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Mom newly diagnosed

kelli0510
kelli0510 Member Posts: 7
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Hi,
My mom was newly diagnosed with Alzheimer’s like 2 weeks ago. I’m so lost. I’m mad I’m angry I’m sad and I’m scared. I’m scared of the future and not knowing what that will look like. I feel like I’m failing my mom. Like I should have been able to prevent her getting Alzheimer’s. I have no help. It’s all on me. I feel so alone. I am trying my best and I feel like it’s not enough. Does anyone have any advice? Is it normal to feel like this?

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  • towhee
    towhee Member Posts: 616
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    Hi kelli0510, and welcome. Yes, it is normal to have those feelings. Your life has changed in a way that nobody wants and that no one is prepared for and usually doctors are no help at all in giving you guidance. This discussion board will give you good advice, there are resources and help available. You can reach out anytime to the Alzheimer's Association Helpline 800 272 3900 for both information and advice. There might be an in-person support group in your area, these can be very helpful. A good resource to start with is the book The 36 Hour Day. Others will be along to say hello.

  • kelli0510
    kelli0510 Member Posts: 7
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    thanks for that information I’ll definitely look into it. Yeah when I took my mom to the doctors he downplayed everything that I was saying and then I asked if I needed to be concerned and if she had Alzheimer’s and he said it was obvious. My mom took donezapril before and it didn’t do anything for her. I asked if she could take something else and he tried to tell me there’s no medications which I know is not true

  • H1235
    H1235 Member Posts: 1,889
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    Welcome. It is so overwhelming. I will attach a few resources for you. I found some comfort in learning all I could about dementia. Having at least some idea of what’s to come and how I might handle it was helpful for me. This group has been wonderful. When I’m faced with difficult decisions or experiences this group reminds me I’m not alone and gives me great ideas on how to handle things. Do you have all the legal things taken care of? She should have a DPOA, medical poa, will and living will. These are very important! Don’t put this off if you have done it yet. As far as medication, I believe there is a new infusion treatment, but it’s not for everyone and it’s no cure. Many take medication to help with symptoms- depression, anxiety, sleep disturbances, hallucinations and sundowning. I’m sorry you need to be here.


    https://www.nytimes.com/2025/10/17/well/anticipatory-grief.html

    https://www.alzinfo.org/understand-alzheimers/clinical-stages-of-alzheimers/

    https://www.consumerfinance.gov/consumer-tools/managing-someone-elses-money/

  • kelli0510
    kelli0510 Member Posts: 7
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    thanks so much for all of this. All I want is to not feel alone. It feels so isolating. I will definitely look into everything. My mom is in rehab now to gain strength from getting sick and they had us fill out what her next wishes are for when the time comes. Is that what a DPOA is? I’m her poa but I don’t think anything is in writing but I know what she wishes are. The sun downing is like no other and it’s hard not having support from my family. I’m left alone to figure all of this out

  • H1235
    H1235 Member Posts: 1,889
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    A DPOA will allow you to make financial decisions and legal transactions for her. If her house needs to be sold to cover her care costs this will allow you to do that. If there comes a time that you believe the best place for her is in assisted living or memory care, this document will allow you to make it happen. Unfortunately most with dementia don’t realize their symptoms or limitations. This means she may not willingly agree to this kind of move, regardless of the necessity or urgency. With a DPOA you can legally sign the paperwork. The living will states her wishes as things progress. Does she want a feeding tube, would she want cancer treatment, kidney dialysis, resuscitation(DNR). A medical poa will allow you to make medical decisions for her if she is no longer able to understand. It also allows doctors to talk with you about her care. She may agree to this now, but as dementia progresses she may get upset and tell doctors she doesn’t want them to talk to you. Without a legal signed medical poa they would not be allowed to talk with you. Everything needs to be in writing signed and notarized! Very important! Dementia care can be very expensive. If you are going to see a lawyer it might be a good idea to talk about finances as well. There may be ways to protect some of her assets. Medicaid is often necessary and can be complicated. Managing someone else’s money is a lot of pressure and you need to keep track of EVERY dollar spent.

  • kelli0510
    kelli0510 Member Posts: 7
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    that’s really helpful. I didn’t know about all of that. I’ll look into it

  • psg712
    psg712 Member Posts: 712
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    Definitely get the DPOA and the health care POA while she can still understand enough to sign for herself. That was one of the best things my mom ever did for herself- she had those documents done while she was of sound mind. Then when she was no longer able to reason and make sound decisions, I was able to step in and help her.

  • kelli0510
    kelli0510 Member Posts: 7
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    I will look into both of those things it makes a lot of sense thanks for the advice

  • StarlightDi
    StarlightDi Member Posts: 5
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    edited January 29

    This is a lot to absorb in just two weeks. You’re not expected to have it figured out yet. Of course you feel lost, angry, sad, and scared. Those are expected responses to something this heavy as you are dealing with a multitude of emotions bursting in every direction.

    And I know you know this, but even though it feels like you should’ve been able to prevent it, you didn’t cause this and you couldn't have. The fact that you’re worried you’re failing your mom is actually a sign of how much you love her and how hard you’re trying.

    Please be gentle with yourself while you process all of this. You are showing up for her even if imperfectly! And we are here with you and standing along side of you in shared circumstances, thoughts and prayers.

  • kelli0510
    kelli0510 Member Posts: 7
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    this means so much to me. I am having a rough time today and just don’t want to feel alone in all of this. It feels so isolating

  • SDianeL
    SDianeL Member Posts: 3,293
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    welcome. So sorry about your Mom. You have received excellent advice already. I will add some resources that will help you care for your Mom: read the book “The 36 Hour Day” and search online for dementia caregiving videos by Tam Cummings or Teepa Snow. They are excellent . Two things I learned here that helped me: 1) never argue with someone with dementia and 2) you can’t reason with someone whose reasoner is broken. You are not alone. We understand how you feel. 💜

  • Sandysdaughter
    Sandysdaughter Member Posts: 3
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    i’m so sorry. It seems so sudden for you. For me it was a big fight for somebody to help me diagnose her because I knew something was wrong with her (my mom) for years. It hurts because you’re losing your mom and at the same time you have to do everything for her. I am also the only one my mom has and I feel so alone, it doesn’t matter how many articles and Help books I read, nobody is giving me the real truth. like watching your mother die in front of you and nobody cares until she’s actually dead. If it helps any, you do come to some peace with that a little bit and it is not your fault! Avoid “remember when” comments, or “don’t you remember” comments. My mom is pretty gone now, but in the beginning, she really liked it when I told her own memories to her; the ones she told me my whole life. She just being around me, even if it’s just sitting on the couch or going shopping; mundane things.

    I’m so sorry you’re dealing with this alone, I feel that. How many times I have cried wanting my mother and everyone feeling my mother is right there, but she’s not.

  • EH404
    EH404 Member Posts: 5
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    so sorry and can relate. My mom has lived in memory care for 6 years and I am her only person. For supportive medical-related support, check out A Mind For All Seasons. Google it. In their paid member community ($25/month) first month free with a code - he usually shares a code in podcast interviews (try JESS that one has worked for awhile- the founder is Eric Collett - I’ll link his Spotify list. Any who, in there you have access to office hours where you can ask their medical team any & all questions. Bring your blood work, your supplements & prescriptions & they will go through all of it with you. They are up to date on ALL the latest research. Amazing people. Wishing you the best- it’s so overwhelming in the beginning. Pace yourself.

  • EH404
    EH404 Member Posts: 5
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    whoops - here’s a Spotify list of Eric Collett’s podcast interviews - he talks about dementia & brain health in general - teaching all of us how to avoid the same outcome of the person we are caring for. I’ve learned a ton from him:

    well it looks like I can’t paste a link here….. Hmm, well if you go find him on LinkedIn - Eric Collett - go to his “Featured” Section & you’ll see a link to a Spotify playlist that is most of the 35+ podcast interviews he’s done in 2025.

  • kelli0510
    kelli0510 Member Posts: 7
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    thanks so much for all of the support. I also am my mom’s caregiver. J have a sister but do her care on my own with no help. It is so isolating and depressing. I feel like everything is falling apart because I’m not in control of anything

Commonly Used Abbreviations


DH = Dear Husband
DW= Dear Wife, Darling Wife
LO = Loved One
ES = Early Stage
EO = Early Onset
FTD = Frontotemporal Dementia
VD = Vascular Dementia
MC = Memory Care
AL = Assisted Living
POA = Power of Attorney
Read more