Chronic Pain members - Welcome, please introduce yourself

PS--Prior to my finding the sympathetic provider in MT I had an MD who did give the hydrocodone that I needed for RA pain and guess what? He had Federal agents coming to his home to investigate him and he had a family. This is beyond excessive in my opinion. My present rheumatologist won't go near the subject of opioids.

@woogie When my friend who had the NDE told me what it is like beyond the veil I was in awe of her experience

I have lots and lots of books about the near-death experience. I, too, have been in awe of the experiences people have had. I have gathered that it is not productive to commit suicide unless maybe there's no hope for recovery. We do not have answers for this. I think it's neat that you actually have a friend who had an NDE! My brother rose up out of his body once while he was sick at home and looked down at his body from the ceiling. My father appeared to my mother after he died. She touched him and he was solid! I've heard of the astral body and think that's what he was in at the time.

@artscaping I am continuing the myofascial treatment. My hamstring is having less pain as are the sides of my calves. I think I’m at session 7 or 8 and I think that is pretty good results. I am using my TENS unit as the pain meds had no effect on my feet pain today but the TENS unit is helping tremendously. It would be much better if the electrodes were Bluetooth to the main TENS unit instead of those stupid wires. I could then get around without tripping on them. Thanks for asking

How do you get your opioids? Do you have a sympathetic provider? I had one in MT but for all I know she could have since been intimidated by the drug police. The small supply of hydrocodone is left from what she gave me and I moved from MT back to MN over 3 years ago.

Hello ellens, @lioness, @faithwalker007, yes, the non-legit substance abusers and their tragic overdoses have caused a great deal of opiophobia in the medical community and also tragically, because of this there is some substandard care going on. If only people understood that patients with legitimate pain do not get high from opiates nor does it really take away our pain rather helps us not to jump or pull the trigger. I have been the victim of stigma on more than one occasion and it has made me feel so awful and has changed my entire life because of it. The judgments and opinions are everywhere. It will take a lot of Education to help people understand but I don't see that happening in the media anytime soon rather only, the opposite is what I see all the time. Never do I see opiates indoors for legitimate pain in the media or talk shows Etc.

Warmest regards to all of you and prayers for relief! Sunny flower 🙏🌹😊

Hi 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

I agree. We do have a small glimmer of hope of the horizon however in the New Hampshire Bill passed called HB-1639-FN. This Bill protects chronic pain care patients and their doctors from the CDC guidelines as well as much more.

I’m in contact and negotiating similar legislation for the state of Wyoming as we speak to protect those with chronic pain here with the backing of the Wyoming Independent Living WYDPAC Committee, WY Council of the Blind, and many more. I’ve already got almost 50 signatures in the petition and it’s only been circulating on Facebook for 4 - 5 days?

I don’t have the money to promote the thing so I’m doing so the sharing and promotion on my own which as you can imagine is not much with my pain level.

Why would Wyoming make a difference? Because most of our state go to out of state providers who are licensed by the State in order to get paid by Medicaid.

Which states am I talking about? South Dakota, North Dakota, Nebraska, Colorado, Utah, Idaho, and Montana.

Wyoming knows how and when to make an impression. We’re sincere, honest and know how things are nil C

@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.