posted
Lately I have been getting really bad headaches on the side of my head near the temples. My veins are sticking out, which they normally don't do. I just had an MRI that was negative. Does anyone have any suggestions to get some relief. Thanks!
John
Posts: 3 | From PA | Registered: Feb 2005
| IP: Logged |
HEATHERKISS
Frequent Contributor (1K+ posts)
Member # 6789
posted
Advil works if you catch the headache early. Some people use stronger rx's.
Once in a while I have to use tynenol sinus which helps alot!!!!
I used to get headaches daily for about three years. And this week they are making a comeback.
Going to take 2 advil now, Heather
Posts: 1974 | From ABERDEEN, NJ 07747 | Registered: Jan 2005
| IP: Logged |
quote:Originally posted by GBexpress: Lately I have been getting really bad headaches on the side of my head near the temples. My veins are sticking out, which they normally don't do. I just had an MRI that was negative. Does anyone have any suggestions to get some relief. Thanks! John
Do you get any relief from OTC meds?
Headaches are the main problem for my 19 year old son. Tramadol/Tylenol takes the edge off of the pain but nothing takes it away.
------------------
[This message has been edited by pab (edited 02 September 2005).]
posted
So sorry to hear of the miserale headaches. I have had Lyme for 29 yrs. and had reoccuring HA for yrs.. Then I got re-infected in '99 and from day 2 my HA were almost daily for 6 1/2 yrs. I would take Ultram and Percocete and some days that would not even touch them. So one day I took Ambien (a sleeping pill) to sleep through it, I took 5 mg and the HA went away and I felt normal. Afterwards I would take 2.5mg and that often worked...yahoo! But the thing that totally (only with herx they return) relieved my HA was taking 1000mg of Vitamin B-12 injections. I take them 2x a week for the fatigue, (I also may have Thyroid cancer). but even when I started at 1000mg 2x a month they went away. After 6 1/2 years!!! Amen!! Also, for quick relief I found emersing my head in cool water helps (or a faucet). Hope that helps...but try any method with the onset of the HA, catching it quick helps. Blessings to you, Shar
Posts: 52 | From Arizona , USA | Registered: Jun 2002
| IP: Logged |
Michelle M
Frequent Contributor (1K+ posts)
Member # 7200
posted
Hi John.
Lymies quite often have marked brain perfusion problems, noted in some study or another on SPECT scanning -- even where their MRI's are negative. In other words, your brain may not be getting enough oxygen.
You might ask your doc for a sample of either Imitrex or Relpax -- as mentioned above, they're vasodilators...they will increase blood supply to your brain. They're not a narcotic or "painkiller" per se, like a Vicodin or anything... but you will notice your headache fading away fast if hypoperfusion is your problem. The catch is that you really can't use them a lot, and you shouldn't use them if you've any cardiac problems.
As a shrieking head pain Neuro Lyme person for a couple years, I can tell you they're about the only thing that would even make a dent in my headaches and I've tried about everything.
Something else to know is that if your headaches are neuro Lyme headaches (as opposed to cluster or tension-type headaches), they WILL GET BETTER! Take heart!
Best wishes for a pain free head..
:-)
Michelle
Posts: 3193 | From Northern California | Registered: Apr 2005
| IP: Logged |
posted
i had one of those god awful headaches the past two days and going into my teeth and jaw. these are typical for me and not much usually works except vomiting it out and rest.
BUT yesterday i tried the aromatherapy scent of PINE in addition to rest and tylenol and the day before advil. in addition to smelling it directly i left the open bottle next to me for like a half hour at a time. every once in a while the scent wafted into me and somehow it made a difference.
some aromatherapy as supplement, i do believe has the potential to work for people in a way that is mysterious and gears toward how smell moves into the brain. but pine may not be the scent for all. i had a dream to use it so i am trying it. i think lavendar is said to be for headaches but i do believe that the aromatherapy scent for you is as individualized as how the lyme affects individuals.
just my opinion.
best wishes.
[This message has been edited by painted turtle (edited 03 September 2005).]
[This message has been edited by painted turtle (edited 03 September 2005).]
Posts: 855 | From United States of Mind | Registered: Aug 2005
| IP: Logged |
johnnyb
Frequent Contributor (1K+ posts)
Member # 7645
posted
quote:Originally posted by painted turtle: i had one of those god awful headaches the past two days and going into my teeth and jaw. these are typical for me and not much usually works except vomiting it out and rest.
BUT yesterday i tried the aromatherapy scent of PINE in addition to rest and tylenol and the day before advil. in addition to smelling it directly i left the open bottle next to me for like a half hour at a time. every once in a while the scent wafted into me and somehow it made a difference.
some aromatherapy as supplement, i do believe has the potential to work for people in a way that is mysterious and gears toward how smell moves into the brain. but pine may not be the scent for all. i had a dream to use it so i am trying it. i think lavendar is said to be for headaches but i do believe that the aromatherapy scent for you is as individualized as how the lyme affects individuals.
just my opinion.
best wishes.
[This message has been edited by painted turtle (edited 03 September 2005).]
[This message has been edited by painted turtle (edited 03 September 2005).]
I've noticed the same thing lately, painted T. My headaches have been radiating down into my jaw. They never did this before lyme, though I've had migraines for years before the bite. I've heard that lavender helps.
John, I've noticed that acidophilus and magnesium have helped, but I am a migraine-type headache. It certainly can't hurt to try, though.
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,
NJ08534USA http://www.lymenet.org/