“The bad news: I don’t have Parkinson’s”

Last week in the Birmingham News, a journalist named Mike Oliver revealed that he was recently given a diagnosis of Lewy Body Dementia (LBD).  He had previously written in September 2016 that his diagnosis was Parkinson’s Disease.  But new symptoms pointed to LBD.

Mike uses the term “Lewy body disease” and describes the condition as being “like Parkinson’s and Alzheimer’s combined.”
He says:

“The disease works and presents like Parkinson’s. In both cases, these proteins kill neurons. It’s just that with Lewy body disease the proteins are killing neurons over a wider swath of the brain. … The big difference is that with Lewy body disease, the dementia comes early, sometimes before any movement disorders are noticed. With Lewy body disease, dementia is often accompanied by hallucinations and REM behavior disorder, which cause people to physically act out their dreams, hitting, kicking or talking.”

Here’s a link to the full article:

www.al.com/news/birmingham/index.ssf/2017/02/im_losing_my_mind_–_literally.html

The bad news: I don’t have Parkinson’s.
Birmingham News
By Mike Oliver | [email protected]
on February 20, 2017 at 12:04 PM

Robin

 

Blogger who has Lewy Body Dementia

Recently a gentleman named Robert Bowles spoke on a webinar about Lewy Body Dementia (LBD).  Robert is a retired pharmacist, who began having neurological symptoms in 2010.  After seeing several physicians, he was diagnosed with LBD in June 2012.  He lives in Thomaston, GA.  In January 2015, he created a website called “Lewy Body Dementia Living Beyond Diagnosis” (lbdlivingbeyonddiagnosis.com).  He seems to post to the blog once a month though he hasn’t posted since December 2016.

Here’s his message on the home page of his website.

Robin

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lbdlivingbeyonddiagnosis.com/index.html

Robert Bowles
Lewy Body Dementia Living Beyond Diagnosis

This website has been created out of a deep love that I had for patients in my pharmacy practice, families, care partners, and others.  My prayer is that with me having a strong foundation in faith as a result of having two Christian parents, having a Mom and Dad with dementia and now with my diagnosis of Lewy body dementia that I will be able to offer insights from multiple perspectives as it relates to dementia.  The resources that are provided should help persons with dementia, families, care partners and others have a better understanding of what it is like to live with dementia and how to care for those living with dementia.  I have a deep passion for better education and understanding for care partners.

As you visit this website, you will be coming into my world of living with Lewy body dementia (LBD).  My goal is to transparently share my experiences with this horrific disease.  I will share the good, the not so good and the ugly in my personal blog.  In my faith blog, I will share how my faith has been my foundation and helped me the most in living with LBD.  There may be things that I write about that you might think are impossible and things that you do not agree with; but, remember you have come into my world with LBD.

June 2012, I received a diagnosis of dementia with Lewy bodies (LBD).  Actually, this gave me peace of mind because I had visited 7 previous physicians and had not received a diagnosis and treatment that was bringing closure for me in regards to the health issues I was experiencing. The peace that I felt was so great that I told my wife 10 minutes after diagnosis, “It is what it is and everything will be OK”

Soon after diagnosis though I begin to think about a patient of mine in my independently owned pharmacy who died with LBD.  I thought about the problems and difficulties that he and his family experienced as it related to his diagnosis.  It seemed as though my death sentence had been issued.  My thoughts were that my life seemed like that of a convicted murderer.  A physician had entered the charges against me, a trial had taken place, I had been found guilty and a judge had announced the sentence — without appeal.  During my initial research on LBD, I found reports of persons living from two to twenty years after diagnosis.

These statistics were not encouraging.  I decided, however,  that I was not a statistic. I acknowledged that I was a human being; born through a miraculous process and created by God with certain inalienable rights.  My decision to live and outdistanced the statistics was one of my God-given rights.  The decision did not mean that I would not have battles, trials and tribulations along the way.  Maintaining the desire to live has been a struggle at times. As I face the many struggles, I rely on my faith in God.  One of my favorite verses of scripture has been a constant source of encouragement to me knowing that I do not travel this journey alone.  Phillipians 4:19, “And my God will meet all your needs according to the riches of His glory in Christ Jesus”.  Also, my wife and entire family are with me every step of the way.

My choice to live with LBD well, drove me into dementia awareness and advocacy.  I wanted others to know that there was life after a diagnosis.  Realizing there was very little information that chronologically sets forth someones path with LBD, I wanted to share mine with the prayer and hope that others with LBD and their care partners might receive benefit.

I wanted others to know there was no stigma in having dementia. I dream for the time when there will be no stigma in having dementia.  I dream for a cure of dementia.  I dream of persons with dementia being better educated about their disease.  I dream of better education for care partners.  I dream for better education and understanding about dementia for family and friends.  I dream of memory cafes in every town and city.  I dream of dementia friendly businesses so that persons with dementia will not isolate because of how that might be talked to.

Individuals with dementia can still do a lot of things.  We all need to be getting this message across.  We just have to accept our diagnosis, find our new purpose and develop strategies of living with our disease well.

There is a lot of work to do in dementia advocacy and helping others understand there is life after diagnosis.

(c) 2015, Robert Bowles

Short podcast on Parkinson’s Plus conditions with Dr. Golbe

This is a worthwhile 28-minute podcast about Parkinson’s Plus conditions, including progressive supranuclear palsy (PSP), multiple system atrophy (MSA), vascular parkinsonism, corticobasal degeneration (CBD), and dementia with Lewy bodies (DLB).

soundcloud.com/world-parkinson-coalition/07-parkinsons-plus-conditions

Parkinson’s Plus Conditions
Podcast by World Parkinson Coalition
Speaker:  Lawrence I. Golbe, MD, movement disorder specialist

Brain Support Network Treasurer Phil Myers listened to the podcast and reports: “This podcast was done a year ago in 2016 as preparation for the World Parkinson’s Congress in Portland.  This is good coverage of all variations of Parkinson’s Plus. It compares each of them to Parkinson’s. It does talk about the lack of direct treatment but does discuss symptom treatments. And it talks about the difficulty of diagnosis.”

I’ve shared an outline of the podcast and a few notes below in case you want to forward to your disorder of interest.

Robin

—————————

1:00 – Dr. Golbe begins a general overview of Parkinson’s Plus conditions

1:45 – PSP discussion begins

5:00 – terrific question and answer on why levodopa doesn’t work in PSP, MSA, etc.

6:00 – MSA discussion begins

8:00 – discussion of dementia in MSA

8:20 – is MSA a prion disease?  He can’t comment on any one study in this format.  He says many diseases are prion-like in that there is a toxic chain reaction.  “Can’t catch MSA.”  Key distinction is that in CJD, the key protein is prion.  Prion protein can be transmitted more easily than other proteins.

11:00 – treatment of MSA symptoms

11:52 – discussion of vascular parkinsonism, which isn’t a neurodegenerative disease.

13:43 – CBD discussion begins.  One-tenth as rare as PSP or MSA.  Those conditions are one-twenthieth as prevalent as Parkinson’s.  Life expectancy similar to PSP and MSA:  between 5 and 10 years, typically between 7 and 8 years.  Lots more tau in CBD than in PSP.

15:10 – MSA pathology

15:40 – DLB discussion begins.  Spontaneous fluctuations that happen in DLB don’t happen in PD.  Levodopa isn’t quite as effective in DLB than in PD.  There’s is a problem that levodopa can cause hallucinations in DLB.

18:00 – general discussion.  There is long-term hope via a double-pronged attack.  First, stopping the protein aggregation or misfolding for a group of diseases.  Second, focusing on each individual disease.

We are further along in PSP given the focus on Alzheimer’s – both are tauopathies.

CBD is more difficult to do research on — because it’s rare and because diagnostic accuracy is very poor (50%).

21:00 – general discussion.  Neglected because they are rare, hard to diagnose, and no biomarkers.  FDA can given these diseases the status of an “orphan disease.”

22:45 – general discussion about how to help these families.  First, accurate diagnosis is important.  Sometimes people are given fruitless tests on the way to a diagnosis.  Second, symptoms can be treated.  Palliative management of symptoms.  Referrals can be made.  Third, at academic centers, treatment trials or research projects are available.  These can give patients the feeling of “fighting back” to help future generations.

25:00 – Dr. Golbe stops speaking.  Podcast continues with comments from hosts Dave Iverson and Jon Palfreman.

Difference between LBD and AD, and how is LBD diagnosed?

The Mayo Clinic has a large clinic in Rochester, MN. The local newspaper in Rochester has a health column where questions are occasionally answered by Mayo physicians. Here are recent questions where Mayo Jacksonville dementia expert Neill Graff-Radford, MD answers. The questions are — What’s the difference between Lewy body dementia and Alzheimer’s, and How is Lewy body dementia diagnosed?

Here’s a link to the article:

www.postbulletin.com/life/health/many-with-lewy-body-dementia-also-have-alzheimer-s-disease/article_856173ba-127d-5e0b-98b8-fd4ecfc4401d.html

HEALTH
Many with Lewy body dementia also have Alzheimer’s disease
by Tom Jargo
Post Bulletin
Feb 6, 2017

Robin

Comprehensive Approach to DLB – Notes from Webinar for Healthcare Professionals

In December 2016, the Lewy Body Dementia Association (lbda.org) hosted a one-hour webinar with Brad Boeve, MD, behavioral neurologist at Mayo Rochester, on the topic of management of Dementia with Lewy Bodies. Note that Dr. Boeve’s presentation was tailored to healthcare professionals.

Dr. Boeve detailed the pathology, neurotransmitters, six symptom groups (cognitive, sleep, autonomic, senseory, motor, and neuro-psychiatric), medications, disease progression, and current research. The webinar ended with a short question-and-answer period.

The webinar was recorded and the video is available on the LBDA’s youtube site:

Comprehensive Approach to DLB Management
Speaker: Brad Boeve, MD
LBDA Webinar, December 5, 2016

www.youtube.com/watch?v=J-0jmH1tInU&feature=youtu.be

Note that Dr. Boeve uses the term Dementia with Lewy Bodies (DLB) throughout his talk. DLB and Parkinson’s Disease Dementia (PDD) are part of the spectrum of Lewy Body Dementia (LBD).

I watched the webinar, and thought it was terrific.

In my opinion, the best graphic is the busy slide shown at the 35:33 time marker. It lists “features” (symptoms) such as cognitive impairment, neuro-psychiatric features, parkinsonism, etc. And it lists medication classes such as AChEIs, memantime, SSRIs, etc. Dr. Boeve indicates whether there is optimism or caution about each medication class for each symptom.

Brain Support Network volunteer Denise Dagan took notes during the webinar but she thinks it’s faster if everyone listens to the webinar! I’ve copied her notes below.

Robin

——————–

Denise’s Summary of

Comprehensive Approach to DLB Management
Speaker: Brad Boeve, MD
LBDA Webinar, December 5, 2016

Dr. Bradley F. Boeve, MD, started with an overview of Dementia with Lewy Bodies (DLB): Lewy bodies are mis-folded alpha synuclein protein. In DLB, they are found in the brain, brain stem, spinal cord and, in some people, the retina, heart, intestines, bladder, sex organs. They affect nerve-cell structures throughout the body. There are no FDA-approved medications to treat DLB.

This ven diagram is a good visual of how symptoms overlap and, therefore, the complexity of treatment.

[Editor’s note: see webinar!]

Dr. Boeve asks DLB patients and caregivers to prioritize the top three most troublesome issues they seek to change at each appointment. When they resolve #1 to a satisfactory degree, #2 often moves up to the #1 position and, together they keep working through symptom relief, rather than tackling everything at once and confusing what’s a symptom and what’s a medication side-effect.

Brain-Behavior Relationships:

Dr. Boeve spoke with brain diagrams about these neurotransmitters and the part of the brain in which they are typically active. In DLB, they find the cells in these areas are living, but for the most part, are not working properly, so medications are helpful to support functioning.

He then went through each symptom group in detail with corresponding treatment options. General notes for each symptom group are above the charts, while notes on specific symptoms are in the ’Notes’ column of each chart.

Cognitive symptoms:

Cognitive symptoms are primarily the result of depletion of acetylcholine. Reductions in other brain chemicals contributes to cognitive impairment, as well as some degree of neuron cell loss.

Start with education & counseling to understanding what’s at the root of these symptoms. Non-medication approaches like, cognitive rehabilitation or occupational therapy (OT).

Neurophychiatric issues:

No medication is needed unless hallucinations are frightening, upsetting, or leading to delusions.

NEVER USE HALDOL, THORAZINE, MELLARIL, and others in this class of drugs.

Motor issues:

Start with physical therapy (PT), gentle exercise, dance, a personal trainer at the YMCA, etc. – as long as balance is okay.

Treating Autonomic Dysfunction

This chart from Dr. Boeve shows several groups of prescription medications and the symptom groups they are often prescribed to treat. Because medications tend to have side-effects (some serious), the chart uses a color scale with those medications having the greatest effectiveness and few ill-effects in dark green and those with the least effectiveness and most ill-effects in orange. Your doctor should have all this information, but its a good visual.

[Editor’s note: see webinar!]

Best advice is to start slow, add one at a time, gradually adjust dose and evaluate the benefit against whether it is making something else worse.

The bright side is that if you try something and you don’t see a benefit, back off that one, change course, try another with the same caution.

It’s worth the effort.

He then went on to talk about the progression of the disease, the direction of research and, finally, questions & answers.

Progression of DLB can be 1-2 years or 10-15, or more, years. No idea why the range is so variable.

Current medications treat symptoms, but none show impact on rate of progression.

Research into Rx to slow progression, delay the onset so person dies before developing symptoms, or prevent DLB, altogether. Dr. Boeve believes medications to slow progression or delay onset will be available in the next 3-5 years. Biggest obstacle to research is lack of clinical trial participants, so get involved, of you can.

“Prodromal DLB” is defined as having early features of DLB

Q&A

Q: Nuplazid?
A: Nuplazid is a new FDA-approved Rx for hallucinations & delusions in Parkinson’s disease. No evidence into the efficacy, safety, tolerability for people w/DLB. Currently, insurances are not covering this, so very expensive.

Q: When is it reasonable to consider discontinuation of cholinesterase inhibitors?
A: No right or wrong way to proceed. Most people, in later stages of illness, have no neurons making acetycholine so there is little effectiveness of the medication. Some people have increased cognitive impairment or hallucinations so doctors are inclined to maintain Rx to avoid the few who have negative effect of stopping the medication because there is no ill effects from taking it.

Q: Marijuana?
A: No research because illegal so no FDA approval. Medical marijuana prescription to treat pain in this doctor’s experience was ineffective, but no data pro or con.

Q: Pain management for arthritis, etc. when over the counter isn’t helping?
A: Ask your neurologist for prescription strength non-steroidal anti-inflammatories, other prescription with opioid effects. Use non-opioids first, then SNRIs have some pain modulating properties. Work with your doctor and keep trying!

Q: What’s in the pipeline with regard to monoclonal antibodies?
A: Monoclonal antibodies directed toward mis-folded proteins is a leading area of research for all age-related degeneration diseases. Phase I & II trials currently, but in the next 1-3 years will be in phase III trials. Challenge is that companies working on parkinsonisms find Parkinson’s disease patients easiest to have access to, so not as much research directed to DLB.

Q: Are seizures common? Are they part of DLB? What to do if they happen?
A: Relatively uncommon (less than 10% have one, or more) but disturbing to CGs and injuries can happen. Medications often have cognitive side effects, so if it is an isolated incident your doctor is unlikely to medicate, but if seizures are regular they will prescribe something, depending on the person’s medical history.

Q: Does the prevalence of lewy bodies in the gut help to understand DLB?
A: Current thinking is that alpha synuclein changes begin around the nasal cavity and along the brain stem from nerves coming from the stomach. Could it be a virus, toxin, or something ingested that starts the process of eventual changes in the brain stem. Avoiding this, if they could find what it is, would prevent infection, if the theory is accurate. Currently NO idea what that could even be!

Q: What are the milestones of the stages of DLB?
A: In recent research, MRI scans show if there is not atrophy in the brain, progression could be slower, but predicting course or progression is difficult, if not impossible.

Q: Is loss of speech communication related to muscle control or cognitive degeneration?
A: The cause is probably both. Use speech therapist because there are physical impairments that can be compensated for with training. Motor control could improve with a dopamine agent.