
- 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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Oct. 9, 2007
Frontotemporal dementia comes to fore
By Angela Lunde
I am finding your stories compelling, full of insight, experience, pain and compassion, and I am pleased to hear how much you appreciate reading the stories of one another.
In a previous posting, I mentioned that there are many forms of dementia, and although Alzheimer's disease accounts for 60 percent to 70 percent of cases of dementia, other disorders that cause dementia include: vascular dementia, Parkinson's disease, dementia with Lewy bodies and frontotemporal dementia.
In the early stages of these diseases, there can be some clear distinctions between each of them. However, late in the disease all dementias appear more alike than different. I bring this up again, because some of you may have seen news stories recently of U.S. Sen. Pete Domenici of New Mexico announcing his retirement because he has been diagnosed with frontotemporal dementia (FTD).
Sad proof yet again, that dementia knows no bounds of status, ethnicity, or gender. There are so many ironies in this disease. In this case the irony is that Sen. Domenici worked so hard for many years for mental health parity, in other words, equal attention and treatment of mental and physical disorders. Now he appears afflicted with a form of dementia that will initially affect his personality, reasoning, and maybe his language but eventually all areas of mental functioning. As with all of you, our thoughts and sympathies go out to the Domenici family.
62 comments posted
May 7, 2008 7:41 p.m.
My husband was diagnosed with FTD 5 years ago, his behavior was so impulsive and his personality completely change and he started acting out. The physician put him on Risperdone. The medication has helped, buthe is certainly not the person he used to be.
- Susan
April 23, 2008 11:06 p.m.
I am wondering if FTD could cause a person to sexually abuse a child. Has anyone had an experience like this?
- Diane
March 14, 2008 6:15 a.m.
My husband, 66, is now in a nursing home, undiagnosed but seems to fit FTD/MND. He also drank CocaCola all day long. Interesting. And suffered chronic back pain all his life and severe leg pain that last few years, progressing through the hierarchy of pain meds. Fell into a coma one night and came out of that but never recovered enough to live at home again. The disease is now progressing rapidly; aphasia, unable to swallow, profound muscle weakness.
- Christina
March 5, 2008 6:43 a.m.
My husband was been diagnosed with FTD three years ago. He is now 58 years old. I have been caring for him full-time for the last 2 1/2 years and I feel lucky that I am able to. He was the funniest, most charming and caring man you'd ever meet. Now that his body holds one of the most horrific diseases we could have ever imagined, I have made arrangements for his brain to be donated for research at the VA/University of Wisconsin brain bank and they will preform an autopsy for us. We all are dealing with the terrible cognitive losses, the uncharacteristic behaviors and the grief of watching our loved one steadily decline. I feel the brain donation is the greatest gift, but it's a way to fight back, too.
- Jeanne from Wisconsin
February 18, 2008 10:23 a.m.
My father has just been dignanosed with ftd. They tell us that in six months if he has any of the front part of his brain it will be a miracle. Will he be able to survive with only the back part of his brain. We have gone through some stages of not knowing immeiated family and aggressive behavior. He has sever pain in his legs. He has short term headaches. The doctors tells us that they will only try to keep him comfortable. He was also diagnosis with spinal stonsis back years ago. We feel now that he may be in final stages.
- Lisa
November 28, 2007 4:11 p.m.
To Dolores: sorry I did not get back to you sooner, my husband is on Aricept 10M, Risperidone .5mg twice a day, citalopram 20mg and at night trazodone 100mg.
- Kathleen
November 14, 2007 6:14 p.m.
Referring to Kathleen's comment My husband has frontaltemporal lobe degeneration. What dementia type medications does your husband take to help him cope?
- Dolores
October 14, 2007 10:18 p.m.
This is off-topic, but I have request for ocnversation: My mother was dianosed with dimentia years ago, at age 52. She's now 60 and in the late stages of what we believe is Early On-Set Alzheimer's. The doctors always had difficultly diagnosing her for some reason. I recently read a news article about sodium benzoate (in soda and many processed foods), that it has been linked to the development of Parkinson's and some cancers. I wonder, have studies been done on Alzheimer's and sodium benzoate? Or, have any of you had family members who developed dimentia or Alzheimer's and also drank a lot of soda. My family has been trying to pinpoint something that could have spurred the early on-set of the disease. Of course, we're not doctors or researchers, but we always wondered if the chemicals in soda could have contributed. She drank tons of Diet Pepsi but was otherwise pretty healthy. Of course, there's always the genetic connection... but I thought I'd bring it up.
- Felicia
October 12, 2007 8:08 p.m.
My husband died recently after a 2 year bout with a Dementia Non-specific diagnosis. His symptoms were dystonia and akathesia like muscle spasms, impaired memory, difficulty swallowing, and some rigidity of his arms. His ability to reason seemed always relatively unimpaired, although he could not express himself well. He always knew those persons important to him. He died after aspirating food and developing lung congestion. He was only ill for 4 months prior to his death, although he had been diagnosed 2 years earlier. i'm still wondering if he was misdiagnosed, and suffered from an agitated depression, and developed dyskinesthias associated with anipsychotic drugs.
- Maryon MacRae
October 10, 2007 9:00 p.m.
Several of the news reports about Sen. Domenici's frontotemporal dementia (FTD)diagnosis said for a year his leg/back were hurting him, so doctors thought it was spinal stenosis, but then his spinal specialist sent him to a neurologist who diagnosed FTD. I am wondering what in the world back and leg pain could have to do with FTD. Does that mean it never was spinal stenosis? I understand the two conditions can co-occur. Has anyone heard of FTD manifesting with chronic leg/back pain symptoms? I ask because my father, 73 yrs old, who likely has FTD, has had chronic back/leg pain for probably more than 15 years. It has been a huge problem in his life. He's had multiple surgeries and been on a succession of narcotic pain meds over the years. The meds probably masked or were blamed for early signs of FTD.
- Bea
October 10, 2007 2:30 p.m.
To Anon. My husband has frontal temporal lobe dementia also, his behaviour and energy patterns are very different - he is agressive, can't reason, acts like a five year old and has taken a big attraction to children (he never bothered much with his own when he had them - so this is very different). He has difficulty putting the correct words in a sentence although he knows in his head what he wants to say. He is in the moderate stage and he was diagnosed at age 68 officially but I noticed signs of funny behaviour about two years before that. A good geratric specialist and proper medication will make it easier for you to live with your mom as she becomes more aggressive and demanding. My husband is reasonably healthy and still goes to lawn bowls and plays curling but his behaviour is bizarre at times.
- Kathleen
October 9, 2007 7:30 p.m.
My mother had what was first called "Early Altzheimers" but it progressed differently. We were told it was a frontal lobe dementia. At her death, age 62, her brain was examined and the disease was determined as Picks disease. How does this relate to FTD?
- anon
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