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» LymeNet Flash » Questions and Discussion » Medical Questions » head, neck & shoulder pain. help..?

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Author Topic: head, neck & shoulder pain. help..?
artbyjessie2
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i'm in agony........ just started working again and it's making it ten times worse.
my head, neck and shoulders are so knotted up they're killing me!
i've tried weekly massages, heat packs, you name it. nothing works.

anything else i can try?
it makes me just want to lie down and sleep the day away...... not really helping me get back into working again....

feel like poop on a stick!
jessie


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Aniek
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See the current thread on shoulder bursitis. I posted what helped me with very similar pain. It took many months, but I bascically need to "prep" my muscles with a muscle relaxer to get anything else to work.
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beachcomber
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Advil softgels.
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Aniek
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quote:
Originally posted by beachcomber:
Advil softgels.

Wow, I'd would've needed about 10 at the height of my pain!


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marblenose
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Hey,
I am in agony in my upper body most of the time. My LLMD has me in muscle relaxers and I use a product called jointritis. I get at the super market which helps temporarily. I also keep a heating pad on my chair at work that I can use if I need to. I am so sorry you have to deal with this. Please know you are not alone.
Blessings,
marblenose

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lymie tony z
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Hey Jessie,
I know most of us use muscle relaxers and I have had my share...an alternative may be a tens unit...if you can get your doc to prescribe one for chronic muscle aches and pains...if not Dr. HO has a mini version for about a hundred bucks on the shopping channels.....I don't know but I don't think the chetes like electricity...or it helps numb out the nerves.......
Just a thought...yes it helps me......zman

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Mo
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Are you being treated for Babesia?

NY is a hot bed for Babesia (and Bartonella)..and I had excruciating neck and shoulder pain that required narcotics..
nothing made it go except treatment for Babesia.

Good Luck,
Mo


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cmichaelo
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Jessie,

It is so upsetting to me to hear about your condition, cause it reminds me so much of my own situation 5 years ago.

And I'm so sorry you're going through this right now.

I have, or actually had, neck/shoulder pains for 5 years. Kept coming back to me. Once I collapsed in the staircase at work screaming in pain.

I took turodol, flexeril, hydrocordone in big quantities to deal with this pain. Had an MRI done. A bulging disc was identified. Considered operation (but didn't thank God.) Learned something called the Alexander technique to teach myself to relax in the neck and keep proper posture. Went to doctors office 4 or 5 times to get a turodol shot in my butt. But it kept coming back.

Then I saw an interview with John Sarno on Larry King live back in August 2000 time frame (I think). And he was also on 20/20 at some point.

Anyway, Sarno has been healing backpain for some 20 years now using a sort of radically different treatment program, or method if you will.

Most people however can't be helped by his method. Not because they don't suffer from the particular type of pain his healing method treats.

No, most people can't be helped because they are not susceptible to the principle behind his treatment method...

which is that your pain is created by your brain and you simply think the pain away.

NO KIDDING.

It is not unlikely that you suffer from what Sarno denotes as TMS (Tension myositis syndrome.) A condition where your brain (your subconscious more specifically) can starve nerves in the spinal cord region from oxygen. This causes pain similar to pinched nerves, sciatica, herniated discs, etc.

And why does your subconscious do this crap?

Because, says Sarno, your subconscious would rather deal with physical pain than emotional pain.

In other words, if you suffer from TMS, it's because you have some sort of significant emotional pain in your life. This kind of emotional pain can range from work related stress, to family problems, and to dealing with a troublesome illness such as Lyme.

So do you suffer from TMS?

I asked myself the same problem 5 years ago. I didn't know. But after reading Sarno's book and totally believing what he had to say, since it made so much sense in my life with all the pressure and stresses I had, I decided to use his method to literally think the neck/shoulder pain away.

It works like a charm for me.

Will it work for you? I can't tell.

But what I do know is that you have nothing to loose by looking into what Sarno has to say.

And if you have an open mind and can absorp some radical thinking AND if you indeed to have TMS, then you are IN LUCK!

Cause you can think your pain away all by your self.

You can say bye bye to all those pills and heating pads and so on....if, but only if, you actually do suffer from TMS AND have an open mind.

And only you can find out.

I believe that you can actually make an appointment to see Sarno. He's down in NY City.

Good luck.

Btw, also see the thread about sciatica:
http://flash.lymenet.org/ubb/Forum1/HTML/031114.html

I have several posts in there about Sarno, including links to his book and some reviews of his work.


Michael


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artbyjessie2
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michael - thanks for the info - that reading is for a day when i have an attention span :-)

marblenose , tony z, - i haven't tried muscle relaxers yet. I'm wondering if I should try them. my massage therapist worked on me very hard (I saw stars) and it did nothing. She said she'd never seen anything like it.

I've got a hot tub and that brings about 10 minutes of relief.

MO - I am being treated for Babesia AND both both strains of bartonella. I didn't know that could be the cause. Good info!

Thanks everyone. I have some good ideas now...


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Aniek
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quote:
Originally posted by artbyjessie2:
i haven't tried muscle relaxers yet. I'm wondering if I should try them. my massage therapist worked on me very hard (I saw stars) and it did nothing. She said she'd never seen anything like it.

That's exactly the same reaction my physical therapist had. He was using a technique where acupuncture needles are put into your muscles to release myofascial trigger points. For most people, the treatment hurts but the next few days they feel great. I never had relief and, one day, my muscle inflammed so quickly he said he had never seen anything like that.

We switched to hands on myofascial relief (no more needles). Once I started a muscle relaxer, we finally saw progress. I have improved more since starting Lyme treatment. But it was a long road to get there.


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artbyjessie2
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do the muscle relaxers have bad side effects? aka, knock you out, make you dizzy, etc?
i'm trying to work -
would be good if i could stay awake :-0

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lymeinhell
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I had trigger point injections of lidocaine shot into the lumps I had developed on my shoulders and back of head.

The lidocaine completely numbed everything and helped bust up the muscle spazms. It's effects are temporary (about 7-10 days), but when done repeatedly and used in combination with Flexeril at bedtime, I got through it. (and oh, the sigh of relief of immediate pain relief.)

I've been told Prolotherapy is a more effective solution.

I still use Flexeril at bedtime only. In the beginning, they make you sleepy and maybe a little dizzy (hence, take at bedtime). You gradually build up a tolerance to it.

And IMHO - the difference between real Flexeril and generic is like night and day. Go for the real thing if you can.

------------------
Julie G.
___________
lymeinhell


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Aniek
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I built up a tolerance to Flexeril. I started by taking 5mg a night, and slowly built to 30mg a night. It took time to not be tired, but it was so worth it.

I do have trouble waking up on the Flexeril. It's the worst part of every day. And I feel hung over if I sleep too much. But it's all worth it. As soon as I hit 20mg, I felt a difference, and when I got to 30mg it was incredible.


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