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pelican Junior Member ![]() ![]() Posts: 6 |
After seeing several doctors and giving up vials of blood, I have finally been diagnosed with Delayed Pressure Urticaria. I get huge hives, mainly on my midrift, extremely itchy blisters on my hands and severe muscle ache approx. 6 hrs. after exercise or muscle strain. I had never heard of this disease, nor had any of my doctors until an allergist came across an article. This disease is not associated with any allergy. I have had it for approx. 9 months, it does seem to be getting better. The doctor does not know what causes it or what cures it, she just hopes it will burn itself out. I read a couple of articles regarding Jane Pauley's mysterious illness and they called it Delayed Pressure Urticaria. Anyone else out there with this disease? If so, do you have any information, i.e., does it go away entirely? what triggers it? I would be grateful for any information. IP: Logged |
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pburgbeanie Member ![]() ![]() ![]() Posts: 35 |
Hi Pelican. I wonder. I had something similar almost 2 years ago. I am diabetic, so everyone blamed it on that. However, I switched to mostly organic cleansers, Dove liquid soap in the shower and dove bar soap as a hand cleanser by the sinks. That actually seemed to help. I was tested for every allergy under the sun and came up negative to all of them. This even cleared up a previously diagnosed allergy to eggs! It took about 6 months to really go away. But I've been fine for a long time now. I do find that I get some mild symptoms of it if I stay in hotels or even sleep at my in-laws home. Hope this helps you. IP: Logged |
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snowanne Junior Member ![]() ![]() Posts: 14 |
Hi..I am suffering from this strange skin rash as well-mine is quite acute--every day I have many areas that flare up. I've had it for 6 months..hoping someday it will go away...I went to a specialist (allergist) and he said its pretty rare..but it may be caused by some trigger if you have been taking penicillin or tetraycline--sure enough mine started after strepth throat last winter! I read from one woman that she was allergic to Yellow Dye 5 & 6. I'm not sure about this....The best thing is to use Benadryl (liquid works in minutes) to stop the intense itching--as you well know its a vicious circle. I used to have long scratches on my hands--it was horrendus! I now take Zytec, a prescription antihistamine daily. Apparently this is the drug of choice for hives. It does make it better, but instead of having the huge welts my skin will just appear red--so at least it looks better! I also found that an oatmeal based body lotion (got at health food store) also worked pretty well--at least to get rid of the intense itching quickly--but the bottom line is that it is not topical--its systemic which is why Benadryl creams don't help---I'm still looking optimistically for this to end--please keep me updated! GOod Luck IP: Logged |
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pelican Junior Member ![]() ![]() Posts: 6 |
Junior Member, thank you for your reply. Your affliction sounds exactly like mine. Good news though, I have been suffering with this for nearly a year and while it's not gone, it is much, much better. The hives are much smaller than they were and they don't itch with the same intensity. The worst itching is on my hands, particularly if I have done yard work or a lot of housework. I believe my hives are related to stress. I have been caring for my father and obviously there can be a lot of stressed involved. After getting a live-in caregiver for him, my hives improved greatly. I have found that Zyrtec works the best for me. Sometimes I only have to take one a week. Benedryl cream helps some, but I find that taking a cool shower relieves most of the itching. I have been told that this is a virus and my Applied Kinesiologist recommended taking L-Lysine and avoiding sugars and alcohol. So far I can't say this is really working for me, but I'm still taking the pills. You can get these over the counter at any health food store. Good luck to you. IP: Logged |
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silverwillow2000 Veteran ![]() ![]() ![]() Posts: 403 |
I've read about this. I came across it while researching b/f's condition. He has Solar Urticaria. His is actually more similar to an allergy than the delayed pressure type. He was on Zyrtec, but it made him too tired. He was switched to something else that works awesome, but he can't pronounce it. (I haven't seen the stuff) He said it's like all consonants & very few vowels or something. Does anyone know of a medication like that? IP: Logged |
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Anonymity Senior Veteran ![]() ![]() ![]() ![]() ![]() Posts: 518 |
My fiance has exercise-induced urticaria. It just stinks, doesn't it?? The follow steps are in the order that my fiance went through them. I don't know if you'll want to do the same things but... 1. If you go to a specialist for this, the doctors will probably do some allergy skin-tests on you (where they apply common allergens, like cat dander, to tiny pricks in your skin and wait to see if your skin reacts). These tests itch and may mildly burn, but they're not actually painful. This may give your doctors a better idea of your overall allergy profile. 2. I would guess that they will then prescribe a bunch of different allergy medicines. You may have to try a whole list, one at a time, before you find one that works. 3. If you try every allergy medicine, and none of them work, then the doctors might try prescribing a medley of non-traditional allergy medicines. Medicines that are often prescribed for something else (say Amitriptyline, a mild anti-depressant) sometimes also have anti-histamine or anti-allergy effects. My fiance was on a whole bunch of drugs that, combined, stopped his hives. Hopefully, however, you won't have to take such strong medicines. If you do, be very careful to learn of all the side effects, etc. of each medicine before you agree to take the medley. Doctors sometimes forget to explain all the side effects of each individual drug. In the meantime, or in addition, I have some hives-tips for you. These are things that I have learned about and my fiance has tried for his hives. Apparently, some of these ideas work for some people some of the time. P.S. I hope this post made sense. If you want more information, search this site for hives and/or urticaria, and a bunch of stuff will come up! IP: Logged |
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catlvr Newbie ![]() Posts: 1 |
Hi everyone! I am so happy to find this site!!! I've had dpu for six years now, and I'm just now getting with an allergist and starting a whole regimine of pills. I'm on Doxepin, Singular and now starting on Sulfasalazine. I read somewhere that this is a drug used for dpu, and so far, it's looking good! I've been on two per day for a few days now, and getting ready to slowly work up to six pills a day. I hate having to take all this medication, but I'll do anything to not swell up in pain! Any words of support are appreciated! Sounds like some of you have been lucky and only needed one or two medications to find relief. That's wonderful! I've done the cold showers too, and I always have a tube of cortizone in my purse. Well, thanks for being here! IP: Logged |
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sapphirefair1 Newbie ![]() Posts: 3 |
Pelican, It is good to know that there are other people out there that are suffering with the same condition. I was told that I had this disorder by a dermatologist. He suggested Benadryl tablets, but they only worked for a couple of hours and made me drowsy, too. My regular doctor prescribed Zyrtec and it works well to relieve the itching and hives. I too, only have to take one every three or four days. However, if I do any significant physical labor, it does not help. I will swell up and have itching feet, hands, elbows, knees, waistline, inner thigh, etc . . . I would like to ask if any of you who have posted have ever heard of these hives attacking your respiratory tract or heart muscle the way it does the rest of the body? The reason I ask is that every now and then I become short of breath with a mild cough. One cough leads to another and before I know it I have to cough to be able to breathe well. After an hour or so of this the coughing subsides and I can breathe just fine again. Also, I have had an episode when my heart seemed to skip beats over a period of several hours, again, this too subsided as quickly as it began. I have contributed this to the hives. By the time I went to see the doctor, it was over and he could not help me much. I would appreciate any insight into this aggravating illness. I tell people that I am "Literally Allergic To Work." That's no lie! Thanks for your time . . . sapphirefair1 IP: Logged |
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pleides Newbie ![]() Posts: 1 |
In reply to pelican I started itching about 3 months ago. Mostly palms and feet. Then raised welts appeared on my skin after pressure or using my hands. One episode I clipped bushes and that night my hands ached so much I had to sit with ice packs for hours. Cant carry shopping bags or wear tight clothes. The itch seems worse on hot days. Also get hive like lumps anywhere on my body as well. Worst areas though are my hands and feet.Three doctors later and after a full range of blood tests found this site. All tests were negative and told to take prednisolone. I wont. Does anyone have more info about this condition please? IP: Logged |
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eastclif Newbie ![]() Posts: 1 |
I was very interested to find this forum. I was diagnosed with dermographism and chronic urticaria about 4 years ago. Until I found this site today, I had never heard of DPU, but it certainly describes what I have. Mine started as severe itching, mainly in my hands and feet, with no redness or hives. Then I started noticing welts and itching, which I eventually figured out were appearing about 15 minutes after pressure. Carrying grocery bags, carrying boxes, kneeling on a carpet or on the sand bottom of a river were the first things I noticed. I started taking Zyrtec (Cetirizine) on my own, just for the itching, and when I saw an allergist, he told me that was the best medication. He tested me for allergies, and although I showed no severe reaction to any of the substances, I had a mild reaction to all of them. He told me the immune reaction in my skin was out of kilter, and that this sometimes occurred after a viral infection. I had recently had a severe viral bronchitis. To confuse the picture, I was living in Australia at the time, and was having severe skin reactions to some kind of insect or spider bite. Anyway the doc told me to keep taking the Zyrtec, and try to stop it every once in awhile to see what happened. He said he had no idea how long the condition would last. A few months after I saw the doc, I went for a facial, which involved "blackhead extractions", and I ended up with huge welts on my face, lasting for about 18 hours. This was when I realised that it was pressure rather than just contact that was causing the problem. Basically, my problems are very mild compared to some people who have written to this forum. I am basically symptom free, except in cases of extreme pressure like a facial. I have tried several times over the last few years to stop the medication, but the longest I lasted was about 36 hours. Then my hands and feet start itching really badly. It's interesting that one person here said they take a Zyrtec every 3 or 4 days, maybe I'll try that, rather than taking one every day like I have been. I'm glad that I have found this forum though, and that I have a more definite idea of what I have. I also now realise the mild reaction I had to all the substances in the allergy testing was likely due to the actual pressure of the skin pricks applying the substances. IP: Logged |
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KellO Newbie ![]() Posts: 1 |
The first time I got my hives were during cheerleading practice 2 years ago. We didnt think anything of it since it was my first time and it wasnt that bad. Then I went to an Amusement park that summer and my whole thigh was swollen, and it hurt to walk, I had to literally have someone carry me. We went to the doctor and he didnt know what it was so, he told us to take benadryl. Benadryl seemed to work fine so when I went to cheerleading camp that summer, it seemed to work ok. That football season I would continuously get hives but not too bad. I would just take benadryl and it helped. It went away that winter and then the following spring while at a cheerleading clinic I got the bumps on my stomach and legs and feet, it was never taht extreme. My Mom was away so I had to call my grandma to take me to the ER. My Dad met us there and the doctor gave me a shot in the butt, to help reduce the swelling. It seemed to help a lot and it made me drowsy so I just slept it off. The next morning my foot was still swollen, so when my Mom came and picked me up we called doctors that specialized in feet, my StepMom is a nurse and she said that we should look into that. We had to drive 2 hours and it took 2 weeks to get into the doctor and when I got there he tested for Lyme disease and Juvenile Arthritis and something similar to that which I cant remember. Those tests came back negative so we still had no idea to what it was. Last summer it seemed to not happen as bad even when I was cheering outside. I had an away game one nite and I didnt feel too good, so I took some tylenol. I woke up the next morning and my ears, neck, legs, feet were swollen and my lips were swollen and my head had a few bumps on them. My Mom had to work that day so I had to wait until she got off work. Throughout the day, it kept getting worse and my face kept getting more and more hives. I looked like one of those Animorphs books, when a person turns into an animal. My Mom got off a lil early and she took me to the ER ((at a different hospital)) and that doctor there said that it looked as if I was allergic to something outside since I seemed to get hives when I was outside for cheerleading. He told us to go to an allergist and perscribed us some Zyrtec. Just about 2 weeks after, I had my appointment with the Allergist they had to take blood my first time and told me to come back in a week so they could start the Allergy tests. After about 3 weeks all of the test were done and I was told that I was allergic to Oak trees, dust, pollen and grass. It stunk because we have Oak Tress all over here. So they gave me shots when I could come in so during the summer I would be more immune to it. I havent been able to go since December because of cheerleading. But I still take the Zyrtec and it seems to help but sometimes (ie Today) it seems to get worse than better. I woke up today and my ears were swollen, my neck and half of my lip was also. I took my Zyrtec last nite around 12 and I took another at 10:30 am. I also took some benadryl at 3. Does it affect anything when I take both meds? It also is taking what seems FOREVER for the meds to kick in. Thanks in advance IP: Logged |
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morganrj Newbie ![]() Posts: 1 |
I can't explain how happy I am to find a name for what I've been dealing with for 15 years. My DPU affects mostly my hands and feet - if my shoes don't fit *exactly* right my feet'll swell... and it's so bad in my hands that I can't leave my arms hanging down (like when you're walking around the mall or something) because my fingers'll swell up. Lately it seems like the attacks are coming more and more often - does anyone else feel like it comes in "waves?" Like I'll be fine for two years but now I'm swelling up every other month. It's also affecting my stomach - when it's really bad I can't even stand up because I'm so nauseous. It's nice to know that there are others out there with this problem... thank you to the host for providing us with a place to share our experiences. ![]() IP: Logged |
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paulie Newbie ![]() Posts: 1 |
hi all, like all you unfortunate people, I to have dermogrpahism (aka DPU.) I have had the condition all of my life and refuse to accept that all we can do as sufferers is to supress this condition by taking anthistamnines, which can cause long term problems when taken to excess. This is the solution in Western medicine and believe it or not this type of urticaria is not taken seriously by GP's. It is treated and classed with the same name and procedure as Ideopathic Urticaria (using anthihistamines). This is thought to be a physcologically induced disorder, in other words people us dermographic sufferers are creating in out little heads My hives I'm sure are caused by food intolerance/allergies, but because I have the condition all of the time, I have no idea what the allergens are, but my condition becomes a lot more severe if i have had consumed preservatives such as Sunset Yellow and Sodium Benzoate. It is for this I have decided to see a NEAT practioner recently. I have only had one appointment, but i will keep you posted on the results, if you wish. I am apparently allergic to a few things, such as Vitamin B complex (in fruit and veg). My only concern is that this treatment is needed for about 40 sessions, as people like us are ellergic to a lot of things. This may cost $500 or £1000 depending where the practioner is from. That would be great if people like me could afford it. Oh well, i'm willing to give it a go for a few. There are also so many other special practioners that we can see, such as herbalists, hypnotherapists, accupuncrists etc but do these people have any idea about this condition, even thought they claim that they can cure it, however so few of us sufferers seem to be have been cured. Interestingly, GPs say that the condition 'burns' itself out eventually, once the body stabilises. Well........23 years and still counting I thought i'd post this message, so that I could contact other sufferers such as yourselves. Even though I wish none of you had the condition, it helps to know that i'm not alone. Ciao for now. [edited to remove link. Please never post commercial websites. [This message has been edited by moderator2 (edited 06-19-2003).] IP: Logged |
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slsowe Newbie ![]() Posts: 1 |
Hi, I have been suffering from Delayed pressure urticaria for 9 years. (I was 16 when it began). If I bump my lip, it swells. If I carry a backpack, my shoulders swell. If I cry, my eyes swell shut. If I wear a pair of new shoes, I can't walk the next day. It took a long time for my allergist to determine the cause. He finally figured it out after taking blood and my arm swelled. The urticaria has seemed to get so much better over the years. When it began I was on 3 different drugs, 3 times a day. The only thing that seemed to make it disappear was Prednisone. Unfortunately, that drug is bad for you. I switched doctors after 3 years and I give him the credit for my symptom free life. I take Zyrtec once a day ... But the drug that made me symptom free is Accolate. Accolate is an asthma drug, but works wonders on patients with Delayed pressure urticaria (so my allergist says). If I go two days without either drug my hives start up. I am posting this ad b/c I know the pain of living with this allergy. When I first got it, I searched endlessly with no results. I hope this helps someone. IP: Logged |
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sheilameehan Newbie ![]() Posts: 1 |
Wow. Hives for only 6 months. I have had them for 5 years. Chronic pressure urticaria. Started with zytrec - 4 a day - didn't completely resolve it, but almost (though my friends thought I was suicidal because I needed to sleep so much). I had some good luck after that working with a homeopathist for about a year in DC, but then I moved and had to find new treaters. I have just started with Dr. Schocket at National Jewish in Denver - he actually specializes in hives (who knew anyone did that!). Apparently some chronic hive sufferers test for certain thyroid issues. If you haven't been checked for that - try it. For those of us who turn up positive on that one, thyroid medicine can help/cure it. IP: Logged |
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ashdelven Newbie ![]() Posts: 2 |
When I was around 10 years old i woke up and my ear was very swollen. For the past 10 yrs. i have been fighting DPU. I have taken every kind of antihistamine and have also been on prednisone a few times. Mine only flares up every couple of years and i was wondering if anyone else's comes and goes? and if so has the space in between breakouts gotten worse or better as you have gotten older? mine seem to happen every 2-3 years. Right now i am having a breakout and i am taking singulair combined with claritin. Has anyone tried this combo? I am so happy to find out that other people can share my experience with this awful disorder. IP: Logged |
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JGorse Junior Member ![]() ![]() Posts: 7 |
I am so pleased to find this forum on DPU - I was beginning to think I was going mad! I have had this horrendous condition for 4 years now - started with the odd "lump" under my feet which itched/burned and generally drove me mad for a couple of days. The urticaria wheals eventually got worse and more generalised over my entire body but this only used to happen every couple of months. Two years ago I caught chicken pox at the age of 36 and the urticaria was extremely severe during the illness. It then disappeared for a few months but is now back with a vengeance. I have now gone from maybe every other week having a bad bout of DPU/generalised urticaria to every single day. This illness is making my life a complete misery (and I'm told by my loved ones, theirs too sometimes!). I have now reached the stage where I can barely open a bottle without my hands swelling, and sometimes have to resort to taking a cushion out with me in case the restaurant I'm going to has hard chairs. As for kneeling down to pick something up - forget it!Reading through other postings on this page, I am interested to read that other sufferers report shortness of breath/nausea. I too get these symptoms, but was wondering if anybody else out there gets occasional chest pains, and more worryingly it appears that when I'm having a particularly bad "wave" of "lumps" I find that the glands all along my neck and up the back of my head are raised and sore. Does anybody else notice this? This normally goes hand-in-hand with a horrible headache - can it affect the brain? (I often feel quite "spaced" when I'm bad) Also, I now know when I'm in for a particulary bad dose as I get extremely hot in the day/night preceding the next batch of lumps. Anybody get that too? I take a combination of Clarityn/Fexofenadine/Atarax most days but they don't really help and I don't like taking such a strong combination of drugs. I have tried just about every anti-itch solution/cream known in the UK and am trying Tea Tree Oil/cream at the moment (it's a natural anaesthetic as well as soothing) and it does appear to help to calm things down a little bit. I really empathise with any of you out there who are suffering too - on the days when I can't walk/use my hands (ususally because I've gone mad and done something daring like walking or vacuuming the day before!)it really feels like I'm on my own and being punished for something! [This message has been edited by JGorse (edited 07-14-2003).] IP: Logged |
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ashdelven Newbie ![]() Posts: 2 |
Well I go back to the dr. this friday to try some new medicine because the singulair that she had put me on hasnt been working. I have been getting the hives really bad on my face lately. Also my knees and feet. So I am worried that the dr. will want to put me back on prednisone which i dont like because of the side effects. Does anybody have any medication they recommend i try? I have done most antihistimines including zyrtec and they dont work. Any magic medicine? thanks IP: Logged |
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booger04 Junior Member ![]() ![]() Posts: 20 |
i have another form of your disease...familial cold urticaria...in other words...im pretty much allergic to the cold...i get the hives, the whole enchilada...only you are lucky youve only had them for 9 months...ive had mine my whole life...i dont know much about yours but there is not cure for mine (hence "familial) its hereditary. i give you my best, hoping that your doctors can rid you of the nusance. IP: Logged |
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pelican Junior Member ![]() ![]() Posts: 6 |
Just an update on my progress with Delayed Pressure Urticaria. Hope this will help those of you out there with the same condition. While there is no known cure, after a year and a half it does seem to be burning itself out. I still have symptoms but they are not nearly as intense as they used to be. At it's worse I took Zyrtec which helped a lot and also aspirin which I was later told I should not take with an antihistimine so I switched to ibuprophen. This helps reduce the inflammation. I have come to the conclusion that mine was triggered by stress. I was my father's primary caretaker and at the time this all started we were going through a rather bad patch. Things have calmed down and so have the hives. I still get them, but they're smaller and not so itchy. I hope this gives you some encouragement...apparently this weird disease does burn itself out eventually. Good luck to everyone and thanks for all your input. IP: Logged |
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JGorse Junior Member ![]() ![]() Posts: 7 |
Interesting that you switched to ibuprofen instead of aspirin. I was told to stop taking ibuprofen as a build-up in your system can apparently aggravate the condition. On the other hand, I was told to apply ibuprofen creams directly to the skin to help with the anti-inflammatory effect! It does help but only to a certain degree. When my feet are seriously bad I find at the moment that the only way I can actually sleep/get any relief is to tie frozen sports injury "gel packs" wrapped in cloth around my feet. The cold does help sometimes. IP: Logged |
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pelican Junior Member ![]() ![]() Posts: 6 |
JGorse, I found that ice packs, etc. helped a lot in relieving the itching. I guess if there was anything to be grateful for was that this all started in the winter and as I live in a very hot climate it was cooler than normal at the time. The very best relief I got was from a nice shower. These were merely temporary symptom relief measures, but after a year and a half it seems to be burning itself out. It's always a comfort to know that most symptoms are gone in the morning also. I rode my bike yesterday...suffered a little for that in the evening but in the morning was feeling fine. Good luck. IP: Logged |
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JGorse Junior Member ![]() ![]() Posts: 7 |
Pelican I'm really pleased for you that your run of this horrible disease seems to have an end in sight! On a bike??? I'm still at the "nothing without a cushion" stage! I'm pretty sure mine too was triggered by severe stress but the specialist here in the UK stated that they don't believe it causes DPU but may contribute to the severity. My DPU has got gradually worse over the past 4 years - am now at the stage where not a day goes by when some part of me doesn't hurt (huge swollen finger today because I carried some shopping yesterday!), and I rarely have a day when I actually feel well. I'm hoping it does eventually burn itself out - maybe one day I can think again of riding my bike! Good luck. IP: Logged |
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sapphirefair1 Newbie ![]() Posts: 3 |
Hello again to all of you. I just stopped in to see a number of new posts on this site. Unfortunately, no miracle cures available. I am still suffering. 3 years now. The Zyrtec controls the itching, but, any strenuous labor leads to an attack. Strenuous labor for me is pushing the nozzle of a spray can for more that 10 minutes, or opening a jar of peanut butter! I have to let my husband pull the weeds in the flower-beds or I will have hands like "The Hulk". When I do have a creative impulse and paint a room, it takes me twice as long, and I suffer with pain, swelling, itching, fever and chills. Rest seems to help. For now, I am still praying for some insight into this illness, and for now, God seems to be saying, "My grace is sufficient for thee". Just wanted to share my thoughts and experiences. Take care. SapphireFair1 IP: Logged |
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pelican Junior Member ![]() ![]() Posts: 6 |
At the risk of sounding Pollyannaish, I just want to say that my symptoms were greatly relieved when my stress level went down. I had to purposely let go of a lot of "stuff" and just let God take over. I am not cured and I still have hives and muscle aches after exertion, but not nearly to the degree that I used to have it and the hives are not nearly as itchy as they once were. I stopped a lot of activities that I used to be involved with just so I could rest, regroup and have some serenity. The Zyrtec got me through the initial symptoms, but now I think this new found peace is helping this nasty disease burn itself out, or at least cool it down. My doctor uses my case as his mystery disease for his medical students. I just keep hoping one of they young doctors will come up with a cure. Right now all they do is suggest ways to relieve the symptoms. Anyway, my best wishes and prayers go out to all of you and I thank you so much for your input. I thought I was the only one in the world suffering with this strange ailment. I'm sorry you all have it also, but as they say, misery loves company and it was a comfort to know I wasn't alone. Good luck to everyone. IP: Logged |
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tlturpi Newbie ![]() Posts: 3 |
I have had this condition since February of last year. It came on suddenly out of nowhere. My lips, face and eyes swell as well as welts on my head, in the back of my ears. I take a regime of hydroxicine, singulair and allegra. (6 pills a day). I also have the cough and the heart palpitations. The cough has been hanging around for about 6 months. I have been to many, many doctors from allergists to endocrinologists (they thought it was my adrenal gland). No luck! So now I just take the pills every day and hope for an episode not to occur. IP: Logged |
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tlturpi Newbie ![]() Posts: 3 |
I have the same symptoms which came on a year ago. Half of my lip, my head (sometimes behind my ears) get lumps and my eyes have swollen shut before. Makes me look very ugly... I have found that you have to stay ahead of it, the meds do not work as well after the swelling has begun. I take hydroxicine every night with singular and sometimes allegra. It seems to work as long as I don't miss one single day. I hope it just goes away as suddenly as it appeared. IP: Logged |
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tlturpi Newbie ![]() Posts: 3 |
I have had the swelling in the face, lips, eyes and head for almost a year and a half now. I am taking hydroxicine every night with singulair and allegra sometimes. This seems to work if I don't miss one single night. If I take the meds 12 hours before I need to get up, I can wake up ok in the morning and not feel groggy. IP: Logged |
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evansgirl Newbie ![]() Posts: 5 |
I have diagnosed myself with DPU based on what I have found on the web. I have to wait until Sept 22 before I can see the dermatologist! I have a digital picture so I can show her when I get there. I made the mistake of breaking in a new pair of shoes when I ran out of Zyrtec, and all He** broke loose! I got a wheal, and a blister on top of that. That was 2 weeks ago. Since then, I have had red raised skin on my foot with TONS of tiny shiny weeping blisters that join up and ulcerate. I can only go barefoot or wear my Dr. Scholls because they don't contact the area. I am now on Zyrtec, Clindomycin, Bactriban ointment, and another ointment for swelling. Has this happened to anyone else? How long until it will go away?? IP: Logged |
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JGorse Junior Member ![]() ![]() Posts: 7 |
evansgirl Interesting that you have tiny weeping blisters - I have noticed only recently (I've had DPU for 4 years now)that I often get the same type of blisters. They are mostly on my feet and particularly where I've had a very itchy patch. I'd be VERY interested if your doc thinks this is all part of this horrible condition. Good luck IP: Logged |
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rain1 Newbie ![]() Posts: 3 |
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rain1 Newbie ![]() Posts: 3 |
I have always been very healthy, until July of 2002, when out of nowhere, I developed DPU. It took quite some time and several different specialists to finally give me this diagnosis. I sympathize with all of the people whose stories I have read. My experiences involve the same swelling, pain, rash, lumps, blisters, and general discomfort. My hives also usually have fever in them and itch intensely. If I scratch them, a burn-like adhesion usually appears the next day. Does anyone experience these same characteristics? In reply to the questions about different helpful medications, I've found the only relief I can get is from taking Prednisone, which of course can bring its own long term problems. My doctor prescribed and EpiPen, which is used in emergency situations during allergic reactions that involve the swelling of the throat. One thing that still seems strange to me, is that this all started the very day I moved into my new house. Doctors have discounted this theory, by saying that this disease is not caused by allergies. Any suggestions would be greatly appreciated. [This message has been edited by rain1 (edited 08-12-2003).] IP: Logged |
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JGorse Junior Member ![]() ![]() Posts: 7 |
rain1 I don't get the cough but I do get quite sharp chest pains and feel quite short of breath at times. I'm sure this is all part of this condition. I've had a really bad weekend - not sure if it's the heatwave we're having in the UK at the moment! I was told by my specialist that this condition can affect the soft tissues of the throat/chest as well as stomach problems, and I too was told that it's highly unlikely that the whole thing is caused by an allergy. Certain things aggravate it (eggs/tomatoes etc) but I was told that I could have allergy tests for ever and a day and they wouldn't find any one thing that I was allergic to. I'm about to try Singulair as recommended by my doc - I know a few people on this site have tried it and it seems to help. Fingers crossed and I'll let you know! IP: Logged |
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EmEm Newbie ![]() Posts: 1 |
hi there!! I have had urticaria for 5 years now, i've tried Xyzal, Piriton, Benadryl (3 a day and one a day) Loratadine, etc, the only ones i know that DO work are Telfast (Fexofenadine Hydrochloride). They actually make me feel cooler, which is something that really bothers me, i get far to warm which starts the whole itchy process of. I've been to the doctors today and i'm starting on Doxepin for night times and Telfast during the day. Although tablets work for a while, they do wear off, i really want to know if anyone knows of a permanent solution. My doctor mentioned that it might be something to do with my thyroid so i had a blood test for that today. Fingers crossed i can pin point it down to something and get it sorted once and for all! All i want is not to be a horrible, red blotchy bride!! lol! Thanks people, Luv IP: Logged |
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rain1 Newbie ![]() Posts: 3 |
This is in response to Emma. I have recently been taking a drug called Bextra. This drug is used to treat another illness, possibly asthma. I have been taking it for about a month, and so far, the results have been miraculous!!! You must ask your doctor... I have been symptom free since I started taking this medication - before this, the only thing that brought relief was steroids!!! Good luck!!! IP: Logged |
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navy Member ![]() ![]() ![]() Posts: 53 |
I have had this since 1985 while serving in the Navy in Panama when my feet hurt for a day or two off and on. I had them x-rayed and they told me my bones were more separted than the average person. Well I guess inflamation would cause them to push apart... I had regular old allergy symptoms for years after that and no real problems until about 1995 when my feet got worse and hands started etc... I now have had it bad for about 7 years after I too moved into my home. I am off work right now due to increased problems. The prednisone I had to take more frequently over the past year is taking its toll. I have respriratory problems and all the common symptoms daily. I especially had problems with dental work and am suprised not to have it mentioned here by anyone else because mine was severe I took sulfasalizine for 5 or so years with good to fair results. I could at least wear a pair of jeans within the first few years then the med stopped working so good. I went up to full dosage and it again worked fair for about 6 months. I changed to 30mg zyrtec, 100mg atarax daily, prevacid and other antihistamines that NO effect on me. I am now waiting to see if Dapsone ( for skin infection started yesterday) works. My derm doc says a specialist in Chicago she contacted recommended it so we will see. I know a lot of you have said that yours is gone and I hate to be negative but I have thought that in the past to, only to have it return with a vengance so consider keeping up the med up even without the symptoms because I didn't and maybe it would have made a difference. Someone asked about muscle pain. I have had two unsuccessful surgeries on my shoulder because of this disease so make sure there is pathology for your pain before you do anything drastic. I beleive this disease can cause a mirad of symptoms because it causes intermittant inflamation anywhere and flu-like symptoms when kicked up. Get yourself a good/caring doctor who definitely know what this is because I didn't and it got out of hand (not for lack of trying). I finally got the yellow pages out and called docs until one personnally called me back with at least knowledge. Most just think it is hives and consider it a nusiance you will have to live with but we all know it is way more than that. When I called for information they all tried to schedule me but I refused to come in unless the doctor confirmed knowledge of this disease (minimum) and better yet if they have experience. I could not find anyone with experiece but my derm doc knows one in another state and is willing to consult him just to help and is very empathetic with my pain too. Finally, I would like to know if any of you have considered this being an infection a possibility and if so have you addressed it with doctors? I tried but they just dismiss my reasoning and I still think it may be because the only real help I got was from antibiotic based drugs. Hope this helped. Navy [This message has been edited by navy (edited 10-08-2003).] [This message has been edited by navy (edited 10-08-2003).] IP: Logged |
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HAIRDOER Junior Member ![]() ![]() Posts: 10 |
Hey I just wanted to let everyone here know that there is more info on the allergy board about urticaria and its many different ugly faces. I have pressure hives and am looking for answers too. Check out the other message board. Also I have angioedema with it sometimes. I just had blood work donw today to test me for Heliobactor pylori infection. If ya wanna know hat that is go to the other board and read up! Lots of hard work done by some members posting some very enlightening brain food for those of us starved for some ray of light at the end of this long road. See ya there.on the allergy board. IP: Logged |
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navy Member ![]() ![]() ![]() Posts: 53 |
I hope it is that for you, it wasn't for me. I had it tested and did have it but my hives are still there without it. Sorry if this disapoints you. I have had just about every test under the sun including repeating the same ones over. I don't hear anyone talking about sulfasalizine. It was my saviour for about 5 years. It did eventually lose it's effectiveness but wow, 5 years. It is a sulfa based antibiotic and anti-inflamatory used for inflamatory bowl disease amongst other uses. Anyway, I came across it while researching in 1997 and brought the article to my doc and he agreed to try it. I was almost symptom free for the first 3 years then mild breakthroughs for the next year or so until just this sept it just stopped working for me. Anyway, it was the only med I had to take for this when I did so considering the mulititude of meds taken otherwise it is worth a try. Navy IP: Logged |
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HAIRDOER Junior Member ![]() ![]() Posts: 10 |
To navy. I found out that my test for the H-pylori infection came back negative. My Dr. was not working today but I got the lab tech to at least tell me that was negative but two other tests they did came back positive but he would not tell me what they were. So I wait again till monday. I know they were testing my liver function and kidneys too. Probably did a CBC and I think my white count was probably high because I have a sinus infection. So I hope to talk to the Doc in a few days. She already had given me a pres. for the sulfasalizine if that h-pylori bug was positive. I am confused about you taking it. You did have the infection but it is gone now? Is that right? And I don't understand why you took it for 5 years. Another question is you say you have flue like symptoms when your hives are very bad. Just wondering what kind of symptoms. I also get the hives internaly. I have had them in my throat, tougne, stomach. I was even tested last winter for strep a couple of times because I could hardly swallow. I have muscle pain when a hive is starting to develop that is large. Like I can feel it aching long before the skin ever turns red and it will swell up like I have hard boiled eggs under my skin. Sometimes it doesn't even itch very much. I had hives on the bottom of both feet today, so no shoes for me today. Do you ever had a hive on one side of your body and have one in the exact same place on the other side? Like I have matching hives on both shoulders one day. I have never had hives that turn into blisters. Some posters on here say they get blisters. So that confuses me too. The hives I get usually last around twenty four hours then decide to move to a new location. And I hate surprises!! Really hate hives that are huge on my face and eyes. I guess that is it for now. I will read more on the allergy board from you and the other sufferers like me too. One more thing though. Did you start taking the dapsone yet? Is it working? Good Luck!! IP: Logged |
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navy Member ![]() ![]() ![]() Posts: 53 |
Hi Hairdooer, First, the sulfasalizine is for the DPU (delayed pressure urticaria) and that I took for five years before it stopped working well. The stomach thing I had but my hives never went away after they treated it. So far the dapsone is not working but I am on 50 mg working up to 150 by 25 at a time every other week so it will be a little while before I know. As for the symptoms, I never had the boils either. I suspect that is boulis something (can't recall the name off hand) but not DPU. As for the muscle aches. I have them way more than I have hives. I get cramps in my sides, calves, arms or wherever. Right now I have little hives on my feet and my calf is all cramped up but you can't really see any of it. That is the worst part about this. Our hives are so deep that they often can't be seen to the naked eye. Fortunately, I have a couple docs that know they won't be able to see them all the time. I don't think they understand the extent of pain but they do get it to some degree. I met with a lawyer last night about social security and he said I have a good case but it will take a while due to the complexity of it and the administrative judges usually award something like this after the board has turned it down. Good news to me because I don't think my heart could take returning to work. The prednisone I have had to take for the last couple of years so I could tolerate massive dental work has me really messed up. Be very careful about that one. I thought I didn't get side effects but they were just sitting in waiting. Good luck and I am here most days if you need to talk or have questions. Navy IP: Logged |
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