Story about Hyper IgE Syndrome .

Hopeful for change

Dec 2, 2


I am adopted - a trans-racial adoptee - and am part of a blended family. I am the only African child, but have three siblings - brother and two sisters. I am the only one with Hyper IgE. I have no knowledge of my biological parents' medical history.

I am being treated currently by Ped Dr Paul Sinclair at a local hospital. He took over my case after our local GP couldn’t help any longer. I have always had problems with my skin – eczema, recurrent staph infections (scalp particularly) and allergies.

Dr Paul has worked very closely with an allergy expert in the hospital and he has diagnosed me with Job’ Syndrome / Hyper IgE and we have started a treatment of Xolair. I am about to have my 5th treatment (150mg a month). But so far there is no difference in my IgE count. But my energy levels have improved so that’s a good thing.

I am fortunate to have found a local company that makes dairy free sugar free candies (hard) and chocolate. Best part is – it tastes just like chocolate!! 

Know someone who should read this story? Share it

0 comments

Login or register to leave a comment


ICD9 and ICD10 codes of Hyper IgE Syndrome

ICD10 code of Hyper IgE Syndrome and ICD9 code

Is Hyper IgE Syndrome hereditary?

Is Hyper IgE Syndrome hereditary?

Is Hyper IgE Syndrome contagious?

Is Hyper IgE Syndrome contagious?

Hyper IgE Syndrome and depression

Hyper IgE Syndrome and depression

Hyper IgE Syndrome life expectancy

What is the life expectancy of someone with Hyper IgE Syndrome?

Latest progress of Hyper IgE Syndrome

What are the latest advances in Hyper IgE Syndrome?

Hyper IgE Syndrome diagnosis

How is Hyper IgE Syndrome diagnosed?

Hyper IgE Syndrome prognosis

Hyper IgE Syndrome prognosis