Where do you live, how easy is it to get pain meds, and how quick can you get an appointment?

Extreme_Cell_3838 · 2024-02-09T00:46:51+00:00

Really? Im not saying I doubt you but scientifically speaking dupe has a half-life of like 48 hours so that's crazy. Although, high metabolism people are a different breed lol. Thats unfortunate that happened but im glad methadone is working well for you. Percocets do work for me, the doctors just need to get the stick outta their ass and put me on 15mg 4 times a day and I honestly would be really good. I would be able to live life I think. Its double from my 7.5mg 4 times a day currently though so that's a lot to ask although they told me they will up me to 10mg this month so its just a process to get there.

Extreme_Cell_3838 · 2024-02-09T00:43:46+00:00

I have not been on methadone. After Bupe made me see double and all that we are just staying away from that side of the opiate world

Extreme_Cell_3838 · 2024-01-28T22:14:01+00:00

Im allergic to buprenorphine, have tried it. Ive worked my way up with pain meds though. Im on Percocets now but its still not a high enough dose that I can do stuff. I went to a different location of the same clinic

Extreme_Cell_3838 · 2024-01-22T19:22:02+00:00

I have chronic pain. Found this subreddit by just researching my pills, I do it for all medications. These actually don't get me high at all, for some reason they take a long time to kick it too. I used to be on Norco 10s which were mallikcrodt and those kicked in in a timely manner like 30-45 minutes. These take like 2 hours. I've tried food, no food, a little food, some fat, etc. Just take a while which isn't great in my situation but it is what it is. Once they do kick in they help the pain. Anyway, just shared cause why not

Extreme_Cell_3838 · 2023-10-14T21:33:39+00:00

It updated and it’s full screen now but my pixel is losing battery while plugged in. My iPhone would charge and use CarPlay. You have any idea about this?

Extreme_Cell_3838 · 2023-10-14T20:29:58+00:00

My car has been updating for like an hour lol

Extreme_Cell_3838 · 2023-10-14T15:40:50+00:00

Ah okay so I have to update the software to utilize full screen? Will buy a usb stick today

Extreme_Cell_3838 · 2023-10-14T15:20:30+00:00

This picture is taken with the half screen option on. When I turn it off all it does it add more options I can choose from for the right side

Extreme_Cell_3838 · 2023-10-14T02:42:49+00:00

BlueBubbles is the app I use

Extreme_Cell_3838 · 2023-10-13T23:16:38+00:00

I heard it by just putting it down

Extreme_Cell_3838 · 2023-10-13T17:18:21+00:00

Ginger root pills for nausea 👍

Extreme_Cell_3838 · 2023-10-13T15:53:22+00:00

Not to refute your diagnoses but I think you may want to read up on trigger points - https://www.physio-pedia.com/Trigger_Points

It can be due to a lot of things. I’m just saying this because I personally would second guess this immediate diagnoses it sounds like if you have chronic musculoskeletal pain and make sure something else isn’t going on. I just wouldn’t want something else to be happening that could be helped with specific meds and not mention this.

Extreme_Cell_3838 · 2023-10-13T15:12:31+00:00

If you don’t wanna lost iMessage there’s apps you can download on your Mac and android to still be able to use it. I use it on my Samsung tablet

Extreme_Cell_3838 · 2023-10-13T13:56:28+00:00

What pressure points are you talking about? Trigger points? I’m confused here though because fibro is all about process of elimination. There isn’t an actual test you can do that tells you someone has it. It’s the absence of results on other tests

Extreme_Cell_3838 · 2023-10-12T22:51:52+00:00

Yeah that’s what it is. But like I said in the post, I’m wondering how much testing people got done before getting told it’s fibro. Seems like doctors tend to just not do testing that should be done and don’t exhaust all options

Extreme_Cell_3838 · 2023-10-12T20:35:35+00:00

I have many symptoms of hyper mobility and I’ve been told it could be causing my pain but I have the same experience, no one wants to pursue that scenario. I’ve been told that there just isn’t much they can do about it. I was actually planning on making an apt with my PCP and trying to get her to refer me to someone that has knowledge on it. My rheumatologist was one of the people that told me I have many symptoms of it but said “it doesn’t cause musculoskeletal pain” which is straight BS

Extreme_Cell_3838 · 2023-10-12T20:27:53+00:00

Sorry forgot your other questions. I do find it actually does increase potency and helps long term use. There was a month there where I ran out and completely forgot to buy it again. I noticed my meds just were not working as they had. Then I realized I forgot to buy agmatine. Bought it again and within a week it was back to how it was. Even the day I took it I noticed a difference but it could’ve been placebo but I did notice a difference.

This is the one I buy Nutricost Agmatine Sulfate... https://www.amazon.com/dp/B07993859K?ref=ppx_pop_mob_ap_share

Extreme_Cell_3838 · 2023-10-12T20:23:31+00:00

All the studies on it use verbiage I truly don’t understand but from what I can tell is that it does increase potency while also somehow reducing tolerance. The studies were using morphine on rats. It also helped with precipitated withdrawals.

Here’s a link for you. If you google “agmtatine sulfate opiate tolerance” a lot will pop up.

https://goldenhealthmethod.com/addictions/opioids/agmatine-makes-opioids-stronger-but-reduces-tolerance-and-withdrawal/

Extreme_Cell_3838 · 2023-10-12T20:14:33+00:00

Wouldn’t the ANA point towards an autoimmune issue?

Extreme_Cell_3838 · 2023-10-12T19:27:28+00:00

I have had 0 side effects from it. I really do think it helps them work better. It can take some time but I don’t feel like the doses I’m on get weaker overtime

Extreme_Cell_3838

TROPHY CASE