View unanswered posts | View active topics It is currently Tue Aug 04, 2020 4:50 am

This topic is locked, you cannot edit posts or make further replies.  [ 3 posts ] 
 Article about Barbara Hutchinson and LBD 
Author Message

Joined: Fri Aug 11, 2006 1:46 pm
Posts: 4811
Location: SF Bay Area (Northern CA)
Reply with quote
Post Article about Barbara Hutchinson and LBD
Some of you may have heard of Barbara Hutchinson and her late husband Bill who had LBD. A few years ago, they drove around the US in a motor home to raise awareness for LBD. Barbara is now living in North Carolina and is still raising awareness for LBD.
Robin ... m=facebook

Cycling turns woman's grief into awareness campaign
Carteret County News-Times
Published: Wednesday, October 20, 2010 3:06 PM EDT
Cheryl Burke

NEWPORT — After watching her husband slowly die from a debilitating disease, one 66-year-old woman is turning her grief into action.

Barbara Hutchinson of this community will ride 100 miles on her bike Saturday to raise awareness of Lewy body dementia (LBD) and money for Lewy Body Dementia Association Inc., based in Atlanta.

She will do her ride at Between the Waters Bike Tour in Onancock, Va.

This isn’t the first time Ms. Hutchinson has traveled to raise awareness of LBD, a progressive brain disease and the second leading cause of degenerative dementia in the elderly.

For the last year of her husband’s life, the couple toured the nation in a motor home speaking to groups about LBD. Her husband, Bill, died Aug. 29, 2007.

“Few people know about Lewy body dementia and it’s often misdiagnosed,” she said. “I want to raise awareness of the disease and see that people are properly diagnosed and receive the proper meds. If people aren’t aware of the disease, they don’t know what to do.

“LBD affects cognitive thinking first; Alzheimer’s affects memory,” she continued. “LBD people lose the ability to use tools and do things. Unlike Alzheimer’s, most people with LBD know their people. Bill knew who I was until the end.”

The three major symptoms of LBD are: fluctuations in cognition, Parkinson’s symptoms and hallucinations. Rapid Eye Movement sleep disorder may be a precursor to LBD years before it shows.

The disease accounts for up to 20 percent of all dementia cases, which in the United States translates to about 800,000 patients.

More than 50 percent of Parkinson’s disease patients develop Parkinson’s disease dementia, which is also a type of Lewy body dementia.

In primary and specialty settings, physicians many times don’t recognize the distinguishing symptoms of LBD. Many times the symptoms are misdiagnosed as Alzheimer’s disease or Parkinson’s disease.

Ms. Hutchinson said the first time she realized something was wrong with her husband was in 2003, when he was 67.

“He walked like an old man and was really stiff,” she said. “He told me he had lost his sense of direction and wasn’t thinking right.”

Being a nurse, Ms. Hutchinson first had him tested for a stroke.

“He had some deterioration, and they diagnosed him with Parkinson’s (which affects motor skills), but it didn’t address his mental problems,” she said. “Then he started having hallucinations.”

They finally found a doctor who diagnosed the disease correctly in August 2005.

“They said he probably had Parkinson’s with Lewy body dementia,” she said.

Unfortunately there is no medication for LBD.

“They treat patients with the same medications used for Alzheimer’s and Parkinson’s patients,” she said. “But it has to be the right balance. The meds used to help the hallucinations of Lewy body can exacerbate the Parkinson’s. And the meds for Parkinson’s can exacerbate the hallucinations.”

Ms. Hutchinson placed her husband in long-term care on Nov. 30, 2005, at the hospital she worked at in Valdez, Ala. But his condition worsened, and she decided in March 2006 to resign from her job and take care of her husband.

“As long as I was with him, he was fine,” she said. “So we decided to load up our motor home and travel from Alaska to Florida raising awareness of LBD. It was the adventure of a lifetime.”

Along the way, Ms. Hutchinson spoke to about 100 different groups, from Lion’s Clubs to churches, about LBD.

While the trip was rewarding, Ms. Hutchinson said there were tough times, as well.

“We had a lot of good times, but there were times when he would collapse,” she said.

The couple arrived at their daughter’s home in Fort Meyers, Fla., in May 2007. Her husband died three months later.

“We stayed at my daughter’s until he died,” she said. “We put him in hospice for the last week and they were wonderful.”

Ms. Hutchinson said her grief was combined with feelings of relief.

“My grieving was watching him suffer and not being able to do anything about it,” she said. “I cried almost every day he was in long-term care.

“We had the most wonderful year when we traveled. He enjoyed going to the meetings where I would speak. He was my most avid fan,” she said.

Following her husband’s death, Ms. Hutchinson drove her motor home to Newport during Thanksgiving 2007 to be near another daughter, whose husband was deployed to Iraq at the time.

Ms. Hutchinson got a job as a registered nurse at Carteret General Hospital, where she worked for a year and a half.

“I retired from there and I now work part-time at Carteret Community College teaching CNA (certified nursing assistant) students,” she said.

Ms. Hutchinson still lives in her motor home and has spoken to a few area groups, including the Morehead City and Newport Rotary Clubs, and at the Leon Mann Jr. Enrichment Center in Morehead City.

She also plans to start a support group for families struggling with LBD.

“I’ve met caregivers of Lewy body people here,” she said. “It’s nice to talk with other LBD caregivers because they understand what you’re going through.”

Ms. Hutchinson also posted a video on YouTube about LBD and the trip she and her husband made across America. That video can be accessed at:

Those wanting to donate to the LBD Association on behalf of Ms. Hutchinson can go to:

Those interesting in taking part in an LBD support group can contact Ms. Hutchinson at 269-9748.

Wed Oct 20, 2010 8:34 pm

Joined: Wed Dec 30, 2009 1:46 pm
Posts: 3213
Location: WA
Reply with quote
Post Re: Article about Barbara Hutchinson and LBD
Barb has been a wonderful spokesperson for LBD! Thank you for sharing this article, Robin. I hope it inspires in the rest of us the same level of commitment.

Pat [68] married to Derek [84] for 38 years; husband dx PDD/LBD 2005, probably began 2002 or earlier; late stage and in a SNF as of January 2011. Hospitalized 11/2/2013 and discharged to home Hospice. Passed away at home on 11/9/2013.

Wed Oct 20, 2010 9:24 pm

Joined: Sat Jul 31, 2010 5:28 pm
Posts: 317
Reply with quote
Post Re: Article about Barbara Hutchinson and LBD
She spoke at a Senior Center that my husband and I belong to. When Del was diagnosed with PDD one of the nurses there remembered her and their plans to tour the country. Nan

Thu Oct 21, 2010 11:23 am
Display posts from previous:  Sort by  
This topic is locked, you cannot edit posts or make further replies.   [ 3 posts ] 

You cannot post new topics in this forum
You cannot reply to topics in this forum
You cannot edit your posts in this forum
You cannot delete your posts in this forum
You cannot post attachments in this forum

Search for:
Jump to:  
Powered by phpBB © 2000, 2002, 2005, 2007 phpBB Group.
Designed by STSoftware for PTF.
Localized by Maël Soucaze © 2010