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I Have Cholinergic Urticaria

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cfm7

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Joined: 15 Feb 2006
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I Have Cholinergic Urticaria
Posted: 02-15-06 17:54pm

The dermatologist told me today I have this, and also possibly keratosis pilaris. She prescribed me zyrtec, which I will take 10 mg of, twice a day. She also told me to get nizoral shampoo (wash my whole body with it) and 1% hydrocortisone cream. Will any of these work. About 6 months ago, I started getting itchy after a hot shower. I started taking very quick showers and it helped. Then, about 4-6 weeks ago, I started breaking out with hives on my inner arsm, chest, and back. Whenever I start to sweat, or get hot. I live in florida, so basically if I walk outside for a minute it will happen. Just sitting in my room playing guitar it will happen, just from the movement of my arms. It comes on extremely fast (i can stand up and jog in place at anytime and it will happen within 20 seconds, but it only usually last for 10 minutes or so. I'm just hoping it won't get too much worse. The doctor I saw a week ago (not the derm.) gave me 10 mg alavert tablets. I've been taking thosr every night, but they haven't helped much. Ithink the dermatologist I saw today said I oculd take the 2 zyrtec tablets and also the alavert everyday. I can't od from that much can i? I wouldn't think I could from an antihistamine. I'm hoping this works because it's just aobut unbearable right now. I'm only 21, and can barely leave the house lately, it's that bad. My hwole upper body starts to burn very badly and extremely itchy as well. What do you guys think?
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paintballrdude

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I Know How You Feel
Posted: 03-20-06 13:58pm

I too suffer from cholinergic urticaria. My case is very severe at times and has affected me to a great degree. I had to drop out of college footbal a couple months ago and I am beginning to miss class more frequently because of this condition. I have been to a regular doctor at an urgent care clinic nearby, a neuro surgeon because my mom was dealing with him at the time and he offered his help, and recently I saw a dermatologist about it. All were basically no help except the dermatalogist who agreed that I have cholinergic urticaria although I had already come to that conclusion. He prescribed me cyproheptadine and I am starting the medication today. Hopefully this will provide me with some relief.

I myself am a very active person, who has many hobbies and interest. From football, paintballing, fishing, surfing, sailboarding or whatever. I live in so cal along the beach so there is always something to do. As I suffer from this condition I am cut off from all of that. Bout the only thing I can do is sit at home on the computer or go to the movies with my gf. Parents are not much help as they don't understand the severity and pain caused by an attack and they cannot understand why I cannot go to work or why I am missing classes. It seems to me I am on my own and I have been doing a lot of research on the condition. There are numerous antihistamines and other drugs that claim they can aid in the treatment of chronic urticaria. It the cyproheptadine does not work, I play on trying to get a prescription for hydroxyzine and acrivastine as well. I'm willing to try anything at this point to get my life back.

It is also very disturbing to hear the condition lasts at an average of 5-7 years. Onset being about 16 years of age and peak being about 22. I am 20 years old and I remember getting small attacks very sporadically at the age of 16 so I guess I meat the description pretty good. My email is pai ntballrdude@yahoo.Com if you have any questions or if you would like to know how the treatment has been going just send me a message and i'll be glad to talk. I hope I helped and i'm sorry if what I said was disapointing.
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Users who thank paintballrdude for this post: aggravated1971 
pimnation

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Joined: 22 Mar 2006
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Location: Waterloo

Posted: 03-22-06 18:45pm

Hey cfm7, I also suffer severely from cholinergic urticaria. They have yet to stop my life as much as they have yours, but then again I have very accepting friends and i've come to terms with looking sort of weird every now and then. As far as living with it I really haven't i've had it since about grade 11 and i'm now in my 2nd year of university. I was hoping by now they would have disappered because I am a very active person with snwboarding, jogging, weight-lifting, soccer, and just life as a teenage guy in general, but no luck. Recently with the end of winter, they have gotten much worse but I believe it is due in part to the thawing of the ground, putting all the crap that was frozen in the snow airbourne. Also the budding of trees and renewal of growing season for most allergenic plants probably worsened the reacitons, which now occur in severe forms over 3 times a day. As far as a cure, well i've seen every specialist and tried every method and nothing works. I am soon entering homeopathic regimens and i'll keep you posted with the results. As far as medicational regimens depending on seasonality the following worked for me:

1. Winter: zaditen (ketofen fumuarte) 6 tablets daily - 3 before bed, 3 mid-afternoon
2. Rest of the year: benadryll (3 a day) and allegra (24 hour non-drowsy - 2 tablets before bed and 2 mid afternoon)

hope some of this helps you and at the least gives you comfort knowing you are not alone.


Sincerely
... Pim brouwers
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ehealthforumuser

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Joined: 28 Nov 2004
Posts: 39

Posted: 03-24-06 23:14pm

Benadryl and all the antihistimine make you very desensitized. Please see my other post about using baking soda to wash all your clothes.
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frustratedgirl

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Joined: 23 May 2006
Posts: 6

Posted: 06-01-06 07:48am

I went to the doctors for the second time today and she was useless. Prescribed me the same drug as is in piriton which I have already tried. I told my parents about it today and they didn't seem to understand how much this condition effects someone. It doesn't sound that painful when described but an attack to me is extremely uncomfortable and distressing. I'm going to try stocking up on vitamin b and c and also shower with hot water frequently to release the histamines. Has anyone tried acupuncture?
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Sean3000

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Joined: 06 May 2006
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Location: UK

Posted: 06-01-06 11:18am

The itching aside, one of the main problems with this condition is that people really just dont understand it, I think its a case of, if you havent experienced it yourself you can never understand how much of a disability the condition is.
A message for frustratedgirl: I personally wouldnt take hot showers or baths, mainly beacuse it will wash /burn away all of your bodys natural oils and moister.
I think with this condition antihistimines may control it but theres nothing you can actually take to provide a 'magical cure' and eventually it the suffering wont be as bad and/or it will go away alltogether. I have come to the conclusion whereby I just accept that I have cu and I try to avoid things that set me off.
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frustratedgirl

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Joined: 23 May 2006
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Posted: 06-01-06 13:52pm

sean3000 wrote:
the itching aside, one of the main problems with this condition is that people really just dont understand it, I think its a case of, if you havent experienced it yourself you can never understand how much of a disability the condition is.

A message for frustratedgirl: I personally wouldnt take hot showers or baths, mainly beacuse it will wash /burn away all of your bodys natural oils and moister.
I think with this condition antihistimines may control it but theres nothing you can actually take to provide a 'magical cure' and eventually it the suffering wont be as bad and/or it will go away alltogether. I have come to the conclusion whereby I just accept that I have cu and I try to avoid things that set me off.


but part of me refuses to accept it, it annoys me so much. It's hard to accept that there is no cure, only things to help control it. I do avoid things that trigger it but I miss doing exercise...I used to love swimming and playing tennis but now I have to avoid doing these. :( I told my boyfriend the other day and he was very understanding and now knows why i'm not so active as I could be! You're right though, I don't think anyone can fully understand if they haven't experienced it. It's like a vicious circle though at the mo, that because it's emotionally stressful this in turn makes me break out cos i'm so anxious about it. :x
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