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Hi everyone, I am a new member to this group. I started my Xolair last February

2007 and

get three shots every two weeks (450 mg. every two weeks). My highest IgE level

was around

6,000 when I started and then they had me on 60 mg of prednisone starting in

December

2006 continuing through May 2007 when I started to taper. That was the worst -

I went into

full Cushing's with the swelling and bruising and vertigo and major depression.

My asthma

had become chronic and nothing seemed to help. I was using my nebulizer more

than three

times a day and rarely slept through the night. I also had to take OTC

antihistamines in

addition to my regular meds - singulair, zyrtec, fexofenodine plus all my

inhalers. Things are

certainly different since starting the Xolair. I still have asthma symptoms but

not as frequent

and still cannot go shopping in crowded stores or go into anyones home who has

cats or

dogs. I thought that I might be able to reduce my dosage after a year or so,

but my allergist

seems to think that I will be on this dose for the rest of my life. My IgE

levels have gone

down to around 4,000 but he said that they are not able to tell what portion is

bound and

which is unbound so they just follow my symptoms. I live in Connecticut.

Anyone out there

from New England.

Anne

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