“Coping with novel coronavirus while caregiving” – Teleconference notes

Today, WellMed Charitable Foundation organized a conference call on how to cope with the novel coronavirus while caregiving, featuring two speakers — Dr. Elliot Montgomery Sklar and social worker Lucy Barylak. Though the conference call was for all caregivers (not necessarily caregivers with one of the disorders in the Brain Support Network community), we listened-in as we thought there would be useful suggestions shared for us all on the emotional and psychological aspects of coping. Indeed, the two speakers discussed how the current pandemic has been impacting caregivers and offered suggestions for regaining some sense of control amid this chaotic situation.

During a recent BSN caregiver-only support group meeting, a caregiver said that her husband was quite panicked about the pandemic, and especially worried that the caregiver would get sick and die.  This question was raised during the WellMed Charitable Foundation conference call.  The advice given was:

As caregivers, this may be the most challenging time for you and your loved one; you will need to be as patient as possible. If they have any form of dementia, you may need to repeat your instructions daily or frequently, or maybe help them yourself more directly than usual. Just because they have dementia doesn’t mean they won’t pick up on your anxiety and the news.  Try to make alternative plans for the loved one’s care if you the primary caregiver do get sick.   Knowing a plan is in place can alleviate some of their anxiety – and yours. Talk realistically with your husband about his concerns.  If your loved one lives in a care facility, remember that staying away is an act of love – you are protecting them. Explore other ways to communicate with them, such as phone or video chat.

For additional questions-and-answers plus suggestions for regaining some sense of control, check out these notes of the conference call.  Lauren Stroshane with Stanford Parkinson’s Community Outreach shared her notes here:

parkinsonsblog.stanford.edu/2020/03/coping-with-novel-coronavirus-while-caregiving-teleconference-notes/

The recording of the call is not yet available on the WellMed Charitable Foundation website.

Robin

How mood and cognition affect Parkinson’s – Webinar notes

In early March 2020, Parkinson Canada offered a webinar on mood and cognition in Parkinson’s disease (PD), featuring social worker Adriana Shnall, PhD.  She provided an overview of mood and cognition symptoms, including depression, anxiety, social avoidance, disinhibition, increased emotion, decreased emotion (which can be a sign of apathy), and cognitive impairment.  Then Dr. Shnall discussed strategies for improving communication and working around these issues.

Though this webinar focused on Parkinson’s disease, all of the discussion of mood issues is relevant to disorders in the Brain Support Network community, which include Lewy body dementia, multiple system atrophy, progressive supranuclear palsy, and corticobasal degeneration.

There was a good question-and-answer about apathy:

Q: Dealing with apathy is a great source of frustration for caregivers. At what point does encouragement on the part of the caregiver turn into nagging?

A: It can be a hard distinction. It is important to push a bit, since changes in the brain make it difficult for the person to take initiative anymore. Pick your battles. If going to see the grandchildren today is really important, but the person doesn’t feel motivated, push for that. If it’s something less important, maybe let it slide sometimes. Giving alternatives so that the person can make a choice is sometimes helpful.

While I didn’t think the discussion of cognition and psychosis was very helpful, I thought the discussion of communication issues was very good and applies to all of us in the BSN community.  Here’s a short excerpt:

What causes difficulties in communicating with someone who has PD?

  • Quieter voice: It can be harder to hear the person
  • Masked face: It can be harder to read their facial expression
  • Mood and cognitive issues: It can be harder for them to engage and express themselves

Strategies for better communication:

  • One-on-one conversations or smaller groups are best.
  • Reduce or eliminate distractions such as TV or music.
  • Sit close, make eye contact, and speak at eye level.
  • Encourage the person to take a deep breath when they start to speak, to help with speech volume. 
  • Give the person time to respond – it can take longer for a person with PD to express themselves.
  • Don’t make assumptions. 
  • Remain calm; smile.
  • Avoid using sarcasm, which can be misinterpreted.
  • Ask one question at a time, to avoid overloading.
  • Ask close-ended (yes or no) questions, which can be easier to answer than open-ended questions.
  • Give hints if the person is having word-finding difficulties.
  • Try to speak in short, simple phrases.

Watch the webinar recording on YouTube here:

www.youtube.com/watch?v=ehgnOj5hAk8&feature=youtu.be

Lauren Stroshane at Stanford Parkinson’s Community Outreach listened to the webinar and has shared her notes here:

parkinsonsblog.stanford.edu/2020/03/mood-cognition-non-motor-symptoms-of-parkinsons-disease-how-it-impacts-relationships-webinar-notes/

Robin

 

AFTD Webinar CBS/CBD: Basics & What You Need to Know

Melissa Armstrong, MD, MSc, Associate Professor of Neurology at the University of Florida (Gainesville) will provide an in-depth look at corticobasal syndrome and corticobasal degeneration. In the webinar, she will discuss the vocabulary used in this disease (what’s the difference between the syndrome and degeneration?), how a diagnosis is made, common symptoms, expected progression, and treatment approaches.

DAY: Thursday, March 19th
TIME: 1 p.m. (PT), 2 p.m. (MT), 3 p.m. (CT), 4 p.m. (EDT)
DURATION: Approximately 90 minutes

AFTD webinars typically fill up quickly and you must PRE-REGISTER for this event, so secure your spot today!

RBD (REM sleep behavior disorder) and other sleep issues – meeting notes

The Palo Alto (California) Parkinson’s Disease Support Group’s February 2020 meeting featured Dr. Emmanuel During, who specializes in neurology, psychiatry, and sleep medicine at Stanford.  He discussed the various types of sleep disturbances that can occur in Parkinson’s disease (PD), such as insomnia, restless legs syndrome, sleep apnea, and REM sleep behavior disorder, along with available treatments for managing these issues. There was also a question and answer session.

Though this was a Parkinson’s Disease support group meeting, these sleep issues are common in all the disorders in the Brain Support Network community, including Lewy body dementia (LBD), multiple system atrophy (MSA), progressive supranuclear palsy, and corticobasal degeneration.  Indeed, REM sleep behavior disorder (RBD) is common in LBD, MSA, and PD.

Lauren Stroshane with the Stanford Parkinson’s Community Outreach attended the meeting and shared her notes below.

Robin

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Sleep and Parkinson’s Disease – Meeting notes
Palo Alto Parkinson’s Disease Support Group Meeting
February 12, 2020
Notes by Lauren Stroshane, Stanford Parkinson’s Community Outreach

The guest speaker was Dr. Emmanuel During, who specializes in neurology, psychiatry, and sleep medicine at Stanford.

Dr. During described sleep as a “blind spot” that often goes unaddressed in medical care. Doctors rarely inquire how their patients are sleeping, so sleep issues often go unrecognized and untreated. Yet the quality and amount of sleep you get every night affects your overall health and quality of life. For many with Parkinson’s Disease (PD), sleep disturbances may have been among their earliest symptoms, before the motor symptoms like tremor or slowed movement started to manifest. Sleep also has the important function of cleaning out toxins in the brain. No matter how well we treat the motor symptoms of PD, if you are not sleeping well, you will not feel healthy.

What types of sleep issues are common in PD?

At night, sleep may be shallow or fragmented. Muscle stiffness can make it difficult to reposition during the night. Sometimes muscle cramps or dystonia occur, which may be painful or disruptive. Frequent urination and restless legs may interrupt sleep, while snoring, sleep apnea, or acting out dreams may worsen sleep quality.

During the day, many people with PD experience brain fog and have difficulty paying attention. Daytime sleepiness and general fatigue are also common.

Fatigue may consist of physical or mental exhaustion. Typically, it occurs when certain neurotransmitters (dopamine, serotonin, and norepinephrine) are low. Causes of fatigue can include poor quality sleep, depression, restless leg syndrome (RLS), and side effects of medications.

Sleepiness is different from fatigue in that it is a difficulty staying awake, like drowsiness. It may be caused by insufficient sleep or sleep apnea, which is when breathing stops repeatedly during sleep. Sleep apnea is a serious condition that decreases the amount of oxygen that the brain receives during sleep, interrupting the sleep cycle over and over. Besides making you sleepy, it also increases your risk of heart attack and dementia. Sleep apnea can be diagnosed at home or via sleep study in a lab. There are a number of different effective treatments available to manage it.

Some medications can cause sleep attacks, periods when a person can’t help falling asleep regardless of the situation. Medications which can trigger this side effect for some individuals include Mirapex (pramipexole), Requip (ropinirole), Sinemet (carbidopa-levodopa), allergy medications, anxiety medications, and some painkillers. Provigil (modafinil) and caffeine are stimulants which can be helpful for managing fatigue and sleepiness in PD, but often, if a medication is suspected of causing sleep attacks, it may need to be reduced or discontinued.

Insomnia in PD

Insomnia, or sleep fragmentation, is also common in PD. Insomnia can either consist of difficulty falling asleep at the beginning of the night, or waking up during the night and having trouble getting back to sleep again. There are a number of ways to manage insomnia, depending on what is causing it.

  • For discomfort in bed due to stiffness or dystonia, sometimes switching to long-acting carbidopa-levodopa (Sinemet ER or Rytary) can help provide on-time overnight.
  • If pain is keeping you awake, try to identify methods to address the pain, such as medication or a heating pad.
  • If you are waking up frequently during the night to urinate (nocturia), the medication can Myrbetriq (mirabegron) can be helpful. Many other drugs for this issue can cause confusion in those with PD.
  • If you address these factors and are still having insomnia, then there are other options:
    • Cognitive behavioral therapy (CBT) can be very helpful.
    • Consult a sleep doctor or neurologist to explore prescription sleep aids.
    • Try over-the-counter sleep aids such as melatonin. AVOID Benadryl and Tylenol PM, which can cause confusion in those with PD!

People with PD sometimes experience circadian abnormalities, in which the body’s internal clock is disrupted and confused. The circadian rhythms in our bodies regulate our cardiovascular, hepatic (liver), pancreatic, adipose (fat), and gastrointestinal systems. Our bodies use certain cues – food, sunlight, activity, and melatonin – to regulate this cycle.

For those experiencing circadian abnormalities, such as from jet lag, Dr. During recommended limiting the use of naps and trying over-the-counter melatonin tablets, 0.5 to 2 mg taken one hour before your desired bedtime.

Restless legs syndrome (RLS)

Restless legs syndrome can occur in the general population but seems to occur more frequently in PD. It is an urge to move the legs that becomes quite uncomfortable until the legs are moved or stretched. This is not the same as leg movements which may occur during sleep – RLS is a bothersome sensation while you are awake, and can prevent you from falling asleep. RLS is typically caused by inadequate levels of iron in the brain.

RLS symptoms can be triggered by rest, boredom, and being in a confined space such as a car or plane. Stretching, massage, walking, distracting, and soaking the legs in hot water can be helpful. Aggravating factors for RLS include smoking, alcohol, coffee, and lack of exercise.

If you have RLS, you may need to get your iron tested and, if it is low, take oral iron supplements at a dose recommended by your doctor. Some antidepressants (with the exception of buproprion) can be beneficial. Other medications commonly prescribed are Horizant (gabapentin enacarbil) and Lyrica (pregabalin), though these tend to be expensive. Dopamine agonist medications including Sinemet, Mirapex, Requip, and the Neupro patch can help with RLS, but must be used cautiously due to the potential to “augment” or dramatically worsen RLS symptoms over time. These medications can also cause serious side effects, such as impulse control disorder (ICD), which consists of compulsive behaviors like gambling, shopping, binge eating, and hypersexuality. Low doses of opioid medications are sometimes used for chronic RLS that does not respond to other treatments.

REM sleep behavior disorder (RBD)

The part of our sleep cycle where the deepest, most important sleep occurs is during rapid eye movement (REM) sleep, when our eyes move but the rest of our body is temporarily paralyzed. In neurologic disease, sometimes the mechanism of paralysis stops working, and our body is able to move around while we are asleep, acting out our dreams. This is called REM sleep behavior disorder (RBD), and it can be quite dangerous due to the risk for injury to oneself and others. People with RBD may flail their limbs, run, fall out of bed, or even throw punches, yet they are asleep and unaware they are doing so.

RBD occurs in 50 percent of people with PD, but can also occur long before the motor symptoms and PD diagnosis. A sleep study in the lab can confirm that RBD is present.

How to manage RBD?

Safety measures can help prevent injury:

  • Move the mattress to the floor and use bed rails to reduce the risk of falling out of bed
  • Padded furniture
  • Window protection
  • Bolster pillow between bed partners
  • Consider sleeping in separate beds or rooms for safety
  • Bed alarm to alert a caregiver if the person is out of bed

Medications can reduce the occurrence of RBD:

  • Melatonin at bedtime (usually 1-10 mg dose)
  • Clonazepam (however, this can be sedating the next day)

A new drug trial is underway for treatment of RBD in Dr. During’s lab. The study drug is sodium oxybate, which has previously been approved for narcolepsy and alcohol withdrawal. Study participants have RBD, have previously tried melatonin and clonazepam, and have been unable to tolerate these medications. To learn more about the study, contact study coordinator Adrian at [email protected]

Takeaways

Parkinson’s disease worsens sleep quality.  Poor sleep leads to poor function during the day!

He recommends the following:

  • Discuss your sleep issues with your doctor
  • Address treatable issues that are affecting your sleep, such as stiffness, need to urinate, insomnia, restless legs symptoms
  • Snoring, brain fog, and headaches when you wake up can be signs of sleep apnea
  • If you have severe restless legs, you may be low on iron
  • If you are acting out your dreams, start melatonin and get a sleep study

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Question & Answer Session

Q: What percentage of people who have REM sleep behavior disorder (RBD) will go on to develop PD?

A: All people with RBD will eventually develop a neurologic disorder. It could be PD, or possibly a type of atypical parkinsonism such as multiple system atrophy (MSA) or Lewy body dementia (LBD).

Q: What types of patients do you (Dr. During) see in your clinic?

A: Dr. During sees patients with PD or other neurologic diseases who have trouble sleeping.

Q: I have dystonia. Is that because of my sleep issues or because of my PD?

A: It is unlikely to be because of your sleep issues. Dystonia is fairly common in PD, but other things can also cause it, so it is important to speak with your neurologist to see if further workup is needed.

Q: Have you found that the quality of melatonin pills is inconsistent?

A: Yes, that is sometimes the case. He recommends a couple brands that seem to be better quality: Nature Made and Naturelle. He also suggested the website Labdoor, which ranks various supplements and minerals according to the quality of their ingredients.

Q: I often crash around 2-3pm and feel like I can’t function anymore. What should I do? 

A: This is common and expected in PD, unfortunately, as well as those without PD! If you are able to nap for 20 minutes or less, do that on a regular basis. If you can’t nap without sleeping too long, instead try going outside and doing something active, like going for a walk. Sunlight and movement will help trigger your brain that it is not time to sleep. Chewing gum also signals to your brain that it is time to eat rather than sleep. And socializing with someone is another tactic that can help wake you up.

Q: Do we only dream during REM sleep?

A: No, we dream at other points during our sleep cycle. However, REM dreams are more complex and memorable. Studies indicate the dreams we remember were typically experienced during REM sleep.

Q: Does sleep position matter?

A: If you have sleep apnea, it is best for your breathing to sleep on your side, and worst to sleep on your back. For other conditions such as RBD, it does not matter what position you sleep in.