We haven't seen her yet, but just got done talking to Dr Browd and everything went well!
I'll post more details later.
Tuesday, December 14, 2010
They just took her back
We won't get any mid-op updates since this one's so quick. I'll post when she's done!
Monday, December 13, 2010
Surgery is tomorrow
Summer had a couple of pre-op appointments this morning. Both went well - she is getting to be such a big girl. She didn't put up a fight for a single test or measurement and was very talkative with the nurses. She even asked one to kiss her head and invited her to our house to meet Rocky and Chloe.
I kept telling Summer "no pokes" all morning...but the nurse at the second appointment made me into a big fat liar. She needed a current blood count, so Summer had to get a finger poke after all. She took it in stride though, and didn't put up much of a fuss.
We finally found out the surgery schedule and recovery details. We'll check in at 1:15pm tomorrow. It's no fun having surgery at all, but surgery that late in the day makes for a miserable morning. Summer can't eat after 6:30am and can only have clear liquids until 10:30am, nothing after that. I think the surgery actually starts at 2:30, but I can't remember for sure. Luckily it's written down somewhere.
The surgery will take about an hour to an hour and a half. She won't need to be in the ICU after and will go straight to the recovery floor. They'll keep her overnight and she'll likely go home on Wednesday. She will be in some pain from the placement of the tube and the incision in her abdomen, but it all sounds pretty manageable.
We don't yet have the full schedule for Boston, but that should be coming sometime today. I did get confirmation that we'll be able to stay at Christopher's Haven starting on January 10th (right now radiation is slated to start on the 11th, so that's perfect timing). I spoke to the manager there this morning, and it really sounds like a great place. We hope to be able to go visit when we're out there for prep stuff in two weeks.
I'll post brief updates tomorrow when Summer goes into and comes out of surgery.
I kept telling Summer "no pokes" all morning...but the nurse at the second appointment made me into a big fat liar. She needed a current blood count, so Summer had to get a finger poke after all. She took it in stride though, and didn't put up much of a fuss.
We finally found out the surgery schedule and recovery details. We'll check in at 1:15pm tomorrow. It's no fun having surgery at all, but surgery that late in the day makes for a miserable morning. Summer can't eat after 6:30am and can only have clear liquids until 10:30am, nothing after that. I think the surgery actually starts at 2:30, but I can't remember for sure. Luckily it's written down somewhere.
The surgery will take about an hour to an hour and a half. She won't need to be in the ICU after and will go straight to the recovery floor. They'll keep her overnight and she'll likely go home on Wednesday. She will be in some pain from the placement of the tube and the incision in her abdomen, but it all sounds pretty manageable.
We don't yet have the full schedule for Boston, but that should be coming sometime today. I did get confirmation that we'll be able to stay at Christopher's Haven starting on January 10th (right now radiation is slated to start on the 11th, so that's perfect timing). I spoke to the manager there this morning, and it really sounds like a great place. We hope to be able to go visit when we're out there for prep stuff in two weeks.
I'll post brief updates tomorrow when Summer goes into and comes out of surgery.
Thursday, December 9, 2010
Surgery Tuesday, Boston the week after Christmas
After my last post, I got a call from Dr Geyer to fill us in on the tumor board's discussion about Summer yesterday afternoon. He had talked to them about periodically draining the cyst up until (and probably during) radiation to keep it small. The smaller the area to be radiated, the better.
In their meeting, Dr Browd suggested instead converting her Ommaya reservoir into a permanent ventriculoperitoneal (VP) shunt that would continuously drain into her abdominal cavity and prevent the cyst from filling up at all. The board agreed that this was a good idea - not only will it keep the cyst at its smallest for radiation, it will alleviate the trauma caused to her brain by the cyst repeatedly growing and shrinking as it fills and is drained.
Dr Geyer gave us a heads up that they were recommending this so we wouldn't be surprised when neurosurgery called to schedule the surgery, but didn't have any details about the surgery itself. He assumed it would be similar to her prior surgeries. I was pretty skeptical at first - I wasn't sure that it was really worth another invasive surgery and all the risks that go with it - so when the neurosurgery scheduler called this morning to set up the surgery, I asked her to have Dr Browd call so we could talk it through.
I spoke with Dr Browd this afternoon and he explained the surgery in a little more detail. He will re-open her scalp along the same incision line (probably not the entire thing, just a smaller part around the reservoir), pop off the Ommaya reservoir and attach tubing. The tubing will be fed down behind her ear, down her neck and into her abdominal cavity, all underneath the skin. He will make a minor incision at her belly button to help guide the tubing down into her abdominal cavity. He wouldn't need to open her skull at all.
The recovery is quick - she'll likely go home the next day, unless she is having trouble managing pain, in which case they might keep her an extra night. After talking to Dr Browd, we felt much better about the surgery and have decided to go through with it. It will provide us some relief, not having to stress about the cyst filling up again, and it will make radiation safer and more accurate without the cyst size continually changing.
We'll have some pre-op appointments on Monday, and the surgery itself will be Tuesday, probably early afternoon. We'll find out the scheduled time at the appointments on Monday.
I also spoke with Anne at Mass. General, and we now have a loose timeline laid out. We will fly out to Boston the week after Christmas for a few days of preparatory appointments. Then there will be a break (a week to a week-and-a-half) before radiation actually starts. During that time, they build custom equipment specifically designed for Summer and her tumor. We haven't decided whether Summer and I will come home during that break or not. The actual treatment will then start the second week of January and continue for six weeks.
I'll have more specific dates and an answer from Christopher's Haven on whether they'll have a place for us sometime tomorrow.
In their meeting, Dr Browd suggested instead converting her Ommaya reservoir into a permanent ventriculoperitoneal (VP) shunt that would continuously drain into her abdominal cavity and prevent the cyst from filling up at all. The board agreed that this was a good idea - not only will it keep the cyst at its smallest for radiation, it will alleviate the trauma caused to her brain by the cyst repeatedly growing and shrinking as it fills and is drained.
Dr Geyer gave us a heads up that they were recommending this so we wouldn't be surprised when neurosurgery called to schedule the surgery, but didn't have any details about the surgery itself. He assumed it would be similar to her prior surgeries. I was pretty skeptical at first - I wasn't sure that it was really worth another invasive surgery and all the risks that go with it - so when the neurosurgery scheduler called this morning to set up the surgery, I asked her to have Dr Browd call so we could talk it through.
I spoke with Dr Browd this afternoon and he explained the surgery in a little more detail. He will re-open her scalp along the same incision line (probably not the entire thing, just a smaller part around the reservoir), pop off the Ommaya reservoir and attach tubing. The tubing will be fed down behind her ear, down her neck and into her abdominal cavity, all underneath the skin. He will make a minor incision at her belly button to help guide the tubing down into her abdominal cavity. He wouldn't need to open her skull at all.
The recovery is quick - she'll likely go home the next day, unless she is having trouble managing pain, in which case they might keep her an extra night. After talking to Dr Browd, we felt much better about the surgery and have decided to go through with it. It will provide us some relief, not having to stress about the cyst filling up again, and it will make radiation safer and more accurate without the cyst size continually changing.
We'll have some pre-op appointments on Monday, and the surgery itself will be Tuesday, probably early afternoon. We'll find out the scheduled time at the appointments on Monday.
I also spoke with Anne at Mass. General, and we now have a loose timeline laid out. We will fly out to Boston the week after Christmas for a few days of preparatory appointments. Then there will be a break (a week to a week-and-a-half) before radiation actually starts. During that time, they build custom equipment specifically designed for Summer and her tumor. We haven't decided whether Summer and I will come home during that break or not. The actual treatment will then start the second week of January and continue for six weeks.
I'll have more specific dates and an answer from Christopher's Haven on whether they'll have a place for us sometime tomorrow.
Wednesday, December 8, 2010
Boston, here we come.
Summer had a HASTE MRI this morning to see if the cyst is still producing fluid. The scan itself went relatively well. Only one parent is allowed back with her, so Jason took her this time while I waited in the waiting room. Summer wasn't happy about being strapped to the table again, but the nurse asked her to help count to 10 as a distraction. She told Summer that when they got to 10 she would be done and could get back up.
Nurse: "1"
Summer: "2"
Nurse: "3"
Summer: "10. 10! 10! 10!"
When the scan was over, Summer told Jason "that was a great nurse!," gave hi-fives all around and said bye to everyone before coming back out to me. Usually when she's upset about something, she won't say a word and buries her head on our shoulders until we leave, so she must not have thought the whole thing was too bad.
We then met with Dr Geyer to review the results and he cut straight to the point - the cyst is bigger than it was at her 11/15 scan, and is only a few mm shy of the 8/11 scan when it was at its largest. So now we know the Interferon didn't work, and we're officially planning on Proton Radiation at Massachusetts General Hospital as the next step.
Dr Geyer drew somewhere between 6 and 7mL of fluid out through the Ommaya today. He said he could have taken more, but would prefer to draw it out in stages. We'll probably take her in for weekly or bi-weekly fluid draws between now and leaving for Boston.
Also before we go, Summer will probably have another VEP test to establish her visual baseline, and perhaps an EEG to spot any potential issues before we wean her off Keppra, the seizure medication she's been on since her last surgery as a preventative measure.
I called our contact at Mass. General and let her know the status. Over the next few days she'll start scheduling and we'll know more specifically when we'll be there hopefully by the end of the week. Sounds like it will be early January. We'll have a few days of preparatory stuff to do there, and then a week or week and a half of waiting until the actual treatment can begin.
I also put word in with her that we'd prefer to stay at Christopher's Haven if at all possible. It looks like a really great setup - a set of fully-furnished apartments across the street from the hospital. The apartments are reserved for families traveling there for proton radiation, but there are only seven of them, so hopefully we can get one.
As unfortunate as it is that Summer will go through radiation at such a young age, the wait-and-see approach was extremely stressful and emotionally challenging for us, so there is quite a bit of relief in having a definitive plan for treatment.
Nurse: "1"
Summer: "2"
Nurse: "3"
Summer: "10. 10! 10! 10!"
When the scan was over, Summer told Jason "that was a great nurse!," gave hi-fives all around and said bye to everyone before coming back out to me. Usually when she's upset about something, she won't say a word and buries her head on our shoulders until we leave, so she must not have thought the whole thing was too bad.
We then met with Dr Geyer to review the results and he cut straight to the point - the cyst is bigger than it was at her 11/15 scan, and is only a few mm shy of the 8/11 scan when it was at its largest. So now we know the Interferon didn't work, and we're officially planning on Proton Radiation at Massachusetts General Hospital as the next step.
Dr Geyer drew somewhere between 6 and 7mL of fluid out through the Ommaya today. He said he could have taken more, but would prefer to draw it out in stages. We'll probably take her in for weekly or bi-weekly fluid draws between now and leaving for Boston.
Also before we go, Summer will probably have another VEP test to establish her visual baseline, and perhaps an EEG to spot any potential issues before we wean her off Keppra, the seizure medication she's been on since her last surgery as a preventative measure.
I called our contact at Mass. General and let her know the status. Over the next few days she'll start scheduling and we'll know more specifically when we'll be there hopefully by the end of the week. Sounds like it will be early January. We'll have a few days of preparatory stuff to do there, and then a week or week and a half of waiting until the actual treatment can begin.
I also put word in with her that we'd prefer to stay at Christopher's Haven if at all possible. It looks like a really great setup - a set of fully-furnished apartments across the street from the hospital. The apartments are reserved for families traveling there for proton radiation, but there are only seven of them, so hopefully we can get one.
As unfortunate as it is that Summer will go through radiation at such a young age, the wait-and-see approach was extremely stressful and emotionally challenging for us, so there is quite a bit of relief in having a definitive plan for treatment.
Monday, November 15, 2010
The news is...no news.
We didn't learn anything definitive from this morning's scan.
The cyst is slightly smaller than we saw in her last scan on 11/3. While it's always good to see the cyst smaller, that doesn't really come as a surprise to us since Dr Browd drew 4mL of fluid right after her last scan. What we can't tell is whether the reduction in size is equivalent to 4mL of fluid, or if it re-accumulated some fluid after the draw.
If you read my last post, you'll know that we anticipated this might be a problem. Dr Geyer had thought that if it had been filling up as quickly as it has done in the past, we would have been able to see it. Perhaps it's slowing down, but it's really impossible to know at this point.
So, we'll have another HASTE MRI on 12/8 that will give us a better apples-to-apples comparison.
The HASTE MRI was very quick. And thank goodness for that - Summer hated the entire 30 seconds of it. But after that, she calmed right down. Apparently the entire thing was MY fault because the second she was done she said "All done. I can see my daddy now please?" From leaving Jason in the waiting room to walking back out to meet him, we were probably gone 2-3 minutes total.
Last week, we got a call from endocrinology to go over her lab results from 11/3. Everything looked normal (even her growth factors, amazingly enough), except her thyroid stimulating hormone (TSH) is still high, which means her thyroid is not functioning at 100%. This is a little bit contrary to what we'd heard before (from the HemeOnc nurse), but I figure we should trust the endocrinologist to know best about the endocrine function...
The TSH is pretty borderline high, but we've been monitoring it for six months now and it's continually high. Since good thyroid function is especially important for brain development at this age, they decided we should start her on some thyroid medication. She takes half of a tiny pill first thing every morning. Piece of cake. They'll retest her TSH levels after she's been on the medication for a couple of weeks, just to make sure it's working.
They also asked us to come in for another stim test - I'm not sure that I wrote about the actual test itself last time we had this done, but it was horrid. Assuming it all goes well, it shouldn't be too bad, but it didn't go very well last time. She'll have an IV injection to stimulate cortisol production, and then blood draws (theoretically from the same IV...but that didn't really work out so well last time) every 30 and 60 minutes to see how she's responding. That test will be this coming Wednesday, and we'll get the results back at our endo appointment on 11/24.
The cyst is slightly smaller than we saw in her last scan on 11/3. While it's always good to see the cyst smaller, that doesn't really come as a surprise to us since Dr Browd drew 4mL of fluid right after her last scan. What we can't tell is whether the reduction in size is equivalent to 4mL of fluid, or if it re-accumulated some fluid after the draw.
If you read my last post, you'll know that we anticipated this might be a problem. Dr Geyer had thought that if it had been filling up as quickly as it has done in the past, we would have been able to see it. Perhaps it's slowing down, but it's really impossible to know at this point.
So, we'll have another HASTE MRI on 12/8 that will give us a better apples-to-apples comparison.
The HASTE MRI was very quick. And thank goodness for that - Summer hated the entire 30 seconds of it. But after that, she calmed right down. Apparently the entire thing was MY fault because the second she was done she said "All done. I can see my daddy now please?" From leaving Jason in the waiting room to walking back out to meet him, we were probably gone 2-3 minutes total.
Last week, we got a call from endocrinology to go over her lab results from 11/3. Everything looked normal (even her growth factors, amazingly enough), except her thyroid stimulating hormone (TSH) is still high, which means her thyroid is not functioning at 100%. This is a little bit contrary to what we'd heard before (from the HemeOnc nurse), but I figure we should trust the endocrinologist to know best about the endocrine function...
The TSH is pretty borderline high, but we've been monitoring it for six months now and it's continually high. Since good thyroid function is especially important for brain development at this age, they decided we should start her on some thyroid medication. She takes half of a tiny pill first thing every morning. Piece of cake. They'll retest her TSH levels after she's been on the medication for a couple of weeks, just to make sure it's working.
They also asked us to come in for another stim test - I'm not sure that I wrote about the actual test itself last time we had this done, but it was horrid. Assuming it all goes well, it shouldn't be too bad, but it didn't go very well last time. She'll have an IV injection to stimulate cortisol production, and then blood draws (theoretically from the same IV...but that didn't really work out so well last time) every 30 and 60 minutes to see how she's responding. That test will be this coming Wednesday, and we'll get the results back at our endo appointment on 11/24.
Subscribe to:
Posts (Atom)