Chronic Pain members - Welcome, please introduce yourself
Welcome to the new Chronic Pain group.
I’m Kelsey and I’m the moderator of the group. I look forwarding to welcoming you and introducing you to other members. Feel free to browse the topics or start a new one.
Why not take a minute and introduce yourself.
Interested in more discussions like this? Go to the Chronic Pain Support Group.
Hello @ beau238, welcome to Connect. Thank you for coming to seek a connection with others who may have had a similar experience with sciatica and irritated nerves.
I'm sorry that you've been through a lot over the years, attempting to find relief. I share your experience with failed epidurals, RFA's, and physical therapy. Through my trials and errors with failed procedures, I finally landed on central sensitization syndrome (CSS). It's a chronic pain syndrome which affects nerves, muscles, joints and sensory input. I attended Mayo Clinic's Pain Rehab Center to better learn how to live with chronic pain.
I'm hoping another member joins the conversation with some advice and experience to share that is familiar with SCS test. Unfortunately, I am not.
Do you have any other options through your pain management team towards finding relief? How do you currently handle your discomfort?
Thank you for your reply. I'm updating my post to include I am a on blood thinner (Aggranox- it's kinda like aspirin on steroids) having suffered a ischemic stroke in 2013. Honestly I cannot distinguish which pain is sciatica related and which pain may be stroke related. I'm ready to rule out an SCS due to the blood thinner.
I'm currently on 7.5mg oxy (4x/day) and 30 mg Cymbalta (1x) and apply Lidocaine 5% ointment. I've also tried various otc ointments and creams without much success. And I exercise regularly. I want to get off the oxy, but fear my options are limited. Lyrica and gabapentin have been eliminated as both left me drowsy and lethargic. My PCP prescribed a low dosage (30mg) of Cymbalta in hopes it won't produce similar side effects. And if successful, we'll gradually increase the dosage. I'm wondering if there are other options available other than what I've described. I am in the process of finding another pain management specialist but have become cautious towards those recommending additional procedures. Your suggestions are appreciated! BEAU238
Chronic pain does not respond well opioids. There is no magic pill — and your pain is real. It may be intensified by central sensitization syndrome (CSS). Mayo’s 3-week outpatient Pain Rehab program is effective. You learn techniques that help you become more comfortable and functional. . . I was skeptical and really did not want to attend. I learned better ways of doing things, gentle exercise that respected my body and how to pace myself mindfully. Am I pain free? No. Am I more comfortable? Yes. I went from walking 1200 steps/day to 10,000+ steps/day. I used to spend a lot of time in bed before PRC. . . Mayo’s Pain Rehab program is effective.
Hello @jojo123456! I'm grateful you shared your experience at Mayo Clinic's Pain Rehabilitation Center, thank you! It's nice to hear when someone benefits from a healthier way of dealing with, and living in chronic pain.
You hit the nail on the head that opiates, and other medications, are scientifically known to increase and intensify pain causing hyperalgesia. I experienced the vicious cycle as I took may different medications in search of, as you say, the "magic pill".
It's a sad reality being stuck in the cycle of wanting to be fixed or helped, and trying anything and everything possible. It's extremely difficult to see your way out to a better opportunity.
Congratulations on being a PRC graduate! Such a huge accomplishment. May I ask when you graduated, and what part of the program has made the biggest, most positive impact on your new "C Life"?
You have tried many ways to handle to your chronic symptoms, and are still hopeful to find suggestions for your path forward. That's inspiring!
My suggestion for you is to take a moment and watch Dr. Sletten from the Mayo Clinic, Jacksonville, explain central sensitization syndrome (CSS). He teaches at Mayo's Pain Rehabilitation Center (PRC), and he and his team do an incredible job.
https://www.youtube.com/watch?v=8defN4iIbho
https://www.mayoclinic.org/departments-centers/pain-rehabilitation-center/sections/overview/ovc-20481691
I'm hopeful that you find a pain management "team". Through my past experiences, I never had a team or group effort that was collectively trying to improve my quality of life, given my circumstances. I benefited greatly from PRC's comprehensive, all inclusive approach on teaching me how to live my best possible life with quality. I gained independence and confidence back, and felt like I was in charge of my well being again.
Do you mind sharing your feedback after watching the videos?
@beau238 My apologies....I attached one video, and one link below the video which is an overview of the PRC program. I'm sorry for any confusion.
That has been my argument. You cannot turn a patient who is in severe pain away from the E.R. and tell them there is nothing you can do for them. That is a sure-fire recipe for someone to harm or kill themselves. They feel hopeless, to begin with, and also frightened that they will be in pain for the rest of their lives. They wonder what is the point. I wonder how many lives could have been saved if they were given the medication they needed to help alleviate at (at least), some of their pain.
Hello there @donfeld, how are you doing? I'm checking in to follow up on Mayo Pain Rehab Center (PRC), and thank you for sharing your helpful PRC experience and insight with me last year.
I graduated PRC October of 2020. It was a rebirth, and gave me my life back. Getting off opiates was the best thing I could have done as it reduced the intensity of my symptoms. Learning how to use my body better through PT and OT, and creating a schedule were my most helpful tools.
If you don't mind me asking, what tools do you find most helpful since graduating PRC?
I think it was the fall of 2017. . .
About at my wit's end ! I've been dealing with chronic Migraines for almost 15 months now. Been to my Local ER Hospital allot. See a Nuero, My reg Doctor and been to pain management . Been admitted in Hospital many times. Have had CT scans and Ct Scans with contrast . Always normal. My Migraines started 15 months ago after passing out 3 seperate times. I've tried infusions, many meds and even give myself monthly shots with not much success ?? And yes i've done Botox also. I just don't know what to do anymore . Anyone that suffers have any suggestions on what i can do ?? I've used up all my FMLA already this year . Unfortunatly still missing work on and off. My employer has been understanding but when missing is to much ??? I've been averaging 3-4 migranes a week. Pretty much always have constant headaches . Thank You