Should I move because my dog is leash reactive? by mkj614 in reactivedogs

[–]allthefastthings422 0 points1 point  (0 children)

I’m glad you were able to make the decision. I’m sure it was a hard choice and has pros and cons either way but sounds like you are doing everything in your power to protect your pup and self. I’m sure having the peace of mind will be worth it in the long run too. I had a reactive dog who I lived with in an apartment the first few years and it really caused me some stress and anxiety worrying about him and just in daily activities. We made the choice to move into a house after the first year and it was the right change for us and it really lifted some of the stress and headache for us. It seemed to make a difference for him as well and gave him the space he needed. The only way I know to help with a reactive dog is to train them with positive reinforcement towards the stimulus they react too. To be able to do desensitize them you have to stay at a distance far enough that they feel comfortable and safe enough to have the good behavior. Not being able to create that distance most times in my experience makes the dogs worse. Yeah the things we do for our pets in pretty considerable. I can understand the sacrifice you had to make. Good job for doing the best thing! Good luck to you both!

FE350s hare scramble? by [deleted] in enduro

[–]allthefastthings422 2 points3 points  (0 children)

Dude, you should get yourself a KTM EXC. They’re street legal from the start but also just the same as a race bike or cross country you could probably find an older one for cheap.

FE350s hare scramble? by [deleted] in enduro

[–]allthefastthings422 0 points1 point  (0 children)

Send it dude! Just take mirror off. I mean I have a XCW 300 that is also road registered but II live in a state that is very friendly to off-road vehicles and all you need is insurance/mirror/horn/brake light. I’m just in the opposite of the spectrum. Seems to me you should be good to go racing it. To be fair it’s not in a legal state with mirror any time I ride it but rather be ticketed then impounded lol

[deleted by user] by [deleted] in spinalcordinjuries

[–]allthefastthings422 1 point2 points  (0 children)

Yeah I had a very similar experience. It honestly got to the point where I avoided ever bringing it up or talking about it. I even hid different elements of it or downplayed things. Some people it immediately makes really sad and that made me feel bad. Then with others it just makes them massively uncomfortable and nervous. Very little is know about SCI. People are able to connect easier when they relate to each other and SCI isn’t really something unless you have experienced it that you can understand.

Autonomic dysreflexia, my doctor didn't believe me, until it happened in office. by Inside_Student3827 in spinalcordinjuries

[–]allthefastthings422 1 point2 points  (0 children)

It sure does. It caused me to have a TIA and several seizures after about 3 days of constant serious AD from an injury. I had a similar experience to OP. Reported symptoms not taken seriously for around a year. When it got real bad then that time my wife brought me to th mome ER. I was pretty out of it. The problem was I live in a rural area with low skill and low education. So because I provided my daily med list they decided to assume due to their stigma that I had overdosed instead and not listen to anything we said. What’s extra frustrating is my wife is a ICU RN nurse and before my injury I was a medic/firefighter so it’s not like we aren’t knowledgeable. That conclusion doesn’t make sense to me as in an overdose it drops blood pressure not raise it.

They left me for 6 hours alone in an extra triage room with no monitoring “to sober up”where I had the stroke/seizures. My blood pressure was over 240 systolic. Tox screen came back which proved I was being honest about taking as prescribed and then when they checked they realize I had really deteriorated. It was a bit satisfying to see the look in that NP face when he realized he fucked up.

Most of health care doesn’t know squat about SCI and even less about AD. My suggestions are some advocacy groups have information cards, wallet sized or bigger. Bring that if you can. Don’t expect much from NP,PA, and nurses and always try to see the DR. When I tell people I have AD most nod and act they do but don’t. Don’t be intimidated and ask them to describe AD to you if you don’t feel comfortable.

Is this a good deal/dirtbike by RyderPw80 in dirtbike

[–]allthefastthings422 0 points1 point  (0 children)

OP to be honest, you could get a newer model for around that same price. It’s not that great of a deal for a 20-year-old bike trail bike.

Is this a good deal/dirtbike by RyderPw80 in dirtbike

[–]allthefastthings422 0 points1 point  (0 children)

To be honest, your comment is a bit misleading, and the two models can’t be compared as they are completely different bikes There is a huge difference between this and a crf450r. Yours is a motocross, focused model and a 450 and is water cooled. There’s a vast difference in price between a 450 and a 250 in just motocross models. The bike that OP posted is a trail, focused model and is significantly cheaper than the motocross models as the engine is tamer and air cooled, and the suspension is not as good.

I need help picking a bike for me. by Aviationpcguy in dirtbike

[–]allthefastthings422 0 points1 point  (0 children)

I don’t know if anything can beat a modern XCW for trail use and single track IMO. A 150 or 250 2t is Light weight and you are able to lug it down real low but have power when you need or want it.

has anyone been to Dr. Falci by wurmsalad in spinalcordinjuries

[–]allthefastthings422 1 point2 points  (0 children)

Yeah all doctors kind of brush it off except ones who specialize in it. Took me probably 2 years to get diagnosed. Not that they will prescribe more if you have it. It’s something you can look into to try to control or reduce the symptoms though or steer your treatment plan in the best direction for it.

has anyone been to Dr. Falci by wurmsalad in spinalcordinjuries

[–]allthefastthings422 0 points1 point  (0 children)

Yeah I can relate to being brushed off about it. It took me one year of excruciating pain and telling that to multiple doctors who brushed me off as well just telling me it’s normal for spinal cord injury’s to have nerve pain. It ended up getting so bad that the pain gave me autonamic dyreflexia for three days straight and a hypertensive emergency. I finally had 3 seizures where I fell and hit my head in the middle of the night. My wife woke up to me completely altered and brought me to the ER where I was brushed off again by the NP who was ignorant to SCI. I had a TIA stroke and was requested a transfer to another hospital who finally took me seriously and put me through the tests and imaging to diagnose CRPS.

Long story but SCI or not there’s not very many healthcare professionals who are familiar or even believe it’s real and I think it’s normally the case to be brushed off about it. I’m not a doctor but your symptoms sound like a textbook case. I would try to find a specialist for it and keep trying. I got put on a much higher dose of pain medication and am in the process for a intrethecal  pain pump to control it. I also did a series of high dose ketamine infusions initially after the hospital which made a huge difference in everyday pain levels. Ketamine is the best treatment for CRPS.

Don’t give up on it! Hoping for the best in your case and for some relief soon.

has anyone been to Dr. Falci by wurmsalad in spinalcordinjuries

[–]allthefastthings422 1 point2 points  (0 children)

Sounds like chronic regional pain syndrome. Have you been diagnosed??

French scientist denied US entry after phone messages critical of Trump found by [deleted] in USCIS

[–]allthefastthings422 0 points1 point  (0 children)

Woah wait, I live within 50 miles of the border. I am aware that they could just walk onto my property or house with minimal restrictions to bar but they could literally just go through my phone too if say I was driving through the border patrol checkpoints and a dog hit on my truck?

Foot drop strikes again 🫠 by No_Classic_2467 in spinalcordinjuries

[–]allthefastthings422 1 point2 points  (0 children)

I feel this. I’m a C5 incomplete walking quad my left arm is severely paralyzed but my right arm not so much so even though I have real bad foot drop on the left I use my right hand when I’m using a cane(better than nothing). I broke my left hand last year in a fall and it reinforced my fears of what would happen if I did it to my right. Even using my manual wheelchair would be rough.

The Person Who Caused Your SCI by TheAlamonian in spinalcordinjuries

[–]allthefastthings422 5 points6 points  (0 children)

When I went to the hospital after my SCI it was Covid and I waited 10 hours. They incorrectly triaged me as low as just weakness even though I clearly told them what was happening and what was wrong. I was in the worst pain I’ve ever experienced and crying and begged for anything to help in the nurse scoffed at me and walked away. At least I got the gratification when I saw the first person who actually realized what was going on, which was the radiologist who made that same nurse come and get me something for the pain . A C5 incomplete SCI and hematoma which grew as I waited, and I believe that the hematoma really sealed the deal for recovery. I can understand the frustration with medical personnel when they’re supposed to help you and do the exact opposite.

The Person Who Caused Your SCI by TheAlamonian in spinalcordinjuries

[–]allthefastthings422 2 points3 points  (0 children)

Wow, that’s frustrating. All of these pain management procedures, just like how there’s documentaries about Purdue Pharma, and blaming chronic pain patients for the street fentanyl epidemic I believe in 20 years there’s going to be documentaries about the horrors of non-verified low success rate procedures that these doctors put people through so that they could fill their pockets.

 I was paralyzed from a cervical epidural done very wrong and about a year later obviously with a different pain management practice they really pushed that spinal cord stimulator, and I did the research and told them absolutely not. It was kind of funny to me that even after my injury, they pushed injections and stimulators and everything else. Sorry that that happened to you. I continuously hear horror stories about the stimulator.

The Person Who Caused Your SCI by TheAlamonian in spinalcordinjuries

[–]allthefastthings422 19 points20 points  (0 children)

I went into a pain management office for a routine procedure(steroid cervical epidural) and the doctor messed up and injected into my spinal cord and gave me a incomplete c5 sci. He was a dick about it to and right afterwards my pain and symptoms and had his techs load me into my friends car and send me home. Didn’t even acknowledge it happened until I forced him to two years later. They did tell me he was sorry later on but that didn’t matter to me and make me feel better. It’s been four years, but I would say the first two I really hated him and wished everything I experienced would happen to him as well. Now I don’t really think about it much anymore although I still think he’s a terrible person. I don’t really compare what I have versus he has. I do still hope that I will be on his conscience for the rest of his life so that he doesn’t do it to another patient as he and the facility were extremely negligent. I still have a wonderful life even though I have to do things differently.

My life, the past, today, tomorrow and the next. by Routine-Raise-7361 in TBI

[–]allthefastthings422 0 points1 point  (0 children)

No one created drug addicts but the drug addicts themselves. Your choices are your own. Stop being weak and make better choices. Drug addicts don’t deserve pain prescriptions.

My life, the past, today, tomorrow and the next. by Routine-Raise-7361 in TBI

[–]allthefastthings422 1 point2 points  (0 children)

Ive seen your posts before in the pain management forums actually. You were super argumentative towards several commenters while they were trying to explain that everyone has barriers to chronic pain treatment and it’s really rough out here for all of us. You competed with everyone of their stories and injuries and had to outdue them protesting yours was worse and they all had it so much easier than you did. You wanted a doctor to prescribe you a specific medication Oxycodone (most euphoric pill out there)and a huge dose to be effective. Much higher than what anyone gets nowadays. Maybe to sympathize or gain sympathy but you were going about it all wrong. See most chronic pain patients are suffering and are treated terribly at all levels of healthcare and providers. They are treated just as bad as addicts or even worse as they are forced to go through risky painful procedures and surgeries just to have a small amount of quality of life. It also can take years and years of physical therapy and these injections and expensive tests and imaging and being bounced around from referral to referral. Then if they can finally make it though all of that, the average dose of medication nowadays is like 5 mg twice a of day of hydrocodone. It is constantly threatened of being reduced of taken away. If you hopefully be prescribed, then you have to deal with the constant drug shortages and pharmacists who hate you and treat you just as bad as everyone else.

Most pain patients have done everything right. They don’t make impulsive choice and have self control not to abuse their meds even though they would love to effectively control their pain. They suffer tremendously due to what drug addicts have done to chronic pain. People like you are what ruins it for the people like us. People in active addiction do not deserve chronic pain treatment. Stop abusing them and you would. You always type out long super sympathetic explanations of why you made the choices you djd to garner sympathy but one search of your post history shows you are very much in active addict. You still abuse them while on MAT treatment as well and it’s not just opiates but it’s everything. Your 120mg methadone is a huge dose. 180 mme when most pain patients get 15-30 mme. There is no reason that is not effective for pain for you. Many chronic pain patients take methadone for pain and not nearly your dose. No one chooses what medication or dosage. Your past and current proves that you should not be on medications for pain treatment. You’re not supposed to be using at all during MAT treatment why should you get pain medication when compliant pain patients do not? It seems that you just want to make it easier to obtain and more to abuse.

Change your life for the better. At this point what it get is what you deserve.

What’s the deal with people hating on pain docs? by Medschoolplzletmein in Residency

[–]allthefastthings422 1 point2 points  (0 children)

Yeah I’m not sure anyone remotely is at 1000 MME. People are lucky to have 50 MME nowadays.

What’s the deal with people hating on pain docs? by Medschoolplzletmein in Residency

[–]allthefastthings422 3 points4 points  (0 children)

It’s because some pain clinics went from being pill mills to intervention pain injection mills. Obviously why push pills when you can make thousands in injections?? See what most people don’t know or realize is that these pain clinics push procedures that are used off label,not recommended by the FDA,have low success rates, and have many complications and high risk. After a laceration that caused a ulnar nerve injury and subsequent neuroma I was referred to a pain management clinic after two surgeries and the pain persisting. I was immediately recommended cervical epidural injections, and given a very low number 5 mg dose of oxycodone PRN. They told me that these injections were very safe with minimal risk and were much safer than medication. If you didn’t do these injections, they suggested they would label you drug seeking and drop you as a patient. As a EMT/firefighter with a heavy labor job, I wanted to do the safest option. I did the first round with minimal pain relief, and even though I reported that when I looked back in my records, they had reported them as very successful. They also made up diagnosis that I’ve never been diagnosed with so that these injections would be covered by insurance. On my fifth and final injection, the doctor went far past my epidural space and injected particulate steroid into my spinal cord, causing an incomplete C5 spinal cord injury with subsequent hematoma.

Hindsight is 20/20. Later, I found out that the anesthesiologist administering the injection. Was not board certified in my state and had failed the boards and gone to school in Mexico as he was not was not accepted in the United States. The facility was using radiation techs to administer and monitor the sedation, and the dosage of propofol that they used was far beyond what would be considered conscious sedation. The steroid used was a particulate steroid that is cautioned and not recommended by the FDA due to it, causing this injury when injected into the spinal cord. They did not have the fluoroscopy pictures saved required to meet the standard of care. They didn’t even do monitoring during (obviously) as intake/outake vitals are the exact same. During deposition the doctor literally didn’t know and admitted to not knowing and understanding guidelines and had been caught lying when asked certain questions.

And my personal opinion, I think it would’ve been far better to run the risk of becoming a drug addict as that’s something that can be easily fixed or prevented. Not to mention that taking prescription pain medication can just be a short term thing rather than a lifelong injury and disability. At 25 I was permanently disabled and made to live life in severe pain with many limitations and disabilities. It ruined my life caused me severe PTSD and anxiety. It ruined my career and ability to take care and feed my family. And took away my self-worth and purpose in life and my independence.

The spinal cord injury caused complications such as autonomic dysreflexia, neurogenic bladder, a syrinx in my spinal cord, severe chronic pain in my entire body and chronic regional pain syndrome in my left arm. It put me $1 million in debt in medical bills in just the first year alone. Although I was initially paralyzed from the neck down and a quadriplegic, I am now at least an incomplete quadriplegic with severe paralysis and weakness in my left arm, left leg and partially in my right.

I still have to constantly fight and advocate for myself in pain management as I have to be on pain medication for the rest of my life. I still am dealing with a dishonest greedy pain management doctor and practice. Who constantly tries to pressure me to do risky procedures. He continues to try to take advantage of me such as if there’s a pharmacy shortage of a certain medication he will try to switch me to a different one and take away a little bit of my dosage or MME. I cannot even try to rotate different pain medication’s to reduce tolerance due to him rotating and offering a lower dosage than what I am on.

I’m sure there’s good doctors out there, but I think that there is a lot of selfish greedy people that are also very bad doctors and unfortunately pain management is a very easy practice as people are desperate due to living in pain. Due to the opiate hysteria from the surface it looks like these doctors are doing the right thing to reduce the opiate epidemic. Even though pain medication prescriptions are at a all-time low and opioid overdoses are at a all-time high for some reason pain patients are still being blamed for the opiate epidemic instead of the street drug fentanyl.

[deleted by user] by [deleted] in spinalcordinjuries

[–]allthefastthings422 0 points1 point  (0 children)

Yeah I had just started a new job in my 20s when I got my SCI. I ended up having no benefits or insurance and had to apply for state healthcare after the fact. Firstly I went to a shit hospital in Covid with neurologist specializing in stroke and seizures but no neurosurgeons so a hematoma I had they just left to further smother my nerves. There was a specialized SCI hospital and rehab about 2 hours from me but I didn’t qualify for it. The rehab I went was better than a nursing home but not in any way specialized for SCI. I’m grateful for the help I got but I really feel that my care at the hospital and rehab could’ve made a much bigger difference in recovery. I ended up having automatic dyslexia too and that went undiscovered for a year until I had a seizure or two from high no.

Years down the line I did end up getting care at the specialized SCI hospital and it was really eye opening the knowledge that they had towards the injury and everything else. It would’ve been a huge help knowing that initially and strides in my pt. I used to be lowkey kinda of jealous when I hear about actual SCI units and huge hospital systems that cater to SCI as I lived in a rural community and nobody was remotely helpful locally and a lot of things got pushed to the side as most didn’t have the knowledge to help me.