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Anyone with this problem should please do contact doctor climent Scott now he will help you too.
I will only advice every other woman TRYING TO GET PREGNANT or have Fallopian tube issues, pcos and other infertility problem too do their research and don’t base your option only on anyone’s advise, I did and it resulted in waste of money and time. contact Dr climent on email: drclimentscott@gmail.com drclimentscott@gmail.com Or his whatsapp number. +2347036879479 because I have discover Dr climent. long time ago and I would have been pregnant earlier if I follow my heart and buy the herbal herbs but I disregard it because of my doctor’s advice and I am annoyed at myself but at the same time I am happy that I made the wise decision by going back to Dr climent, for his herbal herbs. Now I am a strong believer of this herbal herbs natural medicine. Thank You.contact Dr climent for bringing this joy into my home am so happy at last am now a mother of twins am the happiest woman on earth thank god i came back for your herbal herbs i no so many marriages out there finding it difficult to conceive i will surely encourage them to have fate and contact you on your email or number for help contact Dr climent now via drclimentscott@gmail.com drclimentscott@gmail.com Or his whatsapp number. +2347036879479 drclimentscott@gmail.com
+2347036879479 +2347036879479.



Anyone with this problem should please do contact doctor climent Scott now he will help you too.
I will only advice every other woman TRYING TO GET PREGNANT or have Fallopian tube issues, pcos and other infertility problem too do their research and don’t base your option only on anyone’s advise, I did and it resulted in waste of money and time. contact Dr climent on email: drclimentscott@gmail.com drclimentscott@gmail.com Or his whatsapp number. +2347036879479 because I have discover Dr climent. long time ago and I would have been pregnant earlier if I follow my heart and buy the herbal herbs but I disregard it because of my doctor’s advice and I am annoyed at myself but at the same time I am happy that I made the wise decision by going back to Dr climent, for his herbal herbs. Now I am a strong believer of this herbal herbs natural medicine. Thank You.contact Dr climent for bringing this joy into my home am so happy at last am now a mother of twins am the happiest woman on earth thank god i came back for your herbal herbs i no so many marriages out there finding it difficult to conceive i will surely encourage them to have fate and contact you on your email or number for help contact Dr climent now via drclimentscott@gmail.com drclimentscott@gmail.com Or his whatsapp number. +2347036879479 drclimentscott@gmail.com
+2347036879479 +2347036879479.

sillyoldwizard
It began with a ghost-like nerve twinge several months after having a sinus operation (close to the Trigeminal Nerve ) over 20 years ago . Since then , the nerve pain has morphed through various states , firstly Atypical Facial Neuralgia , then Trigeminal Neuralgia , and in the last few years it has become the fully fledged Hemicrania Continua with all its accompanying symptoms . The headaches now cause me more pain than the actual nerve pain itself . When I first had the nerve pain I lost 2 back teeth as my dentist said it might have been root problems .... no luck . Since then , I have tried more or less all the prescribed drugs available on our UK NHS with very little success . One thing which helped a lot when I was experiencing a period of excruciating burning pain was the use of Fentanyl patches . These I still use , and have just started on the last drug available to me , Topirimate . My doctor wouldn't even consider prescribing Indometacin , partly because of my age (72) and partly because of my history of stomach ulcers . At the moment , I have the possibility of Occipital Nerve Stimulation , as well as trying some other alternatives , such as Melatonin and Gliacin . I haven't given up hope , though things are grim at times . Does anyone experience incredible burning in the frontal sinus nerves ? .... a sometime thing for me . I suppose Hemicrania Continua is relatively the new kid in the block , so I'm optimistic . Relief and peace to you all .

Hi Everyone! My name is Twenna Clyton. I was diagnosed with HERPES 2 in April of 2012 when I was 24 years old who just completed my MA in sociology at the University of Northern Colorado where I explored the role of stigma in the process of disclosing a genital herpes diagnosis.I have wanted to get this virus cured, I am happy to share that with you! few weeks ago i came on search on the INTERNET if i could get any information concerning the prevention of this disease, on my search i saw a testimony of someone who has been healed from (Hepatitis B and Cancer) by this Man Dr Gumbla and she also gave the email address (greatgumblaspellhome@outlook.com) and advise we should contact him for any sickness that he would be of help so i told my husband about it the he ask me to write him because this pain has been constant especially in my knees. so i wrote to Dr Gumbla telling him about my (HERPES Virus) he told me not to worry that it was going to be cured!! then i took the medicine he sent me, which few weeks later i started experiencing changes all over me as the Dr assured me that i have cured hence i have taken the medicine and then after some time i went to my doctor to confirmed if i have be finally healed behold it was TRUE. I can understand that lots of people are been diagnosed with this same virus so am excited to be able to share some of my experiences and thoughts about this man that you can as well contact him for help living with genital herpes is not a good thing..HERE ARE HIS CONTACT: EMAIL : (greatgumblaspellhome@outlook.com) OR YOU CAN AS WELL VISIT HIS his website http://eromosalspiritualtemple.webs.com BETTER STILL CALL OR whatsApp HIM viA+2348161850195..GOD BLESS

Hi Everyone! My name is Twenna Clyton. I was diagnosed with HERPES 2 in April of 2012 when I was 24 years old who just completed my MA in sociology at the University of Northern Colorado where I explored the role of stigma in the process of disclosing a genital herpes diagnosis.I have wanted to get this virus cured, I am happy to share that with you! few weeks ago i came on search on the INTERNET if i could get any information concerning the prevention of this disease, on my search i saw a testimony of someone who has been healed from (Hepatitis B and Cancer) by this Man Dr Gumbla and she also gave the email address (greatgumblaspellhome@outlook.com) and advise we should contact him for any sickness that he would be of help so i told my husband about it the he ask me to write him because this pain has been constant especially in my knees. so i wrote to Dr Gumbla telling him about my (HERPES Virus) he told me not to worry that it was going to be cured!! then i took the medicine he sent me, which few weeks later i started experiencing changes all over me as the Dr assured me that i have cured hence i have taken the medicine and then after some time i went to my doctor to confirmed if i have be finally healed behold it was TRUE. I can understand that lots of people are been diagnosed with this same virus so am excited to be able to share some of my experiences and thoughts about this man that you can as well contact him for help living with genital herpes is not a good thing..HERE ARE HIS CONTACT: EMAIL : (greatgumblaspellhome@outlook.com) OR YOU CAN AS WELL VISIT HIS his website http://eromosalspiritualtemple.webs.com BETTER STILL CALL OR whatsApp HIM viA+2348161850195..GOD BLESS

jefferson1957
Hi nice to meet you, am mike jefferson. am a physician with the united states military. i know you are suffering from a few disease that some doctors like myself will tell you it cant be cured, but i have to come to let you know some sickness can be cured through alternative medicine and faith , you just have to try and i assure you its going to work for you. if you are interested or you have any question to ask just send me a mail at mikejefferson1957@outlook.com, but if not you should
just ignore it .thanks

Had severe but intermittent headaches for two years and put it down to teeth, sinus infections, eye strain etc. Went through all the tests, MRI, CT scan, antibiotics and what have you but nothing helped. In December 2012 the intermittent headaches became full-time, all day, every day, non-stop. It felt like someone had punched me in the left temple. My nose was dripping, my head was throbbing, nothing took the headache away. Fortunately I have a GP who takes my symptoms seriously so I was able to walk into her office and tell her that I felt like someone had punched me in the left temple and that I didn't think this was another symptom of the fibromyalgia I had been diagnosed with 18 months before. She phoned the neurologist then and there. I was lucky enough to be able to fill a cancellation appointment with him five days later. He went through all my symptoms and then asked the critical question: "Do you have any relatives with "different" headaches?" Now, I have a niece who has severe migraine-like headaches on both sides of her brain which so far have basically been untreatable. That gave the neurologist the key to my diagnosis for hemicrania continua. He put me on Topiramate and within a week the headache started to recede. 8 months later it is barely there. I HAVE had to make drastic life changes. The medication has drastically altered my sense of taste. I can only eat organically grown food and have become semi-vegetarian (naturally grown meat only and in greatly reduced amounts). If I have to be in large gatherings (funerals, weddings, etc.) I have to bring an iPod with specially selected music to drown out the discordant "noise". There have been so many side effects that I've learned to just laugh about them and cope with the "side effect of the week" rather than get upset. When people say "oh, it's just a headache" I've learned to explain the condition by telling them if I DIDN'T take my headache medication I'd be "Wolverine on steroids" That usually does it.

I've also learned how to walk away from people like that, even if they're my close relatives, because it's not worth the effort to try to explain. My daughter for one thinks my headaches are "nothing" and that I'm being "silly" when, for instance, my husband shatters the air with an extremely loud sneeze. Happened at dinner one night and I just picked up my plate and walked out of the room to eat in the living room. That's what people with HC have to learn - how to cope with the loud things in life that aren't going to change (i.e. like using an iPod). Use the technology at hand, learn how to walk away from the noise, be blunt if you have to when explaining the condition to people who haven't got HC and really can't understand. Be blunt to the person wearing too much perfume or deodorant in the restaurant next to you and ask to be moved to a scent-free area and don't bother to talk in a whisper. THEY are the ones who are stinking not you. If nothing else, HC has taught me to speak up for myself - start off politely and work up to blunt as necessary. sorry if I come off as militant but this HC has really made me become more aware of the screaming kids, the women with their shrieking high-pitched laughs that pollute a room, the heavy perfumes, the smoke-drenched clothing, the general overall "I can do whatever I want and to hell with YOU" attitude pervasive in the 21st century.

I've been doing a lot of reading about HC as my mother suffers from it for about 1 yr now, so many of these stories sound just like her !! she tried Indomethacin & it took the HA away which was a huge relief for about 8 months but could no longer tolerate it as the GI side effects were horrible even with taking Omeprazole. Luckily we stumbled upon a link about a headache specialist in AZ a Dr. Eric Eross, the link was about an all natural alternative called Gliacin a backup for Indomethacin! that was such awesome news! my mom has always been into the all natural alternatives. Boswellia Serrata is Indian frankincense which has been around for well thousands of years. We read a bit more about it on http://www.gliacin.com and http://migraine.com/blog/boswellia-a-potential-herbal-remedy Posted by Dr. Alex Mauskop—February 27th, 2013. We decided to order it and lo and behold it worked for her !! she is so happy we stumbled upon this awesome information!!! I hope others will stumble upon this as we did.
Indomethacin has such scary side effects

Gastrointestinal Risk : NSAIDs cause an increased risk of serious gastrointestinal adverse events including bleeding, ulceration, and perforation of the stomach or intestines, which can be fatal. These events can occur at any time during use and without warning symptoms. Elderly patients are at greater risk for serious gastrointestinal events. (See WARNINGS.)


Everything happens for a reason & I just had to share because I am so happy that my mom found something with little to no side effects that is safe & helps her HC and I hope others will also stumble upon this & get relief. Their ordering team was prompt we received the bottle within 2 days & quick responses to our questions before placing the order.

Thank you Dr. Eric Eross for the Gliacin wonder









October 6, 2012


Hemicrania Continua


As the anniversary of my life changing event nears, I taught that I would conical my situation with hopes that it may help someone.


The morning of October 9, 2011 I awoke with the worst headache I have had in my life. I work for the ambulance service in town and had worked at the stock car track the night before. I taught that I just got too much fumes or took much noise or something. My new headache was very localized to my left eye and temple area. It felt as though an icepick was bring pressed into my head. It did not move. It did not get better or worse...10 out of 10 ALL THE TIME. I was light, smell and sound sensitive and nausea like I had never had before. Any exercise ebacerbated things. Nothing over the counter helped. Hot packs and cold packs gave temporary relief. In my early 20's I had migraines that seemed to be related to my menstrual cycle, I was placed on birth control and the headaches dissipated.


This continued for one first week. I spoke with my Nurse Practitioner, we decided to try Toradol and a burst of prednisone (I have a history of chemical dependency and wanted to stay away from any narcotics.). We agreed that if things did not get any better over the weekend I would jump into a workup.


After an other miserable weekend of the same relentless pain I returned to my NP. We started with all the normal stuff; CBC, Comp, Sed rate, Lyme’s titer, West Nile titer, allergy testing, silac testing. I had testing to see if I was menopausal. I had a Brain MRI and MRA, just because the first thing you think of is a brain tumor. All of which came back normal.


After a discussion with a neurologist, my NP decided to start the “traditional” migraine treatment. I started Meloxicam, Topamax, Verapamil, Ibuprofen, Lexapro ( I had always struggled with depression, and this was the only medication that I took on a routine basis other than Depo Provera for birth control.). I was also started on Effexor to help with my anxiety that had increased over this whole ordeal. We also set up an appointment to set the neurologist at her earliest opening.


Nothing was touching the pain. I was a nurse in a very busy Urgent care clinic as well as an EMT for the ambulance service in town. My average work week was 64 hours...I was very busy, I did not have time for this!!!. After that dreaded day my life consisted of getting up, struggling threw work and collapses on the couch... sobbing in pain until it was time to go to bed. My life had come to a screeching halt. I went from working out and taking dance classes 3-4 night a week , visiting with friends, going to church and having a normal life to a lump on the couch.


While waiting for the neurologist appointment I saw chiropractors, had acupuncture, massage, aroma therapy and was prayed over. Saw a psychologist and a counselor. Had hypnosis. I read EVERY article on headaches I could get my hands on and tried every herbal potion I read about. Just some of them included; high doses of calcium, magnesium, Valerian, lavender, ginger, aspirin and cleanings. I stopped drinking coffee and pop, and drank water until I was floating. I wore magnets. Used light therapy. NOTHING HELPED.


As a side note all the minerals that I was taking and the change in my diet gave me a kidney stone. As if I was not miserable enough I spent a weekend passing that.


Before seeing the neurologist I taught that it would be a good idea see my optometrist. He stated that my exam was normal with the exception of mitosis (constriction) of my left pupil. This finding seemed very benign at the time.


I saw the neurologist on November 21st. Her exam was unremarkable. She had no explanation other than it might be a depression/anxiety cycle. Told me to keep doing what I was doing and check back with her in 1 month.


Meanwhile the only thing that changed is that I was a zombie!! I did not tolerated the Topamax, or as my family refereed to it as “Dope-a-max”. I was gitty, couldn't remember anything and my perception was completely GONE. I was falling, running into things, took the mirror off my car twice and worse of all backed into a car and a pole with the ambulance, in the same day. Thank God no one was hurt. Needless to say my supervisors at the ambulance greatly frouned upon this and put me on Medical Leave. The only good thing about the Topamax was that I lost about 30 lbs, the only thing that I wanted to eat is lemon pudding of all things, which became quite a joke among my co-workers.


By now it was late February. I continued to have constant pain that now was making me very depressed. Another Brain MRI was done just to make sure that there was a tumor growing that went undetected on previous scans.


My NP made another call to my neurologist. She suggested that I see on of her partners who does Botox for pain management. I had 30 injections in my forehead and scalp in early March. The injections did nothing to help the pain. The did however take away my “Crows Feet” which was a nice side note. The this neurologist said that I would need 3 of these treatments 6 weeks apart to know if they would be successful.


The pain remained relentless.


My mood was nonexistent. I had no passion for anything. I was put on medical leave from my clinic job because I was told by my nursing supervisor that I was “grumpy and unapproachable”...She had no idea the life that I was living...or not living for that matter.


On the 195th evening, I was on my nightly Internet search I stumbled upon an article about Hemicrania Continua. Basic a one sided continuous headache. There was no test to diagnosis it other that if the pain is relieved by Indomethacin. Indomethacin is a medication usually used for the treatment of gout. The symptoms that I had were all my symptoms: a relentless one sided headache, light, sound and smell sensitivities, watery eye, mitosis, sweating on one side of head. The pain increased with exercise. A side note was that the pain went away when I ate, some doctors encourage their patients to do a valsalva maneuver (basically bearing down.). THIS WAS ME!!! I (very excited) visited with my NP right away the next morning. I showed her my findings and begged her to try the Indomethacin. I took my first dose at noon, by 12:30 the pain was gone. GONE!!! Praise be to God!


In the weeks to follow I had to learn to adjust the medication, learning I had to take it religiously every 12 hours, 75 mg. I have also learned if I have gone without sleep or have had high stress day I might need to take another dose. I wish someday I will be without the dependence of the Indomethacine, but for know I am working on getting my life back.


Many things have changed over this past year. I lost my job at the clinic, I still say that my supervisor



did not understand what I was going threw. I have fallen into a depression and have constant anxiety, which is making it difficult to find a new job. I had wanted to go back to school but my anxiety got in the way. I do continue to work as much as I can at the ambulance service and have been working as a independent contractor for 2 nursing services.


After finding my diagnosis I have read many article and blogs, I consider my self lucky that I did not need to go years like others have. I only hope my story will help one person from the pain and desperation that went threw.


I have to praise my boyfriend, children and family as well as my Nurse Practitioner to all the support over the past year.






esstar88
I've been suffering from constand daily headaches for the last couple years, with bouts of severe headaches that make it impossible to work or do anything. This year we noticed a new sypmtom that had never presented before; I am now having swelling around my right eye (where the pain is mostly concentrated) which eventually spreads down into my cheek, my eye will swell almost entirely shut. The frequency of the horribly severe headaches, with the swelling, has increased from maybe 1 every couple of months to, 1 every couple of weeks. I have been to a neurologist who has sent me to a rhuemetologist and a neuro-opthomologist. I have had countless blood tests, 2 MRI's, 2 CT scans, and even a spinal tap and the doctors still don't have a clue. Anyone have any suggestions?... I'm at my wits end and I know my boss is too since I have to keep taking off from work. I'm tired of being a pin-cushion and tired of being told "yeah, the swelling is really weird, but I don't know what's causing it." From what I've read it sounds like I could have Hemicrania Continua, but I'm just not sure. Any advice?....

Sheeny
Mine came after been very run down for 6 months coughing with Bird Fanciers Lung then having a very painful nerve condition that worked its way up my body affecting bladder, bowels, heart etc and then back down again within a couple of months. One specialist said it was Post Infectious Sensory Neuropathy the other a bad case of RLS. Now I'm left with this. Any one else develop this after illness like this?

John
I would like to add that after months of Melatonin use, Indomethacin use was not necessary anymore. Just Melatonin, about 3 mg daily as immediate release formulation, suffices to manage my HC.

John
For me Indomethacin worked great for some years, but then it lost effectiveness. Using Melatonin for a few months now, together with Indometacin. This resulted in a huge improvement (on average 90% pain reduction). Time will tell, but I think this combination is worth trying.
In case of severe outburst at night Tramadol helped me out several times. Use this drug as last escape. Fortunately I can tolerate all these drugs, though using low dose Omeprazol to prevent side effects of Indomethacin on stomach and intestines.

Annearchist
Re: Melatonin — I find melatonin really helpful too. I started taking it only at night to help me sleep but now I take it during the day as well. Anne

Annearchist
Re: Ice on forehead / neck — Ice makes the pain WORSE.

Annearchist
Re: Indomethacin — I used to take 50mg 3xof indomethacin daily but now my stomach bleeds. I am getting injections of sensorcaine and steroids and they work really well. I take topiramate and verapamil and they tone down the pain between injections.

Re: T1 Trapezius Nerve — Pain starts in the left Trapezious Nerve up the back side of neck along with sudden preassure behind left eye. Pain then hits sharply across the left front of the head across to the left temple. Sometimes I have numbness on the left side of my face and slight sorness in the left trigeminal nerve in my cheek.

Re: Swelling of eye on affected side — i hace been diagonsed with ht ,but it only affects my eye,as in the pain ,but i have swelling when the pain is bad,i would like to no what could help

cbeale
Re: Toxic working conditions — I started having this problem shortly after I started working in an old building. It's a manufacturing facility and very dirty. I work in a very nice office but am out on the floor frequently.

cbeale
Re: Acupuncture — Accupuncture helped with the pain but didn't help with my sound sensitivity. It was also expensive and not covered with insurance.

cbeale
Re: Indomethacin — I'm taking Indomethacin and have had some relief with the sound sensitivity in my ear. I've been also taking Gabapanten (2700mg per day). That helps the pain.

nick
Re: Indomethacin — complete relief at 225 mg/day but doc says I won't be able to maintain this dosage

bybyemmy
Re: Toxic working conditions — you know i'd love to know!! i've never been sick in my life!! i work now in what used to be an old factoy-very old-converted into medical offices-the lady in the office next to me as had very stange illnesses, i have had lung nodules, liver cysts, a breast lump, all since i came here 2 years ago. girl in the office across from just started with these headaches 6 months ago. i am now being seen at John Hopkins.

bybyemmy
Re: Triptans — No help at all-worse tast in my mouth ever from a med-tastes like you drank a fish bowl-as i would imagine it to taste...lol!

bybyemmy
Re: Topamax — keeps my typical migranes at bay-which the docs say is important so they can tell the difference between these one sided headaches vs. the migranes that i have on occasion 9which are quite different)

bybyemmy
Re: Indomethacin — just started 4 days agao and (knock on wood) first time and many drug and 18 doctors and 16 months later i feel hope and a bit of change in my pain level...

Skip46
Re: Melatonin — I have been using melatonin for two months with significant improvement. Presently I use 3mg-CR every four hours. At night I take 6mg-CR before sleep. I often must take another fast acting dose after about five hours to get a full nights sleep. Other than feeling sleepy and yawning I find my cognitive and executive functions largely in tact.

Skip46
Re: Indomethacin — Moderate relief realized with 75mg-SR two time per day (150mg/ day). Significant relief with 75mg-SR three times per day (225mg / day). Watch for gastric distress including GI bleeds.

winnyninnypoopoo
Re: Indomethacin — Helped a great deal, but gave me pancreatitis. Unable to continue, no other meds helped a great deal, now have an occipital stimulator.

winnyninnypoopoo
Re: Occipital Nerve Stimulation — Permanent Implant - very effective.

jes
Re: Occipital Nerve Stimulation — I've only had the trial occipital nerve stimulator implanted thus far... but now am waiting on the pernament implant... it worked!!! Very well too!! I can't wait for the pernament implant.

sgtmajorpain
Re: T1 Trapezius Nerve — According to research, the nerve trigger point 3/4 up the right-hand (or left-hand) side of the neck is responsible for the EXACT pattern of pain that I experience... Right cheek muscle, behind eye, above right ear, in a ring from the front to upper back right of head, and down the right muscle of the neck.

sgtmajorpain
Re: Temporal Lesion — In my research I found that perhaps rarely, a lesion of a vascular (blood vessel?) in sort of the temporal area, resulted in some HC symptoms, but I've had MRI's and everything and they didn't say what causes HC for me.

sgtmajorpain
Re: Ibuprofen — Best results of all OTC medicines. Any NSAID (non-steroidal anti-inflamatory) drug appears to be fine. But Ibuprofen was better for me than any Naproxen Sodium (which I have swelling of the eyes with), or Aspirin. Non-NSAIDs like Acetominaphen don't do hardly anything at all.

sgtmajorpain
Re: Diclofenac — All anti-inflammator meds have proven effective (for me). Diclofenac was fairly effective. Indomethacin is said to be the most effective (although also one of the most dangerous). I'm actually taking that now, but it hasn't taken effect yet (and I've been taking it for over a week at gradually increasing doses). So, diclofenac so far was the best (better than Ibuprofen).

sgtmajorpain
Re: Neck or head trauma — At the time the HC originated, I was sleeping in an under-sized couch for several months and had my neck at an awkward angle, or compressed in the length of couch, or pressed in a position that cut off flow on the right-hand side.

sgtmajorpain
Re: Toxic working conditions — At the time the HC suddenly originated, I was working in an old building that had a sort of asbestos-like atmosphere. Not sure if that was the cause.

sgtmajorpain
Re: Headache on one side all day long — This pain occurred suddenly on the right cheek muscle area 6 1/2 years ago and felt midly uncomfortable, but has broadened to the whole right head area, still in the original location, but now in the upper right head, front, behind eye, above teeth, back of right, around outer ear, and in cheek muscle. Constant 24/7... Felt in outside of head, not in brain. Responds well to anti-inflamatory medicin like ibuprofen or diclofenac. Just starting indomethacin currently.

jes
Re: Occipital Nerve Block (Steroid) — Indomethacin is a amazing if you can tolerate it.

jes
Re: Headache on one side all day long — The bad thing with this type of headache is that it never goes away... it's 24/7. Also the only treatment that really, really works is indomethacin and some people (like me) are unable to tolerate the indo. I'm currently looking into having an Occipital Nerve Stimulator put in.