Let me preface this by saying I am not a doctor and these are just my thoughts and opinions. Always talk to your doctor if you have any concerns.
The best way that I can describe this terrible disease is that it’s like taking the worst symptoms from Parkinson’s Disease and the worst symptoms from Alzheimer’s Disease and put them together and you’ve got Lewy Body Dementia. It’s a crippling, progressive brain disease that cuts your life short and robs one self of the ability to think and communicate.
Unfortunately, this is an extremely difficult disease to diagnosis as there is no test you can take. A true diagnosis can only be given once an autopsy is performed. Often times, Lewy Body Disease is mis-diagnosed as Parkinson’s Disease or Alzheimer’s Disease. I’ve found there is very little information about Lewy Body Dementia- even in the medical community. Although this is the second leading cause of dementia in our seniors, very few people have ever heard of Lewy Body Dementia. LBD is tricky, too, because it’s often mis-diagnosed, however, LBDers are extremely sensitive to medication. Only certain medications can be given to LBDers or else a horrible reaction can occur sending one in to a terrible downward spiral. Many doctors think their patients are mentally ill, however, it’s not the case at all- it’s the incorrect medication interacting with the LBD.
For a more scientific description, the Lewy Body Dementia Association describes LBD as:
Lewy body dementia (LBD) is a progressive brain disease and the second leading cause of degenerative dementia in the elderly. The clinical name, “dementia with Lewy bodies” (DLB), accounts for up to 20% of all dementia cases, or 800,000 patients in the US. Over 50% of Parkinson’s disease patients develop “Parkinson’s disease dementia” (PDD), which accounts for at least 750,000 patients. (PDD is also a Lewy body dementia.)
Other names for the Lewy body dementias are:
- Lewy body disease (LBD)
- Diffuse lewy body disease (DLBD)
- Cortical Lewy body disease (CLBD)
- Lewy body Variant of Alzheimer’s (LBV)(LBVA)
- Parkinson’s disease with dementia (PDD)
In the early 1900’s, while researching Parkinson’s disease, the scientist Friederich H. Lewy discovered abnormal protein deposits that disrupt the brain’s normal functioning. These Lewy body proteins are found in an area of the brain stem where they deplete the neurotransmitter dopamine, causing Parkinsonian symptoms. In Lewy body dementia, these abnormal proteins are diffuse throughout other areas of the brain, including the cerebral cortex. The brain chemical acetylcholine is depleted, causing disruption of perception, thinking, and behavior. Lewy body dementia exists either in pure form, or in conjunction with other brain changes, including those typically seen in Alzheimer’s disease and Parkinson’s disease.
There are many symptoms of Lewy Body Disease and the thing with LBD is that each person is different and experiences different symptoms. What seems to be common are the following symptoms:
- Fluctuating cognition- variations in attention and alertness. Changes in their decisions, thinking, and memory.
- Hallucinations- mostly visual but can also be auditory. They are often very detailed and life-like.
- Parkinson’s like features- shuffling gait, tremors, expressionless face, stooped posture, etc.
The Lewy Body Dementia Association has good information about the core symptoms, supporting symptoms and detailed descriptions of each symptom. You can read more about it here.

Dear Holly,
Thanks so much for your wonderful blog and for spreading the word about LBD. Keep up the good work!
If you would like LBDA to send you updates when we have new resources on LBD available, please drop me a note with your email address.
Sincerely,
Angela Taylor
LBDA
Thanks, Angela. I’ve sent an email your way. Thanks for checking out my blog.
Hello Angela
Iam a Neuroradiologist , first of all thank you for your explanation, Do you have information about its MRI presentations?.
Reza
Hi Reza,
I’d suggest getting in contact with the LBDA directly. You can try them through the various contacts listed here. (click on the link ‘here’)
I was recently diagnosed with Lewy Body and it has been overwhelming. I am only 61 and am disabled with RA and receive Social security. My husband is still working but we are trying to make it possible for him to retire so I can stay
at home. I am terrified about how quickly this is progressing. We both are.Hoping what we read will help us plan.
Hi Linda,
Thanks for stopping by. I’m sorry to learn of your diagnosis. I hope this blog can give you a little bit of information and insight in to LBD. If you haven’t already, I would recommend getting in touch with the Lewy Body Dementia Association. They have several resources available, support groups, online forums, etc. that might provide some comfort and information. On my blog, I have several links to articles about LBD, other LBD blogs, caregiving news, support groups, etc. They’re definitely worth checking out. I wish you and your family all the best and much strength in dealing with LBD. If there’s anything I can help with, please let me know.
Hi There,
I am a friend of my very good friend Karen,we met last march 09 and first of all we just thought it was forgetfulness but it wasn,t now she has all the terrible things associated with parkinsons and dementia,as you say there is no test,she is on loads of meds sometimes she is quite up there and is her usual very articulated self and then all of a sudden god her love her she shrivells to this helpless being tremors forgetfullness,stairing into space ,can,t ge her words out she says when she can it is so frustrating cause she knows what is going on a round her.
I am glad i have found your support group online cause it is so releiving to express my thoughts on this matter,My gorgeous friend Karen is still in there,i just wish i cauld help her more than i do,She doesn,t rely on me but has a family,but i am always there for her when she needs me,sometimes she will text me and i havent a clue what. it means i have to try and disifer it for myself.
But the nicest thing about this story is she is the kindest ,genourous most intelligent abd caring person i know thats why i am sad for her and when she is ok she is the funniest person i know with a laugh to die for.
Thankyou Collette Campbell
Hi Collett,
I’m sorry to hear about your friend but so glad she has a friend like you to lean on. I would recommend checking out the LBDA’s webpage (www.lbda.org) for more information that might be of assistance to you, your friend and her family. This is a terrible disease for all involved. I wish you and Karen much strength in this LBD journey.
Hi there
This year my dad has be diagnoised with lewy bodies and i have been searching the internet for information with regard to this diseased. i have looked at http://www.lbda.org. can you please advice me where is can get a booklet about lbd.