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Committee Guidelines Validation Therapy-Communicating with the Alzheimer’s
Type
Dementia
Activity Calendars Dementia Care Plan Dictionary.
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Alzheimer's Units Policy and Procedures
Nutritional Concerns and Recommendations for Alzheimer's
and Dementia:
A Guide for Long Term Care
In-services for Long Term Care Staff
Wake Up
Reminisce and Relaxation Videos for Dementia

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show your pride in being a certified Dementia Practitioner!
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Members
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Neil, Carol J. RN MSN
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Wiesen, Marianne LNHA, ADC, Licensed Nursing Home Administrator, Certification
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Canadian Nursing Home Magazine
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Please
feel free to post this newsletter
on your web site or email it to
a colleague. Enjoy the summer and remember
to provide fluids during all activity
programs and through out the day.
Lynn Biot Gordon
LCSW, CDP
Sandra Stimson CALA, ADC, CDP
Lisa Reidinger LNHA, CSW, CTRS, CDP
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SUPPORT GROUPS ARE A NECESSITY IN EVERY
LONG TERM CARE SETTING
Sandra Stimson CALA, ADC, CDP
Executive Director
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There
are several kinds of support groups that
are
held in long term care facilities.
One that benefits the caregivers who provide
care in the home, another is to support the
residents living in healthcare facilities and
finally the support group for families with
loved ones residing in a health care facility.
A variety of support groups should be offered.
A social worker was overheard stating, “we
don’t offer support groups because my
residents and families don’t need it!)
Support groups offer support, provide education
and camaraderie.
Support groups
should be offered to residents, families
and the community,
at minimum on a
monthly basis. It is strongly recommended that
families and residents not attend the community
support groups. One big reason is that families
have different issues and concerns vs. community
care givers. Family caregivers have ongoing
issues related to the facility care, clothing,
medications and discharge. Additionally, they
need emotional support and education related
to their loved one’s diagnosis and end
of life decisions. At times they have concerns
that are facility-specific that would be best
discussed on site, rather than in a larger
community setting. Families of loved ones providing
care in their home have a whole range of different
issues. They are seeking education, emotional
support and tips on dealing with 24 hour care
giving.
Residents should
have their own support group. For example,
it is imperative
to have discussions
and information about dementia. They have many
issues to contend with such as wanderers coming
into their rooms, dealing with disruptive behaviors
and communication issues. Many are afraid they
may one day have dementia. The residents need
to be informed and educated. Often times, the
resident’s are not as patient as they
could be toward a dementia resident. Education
and support offers the residents the tools
to deal with difficult situations. They need
the same kind of education as the families
and the community. Because most long term care
settings now have 60 to 80 percent dementia,
it is imperative that the residents have support
groups. Other topics could be developing self
esteem in the elderly, spirituality, bereavement
or adjusting to nursing home placement. Men
living in long term care settings especially
would benefit from support groups.
Depending on the needs of the group, the support
group may meet monthly or more often as needed.
The group sessions should be about 1 hour.
If you are providing food, you may want the
meeting to run a little longer.
The facilitator
should plan for a speaker several times a
year to
address specific questions,
issues and concerns. A speaker can be someone
from an agency, association, organization,
hospital speaker’s bureau, Geriatric
Care Manager Association, clergy, facility
department head and of course, the social worker.
You don’t want your support group to
turn toxic which can happen for many reasons.
One common reason is a participant who does
all the talking. It is best to address this
head on and utilize a timer or hour glass.
The participant should speak when they have
the timer as it’s important to hear from
everyone. Make sure to explain the rules of
the timer or hour glass. If someone is speaking
too long, simply say, “Thank you for
your input, but we need to move on and hear
from everyone.” Allow time for the participants
to respond to questions or concerns. Remember,
you don’t have to have the answers to
everything. Let the group provide input, as
many have ideas and suggestions. When someone
asks a question, repeat the question and ask
the group for their input.
Be sure to advertise
the date and location of the resident’s
and family support groups in the monthly
calendar, facility newsletter
and on the bulletin boards.
A nice touch
is to provide a journal to the residents
who attend the support group meeting
as they may wish to take notes or write down
their thoughts. Always thank the residents
for coming, as it takes a lot to bare their
soul.
Support groups
should be planned and advertised at times
convenient
to the group you are hoping
to serve. For example, elderly home care givers
would prefer a midweek early afternoon as many
don’t want to drive at night. A light
lunch should be offered. Younger care givers
might want an evening support group due to
commitments of family and work. A light dinner
should also be offered. For your community
support groups you should advertise in the
local paper, local TV stations, Office on Aging
and with your local Alzheimer’s support
organizations. There are many care giver web
sites you may wish to also post your monthly
meetings. If you have a web site, you should
post the information on your site. Try to always
keep the meeting dates and time the same, for
example, the 3rd Thursday of the month at 1:00
P.M.
Always have a table set up with resources,
brochures and current treads for the participants
to review. Offer clean fresh copies as no one
will want to read a faded copy. Let the participants
know they are welcome to leave information
on the table as well.
The facility should
offer support groups for families of loved
ones
with dementia living
on the Alzheimer’s dementia units. These
can be held monthly or quarterly. Let your
families vote on how often they wish to meet.
You should plan the dates of the meetings and
the topics to be discussed a year in advance.
It is recommend that by the 1st week in January
you have posted the dates of the meeting. Families
should not bring their loved ones (from the
dementia unit) to the meeting as this can impede
the flow of the discussion. Always provide
a fact sheet on the topic to be discussed.
Allow time for the speaker and time for the
families to ask questions.
There are many
topics that can be discussed at the community,
resident
and family support
groups. The Alzheimer’s Association www.alz.org
has free fact sheets. These should be downloaded
and kept in your library. Always provide a
fact sheet of the topic you will be discussing.
Each time you meet, discuss one of the fact
sheets. Be sure to have a sign in sheet and
write down the topic on the sign in sheet so
you will remember what you discussed. It is
important to provide seasonal fact sheets as
well, such as “Preparing for the Holidays” and “Recommended
Gifts for the Dementia resident.”
Do not give out names, phone numbers or addresses
of the members of your support group. If they
want to provide that information to another
member of the group, they will. If possible,
print business cards with your name and contact
information. Never give your home phone number.
At every meeting, let the participants know,
that should they have an emergency they should
dial 911. For families of residents or residents
residing in the health care setting, they should
immediately seek out the nursing staff.
For wonderful ideas and suggestions on how
to run your support group please visit www.njgroups.org,
The New Jersey Self Help Group Clearing House
or American Self Help Group Clearing House
http://selfhelpgroups.org or http://mentalhelp.net/selfhelp/
The New Jersey web site has fantastic resources,
such as; How To start a self help group, structuring
a meeting, finding a guest speaker, ground
rules, possible discussion questions, how to
keep the meeting upbeat, providing mutual support,
group evaluations, getting the members involved,
over coming group and member issues, facilitating
the group, etc. If you have never run a group
this is the best web site to go to for lots
of information. You should purchase a 3 ring
binder and download the information and place
in a notebook. In this notebook, you should
also place one of every fact sheet listed (place
in a sheet protector) on the Alzheimer’s
Association web site so you have a clean master
fact sheet. As you find articles and other
resources, add those to your notebook.
Another resource is the Closed Captioned Media.
They have a free catalogue and free in-service
videos. They will mail the videos to you at
no charge. Their web site is www.cfv.org
You should have at least two support group
facilitators so one can fill in should you
not be able to attend the group. Be sure
to keep the support group members names,
addresses, phone numbers, cell phone numbers
and email addresses list updated. Always
obtain an emergency contact number in the
event of an emergency. You never know when
a member may become ill.
If at any time you as the facilitator feel
you are in over your head or become aware of
a potential suicide risk, reach out immediately
for help, guidance and support.
Anyone can be
a volunteer support group facilitator as
it requires;
commitment, patience, good
listening skills, organization and compassion.
If you are presenting a topic that requires
specific knowledge be sure to read about
the topic before the meeting or schedule
a speaker
who is knowledgeable on the topic. If you
want to start a support group and don’t
want to run it by yourself, reach out to
the social
worker, nurse or facility clergy to assist
you with the group. Remember, you are the
facilitator and it’s your job as
the facilitator to insure that the group
runs smoothly.
Long term care communities will find the benefits
derived from the support groups to the participants
are many. What the volunteer facilitator receives
in return is priceless. For facilities that
do not have a support group, now would be the
time to begin exploring who could run your
group, the population to serve and specific
area you wish to address, such as a family
support group for your dementia unit. The support
groups can only benefit your community, facility
residents, staff and families.
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Upcoming
Seminars
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Train
the Trainer Alzheimer's and Dementia seminars
are open to consultants, in-service directors
and
corporate trainers. The seminar provides
all the necessary tools to provide comprehensive
training to staff and community. The student
will be provided with power point disk, over
head copy, master hand out student notebook,
DVD, text books and tests. The modules that
are covered are; Introduction to Dementia,
Diagnosis, Prognosis, Treatment, Communication,
Feelings, Depression, Repetitive Behaviors,
Paranoia, Hallucinations, Wandering, Hoarding,
Aggressive Behaviors, Catastrophic Reactions,
Intimacy, Sexuality, Personal Care, Bathing,
Dressing, Toileting, Nutrition, Activities,
Environment, Staff and Family Support, Diversity,
Cultural Competence, Spiritual Care, End
of
Life Issues and Pain.
Train the Trainer 2007 Dates:
September 29th Philadelphia
October 27th Dallas Texas
November 10th NYC
For those seeking CDP certification, the Alzheimer’s
and Dementia seminars are offered all over
the United States by our NCCDP approved trainers.
NCCDP
will be offering 2007 Alzheimer's and
dementia seminars for those seeking education
or pursuing CDP certification. NCCDP
will be offering 2007 Alzheimer’s
and Dementia seminars on:
September 29th Philadelphia
October 27th Dallas TX
November 10th NYC
The seminar is approved for 7 ceus by NCCAP
for Activity professionals, NJ Social Work
Board and NJ DOH for Administrators. You would
need to check with your state governing body
to see if these ceus will be accepted.
You can visit our web site at www.nccdp.org
and click on the calendar for a list of
other dates and locations. We value your
feed back;
please let us know about the Alzheimer’s
and Dementia seminar you attended. Any organization who wishes to have one of
our trainers present at your next conference
please contact us at nationalccdp@aol.com or
toll free 1877 729 5191.
__________________________________
Facility Trainings: The NCCDP approved trainers
can bring the Alzheimer’s and Dementia
seminar to your facility. Please email us at
nationalccdp@aol.com or call our toll free
number at 1 877 729 5191 for information and
availability.
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CDP
Benefits
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Many times we are asked what
the benefits of certifications are. We have
provided this information and the benefits
for the facility, staff, resident and families.
Link to Benefits of CDP
One important comment we
hear from Administrators regarding staff
who have completed NCCDP Alzheimer’s
and dementia training, “our staff is
providing better competent care and it is directly
related to the NCCDP Alzheimer’s and
dementia training they received.” “Often
times, the only dementia training the staff
received was through videos.” Video training,
all though a great tool should never be used
as the sole way of providing dementia education.
The staffs need to be able to ask questions,
exchange ideas and provide an opportunity to
role play. Health care professionals all have
unique learning styles and not everyone will
benefit from video training. The health care
professionals who have completed training and
certification, take the CDP certification seriously
and implement many of the suggestions and tools
that were provided to them during the seminars.
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Welcome
New CDP’s
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Allen, Dana LVN
Allen, Janese ADC
Allison, Lisa LPN
Andrews, Belinda GNA CNA
Applewhite, Clymesa BS MS
Atwood, Pamela MA
Battle, Tameka CTRS
Bens, Dorothy RN
Blan, Toni CNA HCA
Bojocquez, Carol
Branum, Kimberly RN
Buettner, Sandra ADC
Burns, Dorothy CNA CMA
Carter-Karpel, Trudi CSW
Catherine, Steiner LPN
Chapman, Amy OTR, MSRS
Couliboly, Tracey ADC-P
Crowley, Karon
Dollar, Jacqueline LNHA
Duren, Lauren
Edwards, Diane ADC
Elentukh, Izina
Entzl, Scott MS
Evans, Deborah LPN
Fox, TenaCNA
Franklin, Veronica RN
Friend, Kellee COTA
Fuentes, Minerva CNA HCA
Fuller, Sarah RN
Gonzalez, Leticia CSW
Goulet, Rosemary LNHA
Gray, Janet RN
Guidry, Deana CNA HCA
Hackett, Danuta ADC
Haire, Sandra PT-A
Hale, Jane
Hankey, Rebecca
Heim, Patricia LPN
Hlabse,Jennifer LPN
Ho, Shirline LPN
James, Vicki RN
Jennine, Elardo MA
Johnson, Janice ADC
Jones, Brenda Lynn
Kret, Sandra RN
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Lansdowne,
Eileen
Leeper, PamelaBA
LeGuin, Robin
Leonards, Mary LNHA
Lombardo, Tracy CALA
Loy, Ann LNHA
Lukach, Susan LISW
Lussen,Adam EMT, LPN-c
Malek, Elaine BA LSW
Manasso, Allison CALA
Mares, Jennifer HCA
Maribile, Deborah
Metcalf, Janet
Milbern, Rusti HCA
Minni, Rosemary LNHA ADPC
Myles, Betty BSN
Obertate, Anthony BBA
Pacheco, Cecilia HCA
Peguero, Wanda BS EMT
Ramirez, Veronica CNA
Reinhold, Victoria
Sabo, Julie ADC
Salmeron, Erika RN
Schellhas, Bonnie LPN
Schlachter, Ronald MT-BC
Scroggin, Lori LPN
Smith, Lorie RN NSC
Stacy Lynn, Rotherham BA
Stone, Pamela LPN
Stuttgen, Pamela CNA
Tarsitsano-Amato MA, ATR-BC, Michele
Thomet, Cindy RN
Thyne, Catherine ADC
Tsolakis, Mari LPN
Turci, Francesca CSW
Valdez, Patricia CNA CMA
Valerie, Daniel MSW LSW
Van Wyk, Nancy RN
Vang, Gena LPN
Vivian, Henning-Bailey CTRS
Wade, Tiffany ADC
Whitmore,Addie MS
Wilmott, Trixie RN
Younger, Melanie LMSW
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NCCDP
is proud to welcome our new trainers:
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Carol White MSW ACSW LCSW CDP
Charlene Brosius RN, CDP
Charles Larobis RN BSN CDP
Denise Bishop MSW,CDP
Diane Taylor BSN RN CDP
Edward McMahon Ph.D LCSW CDP
Helena Ford RN, BSPA, CDP
Janice Mullen LCSW CDP
Kathy Strang R.N. BSN LCSW CDP
Kevin Pembrook NHA, NFA CDP
Lynette Krambeer-Morney BA, ADC,CNA, CDP
Maureen Bradley ACC MSS LCSW CDP
Megan Dunfee RN BSN MS
Nancy Bourne RN BSN CDP
Nancy Dondag MA RDT BCT LCAT CDP
Pam Lancaster BS LNHA CDP
Patti Hughes RNC CDP
Sandra Burrows LCSW ACC MSS CDP
Valerie D. Bingham MA LNFA BSW CDP
Valerie Daniel MSW LSW

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COMING
SOON: CEUS ON LINE
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We
are currently in the process of automating
our free cues program. Currently, the free
CEU’s are located in the Alzheimer’s
Care Guide Magazine. Once you read the article
and take the test, the test is forwarded
by mail to the NCCDP corporate office for
grading and a certificate. Once our software
is completed, the CDP’s will be able
to read the article in the Alzheimer’s
Care Guide Magazine or their Activity Magazine
and instead of mailing the test, the CDP
will simply log on to the NCCDP web site
and complete the test online. The test will
be graded immediately and if there is a passing
grade, the CDP will print out a CEU certificate.
Keep watching the web site for details.
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In
The News
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NCCDP
partnered with Fred Sganga Executive Director
of the Long Island State Veterans
Home and wrote an article for publication
in the upcoming fall publication of Advance
Magazine for Long Term Care. The article
addresses policy and procedures for dementia
units. If you do not currently receive this
publication, you can log on to the web site
and sign up for the magazine. http://long-term-care.advanceweb.com/ We recommend the Policy and Procedure manual
for Dementia units at www.activitytherapy.com
web site.
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Associate
Membership and Corporate Membership
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NCCDP offers individual associate
membership and corporate membership on an annual
basis.
The individual associate membership receives
a NCCDP pin and their name is placed on our
web site. The Corporate membership is provided
with a pretty and professional certificate
that can be displayed in your lobby and their
name placed on our home page as well as in
the corporate membership page. Please see our
web site for details.
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Take
Precautions During Community Outings With
Your Dementia Residents
Sandra Stimson CALA, ADC, CDP
Executive Director
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Dementia residents can attend facility trips
as long as precautions have been taken. There
are some residents who would not benefit from
attending community trips because they are
fearful once off the unit or when it is extremely
difficult to bring a dementia resident back
to the unit. The staff should discuss as a
team which residents would be appropriate and
who would benefit from a community trip. The
most important aspect to consider is the safety
of the resident.
Some questions to ask when considering a resident
for a community outing are:
1. Would they enjoy the outing?
2. Are they fearful when off the unit?
3. If they have already taken a trip, did they
enjoy the trip or were their concerns?
4. Is it difficult to return the resident to
the dementia unit?
5. Is the resident violent?
6. What safety precautions would you need to
take when the resident is off the unit?
7. If the resident is in a wheelchair, can
they maneuver their wheel chair or do they
need assistance?
8. If the resident ambulates, do they need
assistance?
9. How much additional staff would you need
if you took this resident off the unit?
10. Does the resident have proper identification?
11. Does the resident (if a wanderer) have
GPS tracking system or Project Lifesaver?
12. What type of setting are you taking the
resident too? For example, apple orchard, diner,
pet shop, etc.
13. Is the resident on a special diet? Are
adaptive devices used?
14. Is the resident on special medications
with time frames?
When ever there is a community outing, the
Director of Nursing should insure that a nursing
assistant is accompanying the residents. At
times, some communities have only taken an
activity staff member. Why take the chance
of something happening? It only makes sense
to insure that there is an appropriate number
of activity staff as well as a nursing assistant
attending the trips. Some assisted living communities
do not utilize a bus driver, which leaves only
the activity staff to drive the bus and monitor
the residents. This is a disaster waiting to
happen. There are safety concerns while on
the bus, such as falls and many concerns once
they arrive at the destination. The biggest
concern of course is someone wandering away
from the group.
The destination should be well thought out.
An activity assistant once took 8 residents
by herself to an apple orchard and parked in
a secluded location. Because of the density
of the apple orchard, she immediately lost
a resident and did not have a cell phone to
call for help. Another facility took their
residents to Statue of Liberty. Anyone who
has ever been to the Statue of Liberty will
tell you how crowded it is. The resident ended
up in New York City and was missing for 24
hours. In both situations, the residents were
found by law enforcement and were unharmed.
They were very lucky.
It is important to pick a destination that
is contained, such as a small diner or a small
pet store. Some of the trips might be a drive
through the park. Large department stores,
county fairs, etc may not be good venues for
the dementia resident. Even if the residents
are not getting off the bus, you should have
adequate staff on the bus to monitor the residents.
Once you arrive at your destination, never
leave your group unattended and constantly
do a head count. If this is someone with a
history of elopement, assign a specific staff
member to only monitor that specific resident.
Be sure that everyone in your group has an
ID bracelet with their name and name of your
community. Some facilities have the residents
all wear facility T Shirts with the name of
their community on the shirt. Plan to have
enough staff to provide safe supervision.
When planning the trip, the destinations should
be a short drive. Once there, allow about 45
minutes to an hour and than return. Anything
longer than that is probably too tiring for
the dementia resident. They would enjoy the
trip much more if it is a short duration.
Always leave with the receptionist and the
nursing departments the names of the residents
and staff who are attending the trip, time
of departure and time of return, name of location,
address and phone number. If you are contracting
for transportation, include the name on your
trip form. Additionally, provide your cell
phone number. Have the dietary department provide
drinks and snacks such as Orange Juice and
Graham crackers. Always carry a cell phone
in case of an emergency. Should there be an
emergency or an elopement, immediately notify
the facility administration staff and 911 if
necessary. If it is an elopement you should
immediately call 911 for assistance. If the
resident has Project Lifesaver, be sure to
notify the 911 operator.
Dementia residents will have an enjoyable
and safe trip as long as safety precautions
are put into place and implemented.
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