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JasonZ
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Apr 26th, 2009 at 1:34pm
 
My name is Jason. I am a 30 year old male episodic sufferer. I have been suffering from this monster for as long as I can remember. Some of my first memories are lying on the floor writhing in pain. And no one could do a thing about it. I have had these for about 27 years or so. I have tried numerous prevention and abortive techniques with some varied relief. I am worried that his is a hereditary condition. I do NOT want my sons to have to deal with the hell of an attack. I usually cycle from the end of September through mid March. I usually will have anywhere from 1 CH per day to ones that last for what seems like days on end. I also have random ones throughout the year with no set time or pattern. They are always in the right eye. I have had them manifest themselves as red swelling in my face. In 8th grade I was accused of getting into a fight due to the swelling. I have been to the hospital countless times. I have tried dietary manipulation and almost every medication for 'migraines'. I was told a few years ago by a concerned co worker that the symptoms appeared to be a cluster headache. His mother was a sufferer. I did more research than I thought possible. And went to my doctor with pages of information and websites to look at. That was 2007. My new doctor (both general practitioners) knew little about CH. I have had scans done in the Army and was told it was migraines. No meds worked. I was told by another doctor it was most likely anxiety. No relief. I had resigned myself to living with the torment of never knowing when my world would come to a screeching halt. Then my friend gave me some direction. Still don't have many answers but at least I now have a name for the demon that has haunted me for my whole life. I am not crazy. It isn't something I am imagining. It IS in my head but not like that. It is not something I do to get out of work or family functions. It IS a disease that has victims. And I am glad to find others that have the same issues. I can take some solace in the fact that I am not alone in this.
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Bob Johnson
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Re: New to CH.com
Reply #1 - Apr 26th, 2009 at 2:26pm
 
Jason, let's take care of the genetic issue first: No good research which shows much of a gene load for CH. Even if there were, worry won't change that potential--but in the absence of evidence--put it aside.

Your long history does not reveal the quality of docs you had or meds, etc. tried and so I'm going to respond as if you were a full blown new case. If this is duplication of your knowledge, get back with specific questions. There is a depth of knowledge/experience available.
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Cluster headache.
From: Multimedia File Viewing and Clickable Links are available for Registered Members only!!  You need to Login or Register (Orphanet Journal of Rare Diseases)
[Easy to read; one of the better overview articles I've seen. Suggest printing the full length article if you are serious about keeping a good medical library on the subject.]

Leroux E, Ducros A.

ABSTRACT: Cluster headache (CH) is a primary headache disease characterized by recurrent short-lasting attacks (15 to 180 minutes) of excruciating unilateral periorbital pain accompanied by ipsilateral autonomic signs (lacrimation, nasal congestion, ptosis, miosis, lid edema, redness of the eye). It affects young adults, predominantly males. Prevalence is estimated at 0.5-1.0/1,000. CH has a circannual and circadian periodicity, attacks being clustered (hence the name) in bouts that can occur during specific months of the year. ALCOHOL IS THE ONLY DIETARY TRIGGER OF CH, STRONG ODORS (MAINLY SOLVENTS AND CIGARETTE SMOKE) AND NAPPING MAY ALSO TRIGGER CH ATTACKS. During bouts, attacks may happen at precise hours, especially during the night. During the attacks, patients tend to be restless. CH may be episodic or chronic, depending on the presence of remission periods. CH IS ASSOCIATED WITH TRIGEMINOVASCULAR ACTIVATION AND NEUROENDOCRINE AND VEGETATIVE DISTURBANCES, HOWEVER, THE PRECISE CAUSATIVE MECHANISMS REMAIN UNKNOWN. Involvement of the hypothalamus (a structure regulating endocrine function and sleep-wake rhythms) has been confirmed, explaining, at least in part, the cyclic aspects of CH. The disease is familial in about 10% of cases. Genetic factors play a role in CH susceptibility, and a causative role has been suggested for the hypocretin receptor gene. Diagnosis is clinical. Differential diagnoses include other primary headache diseases such as migraine, paroxysmal hemicrania and SUNCT syndrome. At present, there is no curative treatment. There are efficient treatments to shorten the painful attacks (acute treatments) and to reduce the number of daily attacks (prophylactic treatments). Acute treatment is based on subcutaneous administration of sumatriptan and high-flow oxygen. Verapamil, lithium, methysergide, prednisone, greater occipital nerve blocks and topiramate may be used for prophylaxis. In refractory cases, deep-brain stimulation of the hypothalamus and greater occipital nerve stimulators have been tried in experimental settings.THE DISEASE COURSE OVER A LIFETIME IS UNPREDICTABLE. Some patients have only one period of attacks, while in others the disease evolves from episodic to chronic form.

PMID: 18651939 [PubMed]
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Current treatments:
Multimedia File Viewing and Clickable Links are available for Registered Members only!!  You need to Login or Register

Here is a link to read and print and take to your doctor.  It describes preventive, transitional, abortive and surgical treatments for CH. Written by one of the better headache docs in the U.S.  (2002)
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Michigan Headache & Neurological Institute for another list of treatments and other articles:

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Lancet Neurol. 2004 May;3(5):279-83.  


Epidemiology and genetics of cluster headache.

Russell MB.

Department of Neurology, Akershus University Hospital, Oslo, Norway. m.b.russell@klinmed.uio.no

Cluster headache, the most severe primary headache, is characterised by unilateral pain, ipsilateral autonomic features, and, in many cases, restlessness. Recent epidemiological studies indicate that the prevalence of cluster headache is about one person per 500. Genetic epidemiological surveys indicate that first-degree relatives are five to 18 times-and second-degree relatives, one to three times-more likely to have cluster headache than the general population. Inheritance is likely to be autosomal dominant with low penetrance in some families, although there may also be autosomal recessive or multifactorial inheritance in others. To date, no molecular genetic clues have been identified for cluster headache. Identification of genes for cluster headache is likely to be difficult because most families reported have few affected members and genetic heterogeneity is likely. Future focus should be on ion channel genes and clock genes. This review summarises the epidemiology and genetics of cluster headache.

Publication Types:
Review

PMID: 15099542 [PubMed]
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The biggest single issue for many, many of us has been finding a good doc. Many neurologists have inadequate training and experience and so you must dig, per this ouline.

LOCATING HEADACHE SPECIALIST

1. Search the OUCH site (button on left) for a list of recommended M.D.s.

2. Yellow Pages phone book: look for "Headache Clinics" in the M.D. section and look under "neurologist" where some docs will list speciality areas of practice.

3.  Call your hospital/medical center. They often have an office to assist in finding a physician. You may have to ask for the social worker/patient advocate.

4. Multimedia File Viewing and Clickable Links are available for Registered Members only!!  You need to Login or Register  On-line screen to find a physician.

5. Multimedia File Viewing and Clickable Links are available for Registered Members only!!  You need to Login or Register Look for "Physician Finder" search box.  Call 1-800-643-5552; they will send a list of M.D.s for your state.I suggest using this source for several reasons: first, we have read several messages from people who, even seeing neurologists, are unhappy with the quality of care and ATTITUDES they have encountered; second, the clinical director of the Jefferson (Philadelphia) Headache Clinic said, in late 1999, that upwards of 40%+ of U.S. doctors have poor training in treating headache and/or hold attitudes about headache ("hysterical female disorder") which block them from sympathetic and effective work with the patient; third, it's necessary to find a doctor who has experience, skill, and a set of attitudes which give hope of success. This is the best method I know of to find such a physician.
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As you have time, explore the buttons (left) starting with OUCH and the multiple internal links there.
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« Last Edit: Apr 26th, 2009 at 2:28pm by Bob Johnson »  

Bob Johnson
 
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cassie
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Re: New to CH.com
Reply #2 - Apr 26th, 2009 at 3:13pm
 
Hello Jason  Smiley
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The best way to predict your future, is to create it.
 
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coach_bill
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Re: New to CH.com
Reply #3 - Apr 26th, 2009 at 8:46pm
 
welcome


                      Coach Bill
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boy i cant wait till it's my turn to give him a headache. paybacks a bitch
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