Parsonage turner syndrome *

Posted by adriennes @adriennes, Sep 9, 2017

I was diagnosed with parsonage turner last November after 2 months of agony, while I am able to function now, I’m still experiencing severe weakness, numbness, pain, this is unusual im told, but having it as a woman is unusual also. Does anyone have any experience with this?

@painful

The pain has been continuous. The pain killers work for 6 hours. I had an MRI and a visit to the Neorlogistat Wellingtons
. They want me back in three month. I am under the care of Andrew Wallace of the Fotrtius clinic in London
He operated on the same shoulder last Feb. Until I went to see him that is what I thought I had. He is top of his field.
He diagnosed me very quickly.
He looks at 2,000 shoulders a year and would see two at most in a year.

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@painful sorry to hear about PTS. Are you on something for nerve pain. I was on nortriptyline for a time and there are many others Drs. can prescribe? Also, I wonder if different supplements might help things like turmeric, quercetin / rutin, other lipoflavins, resveratrol and different combinations of supplements. You can buy these on Amazon or at a vitamin shop. I also take a little hemp seed oil (not CBD). I do think these made a difference for me somewhat in pain level for hip and back pain I have. Some might make pain worse, some better. It might help somewhat with nerve pain.

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Parsonage-Turner Syndrome (PTS), also referred to as idiopathic brachial plexopathy or neuralgic amyotrophy, is a rare disorder consisting of a complex constellation of symptoms with abrupt onset of shoulder pain, usually unilaterally, followed by progressive neurologic deficits of motor weakness, dysesthesias, and numbness.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2926354/

Just for information.

Regards, ElaineD

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@kimchi19

My symptoms are possibly PTS. I had ACDF level 2 surgery Feb. 28th and 3 nerve conduction studies by 3 different neurologists. My left thumb lost all flexion ability 1 month prior to surgery and remains unchanged. My right thumb is weak but still functional. Told to wait 2 years and it may go away. Does anyone have any experience with this disorder?

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Hello @kimchi19, welcome to Connect. There is another discussion with the same name where your question will receive more visibility. I'm tagging our moderator @ethanmcconkey to see if we should move your post to the following discussion:

> Groups > Brain & Nervous System > Parsonage turner syndrome *
https://connect.mayoclinic.org/discussion/parsonage-turner-syndrome/

I'm sure it must be difficult to be told to wait 2 years to see if a symptom will go away. Have you thought about getting a second opinion?

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@johnbishop

Hello @kimchi19, welcome to Connect. There is another discussion with the same name where your question will receive more visibility. I'm tagging our moderator @ethanmcconkey to see if we should move your post to the following discussion:

> Groups > Brain & Nervous System > Parsonage turner syndrome *
https://connect.mayoclinic.org/discussion/parsonage-turner-syndrome/

I'm sure it must be difficult to be told to wait 2 years to see if a symptom will go away. Have you thought about getting a second opinion?

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Yes, I'm flying to Houston to see a neurologist who specializes in PTS to either confirm the diagnosis or rule it out.

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My symptoms are possibly PTS. I had ACDF level 2 surgery Feb. 28th and 3 nerve conduction studies by 3 different neurologists. My left thumb lost all flexion ability 1 month prior to surgery and remains unchanged. My right thumb is weak but still functional. Told to wait 2 years and it may go away. Does anyone have any experience with this disorder?

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Hi @kimchi19 you may have noticed I moved this post to this existing discussion on parsonage turner syndrome so that you can learn from others who have experience with this diagnosis. Simply click VIEW & REPLY in your email notification to get to your post.

I wanted to introduce you @elained @richman54660 and @jjspokane61 as they may be able to offer you support.

Back to you @kimchi19, when will you be going to see the neurologist in Houston?

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@kimchi19

My symptoms are possibly PTS. I had ACDF level 2 surgery Feb. 28th and 3 nerve conduction studies by 3 different neurologists. My left thumb lost all flexion ability 1 month prior to surgery and remains unchanged. My right thumb is weak but still functional. Told to wait 2 years and it may go away. Does anyone have any experience with this disorder?

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Hello @kimchi19 I'm 15 months into my PTS story and I can tell you it DOES get better with time but you have to be patient! Here's somethings to know: 1. If you have hand mobility issues get to a hand PT ASAP. My dominant hand was affected, the index finger became completely rigid. Doing anything became almost impossible. I finally ended up going to see a hand specialist who gave steroid shots and then I started hand therapy. Getting back the use of my hand was a tremendous improvement. 2. gabapentin is a mixed blessing. I would NOT have made it through the most painful times without it, but getting off of it has been challenging. At the most I was taking 1800mg per day ( 6 300mg pills), I tried to reduce by 1 pill/day and could not. The nerve pain would return with a vengence… finally the hand doctor suggested I get 100mg pills so I could wean off more slowly. Since then I've been reducing by 100mg every 2 weeks. I'm down to 900mg daily now. It's still a struggle! The pain is very real and it takes alot of commitment, but I AM going to get off of this medication THIS year! 3. Avoid any surgery if you can. I got impatient with my recovery and kinda pushed my hand doctor into doing a tendon release surgery. It all went well, but I think some of the pain I'm having now is related to that surgery. Probably if I had just been patient I would be in a better place. It's never the best course to have a surgeon digging around inside your body unless it's 110% necessary! 4. It's really hard to let go and let others do things for me! Takes this time to allow others to be your support.

Hope some of that is helpful! Keep us posted on your progress…
JJ

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@josebaltierraiii I'm probably too late to be helpful with your question about whether I would "self medicate" with Gabapentin if I had a relapse… and the answer is… YES I would. I'm not completely off of it yet, but I intend to keep some of the extras around in case on an emergency. It takes days/weeks to get into the primary dr and in the mean time I would self medicate. BUT… one article I read about PTS said that EARLY administration of steroids could lessen the nerve damage done – so THAT would be my first thing to do… call my DR in tears asking for prednisone or just sitting in his office until he has time to see me… hope that helps! You should post an update so we know how you're doing.

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@kimchi19

My symptoms are possibly PTS. I had ACDF level 2 surgery Feb. 28th and 3 nerve conduction studies by 3 different neurologists. My left thumb lost all flexion ability 1 month prior to surgery and remains unchanged. My right thumb is weak but still functional. Told to wait 2 years and it may go away. Does anyone have any experience with this disorder?

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Hi, @kimchi19 I’m sorry for just responding now. I must have missed your post. I have had PTS since February 2017. After a couple of months of trying to diagnose what I had my doctor referred me to an orthopedic nerve surgeon. I had an MRI done of my neck and an EMG. The surgeon assured me that I needed ACDF surgery (cervical fusion) so I agreed to the surgery. Unfortunately, the surgery didn’t help my condition – nerve pain in my right arm and hand. Even worse, two weeks after my surgery I developed the same nerve pain in my left hand. Fortunately, the pain is not nearly as bad as in my right hand, but it is something I live without. 🙂

A week after my surgery I saw the doctor for a follow up appointment and I told him my pain was getting worse. He put me back in the hospital where I had more MRIs and tests. The doctors, a neurologist included, couldn’t find what was causing my pain.

About 6 weeks later I saw two neurologists and the second one performed an EMG and concluded that I likely had PTS. A more recent visit to another neurologist confirmed that I had PTS. I was told that mine is unusual in that the pain doesn’t usually last this long.

Anyone who has PTS will tell you that this condition requires a lot of PATIENCE. I have tried many remedies, but I only get some relief from pain meds, compression gloves, ice, and heat. In the past 6 months I have had some improvement with the use of my right hand and arm, but I am still very limited with what I can do. More than anything, though, is the constant nerve pain that I experience on a daily basis. That has been difficult to live with.

I hope you get better very soon. Just know that you are not alone. There are lots of kind people who are here to help you!

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