Almst six years ago this devil of a disease came into me n my families life...And today it has consumed mine...Everyday is a struggle sometimes...from planning, remembering, normal daily activities are much harder for me...I walk sideways alot...I'm constantly dropping or throwing stuff...I choke on my own spit n anything else most times....no energy...no appetite...can't sleep...my mind raises 24/7...and my eyes ping pong BK n forth all the time...to the point it causes headaches n now with that came seizures....But the worst thing ever is knowing my kids N there future kids have 50/50 chance of being affected...And secondly I'm fighting this fight alone...have really no support...family n or friends...it's like I have the plaque...So please let's spread the word bout it...so we can give the next generation some hope...and peace of mind...


Thank you for visiting my personal fundraising page! With your help, we can help HDSA achieve their mission to improve the lives of everyone with Huntington’s disease and their loved ones.

The Huntington’s Disease Society of America is the premier not-for-profit organization dedicated to improving the lives of everyone affected by Huntington’s disease. From community services and education to advocacy and research, HDSA is the world’s leader in providing help for today, hope for tomorrow for people with Huntington’s disease and their family. 

Huntington’s disease is a fatal genetic disorder that causes the progressive breakdown of nerve cells in the brain. It deteriorates a person’s physical and mental abilities during their prime working years and has no cure.

HD is known as the quintessential family disease because every child of a parent with HD has a 50/50 chance of carrying the faulty gene. Today, there are 30,000 symptomatic Americans and more than 200,000 at-risk of inheriting the disease.

The Huntington’s Disease Society of America is the premier nonprofit organization dedicated to improving the lives of everyone affected by HD.  From community services and education to advocacy and research, HDSA is the world’s leader in providing help for today and hope for tomorrow for people with HD and their families.

Across the United States, HDSA currently supports:
•54 volunteer led Chapters & Affiliates
•41 Centers of Excellence
•65 Social Workers
•160 Support Groups

To learn more about Huntington’s disease and the work of the Huntington’s Disease Society of America, visit www.hdsa.org or call 1-800-345-HDSA.

Please register to walk with me and help make a difference! If you cannot walk with me, please consider making a donation to my personal fundraising page by clicking the ‘Donate’ button at the top of this page. 

Thank you for your support!

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