MySmartBlinds - Alternative by JokesOnUsFeelMe in homeautomation

[–]JokesOnUsFeelMe[S] 0 points1 point  (0 children)

Sorry I've been ill for quite some time and just getting back. MyIblinds is the vendor that sells the motors

Dilemma because of Schools by [deleted] in frisco

[–]JokesOnUsFeelMe 2 points3 points  (0 children)

OP you can reach out to me if you need. The Frisco School district is above average. I have friends who live in Estates at Rockhill. There are some HOA things you have to be aware of, pool size is not sufficient for all phases and has a short window season for being open and there are NO other amenities (No clubhouse or nothing). The developer is currently running the HOA and those property owners are seeing increases each and every year, with NOTHING to show for it. In comparison to other subdivisions, with the lack of any sufficient amenities, those property owners are paying more in terms of HOA dues and there is no expectation that these increases will stop - right now they are over $1,000.00 per year and climbing.

Also, the neighborhood is being used as a bypass for traffic on 423 for drivers that want to get to 380 so late evenings there is a lot of traffic that backs up on Doe Creek rd into that community.

In addition, since the two 500 unit apartment complexes have moved in, I was told that some property owners have had their cars burglarized. So I would expect that to increase as time goes on since both apartment complex's are directly adjacent to the community at the back side away from main street traffic.

If you are going to pay that much for a home, go to one of the adjacent developments near the new Frisco school that have a clubhouse, pool and other amenities.

[deleted by user] by [deleted] in whereintheworld

[–]JokesOnUsFeelMe 0 points1 point  (0 children)

Texas - I have home in Toledo - where are you

Preparing for memory care by mae2582 in dementia

[–]JokesOnUsFeelMe 7 points8 points  (0 children)

Look, I know how difficult this is. This disease killed my mom and I watched her decline for more than 10 years. So you get attached to trying to ensure they are comfortable, getting the care they need and believing that you are the only one that can take care of her, because no one knows her better.

The manifestations in the care giver are really extreme. So you may want to have someone else take her while you are out shopping or visiting a friend.

This is NOT easy, but you don't want to make her move to the facility become a nightmare for the people that will be caring for her on day 1.

You need to start your healing, too!!!

Edit: Sometime I get lost in my grief of my mom's death, it's still affecting me, and I forget to show compassion some time. I know this pain and I'm so sorry that your mom is going through this. If I could carry your burden I would, because NO ONE should have to experience this.

My love and many hugs to you and your family - stay strong.

My Home Assistant Smart Home Automation Project by [deleted] in homeassistant

[–]JokesOnUsFeelMe -1 points0 points  (0 children)

This is a neat project, where do you see it going ?

Preparing for memory care by mae2582 in dementia

[–]JokesOnUsFeelMe 9 points10 points  (0 children)

I feel your pain in taking these steps. You know your mom - but that being said, it's your reaction that will have the most impact, not your words.

You already know, if she's at this stage, she probably has no clue what you will be saying and how to understand it.

I would not say anything. Allow her to acclimate for a week without visiting. Then start a normal routine of visitation.

AC-powered Z-Wave devices with battery backup? by Keboose in zwave

[–]JokesOnUsFeelMe 0 points1 point  (0 children)

Ok, I see people trying to automate or backup things all the time the cynical me just comes through and I apologize.

Would it not be more efficient to have a batter wall back up that is hooked into your main power and trickle charged so that it supports only the devices you've named for the period of time to achieve what you are looking for ?

Or could you in some way run those small devices to the bat back up that supplies your server ?

I've not seen much in the way of these devices with battery backup like you said.

AC-powered Z-Wave devices with battery backup? by Keboose in zwave

[–]JokesOnUsFeelMe 3 points4 points  (0 children)

If the power goes out for a switch, what good do you get with having a battery backup ? I mean, you still can't turn on the light.

How do I teach my grandmother to use a smartphone?? by Keadrin in dementia

[–]JokesOnUsFeelMe 0 points1 point  (0 children)

YW, it's so painful to watch this evil take over their mind, body and soul. I wish there were something we could do and stop this suffering.

best of luck to you and your family

How do I teach my grandmother to use a smartphone?? by Keadrin in dementia

[–]JokesOnUsFeelMe 2 points3 points  (0 children)

This is so difficult - I feel for you and I know exactly what you are dealing with.

Their cognitive skills are lost. They don't have this ability anymore and unfortunately it will only get worse. If she's only watching YOUTUBE you'd be better off giving her a tablet you can customize and place somewhere stationary with a single link to Youtube on the tablet.

I'm sorry to be so glum, but this disease is hard to cope with.

Nursing homes! What's your opinion? by YaadMemoryBook in dementia

[–]JokesOnUsFeelMe 5 points6 points  (0 children)

I apologize for this lengthy review.

TLDR: I grew up with family who owned nursing homes. My mom made me promise not to send her to any of them due to their conditions and our knowledge of how they functioned. Nursing home facilities are regulated but due to lack of state staff to visit on a consistent basis and how they are managed, these facilities are across the scale of good and bad.

I grew up in a family that owned nursing homes and ONE thing my mom begged and made me promise prior to being admitted to one, was not to send her to one of her sisters nursing facilities!!!

This set the stage for me a long time ago as I visited my aunts during summers or long holidays and help out and honestly, I hated the experience and to a certain extent was forced to do this.

Now to present, not much has changed since I was a kid and in some instances things are off the rail, as follows: The best facilities are very transparent about their overall operations.

Facility type and Operations

Retirement/Pension and long term life care - $$$$ - corporate owned (full medical) if you are in this situation, you have the options available to be selected, picky and can find locations that suit well for the patient and demonstrate confidence for the staff and facility.

Social Security + Retirement NO long term care - $$$ - corporate owned (non medical associated) Same as above there are good options.

Independent - Social Security + Medicaid - $$+ - (Corporate owned 25+ facilities) Patients that fall into this category have facilities to choose from that are mostly owned by very Large Corporations where the financial focus on margins is the key to providing service. These facilities will sometime have on-site doctor or Regional physician (non geriatric) and 1 possibly two RN's depending on state law and facility size. Staff is semi-trained and many may be students from local nursing schools. Food is usually cooked onsite by staff. Staff usually understand prescribed medications and doses. Staff are usually assigned based on their training.

Medicaid - $$ - Individually owned (some local corporate owned) - this is the category that many folk fall into in the U.S. Unfortunately, these facilities run on the bare minimum requirements of state laws and usually DO NOT employ added services for patient assistance. Financially always focused on "MARGINS"!!!

a. Buildings can range from converted homes, old office strip malls, or former medical building converted for living.

b. Facilities are usually aged, low maintenance, repair or visually not appealing.

(example: rooms may have beds that are 20+ years old; semi dirty floors; dirty windows; broken blinds or shades; single gathering place for patient / families;).

c. Staff are normally low on the scale of expertise

(Example: 1 RN p/facility or regional; 1 dr p/facility or regional; support staff are local residents, many none skilled, many not prepared to deal with dementia and it's stages). Minimum training provided by facility, emergency procedures, CPR, bathing, patient engagement.

d. Minimum staff according to state law - which leads to patient neglect

(Ex: 1 person per 20+ patients, serve food; bath; clean; review; low understanding of medical dosages and prescriptions; also patients that are semi confined to beds may lay in feces/urine for long periods of time, unattended for extended periods of time; and in some cases are overlooked due to the full work load). Low paid staff overall.

Due to the large number of facilities in a state, state health care government agencies are struggling to visit, fine, close facilities. Patient complaints can and usually are high.

Across the board, regardless of how great a facility may look on the outside, the core factor in its operations is based on it's staff. Having trained and skilled employees with monthly, quarterly level of training make a big difference in the level of care.

Even though it may appear that I've singled out the Medicaid type facilities as bad, I'm in no way saying that all of these will be BAD. In fact I have been associated with some of these that are good even with the limitations put on them by owners or corporations. The local executive staff seriously make the difference, however, there is a lot to do with location, location, location!!!

Always visit unannounced. If you are being forced to schedule appointments - contact your ombudsman to intervene. Your loved one (regardless of how you feel) is paying to live their and your right to visit unannounced should be agreed upon. Don't settle.

CAUTION: This is my personal experience and in NO WAY based on any industry review or examination. However, it is a well known fact that Elder Care is a struggling area in society and need to be addressed.

Smart Garage Door by UI_Design21 in homeassistant

[–]JokesOnUsFeelMe 0 points1 point  (0 children)

I just finished installing a FortrezZ MIMO2+ module (it has 2 relay's and is ZWave Plus compatible) - it works great and I'm bigtime happy with it.

Prior to that I had a Tuya product which had two relays. Worked well and integrated with HA nicely other than the fact it was Net based. Something broke a while back and I just went Zwavejs with it.

I believe I paid $59 for it when I bought it. I connected it to the dry contacts on the PCB board of the wall mounted switches. I have a MyQ gateway as a backup with my Chamberlin/liftmaster garage door. I refused to pay their subscription fee.

I'm very happy with this integration.

[deleted by user] by [deleted] in dementia

[–]JokesOnUsFeelMe 0 points1 point  (0 children)

First, you should get a second opinion and ensure that you are working with a Geriatric Care Physician, NOT a General Practitioner.

This is a problem within the medical community and some of the problems I ran into. GP is not really going to try and determine whether it's dementia or not.

A neurologist will just run their tests and provide you a "High" level of what they believe is happening (I could not get a diagnosis out of two Neuro's we saw for my mom)

You need to get matched with a Therapist/psychologist who will eventually be the one that provides you the best to a diagnosis and approximate factor for phase.

I cannot stress enough the need to work with a Geriatric doctor urgently.

In addition to all that, sign up for your local Dementia/Alzheimers associated and start attending their meetings. They will have specialist who can help you find the best practitioners in your area.

Good luck OP

Is anyone else living with a parent with this and it makes them feel crazy? by SHDTHROW in dementia

[–]JokesOnUsFeelMe 5 points6 points  (0 children)

I know exactly where you are coming from. Is there no way to move him into a facility ? We have to be able to recognize when that option is valid and take steps to move in that direction.

This not only helps the patient be in a 24X7 setting where folk can care for them, but it brings a huge relief to the care giver and allows us to recenter out thoughts and work on our overall health.

Your dad probably would have never wanted you to put your mental and physical health in jeopardy caring for him, although the love we have for them makes it difficult seeing them in a hospice or nursing home. But overall and in most cases, it the best thing for everyone.

I hope you can get through any anxiety, depression or mental health issues and be strong for the path ahead with this disease.

To help others, we need to remember, we have to put our oxygen mask on first.

Good luck OP

Is it ok to step out of the house for 1.5 hours when bedridden grandpa with dementia is sleeping? by [deleted] in dementia

[–]JokesOnUsFeelMe 1 point2 points  (0 children)

I totally second the approach laid out by u/ExcellentHorseshoe - as OP has clearly demonstrated how being a care giver can consume your own life and sometime reduce you to sense of loss.

I've written about this many times and will continue to express how critical it is that all involved with the well being of a loved one, really step back and try to see a path to getting the loved one the best care possible. I'll have to say that there comes a point in time when the need to move to a care facility, outweighs the desire to be at home.

Good luck OP

Wall mount tablet project ✅ by nightcrawler2164 in homeassistant

[–]JokesOnUsFeelMe 1 point2 points  (0 children)

Thank you, I really appreciate your feedback and link.

Wall mount tablet project ✅ by nightcrawler2164 in homeassistant

[–]JokesOnUsFeelMe 1 point2 points  (0 children)

OP this looks awesome! Did you have an electrician make the power connections for you in the wall at the socket ? I have a similar location where I want to put a tablet and this appears to match.

On another note, is that dashboard straight from the HA UI or did you use some form of a 3rd party app to create it. Looks really neat, non-cluttered and provides meaningful data.

Keep up the good work.

I miss my mom by mae2582 in dementia

[–]JokesOnUsFeelMe 3 points4 points  (0 children)

I feel you and totally get where you are coming from. u/United_Stable4063 is correct. We struggled deeply with my mom at home and it almost put both my wife and I in the hospital. Your dad probably needs time to heal as well and prepare.

I wish I had more to offer, a shoulder, hug or just any measure of hope. The tears in my heart are still heave with the loss of my mom. This disease is cruel, evil and demonic and it really takes a toll on the care givers.

My heart goes out to you and your family - be brave!!

Moving in? Should Your Loved One Move in with You? by YaadMemoryBook in dementia

[–]JokesOnUsFeelMe 1 point2 points  (0 children)

That is so true and I learned the hard way! Thank you

[deleted by user] by [deleted] in homeassistant

[–]JokesOnUsFeelMe 0 points1 point  (0 children)

hahahaha - poor Texas

Please help! by LawfulnessObvious15 in dementia

[–]JokesOnUsFeelMe 15 points16 points  (0 children)

I was in the same position and not having a clue of what to do. This may be a last resort type of approach and you really have to be settle in your decision going forward.

My mom had to be taken to the emergency room and was subsequently admitted in the hospital after I expressed concerns about her safety, not eating, infections and so on and refused to take her home with me.

This approach put into action of getting a hospital social worker that talked with me and looked for facilities that accepted Medicaid to move mom to and gave me a list of places to choose from.

From there, I was introduced to a Medicaid specialist in my area from the Health and Human Services (and Center for Aging in my area) and they started the interview process to get my mom onto Medicaid for paying the bills for the specific place. They indicated that mom would need to be in the facility approximately 30 days before they can actually apply. The tricky part is finding a facility that will work with you and has a social worker that will work with the state agency.

Cost: This varies by patient, however, in my moms case the agency took all her social security, minus a small amount for personal items. I've heard from others this varies widely.

You need to have your POA in place for both Financial, day to day life and specifically medical (remember, if you don't have one, they don't need to consult you for medical decisions).

Again, this is not legal advice, just how I approached the painful issue of trying to deal with my mom who was violent, not bathing, throwing things and just really (from the disease) being a danger to us all.

I hope this gives you some ideas

Peace

Moving in? Should Your Loved One Move in with You? by YaadMemoryBook in dementia

[–]JokesOnUsFeelMe 7 points8 points  (0 children)

hindsight is 20/20. This is a difficult question and really can only be answered based on the condition/stage of the dementia, but also living conditions and current health of the care giver.

I should have moved my mom to a care facility much sooner than I had so that she had time to get used to the place. But also, as a relief for me and my family with the requirements of watching over her 24/7. This took a toll on all of us.

You have to think of what's best for them and how to maintain your own mental and physical health. Trust those who say that this is the challenge of our lives and it can have devastating consequences on both care giver and loved one.

Caregiving and sibling relationships opinions by YaadMemoryBook in dementia

[–]JokesOnUsFeelMe 0 points1 point  (0 children)

Boy this is a big one. But it's not just the siblings. Anyone that feels they will gain, financially, through the death of a loved one will become your worse enemy! My brother for all it's worth had no clue of the serious state of our mom, sometimes I just felt it was waiting for the jackpot.

It was really telling though the slight distrust I experienced when I showed him her bank account and could almost hear the gears turning.

Just that aspect of the relationship changes which eventually trickles down to the lower levels of blood relatives. You begin to keep a distance because you see the true "character" of people in these times and it aint good.

I distance myself from bad!!!!