Stage 2: The Freshman Caregiver (by caregiving.com)

November 8, 2016 at 4:22 pm

I Am Beginning to Help

Stage 2: The Freshman Caregiver™

I am starting to help a family member or friend.

Who are you?
You’ve begun to help your family member on a regular basis, weekly, perhaps even a few times a week. Your duties range from errand-running and bill-paying to some assistance with hands-on care.

Your keyword: Find
–Find services that help.
–Find support that comforts.
–Find ways to enjoy your hobbies and interest.

Your Challenge
To discover solutions that work.

Your Purpose
This is your entry into the caregiving role. This is your time to experiment, to get your feet wet and see what works. This is your opportunity to learn how the health care industry works with, or in some cases, against you. Now is the time to shape your caregiving personality: What duties are you comfortable with? What duties make you uncomfortable? How well are you and your caree getting along? What situations would create overwhelming stresses for both of you? (To help you determine your caregiving personality, we’ve included information on how to create your Caregiving Mission Statement.)

This is also the time when you get a feel for the present and future budgets needed to provide the care your caree requires.

In addition, keep up with your hobbies and interests (you may be able only to keep the ones that you enjoy most), ensuring you have made a habit of spending time on your own, enjoying yourself.

As a “freshman caregiver,” what can you do?
1. Learn as much as you can about your caree’s illness, disease or condition.
Consult the local branches or chapters of national organizations such as The Arthritis Foundation, the Alzheimer’s Association, The Cancer Society. What does the future hold for you and your caree?

2. Learn how to provide proper care from health care professionals or from health care videos, manuals or books.
If your caree is hospitalized or receives short-term therapy at a nursing home, ask the staff to show you proper caregiving techniques: lifting, transfers, bathing. If you can, record the therapy sessions so you can refer to your videos when you’re providing the care at home. Or, search the Internet, including YouTube.com, for hands-on care information and tutorials.

It’s very difficult to provide care when you are unsure of what you’re doing. You’ll feel much better when you’re confident of your skills.

3. Join a support group–online or in your community.
It’s so isolating to be a caregiver! Support groups will hook you up with others in similar situations; often, you’ll learn of community resources and options from other caregivers that you were not aware of.

4. Count on regular breaks from caregiving.
Plan for regular breaks–an hour daily, an afternoon weekly, or a day monthly–whatever you can manage. Enlist the help of relatives and community services (such as a volunteer group at your local church) so you can take time off regularly. Relatives can help in many ways–through financial support, social support (calling the caree regularly just “to talk”) as well as respite support.

5. Rely on help from community organizations.
Meals on Wheels, home care agencies and day care centers, to name just a few, may offer services that your caree needs.

Contact your local Area Agency on Aging for a listing of services and organizations in your community. Visit your local medical equipment supply store to find devices and gadgets that enhance your caree’s abilities–and independence from you. Remember, allowing the help of others is a sign of strength.

In addition, ask about local, state or federal programs (like the Veterans Administration’s Aid and Attendant Care Program) that might provide financial assistance for you and/or your caree. As your caree’s care needs increase, so will the costs associated with his or her care. Understanding what programs can help, in addition to understanding what your caree can afford, will help you plan appropriately for the future.

6. Create your rhythm of helping.
You’ll want to find your flow–the rhythm of what you do, what other family members do, what you hire to get done and what your caree does. Keeping the rhythm, which will change and ebb and flow, helps you keep what’s important to you (activities, career, relationships).

7. Keep your caree’s wishes in mind.
When appropriate, ask for his or her input and ideas. Does your caree still feel good about living at home? What does your caree fear or dread? (These are also good questions to ask yourself!)

You may disagree with your caree’s lifestyle choices. You may be incredibly exasperated by your caree’s inability to accept help or make good decisions. Vent your frustations in your journal and to your support group. It’s your caree’s life, which means you want to respect his or her decisions.

If your caree suffers from a cognitive impairment, you’ll want to step in and ensure your caree’s safety. If you struggle to keep your caree safe, consider hiring a geriatric care manager who can help put solutions in place. (You can learn more about geriatric care managers and locate one near your caree here: www.caremanager.org.)

8. Reflect the changes in your journal.
How do you feel now? What are your concerns? Fears? What outcomes are you working toward? What losses have you noticed during this period? What changes in the relationship cause you to feel sad? What changes have given you comfort?

9. Start a second journal that you use to detail your caree’s needs and your caregiving responsibilities.
Note any changes in your caree’s health and condition so that you can confidently discuss your concerns during physician appointments. Use your journal as a caregiving manual, which will help when others step in to provide care. Continue to chronicle your caregiving journey in your first journal. What causes you to mourn?

10. Create a spreadsheet that details your caree’s medical history, medications, hospitalizations, treatments and changes in medical status.
A searchable document, like a spreadsheet, will be handy throughout your caregiving experience. You’ll be able to easily find details relating to important information, such as previous hospitalizations, medication changes and lab results.

11. Create the habit of regularly holding family meetings.
And, if you and your caree share a household with other family members (including children), consider creating House Rules. Rules for the household include:

–Who does what, how and when;
–Guidelines for fights, fun, and festivals (celebrations);
–Schedule of meetings and their purposes;
–Expectations in regard to support, engagement and participation.

12. Manage the money: Develop a budget, keep track of expenses, set up a filing system for bills and receipts.
Keep your caree’s expenses separate from yours and your family’s. Keep track (and receipts) of any of your caree’s bills that you pay. If you’re overwhelmed, consider having a professional, like a financial planner or bank trust officer, oversee your caree’s financial situation, including paying bills.

13. Start a Solutions Fund so you can hire solutions.
The account funds solutions for boredom, breaks and back-up plans. Contribute a monthly amount; allow yourself flexibility in how you use the monthly budget. Use the fund for your caree, for the house, for you.

Use the Solutions Fund for your caree to hire services such as home health, adult day or to purchase games from Marbles the Brain Store or products from The Alzheimer’s Store or activities from eNASCO.

Use the fund for your house (or your caree’s) to hire cleaning service, lawn maintenance, snow removal. The fund buys you services from a counselor or life coach, or for pampering services, adult education classes and activities.

Ask family members to contribute to your Solutions Fund.

14. Have back-up plans and then back-up plans for your back-up plan.
Ask yourself, “What if…” and then create a plan to manage the “What if’s.” If it can happen, most likely it will. Be ready with a plan. A geriatric care manager can be invaluable in developing your back-up plans. (Learn more about geriatric care managers and locate one near your caree.)

15. Help yourself, especially if your caree refuses help.
You may find great resources to help your caree, only to be shut down by a stubborn caree. As you spend more time with your caree, you’ll have less time to keep up with your responsibilities. Hire out services to help you, like housecleaning and lawn maintenance, as often as you can. Even if you can only afford a housecleaning service once a year, do it. And, do it when it will help you most.

In addition, keep up-to-date on community resources and providers. Although your caree may refuse help now, a day may come when you’ll need to step in with help.

16. Build your own paradise of privacy.
Call a spare bedroom or a corner in the basement your own. Add your favorite things (books, chocolate, candles, scrapbook, journal, music, TV, videos, photography, family photos) to make the space a retreat you love to use.

17. You are, and will continue to be, your caree’s most important health care provider.
You have critical knowledge of your caree’s health. More than anyone, you know your caree best, which means you are your caree’s best advocate.

18. Continue to maintain your healthy lifestyle.
Take note when the stress causes too much comfort food or too few walks. One of your best defenses against the impact of stress is a healthy lifestyle.

19. An apple a day…
What’s your apple in this stage? What helps you to feel good on a daily basis? Enjoy your apple every day.


Breast Cancer Survivor Resources in Mobile, AL

October 13, 2016 at 4:47 pm

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Support Groups:

 

“Let’s Talk” Breast Cancer Support Group (Formerly BFF)

USA Mitchell Cancer Institute

Meets First Tuesday of Each Month, 2nd Floor, Multipurpose Room

Noon till 1:00 p.m. RSVP for lunch by calling Cathy Tinnea at 251-445-9802.

 

South Alabama Ostomy and Cancer Support Group

USA Mitchell Cancer Institute

Meets 3rd Monday of Each Month, 2nd Floor Multipurpose Room

5:30 – 7:00 p.m., RSVP Barbara Phillips, 770-312-8638.

 

USA Mitchell Cancer institute – Lunch and Learn Series

Meetings Fourth Tuesday Every Month, MCI 2nd Floor, Noon.

 

“Breast” Friends Volunteer Breast Cancer Survivor Support Group

Meets every 2nd Friday of each month at Providence Hospital. Coordinator Robi Jones may be reached at 251-639-2852.

 

STRETCH – (Strength Through Recreation, Exercise, Togetherness, Caring and Health). American Cancer Society, area hospitals, and the YMCA sponsor this Exercise/Support for Breast Cancer Survivors. A calendar of six week sessions throughout the year meet at Hearin-Chandler YMCA, Tuesdays and Thursdays, 10:30 – 11:30 a.m in Studio B. Must have physician’s written approval.

Instructor Beth Reinert – 251-209-1555.

 

Camp Bluebird – Adult Cancer Camp for 3 –days and 2-nights at Camp Grace in West Mobile, campers enjoy a creative, educational atmosphere and support. Sponsored by Providence Hospital & Telephone Pioneers. For more information, contact Providence Foundation at (251) 639-2050. 2017 dates are April 12 – 14 and October 11 – 13.

 

American Cancer Society events, programs, and services

1110 Montlimar Drive, Suite 420, Mobile, AL 36609     251-344-9858

 

*Relay for Life.

*Making Strides Against Breast Cancer – Bienville Square, 3.5 mile walk to awareness and funds to end breast cancer.

*Gift Items – Wigs, turbans, hats, scarves, and puffs are available by appointment.

*Look Good, Feel Better – Free programs where cosmetologists help female cancer patients deal with the side effects of treatment by teaching them beauty techniques to enhance their appearance and self-image.

*Reach to Recovery – One-to-one support by breast cancer survivors in person or by phone.

*Road to Recovery – Free transportation service for cancer patients to get to and from scheduled cancer treatment appointments.

 

Financial Assistance

 

http://www.cancercare.org/financialOffer limited financial assistance for cancer-related costs such as transportation and childcare, and our oncology social workers can help you find resources.

Call 800-813-HOPE (4673) and speak with a CancerCare® social worker to complete a brief interview. Can be reached from 9 a.m.–7 p.m. (ET) Monday through Thursday, and 9 a.m.–5 p.m. (ET) on Friday.

 

Supplies and Services

 

http://www.careshealthservices.com/about-us.html

LYMPHEDEMA MANAGEMENT * PHYSICAL THERAPY * OCCUPATIONAL THERAPY * COMPRESSION PAIN MANAGEMENT * MCKENZIE MECHANICAL DIAGNOSIS AND TREATMENT OF THE SPINE

WEIGHT LOSS, WELLNESS & NUTRITIONAL SUPPLEMENTS

MASTECTOMY APPAREL & SPECIALTY BRAS

878 Hillcrest Road, Suite A, Mobile, AL 36695, 251-344-4212.

 

http://www.easternshoreop.com

Bras and Prothesis

Mobile location on 2504 Dauphin Street, Suite M, 36606

251-471-0071

 

http://www.advantagediabetic.com

107 North Florida Street

Mobile, AL 36606

251-661-2238

Compression Therapy and Diabetic Supplies

 

http://www.easternshoreop.com

Bras and Prothesis

Mobile location on 2504 Dauphin Street, Suite M, 36606

251-471-0071

 

http://www.advantagediabetic.com

107 North Florida Street

Mobile, AL 36606

251-661-2238

Compression Therapy and Diabetic Supplies

 

Lymphedema Information

MyLymphedema: www.mylymphedema.com

Lymphedema Network: www.lymphnet.org 1-800-541-3259

Lymphedema Awareness Foundation: www.eLymphNotes.org 1-407-324-3255

Juzo – Lymphedema garments: www.juzousa.com 1-888-255-1300

 

 

 

 

 

 

 

 

 

 

 

State Health Insurance Program Coordinator to Speak at E. A. Roberts Alzheimer’s Center

March 3, 2016 at 7:18 am

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James L. Roberson from the Area Agency on Aging will speak to the Dementia Support Group  on 2016 Medicare Updates for Dementia Caregivers at the E. A. Roberts Center on Thursday, March 10, 2016 at 10:00 am. Located at 169 Mobile Infirmary Blvd, complimentary care will be provided during the meeting.

Call 251-435-6950 for more information.

The First Stage of Caregiving

January 15, 2015 at 8:53 am

Number 6The caregiving years have been divided into six stages by Denise Brown and posted on her website, caregiving.com. If you are just entering the caregiving arena, the expectant caregiver stage may be a big help.

Stage 1: The Expectant Caregiver

In the near future, I may help a family member or friend.

Who are you?
You have a growing concern that, within the near future, your family member or friend will need more and more of your assistance and time. You’re concerned because of your relative’s age, past and present medical condition, and current living condition.

Your keyword: Ask
–Ask questions of your caree.
–Ask questions of health care professionals.
–Ask questions of lawyers and financial planners.
–Ask questions of your family members who may be involved in the caregiving role.

Your Challenge
To learn and understand your caree’s needs: health, financial and emotional.

Your Purpose
You expect to become a family caregiver; this is your time to prepare. You should research options, gather information, and provide the opportunity for your caree to share his or her feelings and values. This is also your time to concentrate on taking care of yourself–keeping up with family and friends, enjoying your hobbies and interests, pursuing your career goals.

As an “expectant caregiver,” what can you do?
1. Consult with a good lawyer familiar with eldercare issues.
Find out about durable powers of attorney for finances and health care as well as living wills; start the process to ensure your caree has the necessary legal papers in order. Ask the attorney: What do we need to know to be prepared for the future? What additional documents will we need? What should we keep in mind? (A durable power of attorney for finances and health care appoints an agent to make decisions on behalf of your caree when he or she is unable to. If you live in one state and your caree in another, consider having documents created for both states.)

2. Determine financial situations.
Knowing the financial status of your caree can help determine future health care choices. Determine monthly income from pensions and social security; learn about annuities, stock investments and bank accounts. Meet with financial planners to understand how to ensure investments last as long as possible.

3. Investigate community health care options.
Which home health care agencies offer quality, affordable home care? Which housing options are available–retirement communities, assisted living centers? Contact community organizations to request brochures and pamphlets.

In addition, consider your family member’s current living condition. Will your aging relative be able to reside safely in her home if she uses a wheelchair, becomes bed-bound? What changes can you make today that will prevent future barriers to providing care in her home? Or, are the necessary changes almost an impossibility? If so, what other options do you have: your home, an assisted living facility, a retirement community?

4. Determine the current health care providers.
Be familiar with physicians and learn as much as you can about medications.

5. Concentrate on the reality of the situations.
Keep a realistic view of your situation: What’s the worst that could happen? What’s the best possible outcome? Then, determine what options are available for each of these outcomes.

6. Start a journal; chronicle your feelings, your concerns and your actions.
You may be surprised at feelings of loss. Your preparation of the future allows you to see what your caree–and you–might lose. You both will experience changes in your relationship, your schedules, your amount of freedom. Write down your thoughts about the potential losses–and how you might be able to hang on to them, through minor adjustments and changes, for a little longer.

7. Take time to sort out your own issues.
It’s easy to overlook these issues when life seems easy. Caregiving, especially as it intensifies, will make life hard. And, it’s harder if you have unresolved emotional work as it relates to your caree or other family members.

If you have difficulty standing up for yourself or finding your voice, this is a good time to work with a therapist or life coach to gain confidence in your decisions and your voice.

Do you struggle with the idea of asking for help? Now is a good time to figure out why and start practicing. Knowing how and when to ask for help is a great skill, which will become a huge asset for you.

The Four Agreements, A Practical Guide to Personal Freedom, a book by Don Miguel Ruiz, offers insights about our personal codes of conduct. As your caregiving journey continues, you’ll interact with family, friends and health care professionals who will drive you nuts. This book will give you the tools so you can stay sane.

8. Find your best shape–physically and financially.
Find a work-out routine you like. Maximize the amount of healthy foods you eat. Pay off your debts. Save as much as you can. Uncomfortable managing money? Read books and take classes (online and in your community) to become comfortable. You’ll need to be at your best—physically, emotionally and financially.

9. Learn your caree’s life story.
Document the story in a journal, video or audio recording. Collect recipes, photos, letters, poems and records that reflect your caree’s life and achievements. Ask questions about your caree’s childhood, parents, siblings and first loves. Involve other family members, including children, in the discussions.

10. Begin each day with the knowledge that you have love.
Perhaps the toughest battles in caregiving begin within. Most battles really are about whether or not you are loved—by your caree, by other family members, by friends, by your significant other. End the battle now: Know you have the love. Know it now so you can remind yourself later.

11. An apple a day…
What can you do on a regular basis to keep yourself healthy? Be good to yourself—you are too important today (and tomorrow and every day after that) to let your own health slip. In other words, what’s your apple?

Turning 65- Get answers to Medicare Questions

May 14, 2014 at 6:08 pm

 

SARPC and the Area Agency on Aging invites you to The SHIP Monthly Medicare Birthday Bash!

With so many options and almost daily post cards arriving at your house, the choice can be confusing and a little overwhelming.

Before you turn 65 come to our monthly Medicare Birthday Bash for help.  See flier for more details.

Turning 65 – Birthday Bash flyer 5-14

“Recognizing Health Changes in the Dementia Patient” is the topic for the next Educational Dementia Support Group.

February 27, 2014 at 8:29 am

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E. A. Roberts Alzheimer’s Center hosts their monthly support group on the second Thursday of each month.  In the June meeting, Dana Adair will speak on “Recognizing Health Changes in the Dementia Patient.”   Come at 10 a.m. and join the conversation.

Complimentary care will be provided during the meeting.   Please call 435-6950 for more information.

The center is located at 169 Mobile Infirmary Boulevard in Mobile, AL  36607.

Are you searching for a skilled care facility for your loved one?

February 22, 2013 at 7:29 pm

If you would like to gain insight into the available skilled care facilities (nursing homes) in the Mobile area, I suggest you google Nursing Home ratings in Mobile.  MatchNursingHomes.org is a good place to start.  They offer ratings, bed availability and pertinent information that can help you narrow down your hunt.  Once you find some interesting prospects, call and make arrangements to visit and tour the facility.