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New Message Board Archives >> Oct-Dec 2003 >> Help Please
(Message started by: OldManOz on Nov 17th, 2003, 11:49am)

Title: Help Please
Post by OldManOz on Nov 17th, 2003, 11:49am
I live in a rural area of New Mexico and do not have access to any headaches specialists.  My Doctor has sent me to a neurologist and I have had an MRI – the diagnosis was atypical migraines, but I believe I suffer cluster headaches.  I was hoping that by sharing my symptoms other might help me confirm my suspicion.  I am 57 years old and never suffered anything other than tension headaches until a year ago.  Last fall I began to get sever headaches, they begin with a blurring in my left eye and then I notice a burning or stabbing sensation in my left eye and then a similar sensation in my left nostril.  Then the headache begins.  It behaves in waves with each set of waves becoming more excruciating.  My left eye waters profusely and my eye lid sags.   These always begin late in the day or in the early evening.  I suffered several episodes last fall and then they went away.  This October they returned.  In the last nine days I have had a headache every night except two.  I can control the pain with Imitrex, but it doesn’t seem to keep them from coming back the next day.  Any insights would be appreciated.
Adios
Phil

Title: Re: Help Please
Post by vig on Nov 17th, 2003, 11:52am
Hola amigo,
read all the stuff on the left.
Take the cluster quiz.  
Doctors are admittedly weak with this 'syndrome'

welcome

Title: Re: Help Please
Post by Lori on Nov 17th, 2003, 11:58am
Glad you found us. If you have CH, this is the place to be.
Have you taken the Cluster Quiz yet? (link on left) Read the cluster traits link too. Sounds like CH from what you say, but I'm not a doctor and can't diagnose. I think you can pretty much tell though once you take the quiz but especially from reading the cluster traits page. Imitrex may stop the headache but it's not a preventative. You need to find a new doc, call around the neuros in your area and ask the receptionist if the doc is knowlegable about clusters and does he treat clusters. Make sure you say you are not talking about migraines! You mean cluster headaches and they are different. I mean when you say clusters to some people, they think migraines! it's like..no..they are different! Anyway, to read more about meds..click on the OUCH button (on left) and then click on Cluster Help then on Medications. That will tell you about abortives and preventatives. Read it, print it. Also look at the Oxygen button on your left here.Print that too.

Good luck and let us know how you make out.

Title: Re: Help Please
Post by Leesa on Nov 17th, 2003, 12:00pm
Hello Phil :) As Vig said read all you can at the left of the page and take the quiz dear that will help you a great deal. Then take some time to read EVERYTHING here just be a sponge and soak it all in! I hope this is NOT CH you suffer from but if it is "Welcome to Clusterville" sorry your here but were glad to have in the family!  BTW: JOIN OUCH
Leesa  ;;D

Title: Re: Help Please
Post by don on Nov 17th, 2003, 12:02pm
Look here.................

http://www.clusterheadaches.org/doctors.htm

There are 3 doctors from New Mexico.


Join OUCH while your there.

What did you guys do with Old Mexico ?

Title: Re: Help Please
Post by Kirk on Nov 17th, 2003, 12:54pm
Like everyone else says. Start with everything on the left.
I sure as hell hope its not CH.
My GP was very helpful and has me on Verapamil, O2 and Imitrex.

I wish you had a Beowolf Cluster.

Just whay did you do with old Mexico?

TTFN

Kirk

Title: Re: Help Please
Post by Little Deb on Nov 17th, 2003, 5:25pm
Welcome to a wonderful place with the greatest people for support.
Stay with us!
LD

Title: Re: Help Please
Post by Prense on Nov 17th, 2003, 6:30pm

on 11/17/03 at 11:49:43, OldManOz wrote:
I live in a rural area of New Mexico and do not have access to any headaches specialists.  My Doctor has sent me to a neurologist and I have had an MRI – the diagnosis was atypical migraines, but I believe I suffer cluster headaches.  


Hey Phil!  I live right down the road from you.  

Check your messages...

Chris

Title: Re: Help Please
Post by Prense on Nov 17th, 2003, 6:35pm

on 11/17/03 at 12:02:13, don wrote:
What did you guys do with Old Mexico ?


Opened a Super Wal-Mart!   ;;D

Title: Re: Help Please
Post by Charlie on Nov 17th, 2003, 7:04pm
Welcome. I'm 57 too.....pulling, not pushing 50  8)  It's criminal to get stuck with this horror at our age. Mine began in 1969 when I was 23 but ended for now in 1991 at 45. I know how fortunate I've been.

Your description sounds classic to me. I always ask if they wake one out of a sound sleep as I think it's a sure sign. No one rests or sleeps durning a cluster attack. I agree with the others that you should read all you can here. I learned so much I decided to stick around. I hope you do as well.

Let us know how you're doing.

Charlie

Title: Re: Help Please
Post by BobG on Nov 17th, 2003, 9:20pm

on 11/17/03 at 12:02:13, don wrote:
What did you guys do with Old Mexico ?


It's still there, just changed the name to


California.

Title: Re: Help Please
Post by TxBasslady on Nov 17th, 2003, 10:33pm
;)
Hi Phil,
Welcome to Clusterville !

Like you, I never had anything but the normal headache, till 2 years ago.  But I can still remember the 1st CH!  I only suffered with a few ha's over a year and 1/2.  Then this past August, I went into a full blown cycle.

My dr put me on a Prednisone taper......which ended my cycle.  Luckily, I have been PF since day 1 of the Prednisone.  

Stay around and let us know how you are doing.  Always someone here you can talk to.      8)

Sending you lotz of pf vibes from Texas.          :)

Jean  .......69 days PF.......YEEHAW !!!!!!!!

Title: Re: Help Please
Post by sandie99 on Nov 18th, 2003, 5:22am
Hey Phil! :)

Sorry to hear about your HAs.
I do wish that it's not CH, but to me, some of your symptoms sounds like this devil. I have studied Ch a lot after getting my diagnosis in January, but I'm not a neurologist.
Anyway, I'm glad that you find your way to this place, as this site is a blessing to come to.

I wish you the best with your battle with your HA.

Best wishes & PFdays,
sandie99



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