your purchase will benefit HDSA. Valid on phone orders only.
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!
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.
Given Away: A Sicilian Upbringing
Given Away: A Sicilian Upbringing
by Anna Randazzo
A story of a young girl’s perseverance through the the travails of World War II and beyond. An inspiring tale of the human will to triumph over adversity. 10% of the proceeds from sales of Given Away: A Sicilian Upbringing will benefit HDSA’s mission.
In print: http://www.amazon.com/Given-Away-A-Sicilian-Upbringing/dp/0989481921
An AffaiЯ Worth Remembering With Huntington’s Disease
Price: $25.00 USD
Huntington’s Disease is a progressive, life stripping hereditary disease for which there is no cure. LOVE is the most powerful medicine available in living with and caring for a person at-risk and in the throes of it. This is a Love Story that illustrates how a marriage and a family can live, survive and thrive with an illness. Humor, frustration and sadness are just a few emotions experienced by the reader. True Love prevails as this disease bruises and batters a family’s spirit. Many gifts are discovered during times of illness. Incurable love and intimacy are two such gifts.
This book is the Author’s journey as wife, mother, breadwinner, caregiver and widow/spouse survivor of Huntington’s Disease. It is about creating “Awareness” and giving the families affected by Huntington’s Disease a “Voice” to a situation that few understand including friends, family, co-workers, and the community. Huntington’s Disease is REAL and knowledge of the disease and it’s ripple effect on a family is REAL.
This book speaks to at least four communities, those affected by Huntington’s Disease or any chronic, progressive or terminal illness; the spiritual community, those who find strength through faith in the most trying moments; the therapeutic community, those who treat individuals, couples and families affected by illness; and the medical community, those doctors and other medical professionals, whether in primary care or specialists, who treat the patient, their caregivers or other family members of the illness, which can complicate the healing process.
Book Talks & Signings:
Debbiepausig.email@example.com North Haven, CT, USA 203.985.8246
Purchase a signed copy from me personally at www.debbiepausigmft.com in the “Affair Worth Remembering” tab and order via PayPal, then go to the “Contact Me” tab and enter the code DALLAS15 in the notes section and any special inscription you would like. $1.00 from each book sale will be donated to HDSA. Thanks!
Or-Purchase via Print on Demand through the publisher at: www.Lulu.com/content/15318021
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 firstname.lastname@example.org.
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.
Shattered Dreams–But Hope
By Elton Higgs
Shattered Dreams–But Hope is a distillation of the experiences of Laquita and Elton Higgs in caring for their two JHD adopted daughters. Laquita and Elton have not only shared their own caregiving experiences at a deeply personal level, but they have also offered observations and recommendations to other HD caregivers about coping with the special challenges and stresses of HD. They address the special characteristics and needs of a JHD patient, measures to preserve the mental and physical health of the caregiver, and ways of dealing with the governmental and medical agencies who must be sought to meet the needs of an HD patient and his/her family. But this is also a book for all long-term caregivers, whatever the disablement of the one being cared for. The concluding chapter portrays what two people of faith have learned about suffering, endurance, and love when grappling with the challenge of caring for a loved one day after day, year after year.
100% of the proceeds will go to HDSA.
The Electronic Caregiver Premier Home Monitor and Emergency Response System
The Electronic Caregiver Premier Home Monitor and Emergency Response System
The Electronic Caregiver Premier Home Monitor and Emergency Response System is the most advanced product of its kind. With just a push of the button on the lightweight and waterproof wrist band the ECG Premier gives the wearer immediate two way contact with a trained and certified Emergency Medical Technician. Rapid Response is our 24 hour, 7 day, monitoring Company. The EMT at Rapid Response will contact Caregivers in the order of preference, with 911 also available. The ECG Premier is completely mobile. Whether a trip to the grocer, outside appointment, or simply walking to the mailbox, the Caregiver can be contacted in moments (cell service is required and included), providing the valuable peace of mind so important in today’s stress-filled world.HDSA has partnered with Electronic Caregiver to offer the Premier System at a monthly discount. The usual activation fee is completely eliminated. It is important to know that when you choose the ECG Premier, HDSA will also receive a $50 donation!
There are three levels of service available with Premier, Series #2 is the most cost effective. Want more information? Visit: www.electroniccaregiver.com.
Ordering is easy! You can go directly to the online order form-click on:
You can also order directly from the website. You provide the necessary contact and billing information and the unit is sent to you completely programmed and ready to go. Plug it in and make the initial contact with Rapid Response to activate. You are protected immediately. A Customer Service and Support phone number is available for assistance if required. There are no upfront costs.
IMPORTANT: At the top of the order form is a field labeled “Promo Code”. To receive your monthly discount and guarantee the $50 donation, you must enter the letters: HDSA in all caps. Next please enter Dealer ID. LSM52587.
Geoff Lee is the ECG Representative and support resource. Geoff is available to answer your questions and assist with ordering details. Contact him directly at: (610) 909-4771
Watching Their Dance
100% of the proceeds from “Watching Their Dance” is being donated to HDSA
To purchase “Watching Their Dance” go to Therese’s author website: www.theresecrutchermarin.com It’s also available on Amazon, B&N and in Kindle, Nook, Kobo formate.
Therese Crutcher-Marin, B.S., M.S.
Member on the HDSA Northern California Chapter Board
Author of Watching Their Dance: Three Sisters, A Genetic Disease and Marrying Into a Family Living At Risk for Huntington’s
Synopsis: Watching Their Dance: Three Sisters, a Genetic Disease and Marrying into a Family At Risk for Huntington’s
Would you marry the man you adored if you knew he had a chance of inheriting one of the cruelest diseases on earth?
Therese Crutcher is not a risk taker. Through meticulous planning, she eliminates as much uncertainty from her life as she can. Yet during her senior year of college, blithely planning to marry her beloved John Marin, she is suddenly thrown into turmoil when John’s sisters announce they finally know what killed their mother. Phyllis had Huntington’s disease, an inherited neurological disease with horrible odds: John and his three older sisters have a fifty-percent chance of inheriting this terrible wasting disease, which slowly kills the brain cells that affect movement and cognition. There is still no treatment or cure.
Therese takes the biggest gamble of her life and marries John despite his precarious future. Thus unfolds a life filled with unpredictability, tough choices, and pain, and yet full of love, good times, and great joy. Therese comes to realize that the uncertainty she willingly took on has opened her heart to love more deeply; that acknowledging her world could change overnight has made her life richer. She has learned to overlook shortcomings and to compromise, to let go of anger when she can’t control a situation, to find joy in the simple things. Life is just too precious to waste a moment on small stuff. And though John’s sisters leave this world far too soon, the Marin siblings, she realizes, have taught her about embracing life, forgiveness, and unconditional love.
Visit my Author Website: theresecrutchermarin.com
Visit my Author Facebook Page: https://www.facebook.com/authortheresecrutchermarin/
Amazon Author Page: https://www.amazon.com/author/theresecrutchermarin