PWD Robert Bowles ER and LBD


Emergency Room and Lewy Body Dementia

The spouse of one of my friends with LBD sent me a text this morning because she needed to take her husband to the ER out of state. I quickly sent her links to the LBDA website so that she would have the information to share with the hospital staff. I was able to provide six different links for various situations. She just sent me another text and told me they were at the hospital and the nurse had never heard of LBD.  The nurse told the spouse that the hospital groups ALL dementia under one category.  The spouse relayed to me that “the lack of awareness of LBD among healthcare professionals is scary” and I would agree with that.  The good part is that the nurse was receptive to the information that was provided to her and is asking the spouse before giving any medication to her husband.

Personally, I was given a medication one year prior to my diagnosis of dementia with Lewy bodies (DLB) that took me 15 months to recover from.  I reached a point of sleeping 16 to 20 hours a day and was unable to do anything.  Since my diagnosis, three years ago, I have been given 6 medications that I quickly recovered from, probably since I addressed the possibilities with the physician prior to taking the medication. In each of these situations, the physician agreed to reduce to the lowest dose and I still had an adverse reaction.

On another medication, the physician ordered the maximum dose of a medication over the phone without telling me the dose that he was going to give.  When I picked up my prescription and saw this, I chose to cut the dose in half and still reacted.  This reaction took almost 2 months to recover from.

When I had my cervical disc surgery, I was given medications during surgery that took me 2 and 1/2 months to recover from.  Several months following surgery, I was given a low dose oral steroid dose pack.  Not responding, the physician decided to give me a 12 day, large dose oral steroid pack.  Again, this took 2 and 1/2 months to recover from. My neurologist has told me that he wants to write a paper on my medication sensitivities.

Statistics indicate that one-half of LBD families had an emergency last year. How can you treat what you do not know. We must work harder creating more information/resources/knowledge so that proper care can be given.

Be LBD Strong!

©2015 Robert Bowles


Paulan Gordon at on 04/12/2015 11:24am
It is amazing how little the doctors know about drug interactions and other side effects of dementia medications. I recently saw an article explaining that people on Aricept should never take Anticholinergic drugs. I looked at the list and saw that I am taking three of the medicines daily and have been for years. Mine were Benadryl, Amitriptyline, and Bentyl. The list was in

Linda Foc on 04/12/2015 1:20pm
Robert…may I ask what meds you were on that caused you to sleep so much

Robert Bowles on 05/11/2015 9:24am
It was not medicine. It was the disese.

((Originally posted 2015 April 12 at lbdlivingbeyonddiagnosis))

* Admin issues: SHARE dementia awareness thru buttons below. If interested in receiving notice of future blog postings there is a “follow” button in the upper left corner (MS Explorer) or lower right (Safari and Chrome). Feel free to leave your thoughts in the form of comments, but please filter your comments with truthful loving kindness to all concerned. If there is an advertisement below, I have no control over what is shown. — Copyright exclusively by Robert Bowles Jr on 2015-04/12   (( but if there is font detail like bold and underlining, it is Truthful’s doing in order to easily find quotes in the future )) Registered & Protected


Leave a Reply

Fill in your details below or click an icon to log in: Logo

You are commenting using your account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s

This site uses Akismet to reduce spam. Learn how your comment data is processed.

%d bloggers like this: