Alzheimer’s is often described as a disease of memory loss, but that’s just the surface. The real horror is much deeper; it’s about losing yourself, piece by piece, while still feeling trapped inside your own mind. It’s about families watching helplessly as their loved ones slip away, as their emotions shift unpredictably, and as they become strangers to the people who love them most.
And for some, the greatest tragedy isn’t the disease itself; it’s the system that takes over, deciding what’s “best” for someone who can no longer fight for themselves.
This is what Alzheimer’s really looks like.
Do you have any idea what it feels like to have Alzheimer’s? If you’re like me and you’ve heard all the stories, it will literally break your heart. But stick around because I have good news for you. For example, in the early stages, many sufferers know exactly what’s happening to them. And it’s terrifying.
You hear them say,
- “I can’t trust my own mind anymore. I try to remember a word, and it’s just… gone. It’s like trying to hold onto smoke.”
- “I know I have grandkids. I love them. But sometimes, when I see them, my brain tells me they’re strangers. And that makes me scared of them, which breaks my heart.”
- “I feel like I’m on the edge of a cliff, about to fall into nothingness, and no one can pull me back.”
And as the disease progresses, communication becomes harder. But many sufferers still have awareness, especially of how they are being treated.
They report things like this woman who was moved into a nursing home against her family’s wishes and cried, “I don’t want to be left alone in a place I don’t recognize. I just want my daughter’s hand to hold. Why won’t they let her stay with me?”
Another said, “They keep telling me I’m safe. But why am I so scared all the time?” looking like you could just see the life just draining from her as she asked about being so frightened.
Many people assume that once Alzheimer’s progresses, the person is completely unaware. But studies, and the testimonies of family members show that many still feel emotions deeply. Even if they can no longer say “I love you,” they feel love. Even if they don’t recognize faces, they recognize kindness and cruelty.
And when they are forced into unfamiliar places, when they are taken from their loved ones, when they are drugged into silence, they still feel it.
Alzheimer’s doesn’t just take one life; it destroys entire families.
One woman’s son says, “I lost my mother twice!”
Daniel spent two years caring for his mother, Mary, after she was diagnosed with Alzheimer’s. He left his job, moved her into his home, and dedicated himself to keeping her comfortable. She still had moments of lucidity, moments where she smiled at him and called him her “baby boy,” just like she always did before.
Then, a well-meaning doctor told him that she “needed professional care.” Soon after, Adult Protective Services arrived at his door with a court order. They said that despite his efforts, she was “at risk.” She was taken to a special needs care unit against his wishes.
He visited her every day, but she deteriorated fast. She stopped smiling. She stopped eating. Within months, she no longer spoke at all. He said, “I lost my mother when Alzheimer’s took her mind. But I lost her again when the state took her away from me.”
A woman protested about her dad, “I promised I’d keep him at home.”
Beth’s father, Ron, was diagnosed with Alzheimer’s at 76. He had been a strong, proud man, a veteran, a father of four, and the rock of their family. When the disease set in, Beth moved in with him, determined to keep him home.
Then, one night, he wandered outside in his pajamas. A neighbor called the police, thinking he was confused and lost.
That one call led to an investigation. Within weeks, despite Beth’s protesting all the way, a state-appointed guardian was assigned to “quote” protect “end quote” Beth’s dad. He was moved into a locked-down facility. She was told it was for his own safety.
The last time she saw him, he looked at her with empty eyes and asked, “Where’s my daughter? She said she wouldn’t leave me.” She cried, “They took my dad from his home, and he never forgave me. He died thinking I abandoned him.”
Listen, not all nursing homes are bad. Some genuinely care. But far too many treat Alzheimer’s patients as nothing more than bodies to manage. What is the easiest way to “manage” someone who is confused, scared, or agitated? Sedation. Plus, let’s not sugarcoat this: these facilities have to keep those beds filled, and the legal system can be manipulated to do just that.
Families often notice that once their loved one enters a facility, they go into a downward spiral shockingly fast. Many become unresponsive. Some stop eating. Others develop infections from neglect, urinary tract infections, bedsores, and pneumonia. Yet, here sits the families, powerless to take on city hall, the state, or the feds. If a patient is placed under court-ordered guardianship, families have no say. Even those who still have power of attorney are ignored.
One woman shared that when her mother was placed in a nursing home, she visited every day and tried to advocate for her care. But the staff treated her as an inconvenience. She said, “I came one day and found her sitting in a wheelchair in the hallway, staring at nothing. She had wet herself, and no one had noticed. When I confronted them, they said, ‘Oh, we’ll clean her up now.’ I realized then that they didn’t see her as a person anymore. Just another ‘problem’ to manage.”
It just makes you sick. She fought to bring her mother home, but the facility blocked her. She tried everything she could, but her mother passed away before she could make it happen. Tears falling down her face, she says, “I don’t just grieve her death. I grieve the years she spent trapped in a place where no one ever cared. Not one bit.”
The true tragedy of Alzheimer’s isn’t just the disease itself; it’s what happens to people when the system takes over.
- Families who WANT to care for their loved ones are told they can’t.
- State-appointed guardians take away decision-making power.
- Nursing homes sedate patients into silence instead of providing real care.
- Patients decline faster in facilities, but families are often helpless to stop it.
My name is Wayne Rowland, and I’m here to tell you that all of this is utter BS. You don’t have to be victimized by doctors who are not truthful about what is going on in the first place, though they may not be doing it intentionally.
The system is so messed up, and these “healthcare professionals” are trained by pharmaceutically funded “medical schools,” and what they have told you about Alzheimer’s is exactly what their textbooks dictate they are to repeat.
Now, not that long ago, I thought Alzheimer’s was caused by aluminum toxicity in the brain. Well, since then, I have been doing amazing things with this magical Wayne Water that I developed, colloidal silver water created with Tesla lightning and infused with healing Rife frequencies.
In the beginning, I focused mostly on using it to help heal people who were naturally attracted to me, like those with cancer, severe burn injuries, and highly symptomatic diabetics. They all responded incredibly well to my programs and Silver Water.
I do not promote anything; they just come and find me. It’s like something bigger than me or any of us is going on; then came my first Alzheimer’s patient, and I didn’t have anything to go on. I was flabbergasted and was not feeling one hundred percent confident about this. Still, I decided to trust that there must be a higher source at work here, so I trusted and put her on the same program I used for diabetics, which starts with deworming and my water. Nothing else came to mind.
Fifteen days later, I get a call from her daughter, and she’s ecstatic, saying that her mom’s coming back! Now, this threw me for a loop because I thought that people with Alzheimer’s had lost their neurotransmitters. Well, I don’t know, I just told her to keep going and two-and-a-half months goes by and guess what? Mom’s Alzheimer’s is totally gone. And that was just the beginning.
Ever since then, it’s been the go-to protocol for getting rid of Alzheimer’s, and it works every time. You would not believe it unless you actually saw it for yourself.
What is even more curiouser is, now I wonder about the cause of Alzheimer’s, and it’s looking to me that it’s a parasite and worm problem. It’s interesting, isn’t it, just like my cancer. I treated for worms, and the cancer was gone.
It makes you wonder, right?
Now, you can go fight for change, and God knows we need that. We need to stop enabling bureaucracy and the medical industry to violate the rights of our loved ones, or you can get rid of Alzheimer’s altogether, which is what many thousands of people have done with my silver program.
But if you don’t do that, then get out here and do something about this system that is so messed up that it is unbelievable. Or do it anyway. Take back your loved one’s life yourself, and get out there and change the way we enable all these facilities to line their pockets.
To do that, you need to establish the right of the families to have the final say, not the doctors, some state employees, or the government. If the state really needs to jump in and support someone whose capabilities are slipping away, empower the family, and offer assistance to the in-home family, do that. There is no medical treatment that is better than the care and love of a family can offer at home. You’ve seen what happens when they take them out of the home. This has to stop, if it’s what the family wants.
And in these nursing homes and “care” facilities that these poor people are farmed out to, make them accountable. Enforce the criminality of neglect and abuse of these people. The overuse of medication and neglect must be exposed and stopped.
Patient rights must be respected. Even those with Alzheimer’s have the right to be treated with dignity, not drugged until they die and leave a bed open for the next one.
If you are caring for someone with Alzheimer’s, you are not alone. If you are someone in the early stages, know that your wishes matter. And for god’s sake, if you possibly can, take a look at my program and water.
And if you’ve lost someone, whether to the disease or to the broken system, your grief is valid, and I pray for you and your family, and pray to God that this system can be changed for the better.
Alzheimer’s is cruel enough. The way we handle it doesn’t have to be.
Leave a Reply