
- With Mayo Clinic health education outreach coordinator
Angela Lunde
read biographyclose windowBiography of
Angela Lunde
Angela Lunde is a dementia education specialist in the education core of Mayo Clinic's Alzheimer's Disease Research Center at the Abigail Van Buren Alzheimer's Disease Research Clinic in Rochester, Minn.
Angela Lunde
The transfer of information about dementias, as well as understanding the need for participation in clinical trials, is an essential component of the education core.
Angela is a member of the Alzheimer's Association board of directors and co-chair of the annual Minnesota Dementia Conference. She is a member of the Dementia Behavior Assessment and Response Team (D-BART), a multidisciplinary outreach service assisting professional and family caregivers in understanding and managing difficult behaviors often present in dementia. She facilitates several support groups, including Memory Club, an early-stage education and support series, and more recently, helped to develop and now deliver Healthy Action to Benefit Independence and Thinking (HABIT), a 10-day cognitive rehab and wellness program for people with mild cognitive impairment.
Angela takes a personal interest in understanding the complex changes that take place within relationships and among families when dementia is present. She is particularly interested in providing innovative and accessible ways for people with dementia and their families to receive information and participate in valuable programs that promote well-being.
"Amid a devastating disease, there are tools, therapies, programs and ways to cope, and it is vital that families are connected to these resources," she says.
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Alzheimer's blog
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Feb. 6, 2008
Healing from the pain: Share your story
By Angela Lunde
So many of you have written about the grief and loss you feel. Whether you love someone who lives with the disease of Alzheimer's, or grieve a death, the pain is similar. These feelings have a way of numbing and isolating us and we yearn for some relief from this emotional confinement.
Kent Nerburn ("Letters to My Son"), one of my favorite Minnesota authors, writes, "The question you must ask yourself is not if you will heal, but how you will heal. Grief and pain have their own duration, but when they begin to pass, you must take care to guide the shape of the new being you are becoming. They reduce our lives to chaos, but in return they offer us a chance to rebuild our sense of values and meaning."
Many of you may feel like you are living 'the chaos' right now and that healing is far from reach. Yet, others of you may be on a path toward healing with perspective I invite you to share with us.
84 comments posted
February 22, 2008 11:47 p.m.
My husband is 74 years old. I am 67. He has had dementia for about 4 years. He is on Arisept and Namenda and they seem to be holding off the dementia and possibly the alzheimers pretty well. I have my children near me and they are very loving and supportive and also very helpful. But there is a lonelyness for me to see a little bit of him slip away ever so often. Most of the time I am very able to handle this but sometimes, like tonight, it is so hard. He is trying so hard to hold on to his independence. He is also suffering from massive blood clots in his legs which has caused him to be hospitalized many times. My prayer is that I will stay well long enough to help him here in my home as Jean did. I have the faith that God will see me and especially him through this. Regina
- Regina
February 22, 2008 10:24 a.m.
My mother died of Alzheimer's one year ago today. The disease had her for 8 years. But not only did the disease have her, it also had my dad, my brother & his wife, my spouse & children and me. I've survived depression and have been on a spiritual awakening journey for the past year. God has held us in the palm of His hand but it has been difficult. Loosing myself as I lost mother is something I didn't understand going into the process. What I see now, that was veiled at the time, I just didn't have the energy to keep up with all the details. And when I could get it all done, I depleted my adrenaline reserve. It is a tough rode that is laced with many tender moments. Finding a closer relationship with God is the blessing in all of this. Getting help for yourself is not selfish because you impact many relationships. What you do for your sanity may just preserve the families as well.
- Sandra
February 17, 2008 5:52 p.m.
Thanks and God's blessings to everyone engaged in this blog. Caregivers sacrifice so much, but I think also gain much more than they bargain for, whether the caregiving duty is implied or imposed. At least this had been my experience. Like Di, my father was Mom's sole caregiver, but a brief illness took his life, and my brother and I had to step in. I left a full-time career to help Mom, and feel this is the best(and toughest--or is that the easiest?) decision I've ever had to make. Thus far, the experience has been very rewarding. I have received mixed opinions on giving up "my life" to help with Mom's, but fortunately my husband(whose opinion is the only one that counts) has been very supportive in this endeavor. I am unable to get out to a support group, but this blog had certainly been a great substitute.
- Jean
February 13, 2008 7:19 p.m.
This has to be the most difficult question to answer, as my husband (72) and I have always done everything together. Our lives were intertwined in our family business, our children, grandchildren and our devotion to God & Country with the American Legion & Auxiliary. I have been telling myself that I must start "my Life" but it is almost impossible to think of losing someone you shared 47 years with. He still knows me and our children..and when I come every day he has a big smile and is happy to see me. I take care of some of his personnal needs, for my sake... he seems to love my touch. He is in a great AZ facility where they care for him so well. A special Val dinner is planned for tomorrow for all of us. I don't know if I will be able to handle a new beginning for myself if he passes before me. I also journal quit often. This blog is great and I appreciate reading everyones comments. God bless you all, and give us the strength to go on.
- Mary
February 10, 2008 3:57 p.m.
My mom is 84 yrs. old and as Jean put it, Alzheimer's has had her for about 12 years, probably longer. My dad cared for her single-handedly, with no help, except for my semi-annual visits (we lived 2200 mi. away). Mom came to live with my husband and I two years ago when dad died unexpectedly. I retired from my 30 year career to stay home with her and it really seems to have been a good decision. She is rarely physically ill, and still enjoys getting her hair and nails done, going for rides in the car and "visiting" with friends who occasionally stop by. While we have no other family living nearby, my husband is very good about staying with mom a couple of hours most days so I can go to the gym, take the dog for a walk or go shop. We also have been fortunate to get several hours a week respite care from our local Aging Services. One of the Alzheimer Care facilities in our city provides overnight respite care which has been a godsend. I don't journal, but take lots of pics, la
- Di
February 9, 2008 12:19 a.m.
My husband is 83 years old and has had AD for 6 years now. I still care for him at home with the help and support of my family and friends. He goes to an adult daycare once or twice a week which gives me a couple of days for myself. They love him at the daycare as he is still the genetleman. He is easy to care for and is able to to care for some of his personal needs but is always happy to have my help. What ever I say or do is O.K.with him. It breaks my heart that he doesn't know me anymore. We will have our 60th anniversary in July and by then he won't even know it. Sometimes he will ask for Teresa and I'm standing right in front of him. He thinks of Teresa as the young girl he married. We do a lot of hugging and he is still so loving. Perhaps he thinks he has a new girlfriend. I also keep a jounal on my computer and I am reminded of how much he has lost as I read where he was last year. I think it is good to keep a journal so one can maintain a perspective as changes occur.
- Teresa
February 8, 2008 1:22 p.m.
Susan: My journaling takes but a minute, and is nothing fancy. I'm embarrassed to say that my "journal" is a ringbound notebook that is worn and ragged. Surely you can carve out a moment for yourself even once-a-week to jot down any highlights you may recall? Bring your journal and treat yourself at your favorite designer coffee shop(or like me, at Mom's kitchen table). Hopefully collecting your thoughts and emotions will help you maintain perspective when all seems so out-of-control.
- Jean
February 7, 2008 9:24 p.m.
Thanks, Jean, for this insight. I may not think I have time for journaling, but I can certainly pay more attention to remembering the "real" bits and pieces. Many "bad" days still have positive periods, and the "good" days, or hours, can be delightful.
- Susan
February 6, 2008 8:19 p.m.
Mom is 88 and has had Alzheimer's for 10 years. Or rather, it has had her. At any rate, I share caregiver responsibilty with my brother. Mom is in late-stage Alzheimer's. Thankfully, we are still able to meet Mom's ever-increasing needs in her own home. I have elected to deal with the loss of the person I once knew by getting to know better the person Mom is now. Fortunately, she is delightful, and funny, and still elicits bits and pieces of her personality---the "real" Mom. I have resigned myself to the loss of the abilities she once had and dwell on the abilities she still has, limited though they may be. I find that by journaling my daily interactions I can revisit each day's highlights; despite the ebb and flow of good-days and bad-days, I will always have a written chronicle of those events I hold most dear, which will likely provide comfort in the future.
- Jean
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84 comments posted