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Lyme Disease ForumsGeneral & Supporthead pressure/ neck pain
07/08/2010 03:38 PM
meredithhny
meredithhnyPosts: 37
Member

hi all, was wondering if anyone else gets horrible head pressure/ neckpain?

i do have an abnormal spect scan and sometimes get scared cuz the pressure is sooo much..

the neck pain feels almost cripiling!!

anyone else??

Reply

07/08/2010 03:48 PM  Top
Santinagirl
Santinagirl
 
Posts: 104
Member

Besides what is happening to my feet, the head pressure and neck and spine pain are my 2 worst symptoms. Fiorect works miracles for me tho.

Previous discussions I participated in:
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07/08/2010 06:44 PM  Top
KristenM
Posts: 70
Member

Do you see a chiropractor? I would highly recommend finding a good one!

Even though on most days I don't necessarily need to be adjusted, my chiro stretches me out, does traction on my neck, positioning with my head, and gets to certain pressure points which really help with the head pressure, neck, and back pain.

Ask around about a good chiropractor who knows how Lyme affects the body.


07/09/2010 09:27 AM  Top
zoemajik
zoemajik
 
Posts: 666
Member

Yes!

It went away for awhile while I was on flagyl and Ledum earlier this year - but since stopping, back with a vengeance. It takes constant maintenance to keep it manageable - I hate it Sad

Valerie, Lymphedema group leader and Lyme patient.

I am not a health-care professional. Information and experiences I share should be regarded as such, and are not intended to take the place of medical advice from your doctor.

07/09/2010 10:42 AM  Top
meredithhny
meredithhnyPosts: 37
Member

it feels cripiling....

07/09/2010 11:53 AM  Top
Bettyg
 
Posts: 26614
VIP Member
I'm an Advocate

merdith, i agree w/someone else above.

get a chiropractor that does SUBLAXATIVE treatments and the table being a DROP TABLE. as they push down on you, table drops in those areas so you don't feel all that pressure.

i've been going to one of this special type for 3-5 months now; made great progress.

i don't have head pressure, but severe neck problems from severe falls to my neck/head/shoulder area ... permanent damage.

BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader

NOTE: I DO "NOT" USE CHAT thanks!
**************************************

NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)

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Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.

43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.

07/09/2010 02:32 PM  Top
zoemajik
zoemajik
 
Posts: 666
Member

I would definitely go to a chiro if I could afford one.

I used to work for one, a couple of chronic Lyme patients would come in a couple times/week for relief. (Little did I know - I was one at the time!)

Valerie, Lymphedema group leader and Lyme patient.

I am not a health-care professional. Information and experiences I share should be regarded as such, and are not intended to take the place of medical advice from your doctor.

07/11/2010 04:11 AM  Top
shorelinelyme
shorelinelymePosts: 1252
Senior Member

I completely agree with a chiropractor being able to help with the stiffness, pain etc.. I just recently started going regularly (2-3x/week) and it has made a huge difference for me.

My chiro does neck traction, adjustments, electrical stim etc.. at each appt (covered by insurance!!!) I will be adding in cold laser therapy later.

I look forward to these appts- and love how I feel afterwards!

Jackie


Previous discussions I participated in:
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08/30/2010 05:43 PM  Top
Cinderskenney
Cinderskenney
 
Posts: 20
Member

I just started getting severe head pressure about a month and a half ago, I never had it before but after I was taken off rifampin and put on bactrim again it started up. I am getting an mri tomorrow, am very nervous and tired. Also have nausea and vomiting.

08/30/2010 06:25 PM  Top
VicMac
VicMac
 
Posts: 1649
Senior Member

Head pressure and neck pain has been one of the longest running symptoms I have had. Now it includes a permanent ringing/hissing sound in my head. The neck pain does seem to flare up and be worse at certain times and better at others.

With all of it, for me, there is a definate link to stress and worry. Always makes it worse! Lyme has forced me to simplify my life greatly.

I wish I had solutions for everybody here who is suffering, but I am still hunting for them myself and seem to be more of a student on this board than a teacher. All I have to offer is my experience, support, and prayers based on what I have learned in my recovery. I am not a physician.

Previous discussions I participated in:
Reaching out
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