Thursday, June 14, 2012

The backstory - or the beginning of this new adventure


On April 22 Anny had what appeared to be a first migraine headache that kept her out of school the next day.  She went back to school on tuesday but her teachers told me that she spent most of the day with her head on her desk.  I took her to the pediatrician that night and she had a basic exam.  The dr noticd that her pupils were dilated unevenly and suggested that I follow up with a neurologist.  Since Anny did not have one at the present time I set out to find a dr who worked with the visually impaired. I did and made an appt for may 31st (today, ironically).  She did not feel great for the rest of the week but she was able to go to school every day.  The headaches was totally gone by weeks end and our lives went back to the way they were except that Anny was tired aloha and her teachers said that she was not participating as much. 

Flash forward to two weeks ago when the woman from the commission for the blind who is teaching Anny to read Braille noticed that her pupils were unusually dilated.  I made an appt with the ophthalmologist and she was seen the next day.  The dr said that the issue with the pupils was symptomatic of her visual condition but noticed a decline in her vision.  We had been to the lighthouse for the blind for a low vision checkup the month before and there was no decline noted so I waited for the report from the ophthalmologist to have the two drs speak to each other and reconcile the different results.

We received a call last Monday eve from the ophthalmologist saying that he was working on her report and he realized that the incredible decline in vision was not supposed to happen with her diagnosis.  Her vision went from 20/800 to 20/2400.  He asked us to get an MRI.  At that point I emailed the neurologists office and we moved the appointment to the next day.  She was seen on Tuesday and this dr agreed that she needed an MRI as well. It was scheduled for july 24th.  The first appt thant was available in the hospital he knew that could do one with sedation.  We were told that he would work on getting it earlier but there was no urgency other than getting an answer to the prior months headache and the vision issue before camp began.

On wed she went to school and I got a call that she had a headache and that she was nauseous.  I picked her up and her shadow told me that she was a bit disoriented during the day and was dizzy.  She was quite pale when I picked her up.  On the way home she got her color back and seemed to be feeling better.  We had a discussion about whether to go to 7-11 for free slurpees day or if she should take a nap and then go later.  She opted for the nap. When she woke up one hour later she said that she felt much better and that the headache was gone.  I emailed the neurologist again and asked if the symptoms of her headache were normal.  The receptionist got back to me and said that the dr we had seen the day prior was out of town but that she would get me another dr.  At 9pm we received a return call and whe. I spoke to the dr we discussed that this it be hormonal - she had gotten her period approx 3-4 days after the first headache and here we were one month later and she has a headache again.  The dr said it could be hormonal, it could be migraine but to be sure we should get a cat scan.

I took her to the local er and was told by the er dr that there were some abnormalities on the first reading but that he was waiting for the radiologist to give the final results.  At 2 am the dr calls me to his cubicle and showed me the scan. He started talking about masses, and excess fluid and enlarged ventricles, that he was talking to a neurosurgeon and that we should be transported to Columbia pres in new york.  I was caught unaware and have a good friend who is a pediatric oncology nurse and I called her to speak with the dr and explain to me what the hell was going on.

She explained briefly and told me that the neurosurgeon was tops and also had a great bedside manner.  At 5am one week ago we won't by ambulance to new York.  The neurosurgeon spoke with me and said that there was a large mass on her frontal lobe that was blocking the flow of fluid in her brain and the first step was to put in a temporary drain to relieve the pressure.  That was done last Thursday .  Her diagnosis was that she had a lime size tumor on the left side of her brain that could be safely removed. That was done on Monday in a very long surgery. That tumor is now gone.  There is another mass on the right side of her brain that is inoperable and once she has recovered from this surgery we will need to meet with the oncologist to discuss removal/shrinkage options.  And so the hell continues. She is recovering beautifully and we hope to be home by Friday but first they need to remove the drain so we live day by day.

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