I’m in my third year of caring “full-time” for my completely bedridden mother. I also go to graduate school but can mostly do that from home ( I go into work/school one to two times a week for a few hours). I’ve read a lot on this forum from 40, 50, and 60 year olds who have cared for their parents for decades, and I relate to their experiences more than I expected for how young I am. Do any that fulfill that type have advice for someone just beginning this journey? Careers, children, marriage, etc? It seems like a lot of caregivers already have careers and/or children when the caregiving started, but what about the reverse? I’m especially worried because the women in my family tend to go into menopause around 28, and I expect I’ll do the same (so my biological clock is ticking much faster than most). I don’t want to leave my mother to strange caregivers, but I also don’t want to give up one of the best decades of my life. Looking back, is there anything those long-term caregivers regret? Thanks, Silverbird
Without being morbid, what is the long term prognosis for your Mom? Could she remain in this condition for another 20-30 years?
Is your Mom communicative?
Is this the life you think your Mom would want for you?
Is this the life your Dad wants for you?
What would you like to be doing in 1 year? In 5 years? Can that happen with the current situation? How can you move toward that to make it happen?
If you can carve out a little time for yourself I would really recommend speaking with a professional councilor. You are doing an awesome thing for your Mom, but I am concerned that if it continues much longer it might affect your ability to have good relationships and outlooks. Caregivers are exhausted people. I visit my mom in her NH daily 4 hours and I have to take a nap when I get home. You’re much peppier than I am, but you’ve already realized that you didn’t want to spend the energy to add one more person to your life. You evidently want a partner and children..how much energy will that take?
Us older folks can’t put ourselves in your sneakers, just give you some motherly/grandmotherly thoughts and hugs.
But THANK YOU for calling me Wonder Woman. I get few compliments nowadays and I cherish every one.
Silver, it was a very difficult time for my dad & I. He became a very bitter man and took out his frustrations on bedridden mom and me. I remembered in my late 20's or early 30's, I saw an airplane flying overhead. I had always dreamed of moving off island, find a job and travel around the US, England & Europe. That day, as I watched the plane fly overhead, I started crying so hard. Because I knew that I would never realize my dream. Every year, I thought that this is the year my mom would die. She didn't. I spent 20 years thinking of this. She was bedridden for over 13 years - and only had one very bad bedsore - due to spending a month in the hospital. Mom was on stomache tube, 24/7 oxygen and trache. (Moral of the story: don't let the 24/7 caregiving drown out your dream. I really do admire how far you have gotten yourself. Please don't get lost from that path.)
My advice. Find outside help. When my mom was diagnosed and dad retired, he enrolled mom on the gov't program (for low income family) and requested that they break mom's 4 hour weekly allotment to 4 1-hr visits in which they would bathe mom. He applied for mom the meals-on-wheels program. And somehow, he got enrolled in the NFCS (National Family Caregiver Support program) for himself. This is only for the beginning. Eventually your mom will need more care. Please don't end up like me and my dad where mom became the center of our lives. We worked everything around mom.
Oh, does your mom have a social worker? They are a godsend! Even if we rarely see them - except once a year. But, I do strongly recommend finding outside help. The rate you're going, you will wear yourself out. It will affect your studies.. just like my caregiving affected my work. The hard part is that my dad and I knew that we needed help but we just didn't have the money to pay for it. We didn't qualify as low income. But after paying the bills, mom's pampers, wipes, etc.. we really didn't have much money left for food. Dad would refuse to eat his meals-on-wheels lunch. He would wait for me to come home from work, and insisted we split that measly food between us. It was a struggle...
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Taking care of someone who is totally immobile, is more than a FULL time job. Taking graduate level courses and trying for a social life --- also a full time job. And then there is housekeeping, meal prep, grocery shopping etc. Are you able to carve out any time for YOU?
My father works a fifty hour week, and comes home for about half an hour every day during lunch to help me with diaper changing, etc. He takes extra hours off while I’m having meetings at school. In home care left a year ago due to insurance, because “she wasn’t improving.”
Mother has an undiagnosed autoimmune disease (still undiagnosed after two years at Mayo Clinic) and it was a big success nine months ago that she was able to hold a spoon to feed herself.
Doctors predict she will need care for the rest of her life. If we are incredibly blessed, she may be able to stand after a few years of intensive therapy, but the immense pain she’s in won’t dissipate.
She has food allergies, so I make all food absolutely from scratch, clean the house, order and shop for food... everything. My paltry salary from grad school pays for my undergraduate loans and for medical supplies. That’s considered my “rent” for living at home.
I dated a coworker that I adored for two months a while ago, but it felt like it was just one more person to look after, and i left him quickly.
The caregivers were wonderful. The Agency sent out numerous caregivers so Dad could see if he felt who was a good match. Dad choose two who had a similar childhood as he did, and would laugh at Dad's sense of humor. The two caregivers were with him for over a year, even later when Dad went into Assisted Living. So don't be afraid to try caregivers for your Mom if she and your Dad can budget for this.
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