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» LymeNet Flash » Questions and Discussion » Medical Questions » Any one have a rhizotomy for neck pain

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Author Topic: Any one have a rhizotomy for neck pain
ldsucs
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Member # 16142

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Any one try a rhizotomy for neck pain? Where they burn the nerves in the neck?

I know the bacteria is in my neck, but the pain is getting to me.

Posts: 28 | From tx | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
nyjohn
LymeNet Contributor
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try medical acupuncture or good cranisacral therapy before getting that done!!!!!!!!!

--------------------
do your best to educate the rest because
9 out of 10 doctors don't know jack about tick borne illnesses

Posts: 437 | From shawangunk mountains, ny | Registered: May 2008  |  IP: Logged | Report this post to a Moderator
bettyg
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welcome ld; glad you found us! [group hug] [kiss]


never heard of that!! i agree with 2nd poster! my neck is bad 24/7 too ... i always have FROZEN ICE PACKS ON IT/SHOULDER BLADE AND LOWER BACK.


WELCOME, would you like a FREE copy of my newbie package of 124 pages info galore sent by LYMENET'S PRIVATE MESSAGE system here; includes TREEPATROL'S LINK of his archive of over 1000 links of good lyme info?


I've been completely REORGANIZING it; NOT DONE YET; but up to page 60 since I have now created a TABLE OF CONTENTS WITHOUT PAGE NUMBERS since it changes DAILY! The part NOT organized yet is the last 30 pages of SSDI, ss disability insurance benefits tips/forms!


also, please go to TREEPATROL'S NEWBIE INFO IN MEDICAL; at top being features; mark it as a favorite! over 1000 links of good lyme info. He/I have some duplicates.


most of mine is very DETAILED info on certain things: SSDI/ss diability insurance benefits; FINANCIAL BURDENS; about IGENEX blood testing, symptoms lists for the basic types, NOIR/no infrared SUNGLASSES, etc. and how to use this board!


If you would like my newbie package, please send me a PRIVATE MESSAGE. PMs are the 2 people standing together icon to right of your name. Just ask me to send you lyme package, and I'll get it to you promptly. Thank you!
******************************

we recommend 6-12 WEEKS of doxycycline antibiotics; 2 months symptom FREE before stopping antibiotics.


400 mg daily; 200 mg am/pm each 12 hrs. apart!
***********************************************


so glad you found dr. burrascano's 05 lyme guidelines!


call your dr. and DEMAND MORE! you are now in the LYME WAR CONTROVERSY ... another thing you didn't ask for!


please see BELOW LINK about ACTION ALERTS....CALLING 4 WASH. DC PHONE NOS. GIVING THEM YOUR FULL NAME/COMPLETE MAILING ADDRESS AND TO "PUT LYME DISEASE ON THEIR AGENDA!"!!!!

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=8;t=001271

******************************************

short/sweet version is this:


IDSA, infectious disease society of america, are infectious drs. who:

.. do NOT believe in CHRONIC LYME;

.. treat from 1 day to 3 weeks MAX ANTITIOBICS, AND YOU ARE "CURED"! HOG WASH!!


ILADS, intl lyme associated disease society, are our LLMDS, LYME LITERATE MDS, and they:


... believe in chronic lyme AND TREAT US AS LONG AS NECESSARY!!!


... another controversy; various STATE HEALTH DEPTS. FILING CHARGES on our llmds for treating antibiotics longer than 4 weeks!!!


example: see activism; read about DR. CHARLES RAY JONES, KIDS NO. 1 LLMD IN CONN! starting his 3rd year of charges trying to take away his license!!!

*********************

Also, if you are needing a LLMD, LYME LITERATE MD, please post on board in SEEKING DR. forum. Go to FORUM HOME, right corner click, and then chose seeking dr.


We ask that ALL members post in seeking dr. and START THEIR OWN ``NEW'' POSTS vs. adding on to someone else's because we can NOT keep track of who has been answered and who NEEDS to be replied to ok!

Many of you have been sending me a private message asking for llmd names and have NOT posted on the board. I require you to post online because when you show the state and largest cities nearest you; others from YOUR STATE WILL JUMP IN and give you the MOST CURRENT info that they have.


We have nationwide lists do NOT have most current info! We do what we can, but we depend on members to share all updates, deletions, phone nos. not working or changed, etc. with us. Then we let the others know promptly who have lists!

So thank you for starting YOUR OWN POST in seeking dr! We/I will help you as much as possible over there!  Betty
*******************************************

When you post or reply, please break up your solid, continuous block text [Smile]


welcome to the board! many of us have neuro lyme where we can NOT read long solid block text and be able to comprehend and read it as is.


please edit your post by CLICKING PAPER/PENCIL ICON to right of your name. that opens up BOTH subject line and body text.


now please break up your WORDY SENTENCES into one sentence paragraphs. Then hit ENTER KEY ``THREE`` after each paragraph; we need that space for comprehension.


if you are NOT a wordy person, you can do 2 or 3 total ok. do this for your entire post.

NOTE: you do NOT have to use "", just show the name of person you are responding to, and then type your comment.


IF you need to use "", PLEASE DELETE "BOLD" CODES so it's regular type text we read vs. the DARK, HARSH/PAINFUL BOLDING.


specifically, delete the first 4 characters of 2ND LINE of a ""


[QB] just delete these 4 characters, and BOLDING is GONE! my eyes will really appreciate that; it's one very bad side effect of my having lyme for 38.5 years!! xox


then go to left hand corner and mark box to receive ALL REPLIES, and click EDIT SEND


we thank you for helping us; [Wink] otherwise, we will SOB, SCROLL ON BY, since we can't read to help you. If I see posts like this, I SOB them; to hard on me. I'm also in the early stages of losing my eyesight from diabetes retinopathy. [Frown]

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DakotasMom01
LymeNet Contributor
Member # 14141

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Hi ldsucs,
I didn't have this done in the neck.

However, I had 18 nerves entrapped in my mid to low back, when my spine shifted, because of disk collapses.

I can't describe the chronic pain I was in and living on pain meds. There were no guarentees with spine surgery that it would be better.

I wanted the pain stopped and my life back.

I had all 18 nerves done , close to 5 yrs ago and haven't had pain in that area since.{ before Lyme dx, but was un-dx'd for 20 yrs.}

No Steriods are involved in this procedure. I didn't want to live on pain meds and prednasone, or steroid shots, that didn't last long.

The nerves do grow back, but find another path.

The set up of the procedure will be painful as they have to know they are in the right place, but once its done, they shoot in lydocaine, so you don't feel the cauterization part, then pain is over. I was a little sore for a few days. That maybe cause I had so many done.

My dr was a sports pain management dr, who had a lot of experiance doing this procedure.

Only you can decide, how much pain you can live with, how long you can live with it, and how it affects your life.

Maybe you can find some spinal support boards and see what others who have done it have to say there. The procedure may sound barbaric to people, but not to those it has helped.

If needed, I would do it again. I don't miss that pain!

--------------------
Take Care,
DakotasMom01

Posts: 371 | From NJ | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
   

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