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Female spouse w/young kids looking for mom in similar situation?
I'd love to find a caregiver like myself to exchange texts with, like our own mini support group. This is likely too specific, but ideally it would be a woman whose partner is in the early stages of Alzheimer's (like, very very early stages where most people can't tell) and whose kids are still living at home (our kids are…
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Coping with changing behaviors
My mom has alzheimers and has suddenly become agitated when viewing images of herself or others in a mirror. She is afraid that she's being watched by strangers (images in mirror) or people on tv. She also hides money, thinking others are coming to steal it. She also has no idea whether it's daytime or night. I'm at a loss…
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Struggling to Cope
Hi everyone. I'm 27 years old and two years ago my father was diagnosed with Alzheimer's. Things have been going really smooth. Up until the last few months. He's progressed somewhat quickly and I had a really jarring experience with him yesterday. He's been having conversations with himself which I just let him do, but…
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Bed bound & aggressive -looking for advice
I'm new here and looking for advice. A little background -I help care for my 84 year old father. He has late stage Alzheimer's, bed bound and completely dependent for care. Communication is difficult as his eyesight and hearing are poor and his ability to speak coherently is mostly gone. We are having a terrible time with…
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New to Alz
J & L are new to Alz. We have one support group in 52241 and we are the only active members. Our diagnosis is "Early-Stage" and we are in the upper 80s but otherwise in good health. We have freely shared our diagnosis. We are reading all we can about proper nutrition for dementia. We are active in National Senior Games…
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Guilt around visiting MCF
Hello, I’m a new member and I was referred by a Dr. to connect with some others going/gone through it. I am in my early 30s and I cared for my mom for ~4 years at our family home before it became too difficult for me to care for her. I didn’t have the skills to provide the care she needed nor the mental strength. I was in…
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New diagnosis, new to group. Having a rough ugly cry day.
I have been very emotional, ugly crying today. Today is hard, others are not- those days I am "numb". I am 41, married for 19 years, I have 5 kids ages 8, 10, 17, 18, 20. I have tested positive for PSEN1 which is one of 3 variants known to cause young onset Alzheimer’s. I have had cognitive symptoms since August 2023. I…
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Thank Your Past Self
Please take a moment and think about something you did in the past, that makes your present situation better. When I started caring for my parents, as I began each visit, I made a new note on my phone. It was always titled Thank You! Each time I benefited from one of my past actions, I put a hash tag on my note. For…
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Advice for Going Back to Work
I took FMLA for a year to assist with the new diagnosis of Alzheimers for my mom. It was intermittent FMLA so while I still worked, I was able to take off for appointments, my own mental health, and days that seemed like my mom just needed someone to be with her. I was averaging about 20 hours a week rather than my full 40…
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Not sure what to do.
Im taking care of my grandma who has been diagnosed with dementia, i started taking care of her since i turned 18, this really wasn’t a choice for me but im here and im trying my best everyday however there are things that are popping up making it difficult for me to care for her and i need help, she argues all the time i…
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X2 now
My dad was diagnosed with Alzheimer’s the Monday after Thanksgiving in 2022. Luckily, it has been progressing very slowly. He lives with my mother and is watched by her full time. On Monday, my mom was also diagnosed with Alzheimer’s. It completely threw me for a loop and I am completely devastated. I’m their only son (I…
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Self-care (for the caregivers)
I'm helping to care for a parent (ALZ) with my sister. Mom even lives in a retirement community (still independent living) so day to day I do have my own life. It is still so hard. I went to visit for lunch today and now feel exhausted and can't refocus on work. I can't even imagine how much more difficult if I had her in…
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Is there any other way to relieve agitation besides medication?
My dear grandmother was diagnosed with Alzheimer's last year, and just in the previous few months, she has gotten worse. She has been yelling, berating, and crying lately, more like a manic patient. Sometimes she yells at my grandpa, mom, and aunts over a small thing. We are all heartbroken. And she refuses to take her…
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Medicare and Leqembi
Hi! Anyone out there on Leqembi and have Medicare? My wife is on Leqembi and just turned 65 and signed up for original Part A and B Medicare. We’re wondering how much Medicare pays for Leqembi? And how much is left over for the patient to pay? The first few infusions were given when she was still on my BCBS insurance. So…
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Conflicting Neuroquant MRI and Petscan
I am have started Kisunla infusions, and after my first treatment I had a “ neuroquant MRI” in order to detect if there has been any brain hemorrhages due to the medication. The results fortunately came back negative and the report also mentioned that I do not have brain atrophy. Other MRIs have said I have more brain…
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UTI Test for Incontinent?
Hello. Is there any way a nursing home can test a patient who has Alzheimer's and is incontinent? My mom is 87, and recently, her agitation and combativeness have continued to escalate. She is hitting, biting, scratching, screaming, and, as they said, "speaking in tongues." She sleeps mainly all day and does not eat as…
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Nonstop for my dad. Need suggestions.
My mother has had dementia for 2 years. My father is taking care of her in our own home. Recently, she has been nonstop needing something after helping her just 5 minutes ago. If no one answers right away, she'll throw her cup on the floor, then she will knock her tray down. She also intentionally tries to roll of the…
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Dementia Family Dog Workshop Webinar
I started following this group that’s based in Scotland because my wife who is in the early stage of Alzheimer’s expressed interest in getting a service dog. This free webinar is an “educational workshop to guide families affected by dementia who have, or would like to get, their own pet dog”
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Hospital stay - now what?
My mom (72) has been in MC since August. Minimum assistance w ADLs. Took her to ER on Saturday bc Flu and low BP. They admitted her to monitor her heart rate, oxygen, dehydration and kidney function. Pretty much was severely dehydrated which caused the acute kidney injury and low blood pressure. She’s stable but wheezing.…
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Separating Mom & Dad
Hi y'all. My sister and I are navigating next steps for Mom and Dad. They both have ALZ. Mom is much further along in her journey, she is 80. Dad is 87. They are both in AL but Mom's needs have grown significantly and Dad prevents the caregivers from coming in due to privacy and pride. His sense of logic is dwindling and…
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Rapid Mental Decline in My 65-Year-Old Mother: Desperate for Diagnosis and Long-Term Care Solutions
Hello, I’m looking for guidance about how to get help for my mother, who has experienced rapid mental deterioration over the past year with a cycle of repeated hospitalizations and psychiatric decompensation at home. The situation is placing an unsustainable level of strain on my mother, father and the rest of our family.…
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New here
Good morning everyone. I finally took the step for myself. Talking to someone else about what is happening in my life right now and them knowing how I feel. It’s hard to tell someone who don’t know this disease to every understand. Hopefully I can remember this tool and utilize it. Well, my name is Mia. I been caring for…
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Supporting both parents
Both my parents (79 and 78) live with us in their own attached apartment. My mom (79) is in the very early stages and is still very active. My dad is struggling with her memory changes and becomes angry and frustrated with her. I am looking for how best to support my dad wand how best to support myself as we navigate this…
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I'm learning to accept this new reality
Hey I'm a 35 year old man who takes care of his mother. She lives a few blocks from me and is going through dementia. Early 2024 is when I first noticed signs. My mom is 77 years old, she is my heart, my Queen. She fights me on EVERYTHING and feels I'm taking her independence from her. I don't really get help from my…
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I didn't plan for this:
I am a fairly good planner. I was a project manager, so I know planning for things that can go wrong is wise. I have not planned for the case where I die before my DW. We have wills, POAs, and family members assigned to take over health care and financial matters. However, I have not planned for someone to take over the…
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It's been years since I've gone anywhere.
I haven't left the property in four years. I work night shifts doing chores such as feeding the farm animals. Always waiting for the cover of darkness, and have avoided daytime interactions with everyone for two and a half years. These sacrifices are what we make for our ungrateful dementia family members we care for.
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New to the group: Dad diagnosed with MCI, what now?
First time posting here, glad to have found this group! My dad is a widower and lives alone. In the past few months, his memory and cognitive skills have noticeably declined. Primary care doctor referred us to a neurologist and my dad scored 20 on the MOCA. My dad was very agitated by the appointment, said he didn’t trust…
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Thanksgiving MC
I don’t know what to do about thanksgiving. My mom is in MC. Has been since August. She keeps bringing up Thanksgiving and my sister who usually hosts. My sister and I were hoping that bringing our families together at the MC’s Thanksgiving holiday buffet celebration would help but it hasn’t. She’s fixated on Thanksgiving…
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Compassionate Use or Expanded Access options
Is anyone getting any therapies through Compassionate Use or Expanded Access programs? I saw a comment from someone in a Facebook group who was considering TB006 a compound being developed by True Binding. So it made me wonder if anyone here has considered it or other experimental options that are in development.