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.
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@ellens I had a out of body once. I was on the highway I looked up at a beautiful cloud before I knew it I was up to the cloud I guess my senses took over and I remember saying who,s driving the car like lighting I was back on car
@bustrbrwn22 Hi there, good for you.....how often do you have sessions in a week. Here is what I am doing. I am testing a twice a week series of MFR sessions. Is it possible that I can improve my quality of life by just adding one more MFR session per week? If so, can I hang back from some of the other pain control medications I am taking?
I am already noticing that I can make it much more comfortable with twice a week. However, the first session with greater intensity for the lower body parts led to the upper body complaining because it was ignored. Truly....I was sort of shocked. Anyway....we have now evened up the treatment locations and degree of treatment. Gotta keep those shoulders and that neck happy.
May you be free of suffering and the causes of suffering.
Chris
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1 ReactionHi all!
I am hoping this will provide another resource in everything I've been going through the last year.
Last fall I started experiencing daily sharp, stabbing headaches that would come and go all day long. My GP referred me to a neurologist as I already suffer from migraines and she felt that would be best for treating two headache disorders. Through a process, we got them under control with indomethacin. The initial diagnosis he gave me was indomethacin-responsive trigeminal autonomic cephalalgias. For seven months, I had no headaches, unless by my own fault I missed a dose. In August, the headaches flared up despite the medication, though not as severe as last fall, which has been very discouraging as once again I am in daily pain at various levels off and on throughout the day, and finding a solution has been challenging both on the medicinal side of things and in working with my neurologist. This Tuesday I'll try and SPG block for the first time which I'm hoping will at least provide some temporary relief. Until that relief comes, I will continue moving on one day at a time as that's all you can do.
Rebecca
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4 ReactionsWhen my pain specialist tried to lie and taper me, I involved my US Senator, John Barrasso. I proved that the CDC Guidelines were not written for Chronic Pain patients by the CDCs own warning letter issued after they were released (check the site).
I proved that opioids are necessary for quality of life and I’m not a seeker— I’ve never broken a contract by shopping illegally for my medications, pharmacy hopped, or had another doctor prescribe them.
The decrease was unwarranted, unnecessary, and fully driven by DEA pressure.
Barrasso got involved and it was quickly and forthrightly halted.
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2 ReactionsDear Ones,
I realized that I left out an incredibly important piece of info in this post. That is that the head of the Kaiser Permanente Opiate Oversight Management Team, who happens to be a Psychiatrist (there are many disciplines on the team), met with my husband, PCP and I, quite some time ago, to tell me they validate me and my need for morphine! She was adamant that we knew and understood the team felt this way! I about died of shock LOL!! I have been on pretty much all of the opiates over the past many years (27+) I think.
I wish the same validation, respect and relief for all of you! Warmest wishes, Sunnyflower. 🙏😊🌹
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5 Reactions@rseago87 A suggestion for future reference, is looking into the Michigan Head Pain Clinic in Ann Arbor. I was seen as a patient at the clinic and also hospitalized two times at their inpatient facility. I now suffer from only occasional migraines. Dr Joel Saper was the founding neurologist and patients come from across the U.S. and foreign countries. The first time I was an inpatient for 4 weeks and the second time for 2 weeks. I don't know everything about your circumstances but they were able to help me. I am sure there is information online that might indicate if they would be a source of help for you.
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2 ReactionsHi Renee, thank you for all you are doing to help so many! Bless you girl for your efforts in the midst of your pain! Wow, you are an inspiration! I 've never heard of this before. How can I help if I am able? Warmest regards, Sunnyflower. 😊🙏🌹@lioness, @ellens @jesfactsmon
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2 ReactionsThank you @suzanne2 ! I will look into that clinic as I am researching places to get a second opinion. Thankfully my migraines are pretty well controlled. The TAC headaches are the more significant problem and are much rarer so finding someone who is well-versed in treating them is more challenging but I know there are good doctors out there.
@faithwalker007
Hi, Renee. I'm in a semi-dark place right now because of pain and pain treatment. The neurologist tried to set up a consult appointment to discuss a pain pump implant, but after I sent him a note asking him to expedite the process, he called the doctor he had referred me to, and discovered that no one in central Oregon manages pain pumps. Getting the implant is no problem locally, but the doctors who manage the medication in the pump are 150 miles away. And my wife has voiced her objection to the pain pump implant.
Back to what you said about having a doctor trying to taper you off opioid. I used to take 30mg tid, but after tapering off completely, I only went up to 15mg tid. I've pretty consistently been taking it only bid, to build up a backup supply. This summer my prescription was cancelled 4 months, because the supplement insurance wanted prior authorization. So much for the backup. I know that when I take 30mg, it reduces the pain noticeably. A while back my pcp told me that he wouldn't increase my dose because of tolerance. If I can't get the pump implant, I know that I'm going to need more mscontin.
Did you get the pain specialist to back off and give you the prescription you needed? Can you tell me how much you were taking that prompted the doctor to tell you that?
I guess I need to get an appointment with my pcp and ask him to increase my dose. I'm going to use some of the things you've posted in the conversation.
Thank you for all you're doing.
Jim
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2 ReactionsIt should never be that hard.