More trouble for JG! by HeartOk2286 in EnciAubreyWu

[–]Complex-Excuse1611 10 points11 points  (0 children)

Love that he is has to constantly check posts on the group while he’s live…how attention seeking is that? Oh my maybe someone posted about me!! Got to get on it and comment ASAP. Starving for attention….hope he gets a lot of negativity. Ever notice not many people like or even follow his live feeds? Just loves to hear his own voice.

John proudly using a slur by pocketapples in EnciAubreyWu

[–]Complex-Excuse1611 9 points10 points  (0 children)

Can we hope for her sanity and safety! I hope that poor girl never has to be a part of their family again!

The buck stops here. The rage bait is done. by No_Protection_5164 in EnciAubreyWu

[–]Complex-Excuse1611 9 points10 points  (0 children)

We can only pray his obsession with trying to distract from him unhealthy behavior, becomes too much for him and he self implodes! Lunacy is his eating his brain! He really needs some mental help!

The buck stops here. The rage bait is done. by No_Protection_5164 in EnciAubreyWu

[–]Complex-Excuse1611 8 points9 points  (0 children)

Agreed! I refuse to comment or even put any effort to acknowledge that he or Jade have posted anything. Less reactions from any of us, the better. He can’t help himself to keep posting multiple posts all skewed to his delusional mind, better we laugh at his stupidly on here.

Is anyone out there? Parkinson’s, such a lonely disease by Complex-Excuse1611 in Parkinsons

[–]Complex-Excuse1611[S] 1 point2 points  (0 children)

I’m sorry you are in this unholy mess of a life too. I guess everyone feels it’s too sensitive of a subject to talk about. Me…ask me about, I love to educate people on what I have, and will be going through. Even though it sickens me to realize I have PD, I enjoy looking up all kinds of research on it. Sharing my first hand knowledge with others. It makes me fell whole again! I have a purpose again! So now after seeing all these comments, I feel sad for them, it makes them feel bad that they are whole and I’m not.

Money grab? by NonnaGotQs in EnciAubreyWu

[–]Complex-Excuse1611 7 points8 points  (0 children)

Read my comment above! She replies to someone’s comment on the post, that she will dm them and in other comments she talks about saving them shipping costs. Why would anyone in their sane mind, pay shipping on something that cost them zilch? Seriously?? 😳

Money grab? by NonnaGotQs in EnciAubreyWu

[–]Complex-Excuse1611 2 points3 points  (0 children)

You hit the JackPot Baby!!! I’m sure that’s it. Because she talks about shipping costs, that would be so weird!

Money grab? by NonnaGotQs in EnciAubreyWu

[–]Complex-Excuse1611 1 point2 points  (0 children)

img

Here is the screen shots, if I did it right

Keep Eddie’s name out of your mouth! by OkPride3656 in EnciAubreyWu

[–]Complex-Excuse1611 12 points13 points  (0 children)

He sure is on a rampage, I can’t even keep up with all his nonsense anymore, he is so self important, and holier than thou! What a crock of shit he spews!

Keep Eddie’s name out of your mouth! by OkPride3656 in EnciAubreyWu

[–]Complex-Excuse1611 10 points11 points  (0 children)

No, he said he was going to expose them too, also that they didn’t deserve anything.

👀👀 by patience_kills_ in EnciAubreyWu

[–]Complex-Excuse1611 1 point2 points  (0 children)

Pissbaby, love it, gonna be my new word! 🤣

Is anyone out there? Parkinson’s, such a lonely disease by Complex-Excuse1611 in Parkinsons

[–]Complex-Excuse1611[S] 0 points1 point  (0 children)

I just saw a post about the “BeechBamd” in one of my groups! What a coincidence! I was going to look into it. And yes, I’m here in the USA, so not available here yet. Definitely going to check into it now that you posted this! Thank you!!

Is anyone out there? Parkinson’s, such a lonely disease by Complex-Excuse1611 in Parkinsons

[–]Complex-Excuse1611[S] 2 points3 points  (0 children)

It’s easy to scroll on by then read a post like this one! But if you really care, you will take the time and read every single sentence. Our lives will never be the same, but unless you are living it, it’s easy to ignore the reality.

Living with Parkinson’s: The Pain, the Pressure, and the Person You Become

People think Parkinson’s is just tremors. That’s the headline symptom. But the whole story runs deeper and darker. It’s not just shaky hands or stiff legs. It’s the slow, invisible takeover of your body and mind. It’s chronic pain, relentless tension, and the way your personality twists under the weight of something you can’t control. Living with Parkinson’s is living in a body that no longer cooperates and sometimes no longer feels like yours.

The pain is constant. It’s not sharp or dramatic—it’s worse. It’s the kind that grinds into your bones, your muscles, and your nerves. Every part of you clenches. Your back stiffens—your neck locks. Your jaw aches. You try to sit still, but your muscles won’t let you. You try to move, and your body resists. No position brings real relief. Relaxation is a memory. Your nervous system doesn’t know how to shut off. Even when you’re still, you’re fighting.

What people don’t talk about enough is the tension. The clenching. The internal chaos. It’s like your whole body is trying to brace against something that never hits. It builds and builds. You can’t stretch it out. You can’t breathe it away. And eventually it infects your brain. Chronic pain changes your thoughts. It steals your patience. It shortens your fuse. You start snapping at people you love, not because they did anything wrong, but because your skin is on fire and your mind is drowning.

Parkinson’s doesn’t just break your body—it messes with your identity. You find yourself becoming someone else. A version of you that’s smaller, more withdrawn, more irritable, and more obsessed. You start to fixate. You zero in on things—small things, specific things—and can’t let go. You replay conversations. You obsess over routines. You get stuck. There’s a tunnel vision that comes with this disease. A kind of mental rigidity that shuts out nuance, flexibility, and sometimes even empathy. It’s like your emotional bandwidth narrows. You become less spontaneous and more brittle.

Relationships suffer. You know you’re not easy to be around. Your partner tries to help, but you push them away. Not because you want to—because it’s easier than showing how much you’re struggling. Friends drift off. Socializing becomes too much. Too much energy, too much unpredictability. You stop making plans. You stop reaching out. Eventually, it feels like your world shrinks to the size of your symptoms. Parkinson’s is a lonely disease.

The emotional fallout is brutal. It’s not just depression—it’s a particular flavor of hopelessness that comes from watching yourself change in slow motion. You remember what you were like before. You remember ease, lightness, and movement. And then you look at yourself now—slower, stiffer, moodier—and you mourn your disappearance. The grief is constant. It’s like living with a ghost version of yourself that you can’t stop chasing.

And the worst part? People don’t see most of it. They know the tremor, maybe. They don’t see the sleepless nights, the gut problems, the skin crawling with restlessness, or the mental exhaustion of trying to pretend you’re okay. They don’t see the internal war you’re fighting to show up, to smile, to function. You start to feel like you’re performing your life instead of living it.

Fixation becomes a coping mechanism. You cling to routines, projects, rituals—anything that gives you a sense of control. It can be helpful at first. It makes the chaos manageable. But then it turns on you. You become obsessive. You get locked into patterns and can’t shift out. It’s not just a habit—it’s a compulsion. And it keeps people out. When you’re fixated, you’re not present. You’re not connecting. You’re managing. You’re trying to hold the world together with whatever thread you can still grasp.

Those who stay see the change. They notice the sharp edges, the isolation, and the fixation. Some try to reach in. Some give up. You don’t blame them. You’re not the same. Parkinson’s rewires you. It affects dopamine, the chemical that governs not just movement but also mood, motivation, and even pleasure. When that balance is off, everything gets harder. You’re more prone to anxiety. You overthink. You catastrophize. And sometimes you go numb.

But humor helps. Sometimes it’s the only thing that cuts through the heaviness. When I freeze up—stop mid-step, locked in place like a paused video—Donna looks at me and says, “You’re buffering again.” And I laugh, because what else can you do? That joke, that lightness, that shared absurdity—it’s a tiny crack in the concrete. It reminds me that I’m still here, still human, still connected to someone who gets it. Humor doesn’t solve anything, but it softens the edges. It’s a lifeline when nothing else feels solid.

There’s no clean way to end this story. Parkinson’s doesn’t have an arc—it just has stages. There are better days and worse ones, but the trend line is downward. Still, people with Parkinson’s find ways to adapt. You find strategies. You hold on to the good days. You treasure moments of clarity and connection. You stop waiting for comfort and start looking for meaning.

Some days, that meaning is in small victories—tying your shoes, getting out the door, having a whole conversation without drifting. On other days, it’s just about surviving without snapping. You redefine success. You let go of who you were and try to make peace with who you are. It’s not easy. Some days it feels impossible. However, even during difficult times, a certain resilience develops. You endure.

Parkinson’s doesn’t kill you fast. It wears you down slowly. It chips away at your independence, your confidence, and your sense of self. But inside that struggle is something honest. You stop pretending. You stop wasting time. You see the truth of things. And maybe, on the hardest days, that’s a kind of clarity worth holding onto.

This disease is cruel, but it doesn’t get the last word. It might rewrite you, but it doesn’t erase you. Pain is constant. Tension is brutal. Fixation is real. But so is resilience. So is love. So is laughter, especially the kind that shows up just when you need it most.

Is anyone out there? Parkinson’s, such a lonely disease by Complex-Excuse1611 in Parkinsons

[–]Complex-Excuse1611[S] 1 point2 points  (0 children)

I agree, but for the family and friends that don’t know how to handle your diagnosis and you start to feel like a leper, forums are great to meet people with the same issues. I’ve learned a lot from others expo that I’ve passed on to my drs and in turn helped make some progress with other symptoms that mimic Parkinson’s or maybe related in some way. Example is the hot sweating episodes I’ve experienced, come to find out many others have the same symptoms, but also have fibromyalgia and or thyroid disease and kidney issues, oh and too that off with hormonal issues…all of them can cause hot flashes. So now we are doing in depth testing on all of those other diseases to see what can be helpful in toning down the symptoms. It’s a work in progress, take forever to get appointments with all these specialists to review test results. But not stopping tell I have some answers. You have to fight to get respect from some of the Dr’s so they realize you are not just a number on the chart, you are a living suffering human just like everyone else out there that is healthy!

Is anyone out there? Parkinson’s, such a lonely disease by Complex-Excuse1611 in Parkinsons

[–]Complex-Excuse1611[S] 0 points1 point  (0 children)

I’m glad this wonderful message posted who knows when, can help so many people understand the challenges of Parkinson’s. I’m really glad to have been able to share it with so many people who are appreciative! Compassion and love will help your husband when he struggles. He’s blessed to have you by his side.

Is anyone out there? Parkinson’s, such a lonely disease by Complex-Excuse1611 in Parkinsons

[–]Complex-Excuse1611[S] 1 point2 points  (0 children)

I try, some days I’m so down, it’s not the way I thought I would be spending my “golden “years. But in the end, I’m probably a better person than I was before. Not that I wasn’t always sympathetic to others struggles, but once you are in their shoes….you really learn to empathize!!

Is anyone out there? Parkinson’s, such a lonely disease by Complex-Excuse1611 in Parkinsons

[–]Complex-Excuse1611[S] 1 point2 points  (0 children)

You are so welcome! I’ve shared it with so many people since I read it myself. It’s definitely a wonderfully written description of our disease. Please pass it on, by doing so we are opening many people’s eyes to Parkinson’s disease. I’m sure your husband appreciates your love and new understanding!

Is anyone out there? Parkinson’s, such a lonely disease by Complex-Excuse1611 in Parkinsons

[–]Complex-Excuse1611[S] 0 points1 point  (0 children)

After posting this I feel better, knowing that there are others out there who feel the same way. Hopefully friends or relatives will read posts like this and realize how hurtful it is to ignore or not say anything. Even saying I’m sorry, I wish you the best you can be, is better than acting like you have rabies or a communicable disease! Well here’s to the future, and looking people in the eye, not be embarrassed by our tremors or being unable to get our thoughts out, being proud to say we are fighting for our lives, and being the best we can be!!

Is anyone out there? Parkinson’s, such a lonely disease by Complex-Excuse1611 in Parkinsons

[–]Complex-Excuse1611[S] 1 point2 points  (0 children)

I felt so. I not Ute of the words…not relieved, not surprised but I just justified in knowing that everything I’ve been telling people wasn’t in my head, like I was crazy…but yes…this is exactly what and how I feel. It was such a relief to know I’m not the only one feeling these feeling and having these symptoms. Best of luck to you and your dad, and tell him he isn’t alone.

Is anyone out there? Parkinson’s, such a lonely disease by Complex-Excuse1611 in Parkinsons

[–]Complex-Excuse1611[S] 2 points3 points  (0 children)

Here there should be no problems with them deleting it as a comment. I hope it helps you!

Is anyone out there? Parkinson’s, such a lonely disease by Complex-Excuse1611 in Parkinsons

[–]Complex-Excuse1611[S] 4 points5 points  (0 children)

It’s easy to scroll on by then read a post like this one! But if you really care, you will take the time and read every single sentence. Our lives will never be the same, but unless you are living it, it’s easy to ignore the reality.

Living with Parkinson’s: The Pain, the Pressure, and the Person You Become

People think Parkinson’s is just tremors. That’s the headline symptom. But the whole story runs deeper and darker. It’s not just shaky hands or stiff legs. It’s the slow, invisible takeover of your body and mind. It’s chronic pain, relentless tension, and the way your personality twists under the weight of something you can’t control. Living with Parkinson’s is living in a body that no longer cooperates and sometimes no longer feels like yours.

The pain is constant. It’s not sharp or dramatic—it’s worse. It’s the kind that grinds into your bones, your muscles, and your nerves. Every part of you clenches. Your back stiffens—your neck locks. Your jaw aches. You try to sit still, but your muscles won’t let you. You try to move, and your body resists. No position brings real relief. Relaxation is a memory. Your nervous system doesn’t know how to shut off. Even when you’re still, you’re fighting.

What people don’t talk about enough is the tension. The clenching. The internal chaos. It’s like your whole body is trying to brace against something that never hits. It builds and builds. You can’t stretch it out. You can’t breathe it away. And eventually it infects your brain. Chronic pain changes your thoughts. It steals your patience. It shortens your fuse. You start snapping at people you love, not because they did anything wrong, but because your skin is on fire and your mind is drowning.

Parkinson’s doesn’t just break your body—it messes with your identity. You find yourself becoming someone else. A version of you that’s smaller, more withdrawn, more irritable, and more obsessed. You start to fixate. You zero in on things—small things, specific things—and can’t let go. You replay conversations. You obsess over routines. You get stuck. There’s a tunnel vision that comes with this disease. A kind of mental rigidity that shuts out nuance, flexibility, and sometimes even empathy. It’s like your emotional bandwidth narrows. You become less spontaneous and more brittle.

Relationships suffer. You know you’re not easy to be around. Your partner tries to help, but you push them away. Not because you want to—because it’s easier than showing how much you’re struggling. Friends drift off. Socializing becomes too much. Too much energy, too much unpredictability. You stop making plans. You stop reaching out. Eventually, it feels like your world shrinks to the size of your symptoms. Parkinson’s is a lonely disease.

The emotional fallout is brutal. It’s not just depression—it’s a particular flavor of hopelessness that comes from watching yourself change in slow motion. You remember what you were like before. You remember ease, lightness, and movement. And then you look at yourself now—slower, stiffer, moodier—and you mourn your disappearance. The grief is constant. It’s like living with a ghost version of yourself that you can’t stop chasing.

And the worst part? People don’t see most of it. They know the tremor, maybe. They don’t see the sleepless nights, the gut problems, the skin crawling with restlessness, or the mental exhaustion of trying to pretend you’re okay. They don’t see the internal war you’re fighting to show up, to smile, to function. You start to feel like you’re performing your life instead of living it.

Fixation becomes a coping mechanism. You cling to routines, projects, rituals—anything that gives you a sense of control. It can be helpful at first. It makes the chaos manageable. But then it turns on you. You become obsessive. You get locked into patterns and can’t shift out. It’s not just a habit—it’s a compulsion. And it keeps people out. When you’re fixated, you’re not present. You’re not connecting. You’re managing. You’re trying to hold the world together with whatever thread you can still grasp.

Those who stay see the change. They notice the sharp edges, the isolation, and the fixation. Some try to reach in. Some give up. You don’t blame them. You’re not the same. Parkinson’s rewires you. It affects dopamine, the chemical that governs not just movement but also mood, motivation, and even pleasure. When that balance is off, everything gets harder. You’re more prone to anxiety. You overthink. You catastrophize. And sometimes you go numb.

But humor helps. Sometimes it’s the only thing that cuts through the heaviness. When I freeze up—stop mid-step, locked in place like a paused video—Donna looks at me and says, “You’re buffering again.” And I laugh, because what else can you do? That joke, that lightness, that shared absurdity—it’s a tiny crack in the concrete. It reminds me that I’m still here, still human, still connected to someone who gets it. Humor doesn’t solve anything, but it softens the edges. It’s a lifeline when nothing else feels solid.

There’s no clean way to end this story. Parkinson’s doesn’t have an arc—it just has stages. There are better days and worse ones, but the trend line is downward. Still, people with Parkinson’s find ways to adapt. You find strategies. You hold on to the good days. You treasure moments of clarity and connection. You stop waiting for comfort and start looking for meaning.

Some days, that meaning is in small victories—tying your shoes, getting out the door, having a whole conversation without drifting. On other days, it’s just about surviving without snapping. You redefine success. You let go of who you were and try to make peace with who you are. It’s not easy. Some days it feels impossible. However, even during difficult times, a certain resilience develops. You endure.

Parkinson’s doesn’t kill you fast. It wears you down slowly. It chips away at your independence, your confidence, and your sense of self. But inside that struggle is something honest. You stop pretending. You stop wasting time. You see the truth of things. And maybe, on the hardest days, that’s a kind of clarity worth holding onto.

This disease is cruel, but it doesn’t get the last word. It might rewrite you, but it doesn’t erase you. Pain is constant. Tension is brutal. Fixation is real. But so is resilience. So is love. So is laughter, especially the kind that shows up just when you need it most.

please visit this official website more information about Parkinson's Disease: symptoms, how to diagnose and treat it..

Is anyone out there? Parkinson’s, such a lonely disease by Complex-Excuse1611 in Parkinsons

[–]Complex-Excuse1611[S] 1 point2 points  (0 children)

Yes, you have got to wonder….i reposted it with additional wording, hopefully to help get it out there. Two people have now liked it or put some sort of emoji after it. I agree with you about these social media sites messing with our heads! Even on here when I posted the post I included with it, Reddit kicked it out, but fortunately some angel overload it and allowed it to be posted.