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Thread: Caregiving mother in depression

  1. #21
    Thanks for your replies guys. This is really helpful and inspiring. But the truth is, right now, I can't leave the house because of both family and financial reasons. My mom gets nervous and my dad becomes restless even if I go out after 6 pm with my friends. It will take time for them to give me that much of freedom.

    My parents are not keeping me as hostage or in their control. Apart from this issue, I am quite independent person and have a good time with my sister, dad and sometimes even with my mom.

    Also, I can't leave my mom in the emotional state that she is in. She is already going through identity crisis since my sister left and if I ask to leave too, she might completely break down.

    What I need is some help on how to make sure that my mom is out of this depression. I know therapy is an option, but I need to first get her out of this "rage and annoyance" state to get her to see that she needs help.

  2. #22
    What I need is some help on how to make sure that my mom is out of this depression. I know therapy is an option, but I need to first get her out of this "rage and annoyance" state to get her to see that she needs help.[/QUOTE]


    Sadly, there is NOTHING you can do to get her out of rage and annoyance...she has to see for herself what is going on around her...it has been my experience that when I am over the edge and ready to jump I don't see the crap...often times when I experience my bouts I stuff all the thoughts and feelings and hide them...(put on the happy face so no one knows) now seeing that it is time for me to get back into therapy and a support...
    group...perhaps your Mom is overwhelmed and has lost direction...maybe just show her this post...

    Thank you for posting this, it has really helped me...I took a walk around my house this morning and came indoors in tears...I love to garden. and take pictures of my yard...everything has died...not a flower in bloom...not a butterfly one and last year at any time you could look out and they were everywhere...all I needed to do was water...and I'd tell myself I'd do it tomorrow...that is what depression does...it robs one of doing what they enjoy...

    I hope your Mom finds the support she needs, maybe your Dad can assist with that too...I too worry about what will happen to my son when I'm dead and gone, which is why it is so important for you to do as much for yourself as possible...

    My prayer for the longest time as I crawled in bed was Dear Lord, just let me live one day longer than my son...HOW FRIGGIN SICK IS THAT....today I know he has a life beyond what I could ever imagine and will be okay without me...

    Just keep on, keeping on! hugs to you, judy

  3. #23
    Senior Member canuck's Avatar
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    Not to start a riot but your family doing so much for you is sort of a learned dependence/hostage thing in that you and they are convinced that you can't live on your own. What sort of health issues are you having? Shunt? Cord tethering, Urological or??

  4. #24
    Quote Originally Posted by canuck View Post
    Not to start a riot but your family doing so much for you is sort of a learned dependence/hostage thing in that you and they are convinced that you can't live on your own. What sort of health issues are you having? Shunt? Cord tethering, Urological or??
    They are doing a lot for me, but its not a hostage situation. I am not a simple case of spina bifida, but have many other problems too. I have spina bifida, which is a congenital problem. Also, I have many health issues, like urological problems, kidney problems, frequent UTI, low stamina, low body strength and digestive problems.

    If I go out for 3-4 hours in a day and I find myself unable to even lift a finger the next day. So, its not like I want to be this way. Nobody WANTS to be where I am. But I don't have many options.

  5. #25
    Senior Member willingtocope's Avatar
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    I don't have an answer for you. I'm sort of in the same boat...Primary Progressive Multiple Sclerosis...my wife has to do more and more for me each month. She needed to go have a cataract removed the othe day, and tried to put the normal seat back into our (my...she says) wheelchair van so her friend could drive her. She wasn't able to do it...she came back in the house crying, saying "Its never about me...its always your stuff".

    Could be your mom is going thru that...she needs something that's "about her" and not taking care of you.

    I don't know how you can make that happen...heck, I'm trying to figure out how I can make that happen...but, that sounds like the problem.

  6. #26
    Quote Originally Posted by madmaddmother View Post
    Sadly, there is NOTHING you can do to get her out of rage and annoyance...she has to see for herself what is going on around her...it has been my experience that when I am over the edge and ready to jump I don't see the crap...often times when I experience my bouts I stuff all the thoughts and feelings and hide them...(put on the happy face so no one knows) now seeing that it is time for me to get back into therapy and a support...
    group...perhaps your Mom is overwhelmed and has lost direction...maybe just show her this post...

    Thank you for posting this, it has really helped me...I took a walk around my house this morning and came indoors in tears...I love to garden. and take pictures of my yard...everything has died...not a flower in bloom...not a butterfly one and last year at any time you could look out and they were everywhere...all I needed to do was water...and I'd tell myself I'd do it tomorrow...that is what depression does...it robs one of doing what they enjoy...

    I hope your Mom finds the support she needs, maybe your Dad can assist with that too...I too worry about what will happen to my son when I'm dead and gone, which is why it is so important for you to do as much for yourself as possible...
    Thanks Judy,
    The only time that my mom is really happy is when she is decorating the house and making it prettier. So, that's why encourage her and motivate her to decorate our home.

    You must find something that makes you happy to. And even if you don't feel like doing it, just force yourself to do it. Just tell yourself, "I will do it for 5 minutes. I can assure you, after one or two days, you won't be able to stop yourself from continuing the activity.

    I am sorry about your situation, and hope that things improve soon for you.

  7. #27
    @madmaddmother,

    How are you doing? Just wondering what's going on in life! Let me know.

  8. #28
    [QUOTE=Life&Roll;1396058] It will take time for them to give me that much of freedom.

    Your statement about the parents 'giving me freedom' troubles me, along with your earlier statement that you are 'a spina bifida patient'. You are a person with spina bifida. From my own experience growing up with a significant disability, and my professional experience, I can see how difficult it may be for someone to develop the concept of independent living.

    Our adult freedoms are there for the taking by ourselves, not granted by parents. You are free to stay in the comfort of your home and have others take care of you and make the rules of your life, but at what cost?

    You sound very bright and able to figure out a plan to live an adult, independent life, with caretakers if needed.
    Very best of luck to you!

  9. #29
    Moderator jody's Avatar
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    hi life&roll,
    I have wondered how you are doing.

    I found a blog. I like this guy, he has a lot of great idea's on staying independent.
    http://lifedisabled.com/

    Im not suggesting you move out though, just putting out some links you may be interested in.

    I hope that things are going well and that your mom is feeling less stressed.
    good wishes to you,
    -Jody

  10. #30
    Super Moderator Sue Pendleton's Avatar
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    Quote Originally Posted by Life&Roll View Post
    You must find something that makes you happy to. And even if you don't feel like doing it, just force yourself to do it. Just tell yourself, "I will do it for 5 minutes. I can assure you, after one or two days, you won't be able to stop yourself from continuing the activity.
    Excellent suggestion to apply to yourself also. Believe me, I know mental illness and cued into added dementia before a doctor. Great idea to get your Mom into a doctor with you along. Might ask your Father if he wants to add to any list things he has noticed. Good start. Where I live there are a few 2 person apartments where after rehab and evaluations you are matched with someone else who has a disability. You may need to wait on state funds for this but outpatient OT and PT can also help with just general well being care. How to take care of your skin if a sore develops or rash from utis. Someday you will need to talk a caregiver through these procedures. It's great you get out with family and friends now. Maybe start with laying out your own clothing the night before. Is your closet accessible? Start small and slowly add as you feel able. I bet your Mom and dad would be surprised if you were able to turn out the dinner's salad one night, eh?

    If your Mom is depressed it may be over her fear of what will happen to you when she is no longer there. Once you add a few things she may feel better that you can learn and do some things on your own. That you know how to talk a paid caregiver through your care will also help. If you slowly add to things that require physical effort you'll have some exhausted down days. But as you add to the things that make you, you, like doing your own hair or make up you'll start to feel better yourself.

    Is the bathroom you use accessible to you? To your height and needs not the helpers at home? That and a place in the kitchen made for your height are essential.

    You can do it! And I hope your Mom can too.
    Courage doesn't always roar. Sometimes courage is the quiet voice at the end of the day saying, "I will try again tomorrow."

    Disclaimer: Answers, suggestions, and/or comments do not constitute medical advice expressed or implied and are based solely on my experiences as a SCI patient. Please consult your attending physician for medical advise and treatment. In the event of a medical emergency please call 911.

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