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Sandra Thiesen, Board President

Lynda Crandall, RN, GNP

I am currently in the middle of my 31st year as a nurse and have spent every one of those years working with elders, their families and others who also work in various capacities with this population.  Many of the persons whom I’ve taken care of have had dementias of all types.   From the very start I realized a joy in this work, both in the giving and in the ways I received back from it.  My heart is full of memories that reinforce this has been my calling.  I’ve also experienced Alzheimer’s disease first hand in my own family.  

Seven years ago I was invited to attend a Board meeting for the local Mid-Willamette Valley Alzheimer’s Association’s chapter.  I was immediately taken with and impressed by the dedication of the volunteer Board members and the work they were doing and knew I wanted to be a part of it in whatever way I could contribute.   I strongly believe that we all have an obligation to give to the communities in which we live, and that our hearts along with the unique gifts we each possess will guide where and how we direct our energies and time.  This is unquestionably one of mine.  In November 2003 when the Alzheimer’s Association closed the local office I collaborated with a strong group of volunteers to help form the Alzheimer’s Network in order to continue our work here.  I’ve enjoyed participation as a Board officer as well as working on lots of committees including the Education Committee, the Early Stage Program, Walk committee, Communications Committee, Fund Development and other projects.  I’ve met other volunteers whom I value as friends and who are truly citizens of the highest caliber.  I’ve met people living with Alzheimer’s disease and other dementias (persons with the disease and their families) whom I value as friends and from whom I’ve learned many lessons.   I count my work with the Alzheimer’s Network to be one of the most precious gifts life has offered me.
 

Kathy Belcher, JD, Treasurer

My career choice as an Elder Law attorney first brought me into contact with individuals, families and caregivers affected by Alzheimers disease.  In my practice, I help those affected by the disease with their legal and financial needs, focusing on estate planning and long term care and Medicaid planning. Although this is certainly important, it is not enough.  It is heart-wrenching to watch the suffering that people with Alzheimer‘s disease, their families and caregivers can go through. The fears they experience, the physical and emotional exhaustion of daily caregiving, the isolation and the feeling of being alone.  

People with Alzheimers disease, their families and caregivers need ongoing support to meet their needs.  They need to know they are not alone. They need education and access to resources to help them cope with this devastating disease.  The Alzheimer‘s Network is the only organization working on a local level in Benton, Linn, Marion and Polk counties to meet those needs.  The Network is staffed by dedicated and knowledgeable volunteers who willingly share their time and expertise. The Alzheimers Network is a vital resource to the community and thats why I am proud to be involved with the Alzheimer‘s Network and why I volunteer my time. 

I have been involved with the Network since its formation.  I am a Board member, Treasurer, member of the fund development and public policy committees and speak at education conferences.  I wanted to reach out beyond the areas of my practice.  I wanted to be involved in developing education, support programs and other resources that would help people come to terms or deal successfully with Alzheimer‘s disease.  As a member of AlzNet, I have had the opportunity to work alongside some incredibly talented and hardworking individuals.  It has been really rewarding and encouraging to watch the organization grow as together we strive toward achieving our mission, which is to support the educational, social, emotional, and spiritual needs of individuals with Alzheimer‘s disease, their families and caregivers, as well as raising public awareness of the disease. It can be difficult for any one of us at times to find the time to volunteer.  Working and taking care of family may leave a person feeling like there is little or no time for anything else.  But, there is nothing like the feeling of volunteering for an organization like the Alzheimers Network and seeing the difference you can make in the lives of others.  I would strongly encourage any one thinking of volunteering to jump right in.  Get to know us and see what a difference you can make.

 

Shari Ridings, Vice-President

I am currently working for NW Senior and Disability Services as an Assistant Unit Supervisor at the South Salem Disability Service office. I have specialized in volunteer management through my work at Dallas Retirement Village and Marian Estates.  This is where I first met people with Alzheimer’s and their families, friends, and the staff caring for them.  

In March 1996, I accepted the role of Executive Director of The Alzheimer’s Association Chapter in Salem.  I find it very compelling to see the drastic changes in people’s live, both for the person with dementia and their loved ones, as this relentless disease progresses.  It continues to drive my passion to make a difference in the lives of all those affected.   During the seven years I worked for the Alzheimer’s Association, one of my closest uncles was diagnosed with Alzheimer’s disease.  This brought the personal experience with the journey of Alzheimer’s closer to home.  Many of my friends and church members also have loved ones coping with a family member who has Alzheimer’s.   

In November 2003, I joined the volunteers who founded the grassroots organization, “Alzheimer’s Network,” to continue my work with people with dementia, their families, and caregivers.
 

  Jeanne Dalton

I became involved with this organization as the Education Committee Chairperson in January 2004. I believe that caregiver education is very important.  There is a need to reach as many caregivers as possible.   The more caregivers understand the Alzheimer’s disease process, the easier time they will have caring for their loved ones. Also, education of direct care staff in nursing and other residential facilities will also help them take better care of the person with Alzheimer’s disease.  

We have such a wonderful and dedicated group of volunteers in this area, it is difficult not to catch their enthusiasm. I wanted to join a group that worked for a good cause and help in other ways to provide support to those people struggling to care for others with Alzheimer’s disease. 

In my professional career, I have always enjoyed working with the elderly and with people with Alzheimer’s disease. The elder population is such a diverse and gracious group! I believe that people with Alzheimer’s disease never lose their true spirit and it is wonderful to tap into it. That’s one of the reasons that I teach others so they can see and believe this, too. 

Now, as Alzheimer’s disease has occurred in our family as an early onset disorder, I will learn more than ever the importance of caregiving from a personal perspective.  But I know I will have the help & support of the volunteers of the Alzheimer’s Network.

Robert King

I am new to the Alzheimer’s Network of Oregon Board, but not new to the world of Alzheimer’s Disease. I have spent many years in the retirement community more recently as a Skilled Nursing Home Director working with Alzheimer’s victims ranging from the first hint of the disease to the very advanced conditions. My Mother was one of those individuals that reached the advanced stages and the frustrations we felt every day while caring for her were the same frustrations that thousands of families feel each day while taking care of their loved ones or their good friend.  

Currently, I am working as a Family Services Director with Howell-Edwards-Doerksen Funeral Home, helping families plan their final arrangements. Many of the families that I work with are taking care of a family member with Alzheimer’s disease. Sharing their stories and hearing their frustrations reiterates our need to find a cure for this debilitating disease. It is those stories that encouraged me to become a part of the Alzheimer’s Network of Oregon Association. It is those stories that we need to keep us focused on the possibility of a cure, knowing that this disease will not cure itself. 

I look forward to sharing stories with you and hearing your stories. This is how we get through each difficult day knowing that we are not alone in this journey.

May Dasch

David Rheinholdt

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