Sometimes, as caregivers, we don't know what to ask for, or don’t feel comfortable asking for help or sharing our problems with others — even with family and friends who are close. I put this short list together from my own experience of caregiving as well as from input from some other caregivers I know. The first quote was actually said to me in the emergency room by my dear friend and neighbor, Kelly King. She didn’t know it then, but she was modeling how to be the best kind of friend you can be in a crisis.
“I don’t really know what to say right now, but I’m here if you need me.”
During times of crisis, what a caregiver often needs is presence — the presence of a family member or a close friend — not pity, not small talk, just presence.
“I hate that you have to go through this.”
Simply acknowledging that the situation is difficult can be comforting. A little commiseration can go a long way, as long as it doesn’t turn into a long depressing rant about the situation.
“I’ll pick the kids up for you so you can stay at the hospital.”
In this same vein, any version of this works well:
“I’m on my way to the store. What groceries do you need?”
“I’m on my way to the post office. Do you need stamps?”
The caregiver does not have to ask for help, and a job gets done.
“I’ve been thinking about you. Would you have time for a visit this week? You name the time and place.”
Caregiving can be lonely at times. Some people who feel uncomfortable stay away, and caregivers have little time to go out. Reminding a caregiver that you are still a friend and allowing the caregiver to arrange to meet when and where it’s convenient is respectful and compassionate.
“You are a great caregiver.” “You’re doing everything you can.”
Encouragement can boost confidence and lift spirits. Encourage away!
Comments (25)
Please remember, we are not able to give medical or legal advice. If you have medical concerns, please consult your doctor. All posted comments are the views and opinions of the poster only.
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Family doesn't help us
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After 6 months of intermittent internet searches trying to find any info to help me cope with becoming a TBI caregiver, I am thankful to have found this website. I am still looking for helpful hints on what works when trying to help a TBI loved one learn daily living skills in the home until we can get more help from community resources.
The TBI survivor I have taken into my home is my best friend's daughter who is a 23 year old adult now (my BF was killed in the auto accident that caused her daughter's TBI when she was just 7 years old). This accident happened over 16 years ago, continued outpt rehab after her inpt. care was very inconsistent and already she has made so many improvements since I've taken her in 6 months ago but it has not been without lots of frustration. The time it is taking to get state support so that we can get community resources available to us has left me emotionally spent as I refuse to give up and try to do what I can at home to further her recovery and help her be/do her best, problem is most days it becomes a battle of wills. She says she wants to be better but is not only apathetic towards daily activities (which I know is related to her injury ) but she is so non-compliant to do the things she needs to do to get better.
Appreciate any further resource information/words of wisdom anyone has to offer. Trying to forgive myself for all the times I know I could have done better or different but this situation has just brought a lot of stress (emotionally and financially) for our family and it's hard not to at least expect some cooperation as we try to help her.
Thanks so much for providing a place to at least be able to share, I am trying to find a local support group but no luck to date.
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I wish I could contact the person who left a comment on Feb. 2014. My story is similiar but different. I just need someone to help me. I am a 38 year old female that through God's intervention has been caring for a 45 year old TBI male. Will try to make long story short. 14 years ago...shot point blank twice in head. Paralyzed on right side.
I came into his life when my church started taking out meals to people. A few months into the program he started coming to church with me. He is very limited in speech. A year ago, could only really get out yes and no. He was living alone in a very unsafe place for him to be because his family had abandoned him. He had a legal guardian, but the person took him food and cigarettes once a month and that was pretty much it. For 3 months before God intervened, they hadn't even done that. He went all winter last winter with no water. Well, I won't go into all detail....it was a horrible situation..one that no human should ever go through.
I have super limited information on his background. I have been his legal guardian for almost 4 months now and have him in my home and I am currently staying with my parents right beside my home. We are waiting on results from some tests to get him into a caregiver home program, which I hope I will start finding answers through. I've been going at this blind for 4 months now.
A recent trip to the hospital for seizures (where he basically got kicked out of 2 different hospitals when he would snap and pull all his tubes out) . This guy should have never made it for 14 years alone. But it made me realize that I wasn't capable of caring for him if I couldn't provide for his medical needs. And I realized I hadn't been prepared for what it would bring.
After coming to this site, I realized from one of the "wish they knew" articles..that I had been dealing with him better than even most loved ones care for their families. I'm not bragging, but God has given me super patience with him and a deep love for him. (Friendly)...well, i honestly compare it to a mother's love because I'm super protective of him. I don't rush him ever, but the lack of support for him and for me as far as caring for him has almost brought me completely under (mentally and physically) a few times.
All I'm doing is crying out for help somewhere!! I want someone to talk to. No one understands. You can't be around him for even a couple of hours, days even and understand it. I have support from my family and my church, but no understanding. They tell me what I'm doing is good but no one understand the difficulties I've faced. They think after spending a little time with him they understand how his brain works. I've been with him for 4 months now every single day and he still surprises me with things!! I just want someone to talk to that truly understands. I'd love to find resources to help him but I'm at a standstill.
I won't give up on him but I'm so tired and emotionally drained. I just need help and I don't know how to find it. Thanks. And I was wondering to that person who posted last, it's been a year now since you posted. If you read this...are things working out for you and your friend's daughter? My prayers are with you even if I don't know your name.
Cindy replied on Permalink
You my dear are absolutely amazing and selfless.May God grant you his peace and wisdom.
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Thank you for sharing. My husband had a concussion, brain bleed a few months ago and I cannot tell which is the brain injury and which event issue simply his stubbornness or personality. As a caregiver it is hard to figure out how to give him some responsibility so he feels needed and valued versus overseeing certain responsibilities so that bills get paid and we have some semblance of normalcy for our family.
I have to pray daily that God would clarify that question and provide an answer. I believe God's will is in this for us as a family, but somehow also for those around me as we learn to work together.