This seems to be a question that is not asked enough or we think what we are feeling is not as important as what our loved one is going through. This job we have taken on is a tough one and there are days when I think my "stress rope" cannot be pulled any tighter. Then there are other times that make those bad days just a memory. Do you feel like banging your head against a wall one day? And then the next day your loved one is attentive and loving and comprehends whatever you say? There are some who keep those feelings bottled up within themselves; others take the time for outside resources and others who look at sites such as this for some understanding. I do better when I have someone else to bounce my feelings off of. Let's face it....we aren't superhuman and besides ourselves and perhaps a family to take care of we now have taken on the responsibility of another human who is incapable of taking care of themselves. Do you breeze through the care giving without a problem? If so, I would like to know how you do it, maybe you can offer some new ideas; do you have feelings of frustration and need to talk about those? Come and talk and know that you can speak freely and without judgement and without finger pointing.
I am caring for my mother-in-law and have been for about 1 1/2 years. She has moderate dementia and incontinence. Other than that she is very healthy. Sometimes that short amount of time feels like 10 years and I wonder how long I will be able to do this job. I get so very tired of hearing the same thing day in and day out, but I have to remind myself that to her, each time she sees me, she is offering new information. At times I have no problems communicating with her, but it seems like more and more she cannot retain a thought longer than 5 minutes. We have had to make signs for her so she will know what she can and cannot do. So far it's working, but for how long? Maybe I will have to end up making her a "Book of Do Nots". She is on memory drugs, which don't seem to make a difference. So why do I continue to dole them out to her? I guess I'm afraid of what might happen or how she might act without them. I might have to rent a boat or buy a helmet! Sometimes I see something in her that leads me to believe that she could get aggressive and what would be my reaction to that? At the end of each and every day, after she is tucked into bed, I breathe such a sigh of relief. The "inner beast" is quiet at last, or at least for a few hours.
Pull up a chair and visit........I would like to know how you are coping everyday..be it good or with handfuls of stress.
I just wanted to tale a moment at this early time in the morning before I got back to bed and others get up to start their day to say something.
After being online for most of tonight although not on much during the day, I have found myself thinking about dysfunctional families with parents and/or siblings who use emotional blackmail against us via the ingredients of F.O.G. (fear obligation and guilt).
First, thinking about that led me to coin a new phrase F.O.G.y parents and F.O.G.y relatives. The emotional blackmailers who use Fear, Obligation and Guilt to manipulate and control or at least try to even when there are good boundaries.
Second, thinking about this reminded me how hard it is to make even the smallest choices like taking baby steps in a new direction contrary to the F.O.G.y relative or some other F.O.G.y person(s) in their life is.
Third, thinking about this led me to write a new post in the "On My Mind" section of my wall that says " In offering others help be wisely caring while being empathetically compassionate Let them know you care regardless of their choices."
In seeking to care for other caregivers as a caregiver and to care for my own self, I find tonight's reflections have been a good thing for my own soul.
Book, I hope you find a good female psychologist!
A sad reality of the medical world as it is in so many professions, people are not free or don't feel free to comment about another professional in their profession. There are both positives and negatives about this approach. And you are experiencing the negative of that approach.
My therapist never told me his opinion of my former psychiatrist until after I told him that I was no longer happy with him and had changed to another one. Then, I learn the man has a terrible reputation.
Look to see which of the ones on the list are covered by your health insurance policy. That should eliminate some from the list. Good luck!
Based on what I'm reading, the psychologist have studied more intensely on the human psyche/behavior - psychotherapy and research, personality tests. Psychologists tend to use these tests more than psychiatrists.
Our island is really small. Most physicians and nurses cannot and will not tell you who is the good or bad doctor. Even my niece who is studying to be a nurse said that she now knows the bad doctors in the hospital. But she cannot tell us who they are. Our island is too small. Word spreads fast. I'm leaning more towards a psychologist first - must be female or I won't open up - at all. Learned that from my first therapist, who was male.
Sounds like it was an all around good visit. I enjoyed reading the story of your doctor's visit and glad you felt free to share it.
I wish she had given you more guidance about selecting a therapists because here a psychiatrist does not do actual therapy.They only ask about how you are doing on your various meds and makes needed adjustments of meds like antidepressants. and wants to keep up to date about other meds that you are taking.
I'm used to the term psychologist as a label for someone who is a research psychologist like my wife who has her PhD in Social Psychology but does not practice because her degree is a research degree not a clinical practice degree. This term must also be used of people who are clinically licensed to do therapy.
I'm not sure what the difference is, but my guess is that a clinical psychologist has more training than a psychologist does.
An IMFT sounds a bit more like a specialist in the field of doing therapy who probably focus mainly on marriage therapy and family therapy more than on individual therapy.
You may want to ask her office staff about what the differences are between these categories or ask your insurance company about these fields of therapy.
And even up to this morning, I wanted to cancel my appointment and I was even willing to pay the last minute cancellation fee. I was telling myself that if I go, the doctor's going to think that I'm a hypochondriac. When I was done, the first words she said was that she is so proud of me for coming in. Despite all reasonings to not come in, I still came in. Again, saying she’s glad that I came in. FYI, other than cancer, the next high rate of deaths on this island is Suicide.
After all that, she thawed out. Was very sympathetic and caring. She asked how long have I had depressions. I said since I had PMS. She asked if any in the family has depressions. I said yes. Mom, oldest sis (breakdown and therapy), older sis and her daughter (on meds) , fave sis (therapy and meds). So, her next question was why it took me so long to seek help. I said that I hate taking pills.
She then asked me a question that I thought was odd. Maybe not so odd now – but I’m soooo glad that I answered the way I did. She asked me of my depression, what is the one thing that bothered me about it. I immediately said, “Wanting to quit my job and stay home.” I wonder what would have happened if I said that I was scared that I would kill myself? It’s a very good thing that I’m not suicidal. Just the thoughts only. Would she have had me in lock down for 3 days? {shudder}
She prescribed Citalopram. She said that she's supposed to prescribe 20mg. But she's going to start off with 10mg. I thanked her and said that I'm glad. Whenever I have new doctors, I always tell them that when I take NyQuil I only take 1 pill instead of the recommended 2. I once took 2 and had difficulty waking up. Even at 9am at work, my brain was still woozy. She said very firmly, "Yes, definitely 10mg."
I then brought up that the neurologist actually prescribed me real headache medicines - and not just Motrin. She asked what he prescribed. I said, I don't know. So, she said she will need to send a msg to the neuro for the meds. Then I said, "Oh! One of my friends told me that I needed to bring the medicine with me when I come here." She looked at me. Pause. Then asked me if I got it with me. "Oh, yea! Let me get it out of my purse." By the way, Veronica, she kept praising you for having the presence of mind of telling me that. I told her that since I couldn't remember which Cholesterol Pill that was prescribed to me - here it is. I gave her the bottle. She is very very glad that you advised me to bring it in. The Maxalt-MLT and Citalopram are major conflicts with each other.
Then she automatically got me a referral form for therapy. Therapy?!?! Ohhhh, I don't want therapy. I don't know what to say.
So this is my question. I have a choice of therapists to see. It's a list that I will go down the line and see if they have openings for new patients. In the meantime, I'm trying to figure out which ones to go to.
Do I see a: Psychiatrist? Psychologist? Clinical Psychologist? or a IMFT (Individual, Marriage & Family Therapist)?
Gees, I was trying to make this post short. It's still too long. I even deleted several sentences. Sorry for making a short story of my doctor’s visit.
At the same time, set up an appointment with the urologist. She will accompany oldest sis to the appointment since dad listens to her more than us. She's also going to work on getting dad to agree on giving me POA. I don't know if he will. He's already accusing me (behind my back) of stealing money from his bank account. I'm not exactly crazy about being his POA. To me, it ties me more firmly to him. Where my super sensitive conscience is already ruling my actions, but to have something legal like POA will definitely lock me firmly on this island. I've always told myself that as long as I have no Legal paperwork for dad, I can always pack up, tell bro of next door that I quit and that he needs to do his turn. With POA, everyone will think he's now my problem. At the same time, I'm finding myself stuck when it comes to doing things for him and the company wants me to show my POA. It's a darn if you do and darn if you don't.
Although this respite caregiver is sooo nice to us, I still don't feel comfortable. My gut feelings working. So, I haven't made an appointment for dad yet. I'm gullible. I tend to believe what people tell me. So, I believe her - yet my guts is telling me differently. I have always consistently listened to my head than my guts. So, just now, I went next door and spoke to SIL about the situation. She said Do Not Trick dad to see the urologist. If we do, he will tell everyone (with exaggeration) what we did. If we tell him he's going for the flu shot, then it's only the flu shot. Only see the urologist if he agrees to it. Yeah, right. He refuses to see one - even before he had the stroke.
I lost my wallet once and back to SAM's Club, they were calling my house using the information from my driver's license to look up my phone number.
No activity on bank accounts. My phone # was not in there. Should I call/stop at all the places?
Cannot find a pharmacy bill I was going to pay so I think its in there as well. Grrrrrrr
Best wishes everyone.
Drugs do no heal. They hide symptoms and usually cause more ill health and imbalance.
Embrace the possibility of being in control of your body and your life.
Did you tell the neurologist about your other problems, the depression, osteoporosis and allergies? if you did not call his nurse and ask her to let him know about these. The topomax will help prevent the migraines from ever starting and the Maxalt will head them off before they get a grip or at least make it possible for you to continue to function. Wish they had been available when I was at my worst. As Babalou says give the meds a real chance, They can take several weeks to be come truly effective. DO NOT JUST STOP anything on your own call the Dr. Take exactly as prescribed NOT every other day or what ever crazy idea you come up with. When you see your PCG make sure you tell her that you have seen the neurologist and the meds he prescribed. this may effect what she prescribes for your depression. Again depression meds need to be taken for up to 2 weeks before you begin to see results. Keep away from the herbals if you are using precriptions and the spiritual healers. As the saying goes "Don't mix your drinks" Not saying spiritual healers or Eastern medicine has no place just don't mix things. Tomorrow will be a better day. Much Love Book.
The emotions that you have listed sounds like depression to me which means you need a doctor for meds, a therapist for support, and some boundaries in your life to regain balance.
He asked me if I exercise, especially walking? No, I work full time, then go home to do my shift. I do have a treadmill but within 15 minutes, I'm slamming against the side bars. He said that I'm Not to use the treadmill. I'm to walk around the house - even if it's inside the house (due to bedridden dad.) /// He did the eye check and then the eye movement by following his finger; then touch his finger, touch my nose, touch his finger, touch my nose. He said that my movement was a little slow following his finger. I had to walk forward, with one foot in front of the other. Turn around. Now, close your eyes. (My eyes widened. I tend to get dizzy when I'm standing with my eyes closed.) I closed my eyes. And sure enough, I felt my body swaying. I opened it quickly.
He's prescribed 2 headache medicines. Topamax for the daily headaches that I wake up and go to sleep to. The Maxalt-MLT for when the first sign of the headache appears. Vit.B2, 100mg, take 1 in morning and 1 in evening. I'm to come back in 6 weeks to see if the meds work.
I called up the clinic and set up a consultation with my primary doctor for anxiety/depression. I hesitated on going back to her but... let's see if she will leave me with the same impression as the first time I met her. I've decided to try the meds. Several of you have mentioned to me that you're taking meds for your anxiety/depression. So, I will give it a try. As long as I don't get locked up.
Doc did the knee reflex test. My foot flew up and kicked him. He chuckled and said that I have a fast reflex. He's used to slower ones.
I need to sleep early now. Dad's new schedule is waking up at 5am, ready to eat and start his day.
Some of you had mentioned to me in my message board and even publicly on AC about Tumeric. I was watching the news in which the newsperson said that her friend takes Tumeric daily for her headaches. Her friend said that it's good for inflammation. I've been thinking of buy some for me - so that I can avoid taking those prescription headache pills.
Thank you, everyone, for the encouragement and heartfelt words to me. It's finally got me moving in the right direction - even if it is done reluctantly. I don't know how many months ago, several of you told me to see a neurologist. I finally did. I think it was years ago, that several of you have recommended that I try to get meds for my depression. I'm finally taking steps to do it. And I think it scared me too that I was prepared to quit my job, cancel my appointment with the neurologist that has prompted me to do something. {{{{HUGS}}}} to all of you. P.S... I told myself that just as I have helped others here, now others are helping me. Thank you soooo much.
I know of a family who are strong spiritually. They read the Bible daily, and go to all their religious obligations. Their whole lives are centered on the Bible and God. Their grandmother had Alzheimer. The adult daughter staying with her mom was also getting old and health problems. They put their grandmother in a nursing home. You can do that with your parents - hire someone to come in to the home like Cmag's father, or Assisted Living (where they will be others of their own age with activities aimed for them.) You can try to bring up the subject once in a while.
As for yourself, maybe give yourself a goal. For example, how to help parents maintain their independence so that you can have yours. Then, read up on it on this site by searching (top right of the page) on topics like nursing home, independent living, etc...
You may also try to get them to go to 'adult daycare'. I'd term it differently though. This can provide them to gain friends and enjoy activities with others of their generation. Again, research on this so that you understand what it's all about. And can sell it to the parents. Feel free to come and vent. I've learned that venting with siblings are so different from venting with caregivers.
I'm glad that you have found this place and feel free to open up about things.
How long have you been a widow? Have you worked through the grief over your husband's death? Do your grown children and other relatives ever offer any input about things or ask how you are holding up with all of this responsibility?
What kinds of help do your parents need for you to do for them?
I was glad to read that you are living in your own house. That is a very good boundary and keeps one from feeling in a dependent position which often comes with living back in our parent's home literally.
Given your parent's age, I feel somewhat safe is guessing that you are in your 60's and probably retired. You were ready for a new phase of your life until your husband died and your parents needed you at home. You are understandably angry over this current major unexpected change!
Ever notice that people who care for the elderly in nursing homes and assisted living homes are basically young and work 8 hour shifts which gives them a break for the other 16 hours a day?
My dad who has Alzheimer's and Parkinson's lives at home with three caregivers who are there in 8 hour shifts 3 times a day for every day of the week. He is 89 and their ages range from in their 30ties to in their 40ties.
I think that you have put yourself in an impossible position of being a senior citizen yourself trying to take care of parents who are advanced senior citizens 24/7 which no break except for 3 times a year for two weeks.
Currently, you have 42 days off out of 365 days. Frankly, that is not enough emotional/physical recharge time. At the rate you are going with so little break time you are putting your physical and mental health at risk.
I don't doubt your belief that you are doing what God wants you to do, I just wonder about the how to do it part? I think your feelings of anger each time you return would calm down if you prayerfully consider and seek the best way of how to take care of your parents' needs without totally sacrificing your own needs as a fellow human being.
I believe your anger is trying to tell you that for your own good something must change. I get the impression that your anger leads you into some depression and very often situational depression has anger underneath it which we must face and find out what it is trying to tell us if we are going to overcome it.
Did you know that 1/3 of caregivers die before those whom they are caring for?
Who takes care of your parents while you are gone for two weeks three times a year? Do your parents have any financial resources to pay for extra help? Could they afford to go to assisted living?
I'm not sure that I understand what you mean by keeping your one sister's relationship with your parents unbiased? Unbiased about what or just out of the loop as to the real challenges that you face alone each day? Why doesn't talking to your sister help? Is she a poor listener and does not want to hear what you have to say? Why haven't your tried to talk with your other two sisters or are the relationships there not very close? Have you and your sisters attempted to meet together and discuss your parents' care and realistically look at where things are now, what kind care they need now and that it is beyond just one person to do or have they abandoned you to just do this alone?
I hope you will look for and find some ways to regain balance in your life with some healthy boundaries that take care of you and your health while also taking care of your parents' needs for safety and care. It sounds like to me as if you have thrown yourself under the bus and are tiered of being run over.
I wish you the best. Keep in touch and let us know how things are going!
I was sick last weekend with a head cold and wanted to protect them. So I stayed away for 4 full days, not the usual 1 1/2 - 2 weeks. But I still felt the same way. I know it's got to be tough on them when I am not showing love and patience. But eventually I work through the feelings and settle back into a routine that gives them what they need and love.
They are always so thankful for every little thing I do, whether it's helping my dad buy something over the internet or changing a light bulb. My mom makes comments about how ever can I be so patient with them, how they would be in assisted living if it wasn't for me.
Does anyone else go through this? How do you deal with these feelings that tear up my gut and make me feel so awful?
I am so thankful to have this place to open up about things! I have tried to talk to one of my 3 sisters about this, but it really doesn't help me. She needs to keep her relationship with our folks unbiased. She brings in a fresh laugh with my mom that might be squelched if I always share my feelings & frustrations with her. So here I can be frank about my own issues without hurting my sisters.