#1 ·
Dear everyone,
It honestly saddens me that every single time I sit down to write something here, I first have to offer my condolences to those of you struggling.
At the same time, it serves as a necessary reminder of how much humility I need to maintain. Every day, I find myself sincerely thanking God that my wife is doing so well. We are now in the 21st month since her diagnosis, and she is still like a little girl—cheerful, energetic, healthy, and full of life and hope. It doesn't even feel like we are living with this disease. The only thing that reminds us of its existence is the massive pile of supplements she takes every day.
We have a follow-up MRI scheduled for sometime this month.
No matter how much I read about the hardships patients face or the suffering of their caregivers, it is incredibly difficult for me to wrap my head around the idea that I could find myself in that exact same situation at some point in the future. I can tell you right now, despite all the mental preparation I’ve tried to do, I am terrified of that possibility. Reading about how you all handle these immense challenges fills me with admiration, but it also makes me wonder if I would be capable of being that strong. As time moves further away from the start, my confidence in handling the unknown shrinks. It’s an incredible paradox; I should be purely happy because everything is fine right now, yet the fear persists.
My own procedure went smoothly. All three feeding arteries that were supplying blood to the AVM malformation in my brain have been closed off. For a few days following the surgery, I lost vision on the left side of my left eye due to brain edema caused by the procedure. Fortunately, things settled down after a week, and I've been recovering ever since. Headaches are to be expected, but they aren't a daily occurrence anymore.
I’ve started my rehabilitation by walking laps around Central Park, naturally with my wife by my side.
I am heading back to work next week.
Unfortunately, this story isn't over yet. After the follow-up exam in September, a Gamma Knife procedure is highly likely. We will just have to see.
We continue to hold onto the hope that the AVM will remain dormant forever and that we can somehow avoid the inevitable.
Best regards, and hang in there.
It honestly saddens me that every single time I sit down to write something here, I first have to offer my condolences to those of you struggling.
At the same time, it serves as a necessary reminder of how much humility I need to maintain. Every day, I find myself sincerely thanking God that my wife is doing so well. We are now in the 21st month since her diagnosis, and she is still like a little girl—cheerful, energetic, healthy, and full of life and hope. It doesn't even feel like we are living with this disease. The only thing that reminds us of its existence is the massive pile of supplements she takes every day.
We have a follow-up MRI scheduled for sometime this month.
No matter how much I read about the hardships patients face or the suffering of their caregivers, it is incredibly difficult for me to wrap my head around the idea that I could find myself in that exact same situation at some point in the future. I can tell you right now, despite all the mental preparation I’ve tried to do, I am terrified of that possibility. Reading about how you all handle these immense challenges fills me with admiration, but it also makes me wonder if I would be capable of being that strong. As time moves further away from the start, my confidence in handling the unknown shrinks. It’s an incredible paradox; I should be purely happy because everything is fine right now, yet the fear persists.
My own procedure went smoothly. All three feeding arteries that were supplying blood to the AVM malformation in my brain have been closed off. For a few days following the surgery, I lost vision on the left side of my left eye due to brain edema caused by the procedure. Fortunately, things settled down after a week, and I've been recovering ever since. Headaches are to be expected, but they aren't a daily occurrence anymore.
I’ve started my rehabilitation by walking laps around Central Park, naturally with my wife by my side.
I am heading back to work next week.
Unfortunately, this story isn't over yet. After the follow-up exam in September, a Gamma Knife procedure is highly likely. We will just have to see.
We continue to hold onto the hope that the AVM will remain dormant forever and that we can somehow avoid the inevitable.
Best regards, and hang in there.