“A Presentation on Grief” – CaregiverTeleconnection Notes

What about when you are a caregiver of someone with dementia, and they are no longer the person they were?

In this situation you are grieving the loss of the person that they were. Bill considers it somewhere in between anticipatory grief and grieving a real loss. The person that they once were is now gone, they are now a new person, and that changes the way you relate and communicate with them. The basics still apply – finding someone to talk to, trying to come to terms with the new reality. It is complicated. While you are grieving the loss of the person, they are still there with you, in a different way.

An audio recording can be accessed on SoundCloud:

https://soundcloud.com/caregiverteleconnection/a-presentation-on-grief-march-26-2020

Adrian Quintero, with Stanford Parkinson’s Community Outreach, listened to the audio conference and shared his notes.  See below.

CaregiverTeleconnection is a series of audio conferences offered by the WellMed Charitable Foundation.  You can find information about this service on their website — www.wellmedcharitablefoundation.org/caregiver-support/caregiver-teleconnection/

Robin

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A presentation on grief
March 26, 2020
Audio conference by CaregiverTeleconnection (Wellmed Charitable Foundation)
Notes by Adrian Quintero, Stanford Parkinson’s Community Outreach

Cynthia Hazel helps people with personal development, such as reducing stress, loving themselves more, and gaining skills to help round out their personalities.

Bill Moyer has a long background in grief recovery. He used to work in nursing and medical management and now is a certified hypnotherapist. He was his wife’s primary caregiver for the two years she was battling breast cancer. In 2014, he became a certified Grief Recovery Specialist with the Grief Recovery Institute.  Currently he works as a hypnotherapist, a Grief Recovery Specialist and life coach. He also volunteers with veterans with PTSD and chronic pain. He wishes to dispel some of the misconceptions surrounding coping with grief.

What is grief?

Grieving is how we deal with loss. In this webinar, the loss will focus primarily on decline in health or eventual death of loved one. There are many other types of losses we experience in life.

If your loved one is diagnosed with a degenerative condition, they will be experiencing their own feelings of loss. This might be a loss of independence, freedom, identity, financial security, among others. They may also have feelings of helplessness, anger, fear, or resentment. Your loved one may not be able to drive, or perform ADLs (activities of daily living) without assistance, or fearful of losing their own home. They might be aware of and concerned about the burden they are placing on loved ones. Likely there is awareness of their own vulnerability, including loss of physical or mental function. They could be showing signs of depression or anxiety. Your loved one could lash out, and unfortunately the easiest target is the caregiver.

The caregiver is also grieving. This may include loss of time, independence, earning potential, or relationship changes in the family.

Cynthia shares her own experience:  She is oldest of three children. Her brother was a lifelong smoker since his teenage years. He stopped in his sixties, but had chronic health issues as a result of smoking. He was working as a truck driver and was in a trucking accident while away on the road. He was in an induced coma when she and the family arrived to see him. Cynthia wanted to be able to do something, but she couldn’t and felt helpless. When he came out of the coma the family helped him move to be closer to family. For two or three months everything in her life was slowed down while she helped with his care. Unfortunately, he ended up passing away.  Cynthia took on the process of trying to settle her brother’s estate. Her feelings were “all over the place.” Sometimes these feelings were set aside to try to take care of all the estate work. She was left with a lot of grieving. She felt flat and numb a lot of the time. It took her several years to work it out. Cynthia’s mother has some short-term memory issues. It was hard because her mom didn’t always remember that the brother had passed away.  Cynthia accepted where she was, what she was going through, didn’t push herself to try to make herself recover on any specific timetable.

Misconceptions about grief

Bill says there are misconceptions surrounding grief, and people may offer unhelpful advice. People may offer such things as:

  • “I know how you feel.”  This is both not productive and not true.  Each relationship is unique.  Even if you’ve experienced something similar, it’s not the same.
  • “Oh he’s in a better place,” or “at least she isn’t suffering.” These may be true statements, but it doesn’t address the feelings in the moment, and the immediacy of the loss.
  • Provide advice about staying busy.  It’s simply a distraction, it doesn’t address the grief.
  • Time limits on grieving.  Also not helpful.  As time passes, it doesn’t necessarily mean the grieving passes. The only caveat is, regardless of how long the grieving is going on, if at any time the process causes you to be less able to go through normal routines of taking care of yourself. If these become interrupted, seek out professional help.
  • Advice about replacing the loss – “at least you have family/friends, etc.”  This ignores that you are coping with immediate loss, and that life has been upended.
  • Any other advice on how you should or shouldn’t feel, or should or shouldn’t act.  Those are completely unhelpful, and out of place.

What is helpful to say to someone who is grieving?

Dealing with grief takes action.  It’s a process.  It involves facing the loss, and coming to terms with the current reality.  You are now facing a new reality from here forward.  There is no correct or incorrect way to grieve.  You are going to feel what you feel.  The only caveat is if you’re contemplating harming yourself or others, in which case professional help should be sought.

If you want to help someone who is grieving, simply be there. Listen to what the griever has to say. Be a “heart with ears.” As you’re listening, there’s no evaluation, judgment, criticizing or advising.

Offer to help, but only if you are sincere with your offer.

Help where you can (watching kids, pet care, transportation, cooking, be there with going through estate or dealing with a funeral home, etc.)  Griever may be reluctant to ask for help, or may not be aware of what need help they need.

Things to remember when dealing with grief

  • This is a highly emotional time. It’s good to avoid making any major decisions, especially financial or legal decisions one may regret later.
  • Deal with the emotions. There is no wrong way to grieve (as long as no contemplation of harm to self or others)
  • Get help, seek out someone you can trust and talk to.
  • Allow yourself time- whatever time it takes. Grieve in the way you need to grieve.
  • Try to understand most folks around intend to be of help but don’t know how to, as they don’t know what you are going through.
  • Work towards coming to terms with your new reality.

It’s extremely rare that relationships are all good or all bad. There are usually ups and downs. It’s important to take a close look at the relationship. Remember the good times and take stock of times that were more difficult. The process includes making apologies when appropriate, offering forgiveness. (for anything perceived to contribute to the difficulties). Come to terms with any other difficult emotional components (maybe the person had a difficult childhood, etc.) This helps to release some of the inner emotions, including maybe some of the wishes of things we wish we hadn’t said or done.

Where Bill works, they don’t use the word “closure” with their grieving clients. Losses are life-changing events, and for that there is no closure. They prefer the term “completion.” Complete the relationship as it was, and come to terms with the new reality. The physical relationship has reached its completion, but the emotional and spiritual relationship continues on.

Writing a letter

The Grief Recovery Institute developed the Grief Recovery process. This includes expressing forgiveness, apologies, emotional understanding, and saying goodbye. This can be used for any relationship, including a living person not in our lives anymore.

This process is for the griever, not for the person lost. It is for you to come to terms with the change in reality, and to be able to move forward in a new way.

After writing the letter, they suggest finding someone who can listen to you (a “heart with ears”) read the letter out loud. This can help add to the completion concept. Any symbolic measure that helps you feel like you’re letting it go- could be burning the letter, crumpling it up, burying it, etc. Whatever helps you release and be ready to put energies into what’s to come.

Anticipatory grief (or pre-grieving)

Is grieving now over a potential or suspected loss in the future. It may be an ill family member with a terminal illness. It can also be the result of dwelling on an event that is imagined- one that may occur in the distant future, or may never occur at all.

It is experiencing similar feelings as in grieving process; emotions and behaviors as if the event has occurred, such as sadness, anxiety, fear, sleep disruption, changes in appetite, short temper, inability to focus, etc.

Grieving now over what’s not happened yet robs you the opportunity to enjoy the here and now, the current relationship as it is, or to potentially repair a damaged relationship. Anticipatory grief could interfere with being able to provide adequate care to a loved one. Try to find someone to talk to to help with this. Be kind to yourself, and those you care for. Take breaks, get help. Take time to breathe. Life is complicated, beautiful, rewarding and tragic – often all at the same time.

Questions & Answers

What about when you are a caregiver of someone with dementia, and they are no longer the person they were?

In this situation you are grieving the loss of the person that they were. Bill considers it somewhere in between anticipatory grief and grieving a real loss. The person that they once were is now gone, they are now a new person, and that changes the way you relate and communicate with them. The basics still apply – finding someone to talk to, trying to come to terms with the new reality. It is complicated. While you are grieving the loss of the person, they are still there with you, in a different way.

What about anger when dealing with someone with dementia?

Anger is going to come up, both for the person who is experiencing the changes as well as the caregiver. Again, going back to the basics. Do something to deal with the feelings. It’s perfectly normal to have the feelings, not out of the ordinary by any means.

What about coping with loneliness after a loss?

Try to create some semblance of a normal life. There will be good days and bad days. Even years later it is normal to have days of sadness, missing your loved one. It’s important to find activities you can engage in, and people you can relate to. Find ways you can re-insert yourself into what is now normal life.

 

“Medical Decision Making in the Face of Serious Illness” (and COVID) – Webinar Notes

The Coalition for Compassionate Care in California (CCCC) is hosting a series of webinars on advance care planning. While these webinars are generally for healthcare professionals, lay audiences can still benefit, particularly if you are looking for some ideas on how to raise the topic of advance care planning with a loved one. (The webinars seem to be scheduled for Wednesdays at noon PT. To register, see coalitionccc.org/covid-conversations-education)

The first webinar, on Wednesday, April 8th, was about advance care planning in the time of COVID. It was 70 minutes, including about 15 minutes for questions.

With COVID-19, there is a renewed sense of urgency for us all to start or continue having conversations with our loved ones about our wishes and their wishes. If we have a chronic medical condition or if we are in the vulnerable group, do we want to go to a hospital if that’s needed? Would we want to be placed on a ventilator? For a set period of time (10-14 days, for example)? What if there is a shortage of ventilators, would we forego one for ourselves?

Many of us put off the conversation about advance care planning. But, if we aren’t willing to have this conversation now — during the COVID pandemic — will we ever be able to have it? (I should point out that a single conversation will not suffice. Experts envision continuing conversations as our own medical circumstances change.) During the webinar, the point was made that we have lots of time now to reflect and discuss things with our loved one.

One of the Coalition’s best references for lay people is this conversation guide:

coalitionccc.org/wp-content/uploads/2013/12/CCCC_ACP_Conversation-Guide_June2014.pdf

You can also use the webinar as a guide in your conversations. The recording is here: (registration required)

register.gotowebinar.com/recording/1207588529342067969

Also, I’ve shared my notes below from the webinar. I’ve tried to add in time-stamps in case you want to forward the recording to something in particular.

Much of the webinar was a review of advance health care directives and the POLST form. Here’s what was new to me:

COVID-specific:

#1 – Given COVID, our preferences for ventilation and hospitalization should be discussed.

#2 – “What you should know before you need a ventilator”

nytimes.com/2020/04/04/opinion/coronavirus-ventilators.html

The author of this New York Times article presents several questions we should ask ourselves including:

* what do I value about my life? (This is the usual question.)

* if I will die if I am not put in a medical coma and placed on a ventilator, do I want that life support?

* if I do choose to be placed on a ventilator, how far do I want to go? Do I want to continue on the machine if my kidneys shut down? Do I want tubes feeding me so I can stay on the ventilator for weeks?

#3 – If you have serious lung, heart, or kidney disease, you should be given an opportunity to complete a POLST at this time, because of COVID.

#4 – You can put COVID-specific instructions in Section B of the POLST. (You can find a POLST at capolst.org)

General:

#5 – We should discuss our values, including what can/can’t be sacrificed or compromised. What is acceptable to us? How do you complete this sentence —

“I’d rather die in comfort than _____”
(example – being unable to recognize my spouse)

#6 – I thought that a POLST should be completed by everyone in a care facility. In fact, CCCC is opposed to this. (You can find a POLST at capolst.org. Talk to your physician about completing it, after having a conversation with your physician.)

A POLST should be completed if the person:
– has a serious illness
– is medically frail
– has a chronic progressive condition
– could be reasonably thought of as being within 1-2 years of death. (This is called the “surprise” question for physicians — would you be surprised if your patient died in the next year or two?)

Read all about advance care planning in the time of COVID below…

Robin

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Acronyms used:
ACP – advance care planning
POLST – physician orders for life-saving treatment
HCP – healthcare professional
AHCD – advance health care directive
AD – advance directive
HC – healthcare (as in, HC agent)
SNF – skilled nursing facility
EOL – end of life (as in, EOL option act)

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Medical Decision Making in the Face of Serious Illness
Webinar by Coalition of Compassionate Care of California
April 8, 2020

Notes by Robin Riddle, Brain Support Network

Speakers:
Karl Steinberg, MD, medical director, Hospice by the Sea
Judy Thomas, JD, CEO, CCCC (Coalition for Compassionate Care in California)

Objectives of the call:
* Explain the importance of conversations in advance care planning and POLST
* Describe purpose and content of an advance health care directive and POLST
* Explain the difference between a POLST form and a health care directive
* Discuss how the COVID-19 crisis is impacting advance care planning and POLST.


(1:40) JUDY THOMAS:

Californians can live well in the face of serious illness, including COVID-19

New CCCC campaign: “COVID Conversations”
Importance of having conversations about serious illness (and palliative care)

coalitionccc.org/covid-conversations-toolbox/

Advance care planning (ACP) is a series of conversations over time about:
* what is important to the individual (hopes, goals, and concerns about the future)
* the realities facing the individual (diagnoses, abilities, limitations, resources, treatment preferences)

Benefits of ACP from the person’s perspective
* increases likelihood that wishes will be respected at end of life
* achieves a sense of control
* strengthens relationships (between individual, family members, and healthcare providers)
* relieves burdens on loved ones (such as surrogates)
* eases sharing of medical information around confidentiality (HIPAA)
* provides opportunities to address life closure

Benefits of ACP from the healthcare perspective:
* person-centered care
* avoid unwanted or unnecessary care
* improved family and caregiver relations
* helps to reduce moral distress among healthcare providers. (Moral distress can be expressed as PTSD at a societal level.)

Everyone should have a chance to have their:
* wishes explored
* wishes expressed
* wishes honored

Conversations about serious illness should be happening normally — at kitchen table, in religious settings, etc.

Continuum of ACP process over time (which relies on conversations over time):
* at age 18, complete an advance directive;
* update periodically;
* if diagnosed with a serious, chronic, or progressive illness, complete a POLST form.



(12:12, but he starts addressing these topics at 13:08)
KARL STEINBERG

How is COVID-19 impacting conversations about ACP and POLST?
* created a sense of urgency
* people are actually talking about serious illness, end-of-life, and their wishes
* we have time to reflect and interact with our families (even over Skype or FaceTime)
* threat of death
* lots of media stories
* not business-as-usual
* can’t have face-to-face conversations

Lots of great resources out there, including CCCC, Conversation Project, Prepare for Your Care, CAPC (Center to Advance Palliative Care), and Five Wishes. These websites are getting lots of traffic. And legacy.com.

So much better to plan ahead. We know things are going to get worse.

Ramped up use of palliative care services.

What HCP (healthcare professionals) need to hear from patients:
* surrogate: who is to speak for the patient if incapacitated
* treatment wishes: given COVID-19, ventilation and hospitalization should be addressed; resuscitation (CPR)
* values, goals, preferences: what makes life worth living; what can/can’t be sacrificed or compromised; what needs to be completed before death; what is acceptable to the patient (“I’d rather die in comfort than _____” – unable to recognize my family, for example); special faith-based or cultural preferences

What patients need to hear from HCP:
* ask what they know and what they want to know
* diagnoses
* threats to wellbeing and function
* natural progression of underlying disease process — including COVID-19, based on their specific health conditions
* treatment options and likely outcomes: benefits; risks and burdens; short and long-term results/expected outcomes; alternative interventions/treatments; course of disease with no aggressive intervention; comfort-focused interventions (medications, palliative sedation)


(19:06) JUDY THOMAS

This is a good opportunity to be having these conversations. (The following information is more of a reminder of best-practices.)

What is an AHCD (advance health care directive)? Tool to make healthcare wishes known when a patient is unable to communicate. Allows a person to do either or both: 1) appoint a surrogate decision-maker (healthcare agent) and/or 2) give instructions for future healthcare decisions (treatment).

If you can only do one thing for yourself, name a surrogate!

Choosing a surrogate: willing and able; available; can make difficult decisions; knows values and preferences; will speak for you despite their interests/beliefs. May or may not be the “closest family member.” Can also name whom you don’t want to speak for you.

Who cannot be a surrogate (unless the person is related to the patient): patient’s supervising healthcare provider; any employee of the institution where the patient receives care; any operator or employee of facility where patient lives.

Verbally appointed surrogate: duration of appointment is for the period of health facility stay or 60 days, which ever is shorter. A verbally appointed surrogate has priority over a healthcare agent named in a document for the specified duration.

ACP documents in CA: (three examples)
* CMA’s “My Health Care Wishes”
* “California Advance Health Care Directive” – very easy-to-understand; from Prepare For Your Care
* something prepared by an attorney (“legalistic-looking”)

For an advance directive to be legal in CA, the document is required to have: individual’s signature; date of execution; witnessed or notarized

Witnesses:
* Who cannot be a witness: patient’s HCP or employees of HCP; operator or employee of care facility; the agent named in the advance directive
* ONE of the witnesses cannot be related to patient (by blood, marriage, or adoption) or entitled to a portion of the person’s estate
* If person resides in a SNF (in CA), LTC ombudsman must witness
* Only witnessing a signature (doesn’t need to see the full document)

How can witnessing happen with social distancing?
* CCCC is pushing that a document be honored even if not witnessed. CCCC is working with LTC ombuds.
* Some notaries are setting up remote signature.

POLST (Physician Orders for Life-Sustaining Treatment):
* portable medical order
* provides instructions for specific medical treatment
* legally binding across healthcare sites in CA
* valid only if appropriately signed
* not for everyone. Including not for everyone nursing home or assisted living resident. Designed for those in late-stage illness.

Advance directive vs. POLST
AD: general instructions for future care; needs to be retrieved; many different forms; signed by patient and witnessed (or notary)
POLST: specific orders for current care; stays with patient; single form; signed by patient (or HC agent) and physician


(28:47) KARL STEINBERG

Indications for POLST form: serious illness; medically frail; chronic progressive condition; “surprise” question (would you be surprised if your patient died in the next year or two)

It’s wrong for care facilities to hand out the POLST forms.

If you want current standard of care, which is aggressive care, you don’t need a POLST.

(30:18) Indications for POLST during COVID crisis: Have the conversation! Probably expand the population who could be offered POLST because most people want to know about their prognosis in light of COVID. He doesn’t think we need a COVID-specific form. (Anything COVID-specific can be written in on Section B. Example – Some people may volunteer to forego ventilation if there’s a shortage.) Ventilator issues (10-14 days of ventilation are often needed).

These conversations should be happening for anyone with a serious, chronic condition, even if they aren’t in the last year or two of life.

If you have serious lung, heart, or kidney disease, you should be given an opportunity to complete a POLST at this time, because of COVID.

There has been discussion of blanket orders of “no CPR for all COVID patients.” (He hasn’t heard about this in CA hospitals.)

(34:18) POLST form/Section A on CPR: DNR (or DNAR) doesn’t mean “just let me die”! Section A applies if patient has no pulse and is not breathing — which means that person is dead. (This is stated on form.)

(35:44) POLST form/Section B on interventions: If you have a pulse and are still breathing, Section B is of interest. You can choose full treatment, selective treatment (“no heroics;” most people select this), or comfort-focused treatment (“hospice philosophy”; not so interested in prolonging life but interested in being comfortable).

You can be DNR (Section A) and still get full treatment (including being on a ventilator). Full treatment is everything short of chest compressions and shock. If you check “Give CPR” in section A, you must check “full treatment” in section B.

People should be aware of poor prognostics with COVID-19, ventilators, and chronic illness.

(38:00) Section B – serious questions to ask ourselves if we want to be put on a ventilator during this COVID crisis:
https://nyti.ms/3bS9h6I (Dr. Kathryn Dreger, NYT)
* what do I value about my life? (This is the usual question.)
* if I will die if I am not put in a medical coma and placed on a ventilator, do I want that life support?
* if I do choose to be placed on a ventilator, how far do I want to go? Do I want to continue on the machine if my kidneys shut down? Do I want tubes feeding me so I can stay on the ventilator for weeks?

Section B: Has a “request transfer to hospital – only if comfort needs can’t be met in current location” box. Mainly only applies to nursing homes.

(40:16) Section B: In “Additional Orders,” could say “no ventilator passed 14 days,” “no antibiotics,” “no transfusions.” (This is not always given the weight other things on the POLST are given as these aren’t physician’s orders.) Could write in COVID-specific info here.

(40:50) Section D about advance directives. Patient can orally designate a healthcare surrogate. And “specified orally” can be written on form.

Section C about tube feeding: Has been removed from some POLST forms as it’s not an emergency. But it is important for advance care planning. If you leave anything blank, the default is aggressive care.


(42:50) JUDY THOMAS

POLST Best Practices:
* should be voluntary (Shouldn’t be required for facility placement.)
* not indicated for all patients
* should be re-visited when there is unexpected or significant change of condition
* can be voided by patient at any time
* surrogate decision-makers can void or chance a POLST when circumstances change. (HCP should be involved in discussions.)

POLST is not just a check box form. It memorializes a CONVERSATION!


(44:00) KARL STEINBERG

Pre-hospital DNR form (CMA form) is still recognized. Only relates to CPR. Requires both patient and physician signatures.

Key elements in conversations (from the HCP perspective):
* openness to talk, listen, and trust
* preferences for info and family disclosure
* understanding of their illness
* life goals, including upcoming milestones
* fears and anxieties
* unacceptable states of health, function, or tradeoffs
* not locked in forever to decisions you make today

COVID Conversations that HCP can be having with their patients: (VitalTalk, Ariadne Labs, CAPC, others)
* “Is it OK if we talk about what’s important to you and how the new coronavirus might affect you, so we can be sure we can give you the kind of care you’d want if you got the virus? This conversation can help your family and help us, your healthcare team, if that ever happened. This is a gift to us.”

If OK, then ask:
* “What do you (patient) know about the coronavirus?”
* “What can you tell me about your other medical conditions and how they affect you?”
* “Have you thought about what might happen if you were to get this virus? Do you have any specific fears about it?” (Some people are afraid that there might not be enough ventilators. Some people are afraid that they might be sent to the hospital.)

Then say:
* “It can be difficult to predict what would happen if you got the virus, already being at risk from your [medical conditions]. Many patients get mild cases, and I hope you would be one of them, but I’m worried that you could get very sick quickly, and I think it’s important for us to prepare for that possibility.”

(48:50) Great decisions aids on CCCC website: CPR, artificial hydration, tube feeding, ventilator. Non-value laden. CPR in frail, elder population is not effective but the aid doesn’t say this in that exact language. These aids DO NOT convince people not to have treatment that they are entitled to.

(50:34) Transfer/treatment decisions:
* risks of going to hospital are greater than they usually are because of the virus
* even without COVID, preferable to treat patients in “lowest” safe care location (home, SNF, assisted living)
* issues around access to family visits may influence choices of location to receive care


(51:58) JUDY THOMAS

Managing documents: (photocopies, faxes, and scans are just as valid as original)
* give copy to healthcare agent
* make copies for other loved ones
* discuss with provider/doctor/hospital and place in medical record
* keep a copy
* bring for hospital admission

Person can always revoke directive or appoint a new agent. Best practice is to execute a new document.

If you already have a POLST, review it in light of COVID.


(53:00) Questions and Answers:

Q: How are prescriptions for self-administered medications (with EOL option act) affected?

A by Karl: Probably can’t be used for those with a positive COVID test (since the person won’t likely be alive after 2-week delay). Pharmacies still filling RXs. Doctor visits can be done via telemedicine.


Q: Chances of getting off of vents with COVID?

A by Karl: Probably 30-50% of elders are getting off of vents. Better in the younger population.


Q: If person has a POLST and they are moving to a SNF, is the POLST still good without ombuds signature?

A by Karl: Yes, unless the person wants to change his/her surrogate.


Q: Notary during COVID?

A by Judy: Notaries meeting in parking lots with person in car. Notary has hand-sanitizer and gloves. CCCC is working with state on remote notaries. Docu-sign works for a remote signature. CCCC asking for HCP to honor documents even if not properly witnessed.

A by Karl: Do a video. Not legally-binding but compelling. There are mobile notaries ($40).


(57:27) Q: How can HCP respond to questions about long-term effects of COVID on pulmonary or neurologic systems?

A by Karl: Data being collected now. We know some have chronic disabilities after ARDS (acute respiratory distress syndrome). If elder is already de-conditioned, coming off a vent is very hard and people come off even more de-conditioned.


Q: Can POLST be done via telehealth?

A by Judy: Doctor can sign and note that these are verbal orders that were discussed with patient or surrogate.

A by Karl: “Verbal consent given. Pending signature post-COVID.” Have two people sign as witnesses to MD signature.


Q:  (unknown – question not stated)

A by Judy: CCCC can share probate code for naming a surrogate verbally (if person is going into a care facility).


Q: What determines capacity to make own medical decisions?

A by Karl: If you can understand choices, appreciate differences (and consequences), express your choice, and express your reasoning, then this is what’s required. Ideally, the person says the same thing consistently over time.


Q: What if “do not transfer” box isn’t checked?

A by Karl: If “do not transfer” box is not checked, you go to hospital for any treatment you normally go to the hospital for. If you check box, you want to be treated in place unless your comfort needs can’t be met. Example – person is unconscious with low blood pressure (60/40), this person isn’t sent to hospital as the person is perfectly comfortable.


Q: Always put in coma (sedated) if put on vent?

A by Karl: Normally, yes. Very uncomfortable to be put on a vent. Part of weaning includes lightened sedation.


Q: Do you recommend a pre-hospital DNR?

A by Karl: Use the POLST.


Q: Photographs (on phone) of POLST?

A by Karl: Yes, valid.


Q: Photographs of ACD?

A by Judy: Yes, valid. Copies are valid.


Q: Don’t notaries require a thumbprint?

A by Karl: This is being waived. This is not a legal requirement but a “practice.” Get neighbors to sign in your back yard, if you can’t get a notary.

“That Discomfort You’re Feeling is Grief” (HBR)

This article in the “Harvard Business Review” is about the “discomfort” many of us are feeling at this time, given the pandemic. The author indicates that the “discomfort” is actually “grief.” We are feeling many different types of grief, in fact. One type is “anticipatory grief.” We caregivers are very familiar with anticipatory grief. And, of course those with a neurological diagnosis experience grief as well.

Here’s a short excerpt:

If we can name it, perhaps we can manage it. We turned to David Kessler for ideas on how to do that. Kessler is the world’s foremost expert on grief. He co-wrote with Elisabeth Kübler-Ross “On Grief and Grieving: Finding the Meaning of Grief through the Five Stages of Loss.” … He is the founder of www.grief.com… Kessler shared his thoughts on why it’s important to acknowledge the grief you may be feeling, how to manage it, and how he believes we will find meaning in it. The conversation is lightly edited for clarity.

The article is here:

hbr.org/2020/03/that-discomfort-youre-feeling-is-grief
That Discomfort You’re Feeling is Grief
Harvard Business Review
by Scott Berinato
March 23, 2020

The article is well worth reading, especially for what it stays about anticipatory grief.

Robin

Info on coronavirus for the Parkinson’s community – MJFF webinar notes

Yesterday, the Michael J. Fox Foundation (MJFF) offered a webinar on the novel coronavirus, COVID-19, for the Parkinson’s disease (PD) community, featuring a panel of speakers.  The panelists included Dr. David Aronoff, an infectious disease expert; Dr. Katherine Leaver, a movement disorders specialist at Mount Sinai; Dr. Caroline Tanner, a movement disorders specialist at UCSF; Ted Thompson, JD, Senior VP of Public Policy with MJFF; and Maggie Kuhl, Director of Research Communications with MJFF.

They discussed what we currently know about COVID-19 and PD, how social distancing may help prevent spread, and how to manage challenges and isolation, touching briefly on the potential impacts of the situation on PD research. The webinar ended with a Q&A session.

In a recent Brain Support Network caregiver support group meeting (conference call), one caregiver raised the issue of her husband with Lewy body dementia feeling panicked about the pandemic and worried that the caregiver was going to become sick and die.  This came up during the Q&A in the webinar:

Q: For caregivers of someone with cognitive impairment or dementia, any tips for how to approach or explain what is going on?

A: Use simple language, give reassurance that you are still there for them. They will notice the disruption in their normal routine. Try to make some kind of daily routine or reassure them, reorient them with other topics and activities to provide some relief from the news.

One subject raised during the webinar was:  what if I have Parkinson’s Disease (PD) and test positive for COVID-19?  The answer is:

Like any other illness that occurs on top of your PD, you may notice a temporary change or worsening of your PD symptoms, which is very common. If you have tremor or rigidity, this is likely to be worse. Non-motor symptoms such as anxiety can also temporarily worsen when you are ill. There isn’t a sudden worsening of your actual baseline PD, it’s just that your body is under increased stress due to the virus and has a harder time coping. Once you start to recover and improve, your PD symptoms should return to baseline.  …  PD will not necessarily make your recovery from COVID-19 slower; recovery time will depend on how healthy or frail you are in general.

For further details about the webinar, check out these notes.  Lauren Stroshane with Stanford Parkinson’s Community Outreach listened to the webinar and shared her notes here:

parkinsonsblog.stanford.edu/2020/03/information-on-coronavirus-for-the-pd-community-webinar-notes/

The webinar recording is available on the MJFF website here:  (registration required)

www.michaeljfox.org/webinar/information-coronavirus-parkinsons-community

Robin

 

Apathy (and depression) in Parkinson’s Disease – Webinar notes

Recently, PMD Alliance offered a webinar on apathy in Parkinson’s disease (PD).  Though the webinar focused on PD, the discussion of apathy is relevant to all of the disorders in the Brain Support Network community.

In my experience coordinating caregiver support groups, I have found that understanding that apathy can be a common symptom of a disease, can make the situation more manageable for the caregiver.

The panel of speakers — three movement disorder specialists, two people with PD, and a daughter/caregiver — discussed what apathy means and how it can be confused with depression, as well as some tips and strategies for living with apathy.

The webinar began with a definition of apathy as compared to depression:

Often confused with depression, apathy is a state of indifference, lack of concern or interest, and severe absence of initiative. A person who previously tended to plan or instigate activities may now be content to sit in a corner doing nothing for much of the day. Depression typically involves feelings of sadness or hopelessness, while an apathetic person might feel fine. Depression may also fluctuate, while apathy tends to be fairly constant.

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

parkinsonsblog.stanford.edu/2020/02/are-you-feeling-apathetic-webinar-notes/

Robin