LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Advice for intense migraines?!?!

 - UBBFriend: Email this page to someone!    
Author Topic: Advice for intense migraines?!?!
frustratedNJ
Member
Member # 6603

Icon 5 posted      Profile for frustratedNJ     Send New Private Message       Edit/Delete Post   Reply With Quote 
I was diagnosed just over two years ago with Lyme, Bartonella, and Babesia. My migraines, stemming from both my neck and TMJ are becomming worse and worse. Anyone with ANY advice would be greatly appreciated.

Secondly, does anyone know where I can get any information regarding Lyme getting worse due to a trauma, ie. a car accident?

Thank you and Happy Holidays!
Lisa


Posts: 10 | Registered: Dec 2004  |  IP: Logged | Report this post to a Moderator
Kara Tyson
Frequent Contributor (5K+ posts)
Member # 939

Icon 6 posted      Profile for Kara Tyson         Edit/Delete Post   Reply With Quote 
Hi Lisa,

I get cluster headaches. Something I suffered with well before Lyme.

There are differant types of medications.

You may want to try Imetrex nose spray. It works well but is considered to be very strong and is only given to people who do not have a history of addiction. Some Dr.'s still back away from it.

If you can tell a migraine is coming on you can try Maxalt. It is a disolving tablet.

Also, look at all the herbs and vitamins that you are taking.

Some of these may be causing your migraines. Black walnut and cat's claw can be triggers.

It you are taking a multivitamin check to see if there is B6/B12. The B vitamins can cause headaches.

Also, try to avoid perfumes. The cleaning isle at the grocery store is the worst.


Posts: 6022 | From Mobile, AL | Registered: Apr 2001  |  IP: Logged | Report this post to a Moderator
Lyme Wolf
Member
Member # 5463

Icon 1 posted      Profile for Lyme Wolf     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Frustrated,

I have heard that the antibiotic Rifampin is very effective at treating infections that involve migraine headaches. I would suggest discussing a trial with your LLMD.

Keep on, keepin' on!

-Lyme Wolf


Posts: 63 | From Twin Cities, MN | Registered: Mar 2004  |  IP: Logged | Report this post to a Moderator
flyers999
LymeNet Contributor
Member # 1397

Icon 1 posted      Profile for flyers999     Send New Private Message       Edit/Delete Post   Reply With Quote 
Lisa,

This is probably a long shot but , have you looked at your diet as a cause of your headaches?

I had headaches for years until I discovered that dairy was the culprit.

The most common foods that give people trouble are: dairy, egg, wheat, peanut, soy, tree nuts, fish, and shellfish.

Jack


Posts: 385 | From South New Jersey, USA | Registered: Jul 2001  |  IP: Logged | Report this post to a Moderator
RECIPEGIRL
LymeNet Contributor
Member # 5884

Icon 12 posted      Profile for RECIPEGIRL     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Lisa,

I can relate to face pain, head pain, ear pain, TMJ, etc.


I use RX Elavil in low dose which is an old anti-depressant, but used widely for pain now. It makes the pain go away. It does not cover up the pain. Get the cheap generic.


I've taken Percocet from my Dentist which masks the pain. In an hour or so, the pain is worse than before I took something. I have to take something for the underlying inflammation which is Motrin with snack & then some Elavl.


If I still have leftover pain the next day, I use as low a dose of Elavil as I can. I treat until all pain is gone. If I go to bed in pain then I'll wake up in pain.


My Elavil is 10 mg. tablets. The RX says 1 to 2 tablets. I have a pill cutter to use as needed.


I also take Elavil 10 mg. to sleep & to have restorative sleep. If I don't sleep hard, I'm a super neuro mess.


I've taken Elavil intermittently since the eary 90s. From what I remember, Elavil takes the brain through all phases of sleep.

Sleep is important to keep your pain at a minimum.

Take Care
Jan



Posts: 602 | From Burleson, Texas, USA | Registered: Jul 2004  |  IP: Logged | Report this post to a Moderator
hatsnscarfs
LymeNet Contributor
Member # 6562

Icon 1 posted      Profile for hatsnscarfs     Send New Private Message       Edit/Delete Post   Reply With Quote 
I had frequent and severe migraines several times a week until I figured out which foods were triggering them. There are lists of migraine trigger foods. I'm OK with many of the common triggers but I absolutely can not eat, swiss cheese, peanuts, oranges, preservatives...Also must avoid airfresheners, perfumes, carpet fresh etc.

There are some foods I can tolerate occasionally but if I eat them too often then they trigger a migraine (blue cheese, eggplant, sesame...

I learned which foods caused my headaches over a long period of time. Whenever I would get a headache I woould look back over everything I had eaten and eventually the patterns became very clear. Preservatives like potassium sorbate, sodim benzoate etc.in bread, tortillas, sour cream... were triggering migraines every time I ate out.

I also need to keep my coffee intake under control. If I feel a headache coming on a cup of coffee actually helps stop it.

The other thing that helped enormously is going to the chiropractor regularly. If I start feeling "headachy" I go right away. For me this prevents a full blown migraine from developing.

I've gotten my migraines down from several a week to 1 or 2 year just by avoiding the triggers.

Since getting Lyme I'm on the anti yeast diet and have not had any headaches.

Good luck being a detective.
h&s


Posts: 956 | From MA | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
tabbytamer
Frequent Contributor (1K+ posts)
Member # 3159

Icon 1 posted      Profile for tabbytamer     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Lisa,

Do you get a feeling headaches are pretty common among Lyme patients ?

My cocktail:

At the first sign that a bad headache in coming on I take one Phenergan. It helps a little with headaches but I take it to start calming my tummy (from nausea).

Then, about 20 minutes later I take the Imitrex nasal spray.

If the headache is still going strong, I take one Demerol.

If after all that, and several hours have passed and the pain is still progressing, I take one Toradol 60mg. intramuscular injection.

Usually if the headache goes that far it is one of those combination/cluster headaches from the h-e-double-hockey-stick place. The Toradol works on those 99% of the time for me.

Also, getting in the shower, sitting down, and letting warm water run on my face,neck, and back of my head helps relax me until the meds kick in.

I know a good pain doc if you can come to San Diego. For that matter, he may know of someone is your area. Would you like me to ask? Just e-mail me at [email protected].

------------------
Tabby


Posts: 2098 | From San Diego, CA, USA | Registered: Sep 2002  |  IP: Logged | Report this post to a Moderator
groovy2
Frequent Contributor (1K+ posts)
Member # 6304

Icon 1 posted      Profile for groovy2   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I suffered with migraines for several years.
I am a editor for a TV station and I noticed
a pattern after a while that I was just
getting migraines on weekends. So I figured out what I was doing diffrent on my week
ends. Coffie-- I was drinking about 4 cups
of coffie a day at the station and about 1
cup of weaker coffie a day on week ends.
SO I quit drinking coffie cold turkey.
BIG MISTAKE--13 Day Long Non Stop Migraine.
And then for about a month after that a
lessening head ake about a couple hours a day. Now I havent had one in 5 months.
I switched to tea (1/20th the cafeen in green tea than coffie) Dont do the cold turkey thing --Just taper off the coffie--
I think it has somthing to do with the brain stem swelling that can come from Lymes.
Hope this helps you-- Jay

Posts: 2999 | From Austin tx USA | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
arg82
Frequent Contributor (1K+ posts)
Member # 161

Icon 1 posted      Profile for arg82   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
This post has been very helpful for me. I get terrible headaches a few times a week and as of yet have not found any kind of treatment that consistently takes care of them but I haven't pushed my doctor(s) to trying other treatments. Right now I have Maxalt that I take if it's a bad headache but I'd say it only takes care of the headache 40-50% of the time, most of the time it only takes the edge off, and sometimes it does nothing at all. I've tried Imitrex and Amerge before - Imitrex didn't really help at all and caused a side effect of my throat feeling like it was closing up (which I get with the Maxalt, too, but not as bad) and the Amerge helped for a while but then stopped working.

I've taken Vicodin for the headaches before and that seems to help more than the Maxalt but I'm afraid to ask for such strong meds. I think it would be great for me to find a doctor to deal with all the pain issues. Anyone know of anyone in eastern MA or RI (I'm near Cape Cod, MA)?

I'll look into the Imitrex nasal spray and see if it would cause the same side effects that the oral Imitrex was causing. And I'll try to speak up about the pain at my next LLMD visit in a few weeks.

--Annie

------------------
``The best way out is always through.'' -Robert Frost



Click to join Lyme_Camp

Click here to see my Lyme journal.

Lyme Out Retreat Information Webpage


Posts: 2184 | From Rochester, MA | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
dontlikeliver
Frequent Contributor (1K+ posts)
Member # 4749

Icon 1 posted      Profile for dontlikeliver     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi,

Ive had intense, toxic feeling migraines for years. And, before I knew what was really ailing me, I used to take a double-dose (800mg) of Ibuprofen at the onset and that used to take care of it. (My MD suggested I do this)

When that no longer worked (and later I totally couldn't take it anymore from the stomach pain, but that took years - about 10) - then I started taking Codeine/acetaminophen on prescription - strong ones. They helped which was great, and made me feel "happy", but on the other hand after a while they gave me stomach cramps and itching on my back all the time - so I had to give it up also. I think I used to just take too much too often of these things due to the pain and frequency of these headaches........

.........So, I understand where you're comign from and if you're not already, the above mentioned drugs might help you.

Another thing I used for a while, until it also had no more effect for me, was feverfew drops........later acupuncture. Both worked, but after a while didn't work any more.

So, now I am only "allowed" to take acetaminophen, which doesn't do much. So, what I do now, and the only choices I'm left with really is that, plus I use Chinese White Flower Oil - if you can get a hold of any at a Chinese Grocery store, this does help to take the edge off the pain. It has a cooling effect and really helps me (along with lying down in the dark with a bag of frozen peas on my head sometimes).

I should mention, that since I started Mepron in July, I've had virtually none of these headaches after years of them being chronic. So, once you treat the Babs, it might go away or get much better.

DLL

[This message has been edited by dontlikeliver (edited 21 December 2004).]


Posts: 2824 | From The Back of Beyond | Registered: Oct 2003  |  IP: Logged | Report this post to a Moderator
mjbucuk
LymeNet Contributor
Member # 843

Icon 1 posted      Profile for mjbucuk     Send New Private Message       Edit/Delete Post   Reply With Quote 
for migraines that my one son suffers... we use Migraine-A. The imitrex type stuff never worked for him. He is also on effexor XR which has cut back the # of migraines (he does not have Lyme)

I have CFIDS and used to get horrible headaches that would start in the back of my neck and then work their way up over the top of my head. I take imipramine (tricyclic antidepressant) daily to keep these away.

I noticed that you talk about a car accident, but I am not sure that this reference is about you... I found that if I get a really bad headache (starting in the back of my neck) that using heating pads and massage helps. I never would have gone to a chiropractor... until I found that they can also relieve this type of headache. Try stretching exercises for your neck...

I wish you the best

[This message has been edited by mjbucuk (edited 21 December 2004).]


Posts: 758 | From now TX | Registered: Mar 2001  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 6 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
My constant migraines are gone since Lyme and babesia treatment....and I suspect atenolol also has been helping me. I rarely get migraines anymore. What a blessing!

You can also try a new product, called mangosteen. It works great for migraines! http://www.onmangosteendaily.com/go

------------------
oops!
Lymetutu


Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.