I apologize for taking me five and the half years to write another post! It's ridiculous.
Where did I left off???? Where to begin? Oh yea, Izzy is now 10 years ago. What a blessing!
Most of you known Izzy has half a heart baby in first 5 years of her life. During the next half of her life, she is not only a heart kid but also diagnosed with auto-immune disease, was hospitalized for weeks and weeks. Doctors were confused, she help to take the doctors to a different level of their practices.
"Your daughter is very complex." - Doctor X
"Izzy is very tricky, we need to think through the options of treatment." - Doctor Y
"I don't have the answers right now, I need to reach out to the Immunologists and the Infection Disease specialists and I will get call you as soon as I have the answers. " - Doctor Z
Those are the quotes from the Specialists for the past 5 years but I have to say, they are all very trust-worthy, very caring and very on top of their games. We have good medical team for Izzy here. The Goodmans are extremely BLESSED.
So, what's Izzy's current episode?
Izzy is currently, officially diagnosed with Chronic EVB (Epstein-Barr Virus). To simplified it, it's Mono virus. I am sure some of us had mono virus before, it would take about 4-6 months to recover from it but for Izzy, it might last for a life time due to her auto-immune issues. The virus lives in her B and T cell, if it's not treated or leave it in the system for too long, it would turn a monster. You know what I mean, right?
EVB was found on and off the in her peripheral over the past 4 years but it was now only found in her bone marrow, the number was high. It's messing up how her bone marrow works. She has to have Bone Marrow Biopsy every 2-3 months which also mean she will need to be sedated and as most of you know, Izzy was with half a heart. Procedures under general anesthesia is bad... just bad!!! Besides all those medical reasons, this is one of the procedure she is very nervous about. She fought the drug every time they injects good amount of strong meds in her system. It was hard to see her crying, screaming "No!" to unconscious. I had to tell myself that we are lucky that we have the way to detect and treat it.
I had a long chat with one of her specialist yesterday, they recommended a few options:
1) Sending her to Cincinnati Children Hospital to get treatment, this treatment is targeting T cell which UNC Hospital have no technology to do.
2) Bone Marrow Transplant. This is where her little brother Isaac can help. They need to do some test on Isaac to make sure that they are a match. Yay, super Hero Isaac.
3) Same old treatment we did all the time. Gave her huge dosage of Rituximab which is targeting on her B cell. Which is my less prefer treatment. We been using this method for years, did it work? if it does, she wouldn't be in this situation.
So, here is where we are. I am hoping to get a final decision once all the Specialists agreed with each other.
Whatever it is... Izzy is in good hand. She is loved and taking care by many. :)
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Thought from the parents: Like we always say giving up is not an option, we will do anything to keep her happy and alive. :)
I promise I will stay posting regularly from now on. Thank you for reading and love to all.