Allergies :: How To Establish Trigger? Severe Anaphylactic Reaction
Mar 6, 2015
I had a severe anaphylactic reaction 10 months ago and they have never been able to establish the trigger. I now have to keep with me epi-pens and steroids. I don't have the best memory going and I wondered if anyone in a similar position has any tips that will help me to remember them? I know this sounds stupid but when my wife is with me she always reminds me and so we have them on us, but when I'm at work (I work in various places), I take them with me but if I'm needed elsewhere I have a tendency of leaving them in my locker at base.
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I was taken into hospital with severely painful kidneys, and given morphine as pain relief. Unfortunately this gave me terrible nausea so I was given Cyclizine via IV. Within 10 seconds I went into anaphylactic shock and couldn't breath unassisted. I had to be given adrenalin and was on oxygen for a considerable time. For the next two days I couldn't urinate and had to be catheterized. It was a frightening and stressful experience. The attending doctor told me that it was unheard of for anyone to be allergic to this drug, and that my inability to pee was not connected. I am still trying to recover. More research needs to be done. I believe this drug is dangerous.
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Last night I came up with horrendous lumps, bumps and itchy mosquito type looking rashes all over my body. I have been on Penicillin for about 10 days and only started getting itchy on my scalp maybe a day or so ago, and now these symptoms have seemed to broken out into something very severe!!
The spots keep changing and moving into different spots all over my body, on my face, in my ears, on my knees, arms, hands etc.
The doctor gave me (Prednisone) which is a steroid hormone. This has helped the itching. They say it couldn't have been the penicillin, otherwise I would have reacted far earlier than after 10 days of treatment...
But then I looked at some academic journals, which stated that you can have 'delayed' drug reactions to antibiotics, sometimes a week after first taking them??
I did eat seafood a day or so ago ...but usually am fine eating shellfish etc.
It looks like someone has severely beaten up my legs with a pole! These huge golf ball size hives, very bizarre!
Anyway... my question is...has anyone else had a 'delayed' reaction or unpredictable reaction to antibiotics/penicillin?
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As well as many other side effects, joints, brain fog etc, I was out in my garden for 10 minutes, I had jeans on when I came indoors my legs felt like they were on fire and my tongue has gone tingley, I took my jeans off and I have what looks like severe sunburn all down them, I know this is the cipro has anyone else had this??
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After reading all these posts about Cyclizine, I feel I should add my own traumatic experience from 7 years ago:
(I now know that I am severely allergic to Cyclizine).
Back in the ward after breast cancer surgery with two visitors at my bedside, I suddenly began to feel nauseous. Unable to move my head at the time, I asked a number of times if I could have a 'sick bowl' handy as I felt I was going to be sick. No-one seemed to hear my plea, even though there were lots of medical staff and visitors around in this busy ward. I felt I was speaking loudly but my request still went unanswered. I summoned up the strength to really shout out Please, I need a sick bowl - I think I'm going to be sick. Next thing I saw the nurse half way down the bed putting a needle into the back of my right hand. I asked her what it was for and she replied "Just something to stop you feeling sick". Within seconds of that a strong wave of something went through my head and through every part of me. I started to feel as though my whole body was like jelly and (just as one other poster has described) felt as though I was drowning, couldn't breathe and literally felt as though the life was rapidly draining out of me.
Although I couldn't move my head (or any part of my body), I could see just in front of me and was aware that the woman in the bed opposite me was sitting up and staring at me, as was her visitor. I wanted to shout out Stop Staring at Me, What are you looking at .... but the words wouldn't come out.
There was a rush of panic all around my bed, with doctors having been called and nurses running around but at this stage I couldn't see what was going on - only hear. I heard to my left what I recognised to be the Sister's voice (from having spoken with her earlier) - shouting angrily "Who turned this off?" She was obviously referring to whatever machine I had been attached to there - which had apparently turned itself off!
Then I remember another nurse's voice which I recognized very clearly as an American nurse that I had been chatting and joking with earlier. Although I couldn't see her, I knew it was her because I recognized her loud Texan drawl. She was also the nurse who I had seen (with my tunnel vision) put the needle into my hand. I do believe now that it was her voice that saved my life. Her voice was all I could hear at this stage. She was obviously very close right in front of my face and I remember she kept repeating abruptly and loud: "Don't close your eyes - KEEP YOUR EYES OPEN!" My eyes felt so very very heavy and they kept closing. I so badly wanted to keep them closed - but then her loud voice would bark out the order again "OPEN YOUR EYES!" and with all the strength I could muster I forced them to open each time. It was very hard to do, like I needed a bulldozer to get them to open ... but I managed to do so, only because I could tell from the urgency in her voice that I HAD TO keep those eyes open.
I was also aware that I had been given an oxygen mask and at this stage must have been coming around. The "jelly" feeling had gone and I remember feeling my nose was itchy under the mask. I wanted to scratch it but couldn't move my hands. I'm not sure how long all this was going on, but when the panic was all over I remember the Sister then telling me that I should add 'CYCLIZINE' to my list of allergies. (I am also allergic to Penicillin (as well as some other antibiotics), and this is something I already knew).
I'm not sure that CYCLIZINE should be banned altogether, as it is obviously something that is helpful to others (in the same way as Penicillin is to others), but I do think it should come under the same category as Penicillin and perhaps some sort of pre-test should be done before administering the drug.
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I have a carrot allergy. When I ingest carrots, raw or cooked, I immediately break out in large hives and severe swelling all over my body. Not fun to suddenly have this happen after eating carrots all my life. Okay, I now avoid carrots in all forms, but I would like to know about BETA-CAROTENE. I see it listed as an ingredient in foodstuffs and I want to know if carrot allergy includes beta-carotene? I can't seem to find anything on the net other than beta-carotene is good for you, nothing about possibility of allergy to. Anyone?
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Also interested in hearing about surgery for trigger finger….both positive and negative.
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I had a fall last Friday shortly after arriving in Panama. Result, a badly bruised left knee.Next morning all my old symptoms were back with a vengeance. The only option was to give myself an increased dose of 8mg.Symptoms disappeared.Now getting back very slowly to my old dose of 4.5/. But very very slowly over weeks.I learned my lesson of not rushing it.
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Our 25 year old athletic marathon running/bike riding daughter with good sugar and cholesterol levels most of her life had a massive heart attack recently. Has anyone studied the effects of "insulin" in young adults to see if there is any correlation between taking insulin and heart attacks in young adults?
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I am recovering from foot surgery and am experiencing pain on bottom of foot/heel that is similar to plantar fasciitis. I have other pains related to the surgery that are improving, but this one is persistent. My PT suggested dry needling in trigger points, which is similar to acupuncture. I also have PTTD developing in my other foot, and she suggested it may also help with that.
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I am 18 and back in May I guess I "jammed" my finger. I say I guess because I really don't know WHAT exactly happened. My two dogs got into a little fit and when I was separating the two of them I don't know what I did, but I really messed up my finger. After it all happened my hand hurt REALLY REALLY bad. It also started swelling pretty much immediately. I waited a couple days and then went to the ER because I figured maybe I dislocated my finger or something. They did an X-ray and came back and said there was nothing wrong, and probably a sprain so they sent me home with an ace bandage and some ibuprofen. Fast forward to now.
The swelling in my hand has gone away after about two months of not moving it a lot and keeping it wrapped up. But each time I completely straighten (like I am stretching my hand) out, my ring finger makes a clicking noise and kind of pops up. Moving it certain ways, making a fist, putting pressure, pulling, or grasping something wrong hurts extremely bad. I can feel it move down at the base of my finger (like my last knuckle). It has caused a problem for me because it hurts with most normal things that I do. Even typing this is irritating.
So I finally went to an orthopedic and he looked at my hand and X-rays and said he isn't sure what it is and he recommends me to see a hand surgeon.
I did. I drove almost 2 hours each way to see this doctor and here's what happened in a span of 3 different visits.
He suspected trigger finger even though he said certain symptoms were odd. He gave me a cortisone injection into my left ring finger and OMG that was painful. But to be honest that pain from the swelling of the injection was about as bad as my hand felt right after it happened. But sadly that didn't help. So my doctor sent me to get an MRI. With the results of the MRI, he told me that he saw swelling in my finger and that he thinks is in the sheath but said he doesn't know what is causing that. So he told me he was stumped and should see someone who is more of a specialist and gave me a few names. None of them take my insurance.
So I decided to put all of my info out here and see if someone has had something similar happen or knows what might be going on with my finger.
I will also post below the "findings" on my MRI report.
"There is a focus of marrow edema involving the dorsal aspect at the base of proximal phalanx fourth digit and adjacent dorsal aspect head of fourth metacarpal with a focal small cortical invagination of the metacarpal which may be post traumatic in etiology from previous impaction. No discrete fracture or dislocation is appreciated at the fourth digit IP joints pr MCP joint. The flexor and extensor mechanisms and tendons appear intact. No significant sized joint effusions. No significant degenerative or arthritic bony changes are appreciated. Visualized musculature has normal signal. Subcutaneous tissues are intact."
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I have asthma, we own a cat which we keep downstairs and don't allow it in the bathroom and any bedrooms and for 5+ years I've been having gew build ups in my eyes with some residue on and around the eyes, especially when waking it's a nuisance and at night time my eyes feel very dry and can feel much residue on my eye lashes. I also suffer with a blocked nose especially when waking.
I also suffered with a bad case of eczema this summer, having extreme flare ups on my cheeks (just below my eyes), neck (closer to under the chin), chest and the back of my knees, I also get urticaria especially just below my eyes.
suffering so badly I went for a rast/immunoglobulin test for eggs, milk, wheat and cat and finally received the results. my total ku/l level was over 1,000 and deemed abnormally high. eggs, milk and wheat were all within the 0.01 - 0.1 range with no additional comments. cat was over 100 and deemed very high and higher than the limit
would this be lead to believe cats are the main cause to my allergies and judging by such high readings I would need to avoid cats to get the best clear up of my allergies? we are currently using hypo-allergenic wipes for the cat but too early to see any results
I want dust mites and dogs tested too so I might go for further testing but as of right now it would seem the cat is the number one cause to my high symptoms, would anyone recommend completely avoiding cats with such high results or could there be work arounds? I high feel I will be wanting to move into a cat free home soon which I hope will help a lot
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Ok so I've been trying to get rid of my hives for a little over a week now. This is the first time I've had them. I've gone to the doctor twice and the ER once for them. The doctor gave me 2 steroid shots and gave me some scripts. I'm using Triamcinolone Acetonide cream, I'm on day 4/6 MethylPREDNISolone pills, and I'm taking Hydroxyzine pills 4x daily. The ER suggested that it may be scabies and prescribed me the cream which I've already used and am through with. The ER also gave me a shot of meds that was suppose to kill the scabies if there were any and gave me a shot of benadryl. The ER wasn't sure if I actually had scabies or not but went ahead and treated me for them just in case. I live in my apartment with my boyfriend and he has been untouched. I've washed everything washable in hot water twice now and I've been staying at my grandmother's house until I can get rid of them. But they're still popping up. I haven't changed anything in my diet. I do own 3 cats but have never had problems with them. They are indoor cats and I haven't seen them in 4 days. I haven't changed anything in my daily routine. I'm just completely out of ideas for why/how I've gotten them and why I can't get rid of them. I have another prednisone treatment waiting at the pharmacy for me prescribed by the ER but haven't picked it up yet because I'm still taking the Methyl. I have been to an allergist but all the tests came back negative.
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I am an Australian who has been travelling to USA annually for the last 6 years.
Every time I visit the USA, after approx 4 or 5 days I break out in itchy, red bumps (hives?) all over my torso and upper arms. The outbreak lasts as long as I stay in the USA, and subsides almost completely within 24-48hrs after returning to Australia.
I have stayed at different hotels each time, so I don't think bedding can be blamed, and there is not a particular food I believe triggers this...
What could it be in USA that I am so allergic to, that does not exist in Australia. I travel the world extensively for work and have not experienced the rash in any other region either.
Antihistamines (Benadryl) does not seem to help at all.
Is there some food additives/preservatives that are unique to USA that I may be sensitive to?
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I have to force much effort to speak sometime because extra spit in my mouth like allergy and my word are out of order and missing.
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I am affected by red eye for almost two years and used 3 to 4 steroids prescribed by doctors( But then I was not aware of the rebound effects it can cause ) and one of this steroids (Fluorometholone and Tetrahydrozoline HCl) has really caused some damage in my right eye. On 23rd June I had color Fundus Photography on both eyes And luckily the test shown that it is not rebound effect which I am suffering from. And after some trial and error I have found that it is nothing but Cigarette smoke which is causing all those problems. That is I am an eye allergy patient.
now my medicines are Alcaftadine 0.25% and systane.
How much they can help me to get rid of this allergic problem?
"In fact I would like to know if eye allergy is curable?
And I have heard that by injecting the allergen agent into the eyes starting with a low amount and gradually increasing the amount immunity can be achieved. Is it a option for me to Inject tobacco in this way, while tobacco is poisonous. If no, than what are the alternative treatments. Do not advice to give up smoking. I am not being arrogant here I know it shall be impossible for me.
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Was wandering if anyone has ever had a problem with their mouth due to having pets. I have had this problem since I was 12 and always had a dog on the house.
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I have been breaking out in hives for 11 months. They started shortly after I had some surgery. Sometimes they cover most of my body, and the itch keeps me awake at night. Other times they are tolerable. I have read every blog I could find on the subject looking for some help. Last week I stumbled on some posting on this site which was worth giving a try. In short, it said that dehydration could be causing my problem. Well, I have always had a hard time drinking much water in a day and relied mostly on diet sodas for my liquid consumption. So on Friday, I started drinking 64oz of water each day and am cutting out the soda for now. Well, I am only 3 days into this plan, but it is really helping. I know it will take some time to hydrate my body, but I am very optimistic. I thought I would post this in case there is anyone out there the is struggling like I have been.
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I'm going on a month now prednisone didn't do anything nothing is working and I can't find the trigger of them they constantly burn help!
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I have lumps in my lower legs, shortness of breath (COPD) that is getting worst, even though I haven't smoked in a year. My eyes are not affected, just had them tested. I have been on leflunomide 20 mg for 2 months and lumps are going away. Doctor also put me on O2 at nighttime. My entire itches and that is driving me crazy, I take a baths only every 3 days, and have used all kinds of skin cream, nothing works. I have itches for 5 years, not allergies, that has been ruled out. Sometimes I itch worse than other times. I have also had all kinds of blood tests and the results always come back being OK.
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I was a favourite of the darned 'flu'. We call it rhinitis, hay fever, sinusitis, runny nose, allergy.whatever... I tried it all; Antibiotics/Antihistamines/ cold tabs/ cough syrups, steroid sprays/ cetirizine/loratidine.. Even tried those allergy tests.. What i realised was that my immune system was too weak to deal with so many things that are around. Such as : Dust, mold, cold, fumes, perfumes, pollen.. all these things along with the viruses are a deadly cocktail and it was like poison to me,. Killing me slowly... Even going to a friends' house was a nightmare of sneezes, blocked nose and cough.. . So, i did what anyone else would do. look for a cure, desperately.. And i stumbled upon an ancient exercise regime that they used to deal with flu in the old days.. I started doing that.. Its been about 10 years.. Now, I have strengthen my immune system to a point that these things hardly affect me.. I have modified the exercise to fit around my schedule and lifestyle.. And now it only takes 5 mins everyday.. No chemicals, or medicines or hospital not even, natural products, special food, salt-water, steam... etc..
Just sit in a room and get some workout for my airways.. Never looked back..
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