← Return to CRPS/pain syndrome. is it time for a mobility device. Embarrassed.

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@bebold

Yup. Like you said. Exactly. So yeah, like Disney, putting ourselves last and for what? The next days or week when everyone talks about the great time we all should have been having, I will have let my ego decide to not care about my body. This is exactly the reason for the "is it time" post. Even to just save spoons so the days I go even to PT for 30 minutes, life is done that day. Or psychotherapy - that's it for life that day. Maybe even food unless I drive thru McD depending on energy from rarely more than 4 hours sleep for months now. If you see what I posted below, I need a swift kick before it's all gone. I'm already feeling way older than I should. I am not ready to start the slippery slope.

About aging, I actually have been doing mostly good - esp lamictal helps me some - with depression as well. It's COVID in July of 2020 that brought me to my knees. Tho not literally of course! God forbid me trying to get up.

I'm starting to work with habitat who says they can help me get a walk-in shower, stuff to make life easier just in the normal aging process that is not about sick me. I can't find homecare help that Medicare will pay for so it's all on me to find out how to make it work.

I hear you and thanks for sharing. Funny about the shared childhood experiences. Maybe those hits to our adrenals when we are young leave us wide open to many manner of autoimmune issues. I know I have several. Stress terrible for the adrenals. And no kids get out of their teens without adrenal hits. It's why I also take LDN plus a plethora of supplements since COVID.

BTW, it was my 3rd back surgery for slipped disks via an on the job injury when I was 23 and lifted a patient, that caused my CRPS. I woke from surgery with a huge, bright red, burning foot. The kind like yeah, the surgery 4 hours ago on your back is nothing compared to this FOOT! I didn't know at the time, when they called it causalgia how fortunate I was that it was diagnosed day one. The surgeon knew exactly what it was but just told me, told me it was not curable, it was like this for life now, and walked out. I was still hazy from anesthesia. They know so much more about it now. There was zero treatment. It was assumed he cut or damaged a nerve. I discovered I had a civil war injury and that was it for life. I used crutches for 25+ years and eventually had a few remissions. I was out on depakote for seizures before they even knew it helped pain. I was part of the clinical trial back in the 80s. For Neurontin also. At some points, depression was the worst part of CRPS. 23, career and life gone, I had moved 2000 miles from home for a great nursing job when I was 20 but now, back to my parents house, SSDI, 3 months in a chronic pain unit back when workers comp paid for things. and shortly, totally on my own. By choice. And now 67. Who knew a thing like a pandemic would be my downfall. Feeling hopeful right now tho.

Thanks for sharing. Be

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Replies to "Yup. Like you said. Exactly. So yeah, like Disney, putting ourselves last and for what? The..."

Learned the hard way. Use Word to type a response then copy & paste. Website has malfunctioned a couple of times where it loads forever then errors out.

Wishing you the best. It helps reading about other peoples' journeys. It also gives me an opportunity in this day and age beyond what feels like electronic means to have a real conversation that doesn’t involve tweets or the like in length.

If you could find loophole in Medicaid's handbook, then suing for administrative argument, you may get off cheaply and may get the help you need. Maybe, even have them pay for it, like the story below. Some medical equipment companies accept payment plans. Not sure about medical equipment grants either.

Is there a way to file a reasonable accommodation with Medicaid, and in an extraordinary circumstance such as what I read in your posts, get what you want/need? Google is your friend when looking at keyword searches. Medicaid is a Federal program and they view transparency as important. I can't post websites: "Medicaid Handbook 2022", choose The State Medicaid manual – CMS. By the way, those free attorney consultations that you see on websites or the Yellow Pages can give you access to free information. Educate yourself and fight it if you have to. Use CTRL and F to keyword search within the PDF document or website.

I fought Wyoming Worker's Compensation for years and made them pay for everything. They didn't get out easy. Mayo Clinic alone was $26k out of pocket. Found a loophole when they deny a claim (within your working claim / i.e. many specialist doctors -expensive), you can sue them and they will pay for it. My parents read the handbook and played the game. We won with the exception of not understanding the full settlement terms even with the NY Hospital for Special Surgery saying disability of 25%. They paid a mere 8% disability. Shame on them, stupid me. My point is, educate yourself.

Mental Toughness:

These days I hear from quite a few people that say I am being too hard on myself. I feel I have to stay disciplined in my mind because if I relax it may go away, but generally, short-falls hurt and I do all I can to make things right. That changes a person. Do it enough and the power of brain neuroplasticity begins. Like the saying goes, use it or lose. The same works in reverse and in physical therapy is where I saw this phenomena. I typically listen to YouTube, best motivation or self-motivation, when I feel all depressed, down on myself, abilities, lack of knowledge, low self-esteem, severe flare-up pain which causes a different set of emotions counteracting and causing problems amongst themselves. Yay.

Although not likely true because CRPS does cause mental issues over the long term. My opinion is because the body is in constant flight or fight mode and consciously knowing this reality is a fight between systems. I think to some degree we tend to beat ourselves up when life isn't perfect, doesn't feel perfect, and television, magazines, social media tells us what to think. I believe in a clinical setting and a professional environment you will not be judged. I have a quote I keep close by as a reminder for how far I've come and that life is always changing.

You may not be where you're supposed to be. You may not be what you want to be. You don't have to be what you used to be. And, you don't have to ever arrive. You just need to learn to be the best you can be right now. -Unknown.

Wishing you the absolute best and hope you do make the journey to the Mayo Clinic. The three weeks I was there was a very good experience.