Cure HD
Tax deductible
My name is Leilani Dunmoyer and I live in Sacramento, CA. I'm a wife, mother, marathon runner, and have a passion to find a cure for HD. This is my 3rd fundraiser marathon for Huntington's Disease (HD). It has been four years since I raised money by running the New York City Marathon, so it's time again! This time I'm planning on running our local Sacramento marathon (CIM) on December 2nd 2018 to raise funds for our local HDSA chapter through UCDavis' Center of Excellence . These doctors and caregivers have taken care of my mother and now my brother for many years, and are like family to us.
My Daughter Heather and me with our age group award
HD is a genetic disease that is described as ALS, Parkinson's and Alzheimer's rolled into one. It affects the ability to walk, talk, reason and swallow, and currently there is no cure. If a person has the HD gene, they will eventually develop the disease. Average age onset is between 35 - 50 years old. If a person has HD their offspring has a 50% chance of having the disease. My mother was diagnosed in 2009, and my brother was diagnosed a couple of years ago. I tested positive for the gene also, which means not only will I one day develop the disease; each of my three children also have a 50% chance of having it too.
Learn more about HD
Selfie with mom! She's 85 years old!
I am so grateful for my supportive friends and family, a great God that loves me, and also my running which keeps me healthy and will help me fend off symptoms for as long as possible. Running to raise money and awareness for HD benefits me physically, but also provides a platform to tell people what HD is, and to raise funds for research and awareness.The really exciting news is that for the first time we are on the brink of a potential treatment to stop the progress of HD. There is a phase 3 clinical trial starting soon that has tremendous promise. Dan and I had the great pleasure of attending the national conference this year in Los Angeles.
Also exciting for me is the fact that my daughter Heather (age 24) will be running this as her first marathon! My sister Erika in Seattle also has joined the team!
JOIN US:
I would like to invite any of you out there that would like to sign up and join my team to do it.
* The race is sold out, but through my team you can still join at a discounted rate if you're willing to raise some money for HD.*
There is also a relay division (either 4 person or 2 person) if you don't want to run the whole distance.
My husband Dan and I attending the HD National Conference this year, June 2018
Lastly, please consider donating to my team and the HDSA northern California chapter. Your gift is tax deductible, and any donation amount will be greatly appreciated and put to good use!
Here's a link to join the team: https://www.gofundme.com/cure-hd?teamInvite=znKoFv30SCgXNYXgDbpvs1LkZ3YMa3XYZvPFTLkvRdios1M8fIgeOQ7DonzATydf
My Daughter Heather and me with our age group awardHD is a genetic disease that is described as ALS, Parkinson's and Alzheimer's rolled into one. It affects the ability to walk, talk, reason and swallow, and currently there is no cure. If a person has the HD gene, they will eventually develop the disease. Average age onset is between 35 - 50 years old. If a person has HD their offspring has a 50% chance of having the disease. My mother was diagnosed in 2009, and my brother was diagnosed a couple of years ago. I tested positive for the gene also, which means not only will I one day develop the disease; each of my three children also have a 50% chance of having it too.
Learn more about HD
Selfie with mom! She's 85 years old!I am so grateful for my supportive friends and family, a great God that loves me, and also my running which keeps me healthy and will help me fend off symptoms for as long as possible. Running to raise money and awareness for HD benefits me physically, but also provides a platform to tell people what HD is, and to raise funds for research and awareness.The really exciting news is that for the first time we are on the brink of a potential treatment to stop the progress of HD. There is a phase 3 clinical trial starting soon that has tremendous promise. Dan and I had the great pleasure of attending the national conference this year in Los Angeles.
Also exciting for me is the fact that my daughter Heather (age 24) will be running this as her first marathon! My sister Erika in Seattle also has joined the team!
JOIN US:
I would like to invite any of you out there that would like to sign up and join my team to do it.
* The race is sold out, but through my team you can still join at a discounted rate if you're willing to raise some money for HD.*
There is also a relay division (either 4 person or 2 person) if you don't want to run the whole distance.
My husband Dan and I attending the HD National Conference this year, June 2018Lastly, please consider donating to my team and the HDSA northern California chapter. Your gift is tax deductible, and any donation amount will be greatly appreciated and put to good use!
Here's a link to join the team: https://www.gofundme.com/cure-hd?teamInvite=znKoFv30SCgXNYXgDbpvs1LkZ3YMa3XYZvPFTLkvRdios1M8fIgeOQ7DonzATydf
Co-organizers (3)
Leilani Dunmoyer
Organizer
Arden Town, CA
Huntingtons Disease Society of America Inc (Northern California Chapter)
Beneficiary
Heather Dunmoyer
Co-organizer
Erika Daligcon
Co-organizer