This blog is moving to a new location that better represents our future.
http://www.thewilltosee.com/
We have created the Will to see to be the new home for the blog and to hold all of the info we are discovering about Will's vision. I will be blogging there now and building out that site. Please look there for us. Thanks for following us.
Tuesday, September 1, 2009
Saturday, August 29, 2009
Icky stomach flu
The stomach flu hit our house this week, well at least Jack and I had it. Will might have had a mild version earlier in the week (fingers crossed that he doesn’t get the one that we had) and so far Jim has managed to avoid it. It is really difficult to clean up your child’s vomit when you are nauseous too. (sorry to be so graphic, but anyone who has experienced that will understand). I think we gave it to our friend Karen, so sorry sweetie, hope you are doing better.
So my week of playing catch up became a week of recovering. Oh well, maybe we needed to slow down and spend all of Thursday watching an entire season of America’s Next Top Model. Jack was rooting for Samantha. :)
So my week of playing catch up became a week of recovering. Oh well, maybe we needed to slow down and spend all of Thursday watching an entire season of America’s Next Top Model. Jack was rooting for Samantha. :)
Monday, August 24, 2009
Worst week ever
I can safely say that last week was the worst week of my life. I spent today recovering from a nice but tiring weekend in Lodi for Granny’s funeral and memorial service. Saturday was an emotional but wonderful day. It was nice to have all of the family together, since it is harder to get all of us in one spot at the same time these days. In true Lange style we buried Granny (just as we did with Grandpa) and completely filled in the hole with Grandpa’s shovel. The memorial service at First Untied Methodist Church was a moving tribute to her, full of tears and laughter. She would have just loved seeing all of her old MYFers (Methodist Youth Fellowship) get up and sing for her.
It will take a long time to sink in that she is gone. She was such a big part of my life, since I grew up right next door. As we were getting ready to leave yesterday I thought we need to go say good bye to Granny. I wonder how long it will take us to stop calling it Granny’s house. She touched so many people’s lives. We will miss her everyday.
As if loosing my granny and tests at Children’s Hospital weren’t enough, getting William’s vision diagnosis was devastating. Jim asked me on Friday, “when do you think we will look at him and not be sad?” We are trying to learn as much as we can about this condition and understand the anatomy and how the eye works. It is overwhelming to think that he might not be able to see very well. We all take the sense of sight for granted, since it is so critical to everyday life. I just hope that he is able to see enough to not be limited by it.
Here is to a better week this week.
It will take a long time to sink in that she is gone. She was such a big part of my life, since I grew up right next door. As we were getting ready to leave yesterday I thought we need to go say good bye to Granny. I wonder how long it will take us to stop calling it Granny’s house. She touched so many people’s lives. We will miss her everyday.
As if loosing my granny and tests at Children’s Hospital weren’t enough, getting William’s vision diagnosis was devastating. Jim asked me on Friday, “when do you think we will look at him and not be sad?” We are trying to learn as much as we can about this condition and understand the anatomy and how the eye works. It is overwhelming to think that he might not be able to see very well. We all take the sense of sight for granted, since it is so critical to everyday life. I just hope that he is able to see enough to not be limited by it.
Here is to a better week this week.
Thursday, August 20, 2009
A new normal
During a really long week of tests we have gotten good news and some concerning news. First the good, all of the results that we have received from the tests at Children’s have been normal. We are still waiting on the biopsy and pH probe results.
Today we had Will’s eye doctor appointment to check his nystagmus. She has diagnosed him with Ocular Albinism, which means he has decreased pigment in his eye (mainly retna) which leads to decreased visual acuity. Nystagmus, the side to side eye movements he has, is a sign of this condition as well.
She tested his vision, which isn’t easy with a baby and he can see, but his vision is below normal for his age. He is not to light sensitive, which is good and he has pigment in his iris. So the hope is that he will have a mild to moderate version of this condition. Unfortunately we will not know what his vision will end up like until his is at least 2 or 3.
We are still learning about this condition and what it will mean for him. If he has a mild case then he could have normal or close to normal vision. If he ends up with a severe case he could be legally blind. The doctor thinks he will fall in the middle of the spectrum. She has referred us to another eye doctor to confirm this diagnosis.
Here are a couple of links to some information that we have found so far. As we find out more information we will post it.
http://www.albinism.org/faq/children.html#Anchor-What-52467
http://www.aapos.org/displaycommon.cfm?an=1&subarticlenbr=62
Needless to say we both are having difficulty processing all of this and what it will mean for him. We are hoping and praying that he will be on the mild end of the spectrum to give him the most opportunities. As Jim put it, this is our new normal.
As if Will knew that we needed some hope, he rolled over today. And yesterday the 2nd tooth poked through. He is just an angel.
Today we had Will’s eye doctor appointment to check his nystagmus. She has diagnosed him with Ocular Albinism, which means he has decreased pigment in his eye (mainly retna) which leads to decreased visual acuity. Nystagmus, the side to side eye movements he has, is a sign of this condition as well.
She tested his vision, which isn’t easy with a baby and he can see, but his vision is below normal for his age. He is not to light sensitive, which is good and he has pigment in his iris. So the hope is that he will have a mild to moderate version of this condition. Unfortunately we will not know what his vision will end up like until his is at least 2 or 3.
We are still learning about this condition and what it will mean for him. If he has a mild case then he could have normal or close to normal vision. If he ends up with a severe case he could be legally blind. The doctor thinks he will fall in the middle of the spectrum. She has referred us to another eye doctor to confirm this diagnosis.
Here are a couple of links to some information that we have found so far. As we find out more information we will post it.
http://www.albinism.org/faq/children.html#Anchor-What-52467
http://www.aapos.org/displaycommon.cfm?an=1&subarticlenbr=62
Needless to say we both are having difficulty processing all of this and what it will mean for him. We are hoping and praying that he will be on the mild end of the spectrum to give him the most opportunities. As Jim put it, this is our new normal.
As if Will knew that we needed some hope, he rolled over today. And yesterday the 2nd tooth poked through. He is just an angel.
Tuesday, August 18, 2009
Two busy days
Yesterday morning we left our house for Seattle Children’s Hospital and returned home this afternoon after an endoscopy, pH probe, upper GI and appointment with a feeding specialist. It was a busy two days and we are all very tired. Needless to say you don’t get much sleep when you are in a hospital, but add on to that sharing a room with a family who has an infant and there is even less. Yes, they double up infants. It doesn’t make sense to me either, but that is how it works. Will was able to sleep through the night with everything going on: another baby in the room, nurses in and out checking his vitals every four hours and our roommate’s TV on all night. He is a little super star.
He started off with an endoscopy yesterday morning at 8:45. For this procedure they put him to sleep and then stick a camera down his throat to look at his esophagus, stomach and upper small intestines. They also take tissue samples in all the areas to make sure there isn’t anything going on that they can’t assess visually. The doctor came out with photos (Jim joked that we should frame Jack’s and Will’s next to each other and play pick out your stomach) and said that everything looked normal. He didn’t see any signs of irritation or concern. The tissue sample results will be back in 1-2 weeks.
While they were finishing up the endoscopy they place the pH probe for the 24 hour observation period. It is a probe on the end of a thin tube that sits in his esophagus and measures the pH. If there is any acid left in Will’s tummy when he refluxes or spits up it will register a lower pH. I kept notes on when I he eats, sleeps, spits up, or has any signs of distress. We had to stay at the hospital overnight while it was in, just in case he pulls it out then they can put it right back in.
This morning we did the upper GI, which looks at the anatomy of his esophagus, stomach and upper small intestine. They feed him a bottle barium solution (flavored with cherry syrup) and watch on a fluoroscope as it flows down to his stomach. Pictures are taken every so often, as he is moved into different positions (left side, stomach, right side). He didn’t really like this one very much. All of his anatomy looked normal, so that is good.
The last thing we did today was meet with our feeding specialist. We chatted for a bit and she watched Will feed. She suggested we start using Simply Thick to thicken his formula instead of rice cereal, because the cereal has been clogging the nipples. So far it seems to be working better. She also advised to let him tell us when he is finished feeding and for right now not to start solids. We will check in with her next week to see if we should come back over again.
Overall Will handled all that we have put him through like a champ. Even with all of this stuff he ate a bit better the last few days. The thickening formula seems to be helping, so fingers crossed it will keep getting better.
You may be wondering what Jack was doing during all this. Well we lucked out and had two wonderful people to stay with him, thanks guys. Yesterday my aunt Amy watched him in the morning. Jack got to go wake Riley up and show Amy what a good swimmer he is. Jim came home about lunch time and then they both came over to have dinner with Will and I at the hospital last night. Today Jack’s godfather Alan came over to play. They watched movie and played Hit and Run, one of Jack’s favorite backyard games.
He started off with an endoscopy yesterday morning at 8:45. For this procedure they put him to sleep and then stick a camera down his throat to look at his esophagus, stomach and upper small intestines. They also take tissue samples in all the areas to make sure there isn’t anything going on that they can’t assess visually. The doctor came out with photos (Jim joked that we should frame Jack’s and Will’s next to each other and play pick out your stomach) and said that everything looked normal. He didn’t see any signs of irritation or concern. The tissue sample results will be back in 1-2 weeks.
While they were finishing up the endoscopy they place the pH probe for the 24 hour observation period. It is a probe on the end of a thin tube that sits in his esophagus and measures the pH. If there is any acid left in Will’s tummy when he refluxes or spits up it will register a lower pH. I kept notes on when I he eats, sleeps, spits up, or has any signs of distress. We had to stay at the hospital overnight while it was in, just in case he pulls it out then they can put it right back in.
This morning we did the upper GI, which looks at the anatomy of his esophagus, stomach and upper small intestine. They feed him a bottle barium solution (flavored with cherry syrup) and watch on a fluoroscope as it flows down to his stomach. Pictures are taken every so often, as he is moved into different positions (left side, stomach, right side). He didn’t really like this one very much. All of his anatomy looked normal, so that is good.
The last thing we did today was meet with our feeding specialist. We chatted for a bit and she watched Will feed. She suggested we start using Simply Thick to thicken his formula instead of rice cereal, because the cereal has been clogging the nipples. So far it seems to be working better. She also advised to let him tell us when he is finished feeding and for right now not to start solids. We will check in with her next week to see if we should come back over again.
Overall Will handled all that we have put him through like a champ. Even with all of this stuff he ate a bit better the last few days. The thickening formula seems to be helping, so fingers crossed it will keep getting better.
You may be wondering what Jack was doing during all this. Well we lucked out and had two wonderful people to stay with him, thanks guys. Yesterday my aunt Amy watched him in the morning. Jack got to go wake Riley up and show Amy what a good swimmer he is. Jim came home about lunch time and then they both came over to have dinner with Will and I at the hospital last night. Today Jack’s godfather Alan came over to play. They watched movie and played Hit and Run, one of Jack’s favorite backyard games.
Sunday, August 16, 2009
In loving memory
Oneta Lee Hunter Lange passed away this morning at the age of 87 after a courageous fight with Alzheimer’s disease. She was in the home she loved with her four children by her side. She was known as many things, but to me (and many others) she was Granny. Her legacy will be carried on by her four children and their spouses, her eight grandchildren and their spouses and her five great grandchildren. She was the matriarch of our family and a strong presence in Lodi. When her children where young she lead the youth group at Lodi First Untied Methodist Church and will always be remembered for the amazing ice cream socials they put on. As a member of the Hutchins Street Square Foundation Board she helped shape the creation of Hutchins Street Square into the community center and outstanding facility it is today.
She called me SariAnn and I will forever be able to hear her saying that. When I was growing up she used to watch my cousins, sister and I on Fridays and she would make Yuck Soup with everything in the fridge. She was a master at scrapbooking before it was popular and she would play solitare in her kitchen everyday. She taught me to arrange flowers and wrap presents. Undoubtedly she will be most remembered for her pies and specifically her pie crust. Luckily my sister learned the special techniques and will carry on that legacy.
I am so happy that she got to know three of her great grandchildren, unfortunately the two newest ones were to little and her disease at progressed to much to make a true impression on her. Just three weeks ago she was sitting in my parent’s living room talking with me and holding William. I will hold that memory deep in my heart along with many others. We will all miss her and life will not be the same without her.
We love you Granny.
She called me SariAnn and I will forever be able to hear her saying that. When I was growing up she used to watch my cousins, sister and I on Fridays and she would make Yuck Soup with everything in the fridge. She was a master at scrapbooking before it was popular and she would play solitare in her kitchen everyday. She taught me to arrange flowers and wrap presents. Undoubtedly she will be most remembered for her pies and specifically her pie crust. Luckily my sister learned the special techniques and will carry on that legacy.
I am so happy that she got to know three of her great grandchildren, unfortunately the two newest ones were to little and her disease at progressed to much to make a true impression on her. Just three weeks ago she was sitting in my parent’s living room talking with me and holding William. I will hold that memory deep in my heart along with many others. We will all miss her and life will not be the same without her.
We love you Granny.
Saturday, August 15, 2009
Overfeeding Theory
Well we met with the 2nd GI specialist on Friday. While we like him better, for his compassion to our situation and his overall demeanor, he didn’t provide any more insight into what could be going on. Both GI docs believe that we could be overfeeding William and urged us very strongly to do on demand feedings. We have been doing on demand feedings since his volume has dropped down. I just don’t buy that everything going on with him is because he is just getting full; which is what they are suggesting.
He has dropped his volume in half and he cries or winces in pain when he is burping or right afterward. He also tries to take a couple of sucks and then cries out. My mommy instinct is telling me this isn’t just “overfeeding.” I think there is something going on in his throat. Either there is still some stomach acid left after all the medicines he is on or he is just bothered by the act of refluxing. The last one is a theory that the new GI doc suggested as a possibility yesterday. I had never thought of that one, but it could make sense.
We have decided to add a pH probe to his battery of tests next week, which means we will be spending Monday night at Children’s Hospital. I am not excited about that prospect, but it is what we need to do. During his endoscopy they will place a pH probe in this esophagus to measure the pH changes as he refluxes throughout a 24 hour period. Normally this is done when children are off of their reflux meds, but we are doing it with him on his. We already know he refluxes, we want to know if there is any acid left to bother him when he does.
All of the doctors we have spoken with so far are insistent that there is no way there is any acid left in his stomach, but that assumes that we all have the same amount of stomach acid. If there is acid left we can assume that it is still bothering him and that he is just really sensitive to it, just like Jack. We will just see what the tests show.
He has dropped his volume in half and he cries or winces in pain when he is burping or right afterward. He also tries to take a couple of sucks and then cries out. My mommy instinct is telling me this isn’t just “overfeeding.” I think there is something going on in his throat. Either there is still some stomach acid left after all the medicines he is on or he is just bothered by the act of refluxing. The last one is a theory that the new GI doc suggested as a possibility yesterday. I had never thought of that one, but it could make sense.
We have decided to add a pH probe to his battery of tests next week, which means we will be spending Monday night at Children’s Hospital. I am not excited about that prospect, but it is what we need to do. During his endoscopy they will place a pH probe in this esophagus to measure the pH changes as he refluxes throughout a 24 hour period. Normally this is done when children are off of their reflux meds, but we are doing it with him on his. We already know he refluxes, we want to know if there is any acid left to bother him when he does.
All of the doctors we have spoken with so far are insistent that there is no way there is any acid left in his stomach, but that assumes that we all have the same amount of stomach acid. If there is acid left we can assume that it is still bothering him and that he is just really sensitive to it, just like Jack. We will just see what the tests show.
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