How Am I Supposed To Let Go. Just a short entry.

Hello and thank you for staying connected with me, I hope you are all safe and well.

Letting go. That phrase means so much more now, much more than ever before. Control , now, is a whole new thing as well; just one more thing to relearn and define.

I can’t control the pain. Its horrible and completely unpredictable. Its fast. It has no warning. Its debilitating. It is totally screwing up my plans. Totally fucking with my quality of life, of living well with this disease.

My plan was to slowly succumb to Alzheimer’s. Follow the ” medical path of known trajectory”….. that is not happening, at least in my mind.

I have always known Early Onset moves quicker, but I feel I’ve gotten the short end of the stick, honestly.

In the last 8 months of which I have spent around 5 months on nerve pain meds, this locomotive hasn’t ceased. Three levels of pain, each measured separately in relief, each digging deeper. How do I let go? How do I just release the control and let this happen?

My Alzheimer’s doctor, my Internist, has increased my meds, it’s a brutal amount. I will spend the next days getting used to it. My next few days will be a write-off.

The CBD is absolutely helping, but its expensive and not covered, so I am rationing. I’m getting more today, moving up to 1200 mg bottle. Also, bloodwork, checking on things.

My doctor believes it is progression, it’s the first time any of my 3 doctors have said that, it’s a large and jagged pill, my diagnosis was only 16 months ago, it seems too fast.

To let go is to come into the present, to believe what is and release the past, being willing to allow life to carry you to a new place……holding on means trying to push life into the place of your own making…. that is control and I must let that part go or ride a different wave, a smaller one.

Throughout my journey, I have rolled with the punches, I’ve been happy to make the adjustments and learn new ways to remain happy and living well. The onset of this pain has been like a sucker-punch south paw wallop, the kind that knocks you off your feet. But I have to get back up, it’s only round 2? Maybe 3 or 4, who knows.

My first step, increase my meds. In the big picture, why am I concerned with that? In the small picture, I have to let go of that concern, let that concern wane. Control, it’s never easy to give up control especially when it concerns your own body.

I cannot, easily, formulate the plan, the map in my head, yet, but I’ll get there, I’ll just do it and it will become life. I just hope it helps. The whole point is to live well, I’ll just get on with that. I’ll update you at a later time.

The sunrise this morning is lovely; sitting on the front porch writing this. I hope your day begins happy and ends fulfilled.

Stay well my friends xo Jan xo

From the front porch

3 thoughts on “How Am I Supposed To Let Go. Just a short entry.

  1. Hello beautiful Janet!
    First! I love the photo. It’s beautiful just like you. Next letting go. Yes that is one of the best daily practices we can do. I get it though. Living with this disease is something else — but when something else makes us feel like somebody else. Time to get a game plan and acceptance speech. When we get that way we can’t help it but what we can help is what is it that brings us back to normal. What is it that can comfort us. What is it that we are afraid of. And what is it that makes us feel as though this is too hard for me.

    Me Hong I admire us you writ you share snd you encourage others hit sometimes that great job you’re going remind yourself that you are still able to make a difference every day you write. Ad long as you can still write beautiful one that’s a good thing the rest of the stuff we can’t measure it try to measure. Just keep going keep doing what you know how to do. Enjoy whatever day that you feel like you can. Font focus on the things we are failing in. Just keep on repeating what works for you when it works. Express yourself do what you need to do but know as long as you can remember your name and realize you are breathing. There is a possibility you are still on the game. Love you beautiful . You’re doing great. How do I know because you can still read. Gotcha. Have a day just like you beautiful
    Terry

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  2. I’ve was diagnosed with EOAD in 2014 and Vascular Dementia in 2019. I don’t have a magic answer for you, but what I can suggest you enjoy the little moments like the sunrise you mentioned. Look at photographs or digital photos to spark your memories. Listen to your favorite music and allow yourself to go back to when you first heard your favorites.
    Keep writing! That not only helps you but helps others
    I’m not sure if any of this helps, but I hope it does.
    One day, one moment at a time.
    ~ Brian
    abitofbriansbrilliance.com

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