Guest guest Posted January 22, 2004 Report Share Posted January 22, 2004 In a message dated 1/22/04 5:15:02 PM Central Standard Time, Emeraldsx3@... writes: Has he flared before from strep? Nope, He has only had it twice before,the first causing Scarlet fever because we had no clue anything was wrong and it was left untreated for a couple days.I took him in becuase he had a rash.The second was caught early.Both times were before he was diagnosed.The infective trigger for him was a virus with sore throat and high fever,he even had the white spots on his tonsils,but tested negative. Hugs Becki and 5 systemic Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2004 Report Share Posted January 22, 2004 Patty headaches and the stomach pain yes but not due to meds i dont think but we did find out has a psuedo tumor celebri which caused her to have headaches for 16 straight weeks only relief was a spinal tab and if another series hits her she will have a shunt put in they did alot of tests to locate what the headaches were from 1 doctor took it upon herself and found the tumor had headaches off and on before the 16 week headache Robbin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2004 Report Share Posted January 23, 2004 In a message dated 1/22/04 7:00:33 PM Eastern Standard Time, shelly443142002@... writes: << hello, my daughter takes methotrexate, enbrel, choline magnesium and prednisone, and gets sever headaches to the point where she shakes and then throws up. the always throw it off to a sinus infection, or allergies, but they did a sinus ct last week and it came up negative, so they atre pretty putting it as a side effect to probably the mtx. i wish they could say positively, instead of probably. she also get severe stomache aches that sometimes follow the headaches. they have scoped her throat and stomach and found nothing.. she gets sever heart burn as well. i hope your daughter feels better. it hurts me so much to see young kids in pain, especially when they have other problems such as arthritis.. i hope i have helped in some kind of way. >> Hi : Thank you for your email response. Everything I learn is extremely helpful and I appreciate everyone's advice, personal experience, understanding and many words of wisdom. How have the doctors helped your daughter with her headaches? I know they 'think' it's the MTX, but have they given her a med for her severe headaches? I hope they can pinpoint for sure what it is and help alleviate some of the headache pain. Take care. Patty Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2004 Report Share Posted January 23, 2004 In a message dated 1/22/04 10:25:47 PM Eastern Standard Time, Robbin40@... writes: << Patty headaches and the stomach pain yes but not due to meds i dont think but we did find out has a psuedo tumor celebri which caused her to have headaches for 16 straight weeks only relief was a spinal tab and if another series hits her she will have a shunt put in they did alot of tests to locate what the headaches were from 1 doctor took it upon herself and found the tumor had headaches off and on before the 16 week headache Robbin >> Hi Robbin: Wow, how scary for you both. Is on rGH? I know this is a 'rare' side effect with it, but I worry for in regards to the rGH and a psuedo tumor celebri. Thank God for the one doctor that figured out what was causing her headaches. They didn't figure out what caused it? How is she now? Take care. Patty Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 29, 2004 Report Share Posted January 29, 2004 Barb, I've been on synthroid for 3 years and have never had headaches ----Original Message Follows---- From: " Barbara Schulz " <beschulz@...> Reply-hypothyroidism hypothyroidism Subject: headaches Date: Thu, 29 Jan 2004 15:53:01 -0000 I've been getting headaches for the past few days. _________________________________________________________________ Learn how to choose, serve, and enjoy wine at Wine @ MSN. http://wine.msn.com/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 29, 2004 Report Share Posted January 29, 2004 Thanks, . Then I prob. have another sinus infection happening. Barb K a r e n P <karlynn17@...> wrote: Barb, I've been on synthroid for 3 years and have never had headaches ----Original Message Follows---- From: " Barbara Schulz " <beschulz@...> Reply-hypothyroidism hypothyroidism Subject: headaches Date: Thu, 29 Jan 2004 15:53:01 -0000 I've been getting headaches for the past few days. _________________________________________________________________ Learn how to choose, serve, and enjoy wine at Wine @ MSN. http://wine.msn.com/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 29, 2004 Report Share Posted January 29, 2004 What is in your soy pill in addition to soy? I tried one with black cohosh and it gave me a headache. Soy will also give you a headache. A soy headache for me was along the back of my skull and low down. A progesterone headache was in the front above the eyes. I think that was what was causing them, the product would relieve the pain faster than an asprin. Joan > I've been getting headaches for the past few days. I think they may > be sinus headaches, which means I'm probably getting another sinus > infection. Has anyone had headaches while taking synthroid? The > only other thing I have added to my medicinal mix is the soy- > menopause pill, but I've only taken that for a few days. > > Any ideas? > > Barb Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 2, 2004 Report Share Posted February 2, 2004 In a message dated 2/2/04 5:15:59 AM Central Standard Time, boundforlondon@... writes: MTX and they couldn't get the same brand in anymore so it came in this huge vial this time. And the literature mentions nothing about arthritis. Hmmm, makes me think I should have checked the expiration date. Hi e, Good luck at finding the source of the headaches. has been on 3 differant MTX's one had no mention of arthritis what so ever.I paniced called the rheumy and named the ingrediants.All was fine.I assume Joe got a big vial with 4mls or 100mg of MTX. Hugs Becki and 5 systemic Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 2, 2004 Report Share Posted February 2, 2004 Hi e, I feel like we've been really lucky, as far as not having problems with the headaches that are mentioned so frequently here, in kids with JRA. He has headaches only occasionally. Rarely, really. It's so hard to know whether it's from the disease or possibly a side effect of one or another of the meds, or something totally unrelated to either. That is a somewhat higher than normal dose of MTX for arthritis but I've read and posted (long time ago, though) studies suggesting that a higher dose may be more effective for those whose arthritis symptoms aren't being adequately controlled, as long as the liver profile is okay. I guess lowering the dose might be one way to find out if the headaches subside. Or maybe switching to a different type of birth control pills, if that's possible, to see if they resolve? It can be worrisome to pick up a regularly ordered medication from the same pharmacy you always use and only later, to notice that it has a different, unexpected, appearance. A different color pill, a different shape sometimes, etc. Most times the pharmacist has put a sticker on ours when that happened, saying it's the same med despite the different look. Once or twice they've forgotten to make note of it and I've gone back just to be sure. To be on the safe side. We don't get any liquid meds from the pharmacy, though. But I can see how you might be worried about whether or not the product was still fresh, in case that might have caused the headaches. Wish I could be of more help. I hope you'll find out the cause of Joe's headaches and be able to reduce them. Take Care, Georgina bound for london wrote: > I know I have seen recent posts about headaches from others. Our rheumy > said this is a side effect of the MTX and one reason why we should > reduce it (she is at 25mg injectable weekly). Anyone else know of this? > I read the insert and it does list headache as a side effect but then > there are so many side effects listed. weird thing is my daughter is the > only one at this pharmacy on the MTX and they couldn't get the same > brand in anymore so it came in this huge vial this time. And the > literature mentions nothing about arthritis. Hmmm, makes me think I > should have checked the expiration date. > > So, any ideas on the headaches. Med related or just another feature of > JRA? He also said it could be the birth control pills but without them > she cycles every 2 weeks with only a few days off. That is new since > JRA. ARGH!!! Poor kid. No wonder she is so emotionally labile. Well, I > am once again off topic and need sleep. LOL > > e, mom to joe 17 poly > Current meds: Prednisone, MTX, Celebrex, Enbrel, Vitamins, Folic Acid, > Protonix, Tums, Low-ogestrol, Ultram, Tylenol, Celexa (and my brain is > slipping cause I'm sure there is something else) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 15, 2004 Report Share Posted August 15, 2004 n gets headaches all of the time. We have brought her to many specialists and they were labeled as chronic daily headaches. No medicine was prescribed, for the neurologist said that you get a rebound effect from the drugs with these types of headaches. When she flares she gets the headaches. They are 24/7. With n, I would definitely say that the headaches are part of her disease. (n, 15, systemic) headaches > Hi All: > I rarely post anymore, though I do keep up somewhat with the reading. > > My daughter Mickey, now 10, (systemic onset at 3) has been getting a lot of > headaches lately. Her pred is down to 1mg/day, .8cc of methotrexate once a > week, 25mg indomethacin 3x/day. Folic acid, calcium, etc every day. > > I myself get migraines, and it looks like the poor kid may have inherited > this tendency. But as bad headaches are one of the symptoms of MAS, could > someone please refresh my memory on the other tell-tale signs? I am doing a > search of the archives, but any information would be appreciated. Does > anyone else's child suffer from regular headaches? > > Thanks, > > Lynn > Mom to: > Mickey (10), systemic jra since 3 > Kinsey(8), wonderful sister to Mickey > ----- > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 15, 2004 Report Share Posted August 15, 2004 Hello Lynn, I also have systemic, aka still's disease. I have had problems with migraines and also I hear a lot of others at the still's disease board of having problems with headache's as well. I do believe there is a link between them and the arthritis. Just the other night I had a real bad one, I haven't had one like this in over a year. But also I believe mine are also due partly to my neck. > Hi All: > I rarely post anymore, though I do keep up somewhat with the reading. > > My daughter Mickey, now 10, (systemic onset at 3) has been getting a lot of > headaches lately. Her pred is down to 1mg/day, .8cc of methotrexate once a > week, 25mg indomethacin 3x/day. Folic acid, calcium, etc every day. > > I myself get migraines, and it looks like the poor kid may have inherited > this tendency. But as bad headaches are one of the symptoms of MAS, could > someone please refresh my memory on the other tell-tale signs? I am doing a > search of the archives, but any information would be appreciated. Does > anyone else's child suffer from regular headaches? > > Thanks, > > Lynn > Mom to: > Mickey (10), systemic jra since 3 > Kinsey(8), wonderful sister to Mickey > ----- > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 15, 2004 Report Share Posted August 15, 2004 Hi Lynn, The first time that Robbie had headaches since diagnosed with JRA was when we added cyclosporine - and it caused him to have hypertension (more likely the combination of prednisolone and the cyclosporine - since it is a side affect of both medications - when we taper the steriods we end up tapering the lisinopril as well - when the steriods go back up, so does the hypertension and the lisinopril dose) - He never had problems with hypertenision previously though on just the pred. I have noticed that he has had complaints of headache on top of his other symptoms during the last two flares - but they have been been in concjunction with his other severe systemic symptoms ( " all over " pain,fever, rash, lethargy, etc.) Robbie also complains of abd pain during his flares. The MAS symptoms I remember reading about in addition to the headache are flu like symptoms - much of the symptoms are such that it is the combination of a lot of symptoms that alone would seem insignificant. With your history of migraines - nausea and vomitting would seem to go hand in hand with them - at least they did for me - my migraines stopped about 12 years ago - for no apparrent reason that I have been able to identify - but I know how painful and miserable it can be. I would think if Mickey is having flu like symptoms along with the headaches that it would bear looking into. At Robbie's second arthritis related hospital admission, and the one where they agreed on his SoJRA diagnosis - he was admitted with " probable JRA and MAS " It was months before I was able to find out what the MAS was - but all I know is that Robbie was so very sick when admitted that time that I couldn't begin to sort what symptoms actually went with what, he was lethargic, didn't want to be touched, didn't want to be moved - there hardly seemed to be an internal organ not inflammed in one way or another, it appeared he had strep(though he didn't), ear infection, and conjunctivitis on top of the enlarged liver, spleen, lung involvement and irregular heartbeat. The rash showed up later. I hope this is of little help - there is a clear description of MAS in one of the archive posts. I hope that Mickey feels better soon. I do agree with n that headaches for many seem to be connected. Val Rob's Mom (6,systemic) In a message dated 8/15/2004 11:03:29 AM Eastern Daylight Time, " WILLIAM PRICE " <bc.price@...> writes: >n gets headaches all of the time. Â We have brought her to many >specialists and they were labeled as chronic daily headaches. Â No medicine >was prescribed, for the neurologist said that you get a rebound effect from >the drugs with these types of headaches. Â When she flares she gets the >headaches. Â They are 24/7. Â With n, I would definitely say that the >headaches are part of her disease. Â (n, 15, systemic) > headaches > > >> Hi All: >> I rarely post anymore, though I do keep up somewhat with the reading. >> >> My daughter Mickey, now 10, (systemic onset at 3) has been getting a lot >of >> headaches lately. Her pred is down to 1mg/day, .8cc of methotrexate once a >> week, 25mg indomethacin 3x/day. Folic acid, calcium, etc every day. >> >> I myself get migraines, and it looks like the poor kid may have inherited >> this tendency. But as bad headaches are one of the symptoms of MAS, could >> someone please refresh my memory on the other tell-tale signs? I am doing >a >> search of the archives, but any information would be appreciated. Does >> anyone else's child suffer from regular headaches? >> >> Thanks, >> >> Lynn >> Mom to: >> Mickey (10), systemic jra since 3 >> Kinsey(8), wonderful sister to Mickey >> ----- >> >> >> >> >> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 21, 2006 Report Share Posted March 21, 2006 Hi there, I am not a headachey person, but I had a time in my life, around age 19, where I was stricken with them. It was like my head was in a vice and was being squeezed, kind of where the temple areas are. I remember the pressure would build and become unbearable and I wept almost daily. I do not recall painkillers helping me and I wanted to die. EVERYDAY I had them. Then, I went to someone because I was always ill and suffering depression etc. I was shoved on antidepressants which did no good, I thought of suicide. I had symptoms all over the place that made no sense to me. Finally through a friend, I went to a doctor who put me on new diet. I did not want to do it because I liked my sugar, but I was desperate. I found it hard to adhere to this diet and the withdrawal at that time was so bad, I cried and paced the floor because of my love of sugar and other foods. I stuck to it and had NO sugar and no yeast and no gluten/wheat. The headaches worsened in one way for the time I was withdrawing/detoxing as the toxins in and around my brain began to come loose and I felt wretched. I think I smelt also, but by the end of two weeks or so, I noticed a change in myself that was marked. The improvements were amazing. My quality of life almost returned, my appearance changed and became youthful (and I was already young, yet looking old/haggard because of illness). My hair and skin and eyes changed in quality and became healthy. I looked like a different person. Though I was still ill in one way (I suffer with mercury toxicity), the other symptoms were GONE. NO MORE HEADACHES!!! Even my asthma died down, though occasional wheezing. I do not know whether the headaches went from me giving up gluten/wheat or the sugar or what it was, but they never returned. I cannot promise the same will happen to you, but please believe me, the diet is worth everything. IT might be the only thing to ever help as it was for me. Nothing else helped me. No amount of medication for this or that did a darned thing. Though I am ill again, due to other problems with toxicity, so am trying to start from scratch, though I have underlining toxicity now that is going to have to be dealt with. The candida diet, giving up wheat/gluten is probably keeping me sane. I hope this in some way encourages you that given a chance, the body can begin to release the stored poison and rebuild itself with new tissue/cells etc. Eating sugar here and there, thinking it's not a big deal will not allow this process to take place. I tried that. You have to give it up completely so that the candida cannot keep surviving on the bits you might still be having. Oneday you might be able to have bits again here and there without getting ill, but initially you have to give it up. > > Hi, I am new to this group but not new to candida. I have systemic > candida, Fibromyalgia, CF, IBS and the list goes on. I feel that it > is all caused by overgrowth of yeast, but try and tell a Dr that. > Does anyone out there suffer with this horrible headaches that last > for weeks or monthes and there is no pain reliever that helps. I feel > all alone and scared that this pain i feel will drive me crazy. Any > suggestions? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 22, 2006 Report Share Posted March 22, 2006 Hi, what is your name? Welcome to our group my friend. I answered your questions below offline, so I hope you read my main article and start on the diet right away, one step at a time. All of your symptoms are related to candida overgrowth. Many of our members have turned their symptoms around, even headaches, on our candida program. Eventually you will regain your health and the headaches will stop - it takes persistence and hard work but it is worth it. The best in health, Bee > > Hi, I am new to this group but not new to candida. I have systemic > candida, Fibromyalgia, CF, IBS and the list goes on. I feel that it > is all caused by overgrowth of yeast, but try and tell a Dr that. > Does anyone out there suffer with this horrible headaches that last > for weeks or monthes and there is no pain reliever that helps. I feel all alone and scared that this pain i feel will drive me crazy. Any suggestions? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 22, 2006 Report Share Posted March 22, 2006 The best headache cure for me I got from the macrobiotics. You heat some water in a pan, and have some folded washcloths or small towels. Soak the towels in the hot water -- as hot as you can stand. I myself heat the water to boiling, let it cool slightly, then wring the towels with the use of tongs and spoons. It keeps cooling as you wring the excess water out and (if necessary) refold them. You can add fresh ginger juice to the water; though I am so lazy I skip that part. Have 3 hot moist towels folded one on top of the other. Put the towels on the part of your head that hurts. The towels should feel hot. You don't want to burn yourself of course. But as hot as you can stand. After a while the towel on your head will cool, and then you take the one on your skin and put it on the back of the pile so that the towel in the middle is on your head -- that one will be hot. Until that one cools down. When they are all cool, you can wring them out and resoak them in more hot water if necessary. This works much much better than any asprin or ibuprofen or any other drug. It opens the blood veins and relaxes the muscles. A hot shower can help too. But you need to dry your hair quickly afterwards, so your head doesn't get cold again. Another thing I like to do is to rub Tiger Balm on the part of my head that hurts. That helps alot though not as thoroughly as the hot towels. Hot towels are also good for dry eye syndrome; I make them a little less hot for directly on my eyelids. Good luck! - T Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 22, 2006 Report Share Posted March 22, 2006 Here is one I like to do. I lie down and put a cold pack behind my neck and a heat pack on my stomach. Crazy as it sounds it works even on the worst migraines. Jeanne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 4, 2006 Report Share Posted June 4, 2006 > > It has been a while, but is there a possibility that dizziness and bad bad headaches can be caused for a flare with AIH? Before I was diagnosed with AIH/PBC overlap, I used to get disabling headaches that would last for days - averaging 2-3 days. Not being prone to headaches, they really upset me. The worst pain was near the left temple. Nothing helped them. Once I was diagnosed and put on pred and imuran, I haven't had them since. So though I can't say for sure it was due to AIH, it seems too coincidental not to be the cause. Take care, Sandy C. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 4, 2006 Report Share Posted June 4, 2006 Sandy, thank you so much. I am just about ready for hubby to takeme to ER and see if I can get some relief. Not only are the headaches bad, but the pain in the right side is driving me mad! Debby [ ] Re: Headaches > > It has been a while, but is there a possibility that dizziness and bad bad headaches can be caused for a flare with AIH? Before I was diagnosed with AIH/PBC overlap, I used to get disabling headaches that would last for days - averaging 2-3 days. Not being prone to headaches, they really upset me. The worst pain was near the left temple. Nothing helped them. Once I was diagnosed and put on pred and imuran, I haven't had them since. So though I can't say for sure it was due to AIH, it seems too coincidental not to be the cause. Take care, Sandy C. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 4, 2006 Report Share Posted June 4, 2006 Hello, my doctor put me on Zomig nasal spray for my headaches, and it is the only thing that works. It makes my nose burn alittle and dripps down my throat and taste terrible, but the headache is gone. [ ] Re: Headaches > > It has been a while, but is there a possibility that dizziness and bad bad headaches can be caused for a flare with AIH? Before I was diagnosed with AIH/PBC overlap, I used to get disabling headaches that would last for days - averaging 2-3 days. Not being prone to headaches, they really upset me. The worst pain was near the left temple. Nothing helped them. Once I was diagnosed and put on pred and imuran, I haven't had them since. So though I can't say for sure it was due to AIH, it seems too coincidental not to be the cause. Take care, Sandy C. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 4, 2006 Report Share Posted June 4, 2006 I think that I am going to see my GP tomorrow is I can get in the AM and see if I can get something to kill the pain. I am willing to do anything. The Imitrex is not touching the headache at all. All I want to do is to sleep...this is NOT normal for me Debby [ ] Re: Headaches > > It has been a while, but is there a possibility that dizziness and bad bad headaches can be caused for a flare with AIH? Before I was diagnosed with AIH/PBC overlap, I used to get disabling headaches that would last for days - averaging 2-3 days. Not being prone to headaches, they really upset me. The worst pain was near the left temple. Nothing helped them. Once I was diagnosed and put on pred and imuran, I haven't had them since. So though I can't say for sure it was due to AIH, it seems too coincidental not to be the cause. Take care, Sandy C. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 4, 2006 Report Share Posted June 4, 2006 Debby Glad to see that you are going to the doc tomorrow. If it stays this long it needs to be checked. Will keep fingers crossed that it is not a flare up causing it. Good luck, let us know how you do. Thinking of you Marie (Ont) > > > > It has been a while, but is there a possibility that dizziness and > bad bad headaches can be caused for a flare with AIH? > > Before I was diagnosed with AIH/PBC overlap, I used to get disabling > headaches that would last for days - averaging 2-3 days. Not being > prone to headaches, they really upset me. The worst pain was near the > left temple. Nothing helped them. > > Once I was diagnosed and put on pred and imuran, I haven't had them > since. So though I can't say for sure it was due to AIH, it seems too > coincidental not to be the cause. > > Take care, > Sandy C. > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 5, 2006 Report Share Posted June 5, 2006 I had headache on my right side that was disabling. I used to wake up with headache at night as well. I had this headache and felt extremely tired and that is why I thought something was wrong and went to see a doctor. Of course they found out that I have AIH. Personally I don't think headache is from AIH because I have been doing these very slow stretching excises for a week or so and my headache is gone. Before starting these exercises, I tried all sorts of pain medication but nothing worked. So I turned to oriental medicine. I tried pressure points (like acupuncture but without the needle) and these slow stretching yoga like exercises. My tiredness has diminished greatly. Only symptom I feel is the tingling on my right shoulder. I guess that is from inflammation of the liver. I hope your headache will get better soon! Kim from PA tdcc2000@... wrote: Sandy, thank you so much. I am just about ready for hubby to takeme to ER and see if I can get some relief. Not only are the headaches bad, but the pain in the right side is driving me mad! Debby [ ] Re: Headaches > > It has been a while, but is there a possibility that dizziness and bad bad headaches can be caused for a flare with AIH? Before I was diagnosed with AIH/PBC overlap, I used to get disabling headaches that would last for days - averaging 2-3 days. Not being prone to headaches, they really upset me. The worst pain was near the left temple. Nothing helped them. Once I was diagnosed and put on pred and imuran, I haven't had them since. So though I can't say for sure it was due to AIH, it seems too coincidental not to be the cause. Take care, Sandy C. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 8, 2006 Report Share Posted June 8, 2006 I did finally see my GP and had the labs done. The liver counts were somewhat elevated, but no worse than they have been in the past. The only problem that did show up was the protein levels, globulin serum and indirect bilirubin. These were elevated more than normal. I have not sent them to my GI but may tomorrow. The good thing was that my CBC looked better than ever before! WHOOHOO! Now just to get the liver back in line! Anyway, thought I would let you know. The headaches are still there, but not quite as bad as before, so maybe they will all go away soon! Debby [ ] Re: Headaches > > It has been a while, but is there a possibility that dizziness and bad bad headaches can be caused for a flare with AIH? Before I was diagnosed with AIH/PBC overlap, I used to get disabling headaches that would last for days - averaging 2-3 days. Not being prone to headaches, they really upset me. The worst pain was near the left temple. Nothing helped them. Once I was diagnosed and put on pred and imuran, I haven't had them since. So though I can't say for sure it was due to AIH, it seems too coincidental not to be the cause. Take care, Sandy C. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 8, 2006 Report Share Posted June 8, 2006 Do you have any other symptoms with your headache like sinus pain, post nasal drip?? Does Sudafed help?? I found that since my liver problem I also developed a non-allergic-rhinitis (?), and I have been taking Nasacort Nasal Spray and Saline Nasal Spray for it and I do not get the headaches very often lately. But I found out that I had that problem by reponding to Sudafe/Sinutab meds and went to an Allergist (on my own) who did all the tests for allergies without success, but gave me the right medicine anyway. Later when it flared up again, I even had a head x-ray that showed a mass in my sinuses and had to take prednisone and antibiotics for 2 weeks. I seem to be OK since, at least in that department! By the way , my blood work did not show the sinus infection! Sometimes we concentrate on the liver problem so much, that even the doctors forget to check for other things. Clara from OR [ ] Re: Headaches > > It has been a while, but is there a possibility that dizziness and bad bad headaches can be caused for a flare with AIH? Before I was diagnosed with AIH/PBC overlap, I used to get disabling headaches that would last for days - averaging 2-3 days. Not being prone to headaches, they really upset me. The worst pain was near the left temple. Nothing helped them. Once I was diagnosed and put on pred and imuran, I haven't had them since. So though I can't say for sure it was due to AIH, it seems too coincidental not to be the cause. Take care, Sandy C. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 9, 2006 Report Share Posted June 9, 2006 I also have a lot of problems with sinuses and other respiratory problems: ear infections, pneumonia. Nasacort does help -only use it once/day at bedtime. I'm currently finishing uo a round of antibiotics and steroids. My liver does not make enough IgA which helps fight upper respiratory infections. You can buy over the counter nasal sprays but only use them twice a day (I'm told that it can be addictive). Clara Shelton <cshelton33@...> wrote: Do you have any other symptoms with your headache like sinus pain, post nasal drip?? Does Sudafed help?? I found that since my liver problem I also developed a non-allergic-rhinitis (?), and I have been taking Nasacort Nasal Spray and Saline Nasal Spray for it and I do not get the headaches very often lately. But I found out that I had that problem by reponding to Sudafe/Sinutab meds and went to an Allergist (on my own) who did all the tests for allergies without success, but gave me the right medicine anyway. Later when it flared up again, I even had a head x-ray that showed a mass in my sinuses and had to take prednisone and antibiotics for 2 weeks. I seem to be OK since, at least in that department! By the way , my blood work did not show the sinus infection! Sometimes we concentrate on the liver problem so much, that even the doctors forget to check for other things. Clara from OR [ ] Re: Headaches > > It has been a while, but is there a possibility that dizziness and bad bad headaches can be caused for a flare with AIH? Before I was diagnosed with AIH/PBC overlap, I used to get disabling headaches that would last for days - averaging 2-3 days. Not being prone to headaches, they really upset me. The worst pain was near the left temple. Nothing helped them. Once I was diagnosed and put on pred and imuran, I haven't had them since. So though I can't say for sure it was due to AIH, it seems too coincidental not to be the cause. Take care, Sandy C. Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.