As the largest resource of information specific to women's brain health, we are sure you will find what you are looking for, and promise that you will discover new information.
Published on: June 7, 2013
by Jan Dougherty for Huffington Post:
Joan Byrd grew up in a family of six. She and her siblings were raised to stay connected with one another no matter where they went. Each year, Joan would make the trek from Phoenix to Washington, DC to visit her older sister. After a case of shingles put her sister in the hospital, Joan learned her sister was also suffering from dementia. Her sister, who lived alone, never told anyone about the condition.
Her sister’s husband had passed away and she never had children, so the responsibility fell on Joan to provide the critical care her sister needed. Over the next few years, she got her sister’s affairs in order — everything from paying outstanding bills to making sure she had food to eat. And, Joan did this from her home in Phoenix and through visits to DC.
Joan is one of the many caregivers who provide support from across the country. According to the Alzheimer’s Association, more than 15 million caregivers provided more than 17 billion hours of unpaid care valued at $216 billion in 2012. Whether you find yourself caring for someone who lives across the country or assisting someone who lives closer, providing ongoing care for family members or loved ones with dementia is a challenging, and often exhausting long-term job. And, due to dementia’s progressive nature, caregiving can last 10 years or longer.
In the past, generations of families were able to divide caregiving tasks and responsibilities because they were larger and often lived in the same town. Today’s families are often smaller and may be spread across the country, communicating by telephone, email, Facebook or Skype.
Family members providing direct care are often isolated, and family members who don’t see the day-to-day may not understand the effects or severity of the dementing illness. This can lead to conflict, frustration, and long term dysfunction despite the best intentions of all family members.
It is important to remember that your job as a distance caregiver is to ease the burden on the direct caregiver and make the person with dementia feel at ease. It’s crucial for long-distance caregivers to understand the disease while offering meaningful help.
Here are some ways for distance caregivers to stay involved with the direct caregiver:
• Set a schedule and call the caregiver directly. Be a good listener. Use phrases like “Help me to understand,” “This must be difficult for you,” “You must be tired (frustrated, etc.),” and “What do you want to do about that?”
• Ask for copies of the medical reports so you can better understand the person’s condition.
• Read the latest information on Alzheimer’s disease or related dementia and methods of care to keep yourself in the know.
• Consider attending a caregiver support group to discover solutions for some of the problems associated with caregiving.
• Inquire about the caregiver’s health and whether they are able to get out at times.
• Offer to contact the local Area Agency on Aging to help find respite services and day programs.
• Offer to trade places for a weekend every few months so the caregiver gets a “free vacation” and you provide the necessary care.
• Always remember the important milestones in a caregiver’s life, like birthdays and anniversaries, as special days tend to be the most difficult for caregivers.
And here are some tips to stay connected with a person with dementia:
• Send cards or letters frequently.
• Speak directly to the person with dementia on the phone or via Skype. Have favorite stories of the person’s life you can share during the call.
• Always remember birthdays, anniversaries or other special occasions.
• Send photos with labels on the back that identifies everyone in the picture. In addition to pictures of family members, send images of your home, your new dog, or a vacation that speak about your life.
• When visiting, don’t forget to build in leisure time to spend with the person. Try to stick with the person’s regular routine to avoid agitation or confusion.
• Depending on the person’s condition, dinner at home may be less stressful than going out. Listen closely about limitations and try to keep activities to no more than 90 minutes.
• If the person doesn’t communicate well, listen anyway and keep talking. Don’t expect the person to remember the activity. You are doing this for moments of enjoyment, not to create new memories.
Remember, it’s the little things that count as you assist in the care of a loved one with Alzheimer’s or a related dementia from afar. Because caregiving is sometimes overwhelming, it’s important to appreciate the support of everyone in the situation which helps overcome the unique challenges in care for your loved one.
Thirty-six million people worldwide suffer from Alzheimer’s disease and dementia. In Canada, 25,000 new cases are diagnosed each year. Those sobering numbers have researchers around the globe racing to come up with new ways to...
he Food and Drug Administration issued new guides on drug development for neurological disorders. This sets the stage for possible treatments for Alzheimer’s. The disease-oriented development guide documents will provide details on how researchers...
For young adults with autosomal dominant Alzheimer’s disease (AD), molecular markers can identify changes associated with the disease before clinical onset, according to a study published online Feb. 12 in JAMA Neurology. Yakeel T. Quiroz, Ph.D., from Massachusetts...
The material presented through the Think Tank feature on this website is in no way intended to replace professional medical care or attention by a qualified practitioner. WBHI strongly advises all questioners and viewers using this feature with health problems to consult a qualified physician, especially before starting any treatment. The materials provided on this website cannot and should not be used as a basis for diagnosis or choice of treatment. The materials are not exhaustive and cannot always respect all the most recent research in all areas of medicine.