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Hi a: I'm curious to know if you had success with the Zyrtec and Zantac

why you didn't go back on it? If it was successful the first time around it

might be again.

I have been off and on it over the last 6 years. I have gone into remission

every year since I developed hives. My outbreaks have lasted anywhere from 4

to 8 months. My remissions are getting longer although this past year I have

had to take my meds every couple of days for intense itching. I do continue

to get occasional hives but they seem to be limiting themselves to the

corners of my eyes and my ears. My last major flair was last November after

putting the cedar garland around my front door. This flair lasted 36 hours.

I suspected maybe the cedar but had no problems taking it down. We will see

what happens this year.

The way I knew I was going in to remission was once the hives seemed to be

settling down I would try to wean myself off the meds. Dropped from 2 doses

of each a day to one. Typically I wouldn't have made the 12 hour mark

without going insane from the itching. Eventually was able to get past that

mark and then went to every other day and one day was able to finally stop.

Hang in there!

Barb

London, Ontario, Canada

May the wind be always at your back.

mtnbiker@... mountainbiker41@...

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Thanks Barb, I'll try to hang in there!

The reason I wanted to try something different than Zyrtec/Zantac is because

they eventually seemed to stop working. The only thing that really controlled my

hives was my change in diet (low histamine/lo salycilites). I still got some

hives, but when I went off the meds there seemed to be even fewer. I was never

totally hive free, maybe one or two days a week, if that. But I was doing really

well. I'll keep you posted on the Doxepin... had my first one last night. This

morning I'm better (about 30 hives) but I sure am sleepy.

When Zantac/Zyrtec stop working, if you make a pause in taking them, can they

work again?

Take care, a

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Hi a: I'm fighting a head cold and wrote my response after I worked the

afternoon shift and realized that I screwed up my message. My bad days of

hives are becoming a distant memory and I gave the wrong information.

When I first got hives I tried Benadryl but couldn't function and still

work. All I wanted to do was take care of was the itching. I tried self

medicating for 2 weeks before I saw the Dr. He immediately put me on Zyrtec

(Reactine here in Canada) 10 mg twice a day. I had 100% relief from the

itching within 2 hours of the first dose. Although it took care of the

itching it didn't do a thing for the hives. I didn't really care because the

itching is what drove me insane. I was seeing my Doc every week and when I

started to get swelling around my eyes and lips he tried me on Prednisone. I

stopped the Zyrtec but lasted only about 3 days before I started ripping my

skin off from scratching so much. I resumed the Zyrtec and stayed on the

Prednisone. I definitely have the horror stories of side effects from

Prednisone. I think I even scared my Doc I was so sick taking it. I was only

on it for 19 days but it seemed like a lifetime. It's the closest I've come

to feeling like I might be checking out. I developed my first migraine while

on Prednisone and continue to get them now. Not often but can be quite

debilitating to say the least.

During this first outbreak (which lasted 8 months) I also added Zantac on

the advice of a dermatologist. I don't recall that it made any difference.

When my second outbreak started I took the Zyrtec again and it continued to

take care of the itching. I just decided to let the hives do what ever they

wanted to as long as I didn't itch. That is how I carried on with each

subsequent outbreak until year 5. The Zyrtec was offering about 75% relief

and by this time I had found this group and learned about the Z/Z combo. I

went back to my Doctor and told him about the combo and he said he had heard

of this combo so had no problems writing a script for me. Adding the Zantac

brought the itching under control again.

Here I am in year 6 and as I said I have continued to take the Z/Z combo

every couple of days. It continues to offer me relief so I can't really

comment on your question as to whether meds stopped working whether taking a

break from the them would allow them to start working again.

I used to know that I wasn't over this completely because I just had this

feeling in my skin. Hard to describe! That feeling has changed though. Do I

think it's totally out of my system? No, because I continue to get the odd

hive but it has definitely changed and I do feel that I might be one of

those ones that they just suddenly disappear as quickly as they came.

Barb

London, Ontario, Canada

May the wind be always at your back.

mtnbiker@... mountainbiker41@...

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  • 1 year later...
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Sounds like a good plan. I have my endocrinologist appt set up for Aug. 21st and my consult with adult doc. number 1 on Sept. 4th. Let me know how your appt goes. I'll be thinking of you.

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Guest guest

, I haven't found out much more about the G-tube. My PCP was

consulting with a GI specialist here, who is familiar with me and my

" situation " . He felt it was best to send me to a GI specialist at the

University of Iowa Hospitals and Clinics. This is where all the " big

wigs " are! :-) My appointment isn't until Sept. 2. So, I have a

waiting period. I am playing things by ear right now!

Thanks and smiles,

a

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  • 2 months later...

,

I think it is to late for letting the principal bully me, but it is partly my fault. I need to stand up for myself more. Thankfully it is for just 2 hours tomorrow.

Thanks for mentioning about the SLE and migraine medications. If it is okay with you, I will be mentioning this to my neuro. He is sort of "new" to all of this, although he thinks he knows a lot about it. I didn't think that the nubane, however, was one of the 9 migraine meds. That is what seemed to have caused my reaction or SLE or whatever it was. The neurologist seems to think it was a combination. He was still giving me Imitrix though. Since I have been out of the hospital, I have only taken one dose of that and that was the day I got out, on Monday. I have not taken it since and don't think I will ever take it again. The migraine is not gone, but the Naproxen seems to help the migraine more than anything else. I am supposed to be going up on the Topomax as a migraine preventative, even though it makes me feel sort of "out of it". Does it affect any one else's blood pressure? I am on B2 as a preventative, but just started it in September after seeing Dr. Peltier. Neurontin, believe it or not, had been doing a good job at keeping my migraines at bay. Thanks for all your help. I am so glad that I have this group and people like you to come to!

Smiles,

a

a,I hope you don't let the principle bully you into coming back before you are ready. I wanted to let you know that I mentioned your SLE after taking the migraine med while I was at my neuro appointment the other day. Our local neuro said he would never let anyone that has SLE take any of the 9 migraine meds because of them being vasel (sp) dilators. Dr. Cohen also said that mito patients should stay away from them as well. I hope the seizure med helps prevent the migraines. Do you take the B2 as a preventative?Hugs,

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,

I think it is to late for letting the principal bully me, but it is partly my fault. I need to stand up for myself more. Thankfully it is for just 2 hours tomorrow.

Thanks for mentioning about the SLE and migraine medications. If it is okay with you, I will be mentioning this to my neuro. He is sort of "new" to all of this, although he thinks he knows a lot about it. I didn't think that the nubane, however, was one of the 9 migraine meds. That is what seemed to have caused my reaction or SLE or whatever it was. The neurologist seems to think it was a combination. He was still giving me Imitrix though. Since I have been out of the hospital, I have only taken one dose of that and that was the day I got out, on Monday. I have not taken it since and don't think I will ever take it again. The migraine is not gone, but the Naproxen seems to help the migraine more than anything else. I am supposed to be going up on the Topomax as a migraine preventative, even though it makes me feel sort of "out of it". Does it affect any one else's blood pressure? I am on B2 as a preventative, but just started it in September after seeing Dr. Peltier. Neurontin, believe it or not, had been doing a good job at keeping my migraines at bay. Thanks for all your help. I am so glad that I have this group and people like you to come to!

Smiles,

a

a,I hope you don't let the principle bully you into coming back before you are ready. I wanted to let you know that I mentioned your SLE after taking the migraine med while I was at my neuro appointment the other day. Our local neuro said he would never let anyone that has SLE take any of the 9 migraine meds because of them being vasel (sp) dilators. Dr. Cohen also said that mito patients should stay away from them as well. I hope the seizure med helps prevent the migraines. Do you take the B2 as a preventative?Hugs,

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