Cdz19,
i was prescribed cyclosporine by my
allergist last spring. I took it for a
few days until I compared the risks to the
benefits of taking it. When I took my
prescription to the pharmacist, he
actually questioned that my allergist
prescribed this medication on an
outpatient basis. It is typically used
for transplant patients. Cyclosporine
suppresses the immune system making you
more susceptible to infection. You are
at a higher risk of cancers, viruses, etc.
I felt the risks were much too high.
I stopped taking it immediately. I have
heard it does help with cu though. Just
some insight on what I have found. I
hope this helps a little.
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CDZ19
New User, Becoming EHEALTHy
Joined: 21 Jan 2006 Posts: 31 Location: St. Louis, Missouri
Cyclosporine Posted: 02-02-06 23:30pm
Bsmith16,
yeah i've been on cyclosporine for about
ten days...And it's not working at all.
Today I tried to go running, but I
couldn't finish off the mile because the
itching was too unbearable...
If anything I could gain from the
experience, after not excersing for a
while, it was good to know that I still
had the will...
But yeah, I think i'll stop taking it and
go with the herbal solutions...I hear good
things about herbal medicines when it
comes to cu...Do you or anyone else know
anything about herbal medicines?
It sounds like if I keep taking this
medicine...I'll only keep hurting
myself...And i've been on it for ten days
and have seen no improvements. I dont'
need a disease in addition to this...It's
annoying enough as it is.
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josh6552
New User, Becoming EHEALTHy
Joined: 30 Jun 2005 Posts: 24 Location: Tampa, FL
Posted: 02-04-06 22:40pm
Wow. I didn't know I had all these
replies. I was just searching google
arbitrarily tonight for cholinergic
urticaria cure and came across my own
post.
Well, my zyrtec worked perfect but I
couldn't afford so now i'm using loradine
and it works as good. When ever I get
some spare money, i'm going to try the
online drug presciption at the website www.Urticaria.Com.
Hopefully, I will be hives free one day,
but untill then I must live with constant
unbrearable itching (only when the meds
wear off). Just to say...When I was 16
and 17 and never ever had a problem with
my body...Now it seems a bomb has
exploded...Lets see.
I'm now 20 I now have to worry about the
cu, surgeries of sorts, skin cancer (where
I had a moles surgically removed but came
back non melanoma, and I don't have that
many moles, either). Anyways, I hope you
people with cu will seek a definite
cure.
Sincerely,
josh
|
CDZ19
New User, Becoming EHEALTHy
Joined: 21 Jan 2006 Posts: 31 Location: St. Louis, Missouri
Herbal Meds? Posted: 02-05-06 01:35am
Zyrtec, claritin, and cyclosporine have
been utterly useless!!!
There was a short time back in december
when I was taking prednisone and it worked
like a charm, not an ounce of itching at
all...
Anyway, I hear good things about herbal
meds...Does anyone know where I can obtain
them?
|
mattyc82
New User, Becoming EHEALTHy
Joined: 01 Feb 2006 Posts: 2 Location: Boston
Possilbe Meds Posted: 02-10-06 17:39pm
Hey guys,
i saw an allergist last week and was
perscribed hydroxyzine hydrochloride which
is atarax, an anti anxiety and
antihistamine. I'm taking this as well
as zyrtec and it seems to be working
really well. I'll check back with new
results in a few days. I definately
recommend this med.
|
josh6552
New User, Becoming EHEALTHy
Joined: 30 Jun 2005 Posts: 24 Location: Tampa, FL
Posted: 02-11-06 10:37am
When I was on hydroxyzine it was 100%
effective but since it's supposed to treat
anxiety too, it would absolutely kill my
concentration, slur my speech, make me
feel like I didn't care for anything. The
docotor never told me about that it treats
anxiety..
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Slartibartfast
New User, Becoming EHEALTHy
Joined: 11 Feb 2006 Posts: 1 Location: United Kingdom
Posted: 02-11-06 14:02pm
Hi,
i've suffered from cholinergic urticaria
since I was 14, daily. None of the h1
antihistamines were very effective, the
combo h1 and h2 blocker also proved
useless. At 21 years of age I visited
one of the top specialists in the world in
london. I was put on low dose stanozolol
for two weeks along with fexofenadine.
There was a dramatic improvement after
this treatment. I've been told that
another course; perhaps two, will be
needed for complete remission.
|
CDZ19
New User, Becoming EHEALTHy
Joined: 21 Jan 2006 Posts: 31 Location: St. Louis, Missouri
Cu Posted: 02-21-06 21:38pm
I came back from my allergist today...And
i'm not allergic to any foods.
Meaning that whatever the cause of my
itching/hives are, it has to do with
either stress or diet.
But what's weird is the fact that when I
eat certain foods, my face and scalp get
itchy...
Does anyone else know what i'm talking
about? What's the deal?
|
cfm7
New User, Becoming EHEALTHy
Joined: 15 Feb 2006 Posts: 10
Posted: 02-27-06 21:35pm
Hey guys, I don't have time to read all
the replis right now, so sorry if I ask
osme things that have been answered. I'll
read the whole thread later tonight.
So i've been diagnosed with cholinergic
urticaria by my dermatologist. Like i've
read on the internet, I have the typical
symptoms. When my body temp. Rises or I
get really stressed, I break out in
extremely painful and itchy hives. My
regular doc gave me alavert and it did
nothing, so I saw a dermotologist, and she
prescribed me a larger amoutn of zyrtec.
Neither have don e anything. I have
another appointment with her in 2 weeks.
For a couple days (while I was moving and
working hard), I noticed it would happen
off and on during the first couple hours
of moving, and then it would be ok the
rest of the day. For a couple days this
happened and I thought the zyrtec was
working. However, it came back and it was
worse than ever. I have't gotten a chance
to try it, but could I potentially
exercise hard in the morning and suffer
the pain badly for a little bit, and then
have it go away the rest of the day? I
read something aobut this maybe working,
something about the histamines all being
flushed out and the body not having any
left to release for the day, thus
eliminating the symptoms. If this works,
i'd def. Want to do it until I can get on
some right medicine. I would hurt
extremely bad, but it would be worth it to
get rid of it for the day. Right now it's
so bad that I can barely leave the house
or be active at all.
What do you guys think?
|
CDZ19
New User, Becoming EHEALTHy
Joined: 21 Jan 2006 Posts: 31 Location: St. Louis, Missouri
Posted: 02-28-06 01:14am
Hey guys, I just ordered a medicine called
lacitrex today...Apparently it's supposed
to be really good for cu and no one's said
anything bad about it...
It's supposed to get here about wednesday
or thursday, i'll let you know how
everything goes.
|
cfm7
New User, Becoming EHEALTHy
Joined: 15 Feb 2006 Posts: 10
Posted: 03-01-06 02:12am
Does anybody hgave it on their legs too?
I've had it for a couple months, and today
for the first time my legs got it too.
Does this mean it's getting a lot worse?
I'm desperate.
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bsmith6
New User, Becoming EHEALTHy
Joined: 09 Jan 2006 Posts: 9 Location: Dewitt
Posted: 03-01-06 09:21am
I can always tell when I am going to have
a bad outbreak as it usually starts
itching really bad on my legs. If I skip
workouts for a few days my legs are the
first to get itchy. I have been able to
control the itchy legs by sweating a
couple of times a week. I have also just
purchased a steam room for my house.
This will allow me to sweat everyday and
hopefully ward off any major outbreaks.
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phatfred
New User, Becoming EHEALTHy
Joined: 01 Mar 2006 Posts: 1 Location: Houston
Thanks! Posted: 03-01-06 16:13pm
For the most part, a lot of the
descriptions fit my... "condition" to the
dot. Went to an allergist about it and he
called it something different but pretty
much gave me the same meds others have
had. I was on zyrtec for a while but
eventually it stopped working. I'm on
hydroxazine (atarax) which makes me feel
so tired and groggy I usually don't bother
tanking it.
Mine isn't too bad in the summer but kicks
in from fall - spring usually. At the
moment i'm just glad i'm not the only one
out there with my condition and I would
really like to hear more the med you got
cdz19 when ever you can get some info.
For the mean time i'm gonna try the
running thing since I feel alot of times
it is because of not being able to sweat
very well. (i sweat when I work out but
it always happens b4 I actually start
sweating as if the hives are trying to
restrict my body from doing so)
thanks again for everyone who has posted
and if anyone gets any information about
any herbal remidies please share for it
would be greatly appreciated.
|
CDZ19
New User, Becoming EHEALTHy
Joined: 21 Jan 2006 Posts: 31 Location: St. Louis, Missouri
Lacitrex Update Posted: 03-05-06 00:18am
So far so good...
I'm quite surprised really...
I got the medicine on wednesday after
having a major breakout that day, which
caused me to stay home the rest of the day
and made me miss class...The timing
couldn't have been anymore perfect.
I had a mid-major attack on thursday, but
after that, there was nothign else the
rest of the day, my attacks seem to happen
around 12 everyday...Well 12 rolled around
and I was just as calm as a cucumber, not
a hint of itching, and I was even laughing
hysterically while out in the sun...So I
had stress and sun in that situtation, and
no itching.
After that, friday and saturday have been
nothing but utter peace...A few "prickles"
of itching here and there, but after
applying the solution to these places, it
quickly wears off.
I'm still weary though...After having cu
for so long and going through 8 different
medicines, it's hard to believe that this
particular medicine is actually working.
I still walk around thinking about it
sometimes, dreading certain days and
times, fearing that it may happen...But to
no avail, thankfully.
I guess i'll ask a few questions to the
people who sell this stuff, but for now I
guess i'll treat it as if i'm
rehabilitating from any other
ailment...I'll give it time to really set
into my body before I try working out, or
trying anything really extreme again.
It's still early, and i've only had the
medicine for 4 days...So only time will
tell.
I wouldn't advise anyone to buy it unless
you've got nothing else to go on, and no
other medicines you've been given so far
have been working...It's worth a shot.
It's completely natural, and i've had no
side effects. If anything, you feel
calmer...But I guess that's to prevent
stress, which creates the hives in the
first place (in my case, my cu arises from
stress)
i hope this helps, and good luck to you
all in your ongoing war against the
dreaded cu.
|
CDZ19
New User, Becoming EHEALTHy
Joined: 21 Jan 2006 Posts: 31 Location: St. Louis, Missouri
Posted: 03-05-06 00:42am
Oh and for reference here are all the
medicines i've taken up until this point:
all of which either didn't work...Or
worked for a bit, but then my immune
system fought it right off.
|
cfm7
New User, Becoming EHEALTHy
Joined: 15 Feb 2006 Posts: 10
Posted: 03-05-06 03:29am
Hey, what form of it are you taking?
Pills? Which "kit" did you get? Did
insurance cover it?
|
CDZ19
New User, Becoming EHEALTHy
Joined: 21 Jan 2006 Posts: 31 Location: St. Louis, Missouri
Posted: 03-07-06 15:39pm
Cfm7: they're pills, and I don't really
know about the insurance part...It's just
there for you to purchase.
It's made completely of herbs, and I got
the kit with only one bottle of topical
solution and pills.
Hope that helped
|
Dreammaker411
New User, Becoming EHEALTHy
Joined: 07 Mar 2006 Posts: 2 Location: Washington, DC
Cholinergic Urticaria Posted: 03-07-06 16:44pm
Cdz19 i'm new to this forum and was
wondering if the lacitrex is still working
for you? I have been considering
ordering it myself. I have have had cu
for the past 4 years and have taken many
of the meds mentioned on this board and
would much rather use a holistic
product/remedy.
"dream"
|
cfm7
New User, Becoming EHEALTHy
Joined: 15 Feb 2006 Posts: 10
Posted: 03-07-06 21:17pm
Hey guys im wondering how bad if gets for
all of you. Ive only had it a couple
months and its been getting worse and
worse. Now I get it all the way down to
my ankles and the pain is unbelieveable.
Im 21 and always have had a high threshold
for pain but this is unbelievable. If I
dont jump in the shower it feels like im
going to pass out and I eventually will.
The visual aspect of it is getting worse
too. I can now feel the hives rising off
my skin. How bad does it get for you
guys? If you stay inside and manage to
not have an attach for a few days, does it
make the attack worse once you get it?
Like its been building up? Maybe I
shouldnt put it off for so long because it
seems like its 10x worse when I do. How
am I supposed to lead a life with this
stuff
|
skippy
New User, Becoming EHEALTHy
Joined: 07 Mar 2006 Posts: 1
Posted: 03-07-06 23:06pm
Hello everyone.
Just found this forum. I believe that I
have cu. My doctor is skeptical. She
says that cu is rare and she believes that
I simply have dry skin.
Whever I go into a heated building from a
cold (during winter), experiance emotional
stress (could be as simple as someone
calling my name in front of a large group,
or seeing a girl I like smile at me), or
go for a run or to the gym to lift, I get
very very intense, painful itching feeling
on my scalp, back and chest.
During the summer, I only notice it if I
go for a run. It starts within 5 min and
ends after I begin sweating.
During the winter, I notice it for all of
the above stimulents, and it is much more
intense than in the summer.
The thing is, I dont know if I get hives
or not. I certainly dont swell up or
anything, but I do have redened skin in a
streaking pattern with small red bumps.
The red areas and the bumps dissapear
before my workout is over.
When I go for a run, it usually starts
within 5 min, and ends at the 15min mark.
I am usually sweating by then. As soon as
I am sweating all over, I no longer
experiance it.
If I run in the morning, I can go back and
forth from the cold outside to inside with
no problem for a while. I'm not sure how
long this period of remission lasts, but
its less than 10 hours.
A few months ago, I ran 4 times a day,
evenly spaced. I made sure to sweat each
time. I hardly noticed anything.
But...Not that im back in school I dont
have that much time.
Antihistamines dont do anything.
Im going to try and get the doctor to let
me run in place at my next visit so she
can see the sighns and tell me if they are
hives or not. I will let you all know my
progess.