Note to medical writers and assignment editors: To arrange interviews with UA ALS researchers and ALS patients and/or family members, please contact Jean Spinelli at 520-626-7301.
The 13th annual Himelic Memorial Dinner and Golf Classic supports vital scientific research with the goal of improving our understanding of amyotrophic lateral sclerosis (ALS, also known as Lou Gehrig's disease after the baseball legend) and developing effective treatments that ultimately will lead to a cure. This progressive, fatal neurodegenerative disease can strike people from all walks of life and of any age, most commonly between ages 40 and 60, but sometimes younger and older as well.
Proceeds benefit ALS research at the Jim Himelic Neuromuscular Research Laboratory at the UA College of Medicine-Tucson department of neurology and at Southern Arizona's only multidisciplinary clinic dedicated to the care of patients with ALS, the MDA/ALS Center at The University of Arizona Medical Center-South Campus, 2800 E. Ajo Way, Tucson.
The price for golfing, dinner, the auction and dancing is $175 per person and $700 for a group of four. For dinner, the auction and dancing, the cost is $75 per person after May 16.
For more information or to make a contribution, contact Diana Himelic Dawley at 520-907-5235 or email@example.com.
Like the saying "mighty oaks from little acorns grow," great medical discoveries can grow from a little seed money – funds that allow researchers to conduct the preliminary research necessary for obtaining larger government and private grants.
Those grants then nurture the research as it ultimately "grows" into more effective treatments, and possibly cures, for many diseases.
That's what one family had in mind for amyotrophic lateral sclerosis, or ALS, research at the University of Arizona and elsewhere with the creation of the Jim Himelic Foundation, or JHF.
The family's goal is to raise $1 million in seed money to fund UA preliminary research on ALS, a progressive, fatal neurodegenerative disease.
When ALS, commonly known as Lou Gehrig's disease, took the life of Jim Himelic, a friend of the Tucson community and much-respected juvenile court judge, in 2000, his family, friends and colleagues established the foundation.
"The family's initial investment has led to our researchers being able to gain some large research grants," said Dr. David Labiner, who heads the UA neurology department.
ALS most commonly affects people between the ages 40 and 60, but also those who are younger and older. Although some survive longer, the average life expectancy following diagnosis typically is two to five years.
The foundation continues to raise funds for ALS research and, since beginning its support of UA research in 2001, has raised $832,000 through its annual Himelic Memorial Dinner and Golf Classic. The event is being held May 31 and June 1 at the Westin La Paloma Resort in Tucson.
Also, JHF supports physicians at the MDA/ALS Center at The University of Arizona Medical Center-South Campus clinic, opened in 2008. The center is one of only 42 facilities at major medical institutions in the country designated by the Muscular Dystrophy Association as MDA/ALS Centers, indicating the high level of expert medical care and clinical research taking place there.
During each clinic visit, patients meet with a physician, physical therapist, occupational therapist, respiratory therapist, speech and language pathologist, dietician and an MDA health-care services coordinator – all in one location.
Also, at the MDA/ALS Center, the foundation is working with neurologists Katalin Scherer and Holli Horak, both UA associate professors of neurology. There, Scherer and Horak apply ALS research in a clinical setting.
JHF hopes to fund local and national multicenter clinical trials, based on the ALS patient base of Southern Arizona, with the help of the ALS clinic established and directed by Scherer. Horak joined the clinic in 2010.
Earlier, in 2004, the UA College of Medicine-Tucson's neurology department's stem cell laboratory officially was named Jim Himelic Neuromuscular Research Laboratory in recognition of the JHF funding support.
Additionally, the foundation supports investigations at the laboratory, including research by Daniela C. Zarnescu, a UA associate professor of molecular and cellular biology and neurology.
JHF seed money has enabled Zarnescu to gain several national grants to continue her research, including two three-year grants from the Muscular Dystrophy Association totaling nearly $800,000 and a two-year grant for more than $420,000 from the National Institute of Neurological Disorders and Stroke.
Zarnescu is modeling ALS in the fruit fly, Drosophila, a powerful genetic model that harbors several genes similar to those linked to human neurological and neurodegenerative disorders.
Using this model, Zarnescu's team recently completed a drug screen for compounds that alleviate ALS-like symptoms, including motor dysfunction and reduced survival. Efforts are under way to select promising compounds with therapeutic potential.
"The seed money provided by the Jim Himelic Foundation has allowed my lab to develop an ALS research program focused on understanding the mechanisms of this devastating disease as well as developing therapeutics," Zarnescu said.
She also noted that the funds support undergraduate and graduate student researchers at the UA.
"This type of support is particularly important in these difficult funding times and has enabled us to develop new disease models and drug screening strategies that are now beginning to pay off both in discoveries as well as in increased private and federal funding for the lab."