D.G. Fulford understands what it's like to be a designated daughter. She moved home to Ohio to take care of her mother when she needed help. From this experience she wrote her book Designated Daughter – The Bonus Years With Mom. The newly featured book in the Getting Better All the Time group, this story shares all of the tips and lessons D.G. learned as she sat by her mother's side.
Gather is looking for 10 lucky members to write a review of the book. Tell us if you're a designated daughter in the comments below and we'll randomly select 10 reviewers!
Comments should be made by Monday, June 30th. All reviews should be posted by Thursday, July 31st.
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Comments: 31
Here's a poem I wrote the morning of the day she died. We'd been on Hospice watch for only 8 days.
TO MOTHER
Frail bird
Tethered by the air you breathe.
Bruised and battered by the storms
of life and death.
I feed and smooth blankets
read and wash and weep.
I would take you to the window
Hold you up with trembling hands
Sing a bon voyage and watch you fly.
Sandra F.
March 28, 1997
On Valentine's Day, I was allowed to see my dad's heart because they were unable to close his chest for several days so it was visible under a dressing. It sounds awful, but to see that beating heart gave us hope and it was a gift we all needed. Later, at the rehab, days meant therapy so I got to watch, participate and encourage that part of the recovery.
Now we go to doctors' appointments and out to lunch sometimes, I tote his walker around and remind him to take his pills. Sometimes I think I act more like a parent than a kid (OK I am 45, but still, everyone needs their dad).
To see her so vulnerable, in needing so much help. It breaks my heart still to think about it, but I am so glad that I was able to be there with her. To love her through it all, to help in all the ways I could.
She lost her battle with cancer, the day after Christmas - but the time we spent together was wonderful, unmeasurable.
I also spent three weeks in a motel taking shifts with the family when my mother in law was dying of cancer in a hospital bed. I took the night shift so the others could sleep. It seems that the night time is when she would get the worst and it was always on my watch. I read scriptures to her and held her hand even after she went into a coma.
This is no uncommon for me and my husband. We are always the one who cares for the sick in our families. When we purchased our new home, we made sure it had an extra bedroom and bath for our aging parents.
We moved back home to help my folks when my dad was dying of cancer in 2001. Now my mom is 79, and she is glad to have us living here. Her and I spend a lot of time together , going out to lunch, playing Scrabble, and even playing the Wii - she loves it!
I would look forward to reading your book, and crying with it.
She was also always there for us when we were ill. I remember how she'd hold my hand and tell me how she wished she could take away my pain.
About ten years ago, it was my mother who became ill ' that day all children dread had arrived. You see she had a major stroke and the one that had always been there for us was the one now needing our help.
She was dangerously ill and to make matters worse, she had lost her memory too. I remember walking into the hospital from work, fearing the worst. When I saw my mom on the stretcher, unconcious and helpless, it made me wish I could take away her pain.
This was the day I also realized that I had suddenly become the designated daughter. Nowhere in my college or graduate education did I learn what to do when my mother burst into tears during a discussion . Or how to be patient when she realized she had lost her vocabulary and had to learn how to speak again. Nor did anyone tell me how to handle the emotions that would accompany seeing my mother fall and not being able to ever get up again , getting whisked away by EMTs,and ultimately watching her struggle with a walker..and finally watching her learn to rely on me. We should all have required courses in gerontology. Then at least we might not be shocked and scared when the parent who once seemed strong and smart and capable . . . isn't. I know about broken hips, hearing aids, orthopedic shoe, walkers, and physical therapy.
What I don't know is where my mom went, or even who she was before the words that might enlighten me disappeared. I know she loved me, and I guess that will have to do.
This can be a very lonely place but she has not only been my mother all of these years but she's also been my best friend. Losing her as she once was has been very difficult and I've mostly not dealt with the emotions because I'm too busy being strong. She deserves that! She deserves the best of everything and that includes the best part of me!
Even though we live very far apart (after never even living in separate states for more than a few months) I talk to her every day. I fly out and take care of her/visit with her every few months for 3-4 weeks at a time. I am a caregiver, I am her power of attorney. I am the 29 year old daughter of the 55 year old woman who has been reduced to child-like qualities. This woman, my mother, has always been the pillar of strength for everyone around her through her whole life. She's always been independent since a very young age because she had to be and now she can not do things for herself. It's devistating to see how it's broken her soul. I would give ANYTHING to make her better, to heal her.
Currently we are trying to find a way for her to live with us if she chooses to do so. Her insurance will not transfer out here and you have to be on Social Security Disability for 2 years before they will put you on Medicare. With the market the way it is we can't even sell our home to move out to her.
We just keep trying to move forward each day with a positive attitude. Many of my days and nights are spent doing research on new treatments for stroke patients and anything that might help aphasia.
Even with all the problems and deficits she has now, she still has the loving and caring way about her that's she's always had. She still wants to give and I think that's part of what frustrates her the most.
I will always be there for her just as she's always been there for me but now I suppose I need to find someone who can be there for me. This has been a very lonely last year and a half.
been there, done that, got the t-shirt.... took care of Ross' mom for 5+ years ... harder to NOT be the caregiver than it is to actually do it, though, I think ... my Dad needs care now... but his second wife doesn't want my help. It's more frustrating than anything I ever went through with Doris.
I worked for an agency that supported the elderly in their home care and such. I saw the behind the scene working of so many designated daughters taking care of their mothers. Whats sad is when the tables turn and the mothers are taking care of their aging daughters.
I was one of 5 designated daugthers many years ago in taking care of our mom prior to her passing. That was 24 years ago when I was 24 years old. But it wasnt just when I was 24, we took care of my mom for the previous 12 years before she died. Sometimes I wish I had been older and more wiser because now that I have worked for an agency for the aging there would have been so much more that could have been done for her.
So if you have an aging loved one that needs help there are alot of support groups out there.. and agencies that can help. You dont have to do it all alone.
Thank you Christine M. for having such a wonderful offer to people! It is so needed!
We've had ER visits for pain, numerous doctor appts., etc., etc. She will probably live to be 100 and as much as I love her, I have such mixed emotions about being the "designated daughter" As someone once said, "getting old is not for sissies". That is certainly true...for the Mother AND the Daughter.