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I. How We Work in Washington. Based on your preferences, we provide you with information about one or more of our contracted senior living providers ("Participating Communities") and provide your Senior Living Care Information to Participating Communities. The Participating Communities may contact you directly regarding their services. APFM does not endorse or recommend any provider. It is your sole responsibility to select the appropriate care for yourself or your loved one. We work with both you and the Participating Communities in your search. We do not permit our Advisors to have an ownership interest in Participating Communities.
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III. When We Tour. APFM tours certain Participating Communities in Washington (typically more in metropolitan areas than in rural areas.) During the 12 month period prior to December 31, 2017, we toured 86.2% of Participating Communities with capacity for 20 or more residents.
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V. Complaints. Please contact our Family Feedback Line at (866) 584-7340 or ConsumerFeedback@aplaceformom.com to report any complaint. Consumers have many avenues to address a dispute with any referral service company, including the right to file a complaint with the Attorney General's office at: Consumer Protection Division, 800 5th Avenue, Ste. 2000, Seattle, 98104 or 800-551-4636.
VI. No Waiver of Your Rights. APFM does not (and may not) require or even ask consumers seeking senior housing or care services in Washington State to sign waivers of liability for losses of personal property or injury or to sign waivers of any rights established under law.I agree that: A.I authorize A Place For Mom ("APFM") to collect certain personal and contact detail information, as well as relevant health care information about me or from me about the senior family member or relative I am assisting ("Senior Living Care Information"). B.APFM may provide information to me electronically. My electronic signature on agreements and documents has the same effect as if I signed them in ink. C.APFM may send all communications to me electronically via e-mail or by access to an APFM web site. D.If I want a paper copy, I can print a copy of the Disclosures or download the Disclosures for my records. E.This E-Sign Acknowledgement and Authorization applies to these Disclosures and all future Disclosures related to APFM's services, unless I revoke my authorization. You may revoke this authorization in writing at any time (except where we have already disclosed information before receiving your revocation.) This authorization will expire after one year. F.You consent to APFM's reaching out to you using a phone system than can auto-dial numbers (we miss rotary phones, too!), but this consent is not required to use our service.
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I am working on state assistance for a SNF. My dad has gotten aggressive... I need my mom to be away from him so his Dr. is suggesting a behavioral health unit first then a SNF. What are these places like? Does anyone have experience with them?
Lookin4help, we had to remove her from the facility that day. They left no choice, us or the police. We took her to our house and it was several months before she was able to go to a facility that was a mental ward, no beds.
It was incredibly difficult, my mom had 2 young kids and a teenage boy on top of both her parents.
What I remember most about the facility is the door knobs were 3/4 of the way up, crazy people never look up. (No offense meant, that's what we were told) this was in the 70s and things have come a looong ways.
She stayed there until a more modern facility opened up right around the corner from our house.
It wasn't my grandma anymore for many many years before she died, it was harder on us then her, she wasn't home any longer.
Dad is at behavioral now he was at va nursing home dad has PDD it has progressed so much in last few months he has very little trimmer but his feet would get stuck to floor and he shuffled his feet very unsteady also sundowners set in. I couldn’t work and take care of him and he got to wear he couldn’t be alone anymore I stressed so much over all this. So he went into VA nursing home his doctor put him on sinement and he is not as rigid and walks good but that’s just it he became confused real bad he was only confused at nite with the sundowners but no he is confused all the time and walks all the time it’s like he doesn’t know what to do with himself it’s like he is so nervous. We the VA sent him to BH unit they took him off serequil and is giving depakote and going to lower sinement. The VA doesn’t like him walking with walker he was the only one not in wheelchair and they all the sudden said that he was having behavioral issues I have seen no proof and nurses said they never have any trouble with him. So they sent him to behavioral health. They have had no issues with him. The VA wanted him out they have ran threw his money now getting on Medicaid they wanted him out. They stated he was a fall risk its crazy you can’t believe. He was so isolated there you never see a nurse and they just walk by you and act like you don’t exist my dad said. I am looking for a secured unit now with dad sundowners and able to move around he might go in wrong room that hasn’t happened but once but he is sleeping 8 hours now and that’s a lot better. i do wish they could get something to help his manic walking but I don’t want him drugged up. It’s so hard I know you understand. I am so tired I feel as though my dads so lost he is a small helpless 74 year old man love him so so much. I am not ready for this just los mon 2 years ago. I am in this by myself just doing and learning anything I can to figure this out. thank you
This is happening to me right at this moment I was like you scared, hurt, but let me tell you it’s the best thing I could have ever done. Dad is so much better and I found that a nursing home is not so good for him since he has progressed so much. He was so isolated roaming in fear nurses walking by never communicating but in smaller facility at the behavioral place he is so content. So I am looking for secured memory care right now I feel so much better now knowing what direction I need to be looking into. The last month has been so so hard, my job,marriage I couldn’t function with worry. I was at my lowest point I can’t even explain it. I want my dad safe he is not going to get better that’s what I have to over come. But as I talked to other people a smaller secured unit they do better, it’s like they feel safer. I have seen this for myself with help of some friends. Hope this helps. I am looking at facility’s now. Let you all know about my journey hope this helps
My mother spent some months in a geriatric psychiatric hospital when she was in early stage vascular dementia, was paranoid, had delusions and was suicidal. She was thoroughly evaluated there and an anti-psychotic was recommended, She refused them for months until the delusions became so distressing to her she finally agreed. Fortunately the meds worked very well for her and she was quickly discharged to an ALF. Her experience in the geri psych hospital was good apart from her illness and her behaviour has been much more manageable since.
I believe in an SNF that there is usually a separate floor for those patients that have behavioral health issues. I know the facility my late mom was at had one.
I have an example - my parent was kicked out of an Assisted Living and went to Behavioral Health for 14 days. Now parent has been happily living in a Memory Care facility and life is a thousand times better for everyone. But is was hard to see parent in Behavioral Unit while they were adjusting meds to find the right combination.
If he is a danger to your mom or anyone else, he really needs help beyond what a non professional can provide.
This disease is so awful, it makes us choose the lesser of two evils more than seems bearable.
Do what his doctors recommend for his well being as well as that of your mom. Let them find the meds that calm him.
Dementia aggression is very dangerous as there is no reasoning with an individual that has super human strength, his brain is broken and he is in a fight or flight mode, adrenalin is maxed out so he is capable of unimaginable damage to others.
My grandma beat up 6 nurses in one fight, I saw the damage and it freaked me out how hurt these woman were, black eyes, swollen faces, jaws, lips, even a busted nose. We were called the moment she was restrained and told to come get her, right now. Uh, thanks! Imagine a man against one woman in that kind of thing, I'm afraid it would be a tragedy.
God bless you and your family on this journey of dementia and may you all be safe and cared for.
My dad just got out of his first trip to behavioral health he was there 23 days.My dad has Parkinson with dementia and has recently had couple of episodes of aggression he has never done that. VA sent him there they worked on meds to get him less aggressive and the very day they let him out he was hallucinating that was new, they assured me it takes time he went back to SNH VA that was 5 days ago and they sent him back today. They said he needed memory care now. He is not the same now, and the SNH Veterans won’t take back because they have went threw all his money and fixing to start Medicaid first of the month so I don’t know what’s next. sometimes we don’t have a choice on the matter the doctors know more I know it’s hard because I have felt like I have just been battling for dad for months. Dementia patients it’s hard I think to get a base line because there just isn’t much that can help the desease because it changes. BH in those 23 days that dad was there seen other family’s that things with there loved ones turned out great. Don’t give up, I am with ya helps to talk
Our Dad was admitted to a geriatric behavioral unit in a major hospital for assessment. He was there for several days and assessed for capacity to make his own decisions. From there the social worker and case manager helped to get him into a SNF as a rehab patient for a few weeks. For those who say never let your loved one go into a facility-my Dad was aggressive to his children and refused any/all help at his apartment. I think it is sometimes the only option. My Dad is almost 91, has vascular dementia with paranoia and hallucinations. He was eating rotten food and rinsing our disposable diapers to reuse them when he was on his own. And taking taxis to get payday loans. And drinking and hoarding. His neighbors were calling APS. No one could have had him at their home-no one. No one could stay with him-believe me-20 minutes with him and you would put yourself in a nursing home.
We had experience with a “mental” unit when one of my parents needed medication adjustments. Honestly, I think the experience turned out to be harder on me then on my parent. My mom had absolutely zero memory of being there for a week, she couldn’t wait to go back to the memory care place, and my dad couldn’t wait for her to get back to the memory care place. Although I’m not usually a big fan of drugs, after seeing what happens to people in the moderate and late stages of dementia and Alzheimer’s, I’m all for using something to make the patient less agitated and more able to function and for anything that will reduce their hallucinations or aggression. If you need to use such a facility in order to get one parent separated from another parent for safety reasons, do it! It becomes very difficult to remove an unwilling parent unless they are a danger to themselves or others and I’m sure you don’t wish to have your parent arrested first in order to be admitted under those circumstances.
My daughter says its like guality over quanity thing. Yes, the medication might make them dopey but the alternative is them being agitated all the time. Not good for them or the people around them.
I thought Behaviour units were for finding the right medication to help the violent behaviour. I think for Mom and your safety its a good idea.
When it comes to medication its finding the right one. My daughter says it takes 30 days to see if a med will work. Every person is different so its adjusting to get the right dosage. Then, if its found that med doesn't work, they have to try another.
We have had horrible luck with them. They drugged my Dad up whenever we weren't there, and when we came back the next day, he was always gorked. Investigate ketogenic diets for dementia. It worked fantastic for my Dad, until he had a fall and they moved him to a SNF where he picked up MRSA, VRE, C-diff, pneumonia and was finally allowed to dehydrate and starve for a short time when we all were sick with colds and were advised to stay home. Best to keep them at home. Vets can apply for Aid and Attendance to pay for home care.
The unit is probably attached to a hospital. Depending on the size of the hospital elderly people may have their own unit separate from other units. It's difficult to say what it's like but in general there will be a routine for your dad, 3 meals a day, snacks, he'll get his medication, he'll see his doctor but probably not everyday. There will be other elderly people there, some in various stages of dementia, some not. There will be activities but it won't be too structured. There will likely be a communal TV, he'll have assistance with showering but not everyday. There will be nurses and CNA's, he'll probably be able to wear his own clothes as opposed to a hospital gown, you'll be able to visit him while he's there.
When I was in school we did rotations through behavioral health facilities. I never saw anything alarming. Sometimes it was sad but I can understand why the doctor suggested it for your dad if he's become aggressive towards your mom. Sometimes it can take a while to get a bed in a SNF and a behavioral facility can be a good place to keep your dad and your mom safe while trying to find a more permanent solution.
By proceeding, I agree that I understand the following disclosures:
I. How We Work in Washington.
Based on your preferences, we provide you with information about one or more of our contracted senior living providers ("Participating Communities") and provide your Senior Living Care Information to Participating Communities. The Participating Communities may contact you directly regarding their services.
APFM does not endorse or recommend any provider. It is your sole responsibility to select the appropriate care for yourself or your loved one. We work with both you and the Participating Communities in your search. We do not permit our Advisors to have an ownership interest in Participating Communities.
II. How We Are Paid.
We do not charge you any fee – we are paid by the Participating Communities. Some Participating Communities pay us a percentage of the first month's standard rate for the rent and care services you select. We invoice these fees after the senior moves in.
III. When We Tour.
APFM tours certain Participating Communities in Washington (typically more in metropolitan areas than in rural areas.) During the 12 month period prior to December 31, 2017, we toured 86.2% of Participating Communities with capacity for 20 or more residents.
IV. No Obligation or Commitment.
You have no obligation to use or to continue to use our services. Because you pay no fee to us, you will never need to ask for a refund.
V. Complaints.
Please contact our Family Feedback Line at (866) 584-7340 or ConsumerFeedback@aplaceformom.com to report any complaint. Consumers have many avenues to address a dispute with any referral service company, including the right to file a complaint with the Attorney General's office at: Consumer Protection Division, 800 5th Avenue, Ste. 2000, Seattle, 98104 or 800-551-4636.
VI. No Waiver of Your Rights.
APFM does not (and may not) require or even ask consumers seeking senior housing or care services in Washington State to sign waivers of liability for losses of personal property or injury or to sign waivers of any rights established under law.
I agree that:
A.
I authorize A Place For Mom ("APFM") to collect certain personal and contact detail information, as well as relevant health care information about me or from me about the senior family member or relative I am assisting ("Senior Living Care Information").
B.
APFM may provide information to me electronically. My electronic signature on agreements and documents has the same effect as if I signed them in ink.
C.
APFM may send all communications to me electronically via e-mail or by access to an APFM web site.
D.
If I want a paper copy, I can print a copy of the Disclosures or download the Disclosures for my records.
E.
This E-Sign Acknowledgement and Authorization applies to these Disclosures and all future Disclosures related to APFM's services, unless I revoke my authorization. You may revoke this authorization in writing at any time (except where we have already disclosed information before receiving your revocation.) This authorization will expire after one year.
F.
You consent to APFM's reaching out to you using a phone system than can auto-dial numbers (we miss rotary phones, too!), but this consent is not required to use our service.
It was incredibly difficult, my mom had 2 young kids and a teenage boy on top of both her parents.
What I remember most about the facility is the door knobs were 3/4 of the way up, crazy people never look up. (No offense meant, that's what we were told) this was in the 70s and things have come a looong ways.
She stayed there until a more modern facility opened up right around the corner from our house.
It wasn't my grandma anymore for many many years before she died, it was harder on us then her, she wasn't home any longer.
What is happening with your dad?
its crazy you can’t believe. He was so isolated there you never see a nurse and they just walk by you and act like you don’t exist my dad said.
I am looking for a secured unit now with dad sundowners and able to move around he might go in wrong room that hasn’t happened but once but he is sleeping 8 hours now and that’s a lot better.
i do wish they could get something to help his manic walking but I don’t want him drugged up. It’s so hard I know you understand. I am so tired I feel as though my dads so lost he is a small helpless 74 year old man love him so so much. I am not ready for this just los mon 2 years ago. I am in this by myself just doing and learning anything I can to figure this out.
thank you
I was at my lowest point I can’t even explain it. I want my dad safe he is not going to get better that’s what I have to over come. But as I talked to other people a smaller secured unit they do better, it’s like they feel safer. I have seen this for myself with help of some friends.
Hope this helps. I am looking at facility’s now. Let you all know about my journey hope this helps
This disease is so awful, it makes us choose the lesser of two evils more than seems bearable.
Do what his doctors recommend for his well being as well as that of your mom. Let them find the meds that calm him.
Dementia aggression is very dangerous as there is no reasoning with an individual that has super human strength, his brain is broken and he is in a fight or flight mode, adrenalin is maxed out so he is capable of unimaginable damage to others.
My grandma beat up 6 nurses in one fight, I saw the damage and it freaked me out how hurt these woman were, black eyes, swollen faces, jaws, lips, even a busted nose. We were called the moment she was restrained and told to come get her, right now. Uh, thanks! Imagine a man against one woman in that kind of thing, I'm afraid it would be a tragedy.
God bless you and your family on this journey of dementia and may you all be safe and cared for.
He is not the same now, and the SNH Veterans won’t take back because they have went threw all his money and fixing to start Medicaid first of the month so I don’t know what’s next.
sometimes we don’t have a choice on the matter the doctors know more I know it’s hard because I have felt like I have just been battling for dad for months. Dementia patients it’s hard I think to get a base line because there just isn’t much that can help the desease because it changes.
BH in those 23 days that dad was there seen other family’s that things with there loved ones turned out great. Don’t give up, I am with ya
helps to talk
For those who say never let your loved one go into a facility-my Dad was aggressive to his children and refused any/all help at his apartment. I think it is sometimes the only option. My Dad is almost 91, has vascular dementia with paranoia and hallucinations. He was eating rotten food and rinsing our disposable diapers to reuse them when he was on his own. And taking taxis to get payday loans. And drinking and hoarding. His neighbors were calling APS.
No one could have had him at their home-no one. No one could stay with him-believe me-20 minutes with him and you would put yourself in a nursing home.
When it comes to medication its finding the right one. My daughter says it takes 30 days to see if a med will work. Every person is different so its adjusting to get the right dosage. Then, if its found that med doesn't work, they have to try another.
When I was in school we did rotations through behavioral health facilities. I never saw anything alarming. Sometimes it was sad but I can understand why the doctor suggested it for your dad if he's become aggressive towards your mom. Sometimes it can take a while to get a bed in a SNF and a behavioral facility can be a good place to keep your dad and your mom safe while trying to find a more permanent solution.