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
New User, Becoming EHEALTHy
Joined: 20 Mar 2006 Posts: 3
Thanks: 1
Thanked:0
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
New User, Becoming EHEALTHy
Joined: 22 Mar 2006 Posts: 3 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
New User, Becoming EHEALTHy
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
New User, Becoming EHEALTHy
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
New User, Becoming EHEALTHy
Joined: 06 May 2006 Posts: 35 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
New User, Becoming EHEALTHy
Joined: 23 May 2006 Posts: 6
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