We've made the move to OU Children's Hospital. It's a completely different environment, but then again, we didn't pick this hospital for its paint scheme or floor plan and layouts. Ellie's geneticist saw her last night at 11:00 PM, so the move has already shown itself to be beneficial.
As some of our first updates stated, Ellie's disorder is devastating. NonKetotic Hyperglycinemia (or Glycine Encephalopathy) is an extremely rare metabolic disorder that is destructive to the body even when on an aggressive medicine regime. I lead with that to say this: Ellie is experiencing more and more seizures. They are coming harder and longer. We are adimently trying to counter them with the appropriate meds but this is proving difficult.
We are still fighting for our daughter. We love you and thoroughly appreciate your prayers, thoughts and support.
- MFM
Friday, April 14, 2006
Thursday, April 13, 2006
April 13, 2006
The last 2-3 days have been very difficult. Elizabeth has experienced some seizures. They are partial or focal seizures... lasting anywhere from 5-20 seconds. That could be a reaction to some of the new medicines she is on or an advancing of her condition. It's too difficult to tell right now.
The other difficult news has been that her veins are growing tired faster and faster from the many IV sticks. So much so that she had to undergo surgery today to place a catheter style main-line in her chest. This will allow her once again resume IV feedings and IV medicine.
The bigger news of all this is that we are trying to get her transferred to OU Children's Hospital. Her specialists are there and being a college, they naturally have more specialists in all the other areas as well. The reason why we haven't been there the entire time is, bed space. OU Children's bed space almost always fills up faster than Baptist so we always get diverted to Baptist.
We'll keep you all updated as soon as something changes.
The other difficult news has been that her veins are growing tired faster and faster from the many IV sticks. So much so that she had to undergo surgery today to place a catheter style main-line in her chest. This will allow her once again resume IV feedings and IV medicine.
The bigger news of all this is that we are trying to get her transferred to OU Children's Hospital. Her specialists are there and being a college, they naturally have more specialists in all the other areas as well. The reason why we haven't been there the entire time is, bed space. OU Children's bed space almost always fills up faster than Baptist so we always get diverted to Baptist.
We'll keep you all updated as soon as something changes.
Monday, April 10, 2006
April 10, 2006
This is going to be one of the weirdest and funniest posts ever but... Ellie Kate pooped last night. She did it all on her own, with no help from Glycerin, enema, suppository or the like. Her stomach was battling all night last night, causing her quite a bit of pain and discomfort... but after a few hours, she finally got some relief. Hopefully this is a sign that things are not only moving around in her system but moving through her system.
This may or may not be a news flash but Ellie Kate is a fire cracker. This morning she decided that she was tired of where the IV was so she pulled it out. This isn't the first time she randomly started pulling at her tubes and lines. So she spent a good part of this morning being held down by a team of nurses while they found another place for her IV (her foot). I'm not sure if there is a weight-lifting competition for 4 month olds but EKM would win if there was such a thing. She is ridiculously strong. But she is way cute, and by way cute, I mean totally beautiful.
Once again, we'll meet with our handful of doctors and update this page as we get updated.
Here are some prayer suggestions for those with the time:
(1) pray that EKM will continue to have movements, which in turn will eliminate all the barium in her system.
(2) pray that her system will return to its normal motility and function.
(3) pray for her momma, Ryan Elizabeth... this has been a long and grueling ordeal for Ryan. She is very tired and wants to take EKM home.
(4) pray for Conner, he's tired of not having his parents at home.
- MFM
This may or may not be a news flash but Ellie Kate is a fire cracker. This morning she decided that she was tired of where the IV was so she pulled it out. This isn't the first time she randomly started pulling at her tubes and lines. So she spent a good part of this morning being held down by a team of nurses while they found another place for her IV (her foot). I'm not sure if there is a weight-lifting competition for 4 month olds but EKM would win if there was such a thing. She is ridiculously strong. But she is way cute, and by way cute, I mean totally beautiful.
Once again, we'll meet with our handful of doctors and update this page as we get updated.
Here are some prayer suggestions for those with the time:
(1) pray that EKM will continue to have movements, which in turn will eliminate all the barium in her system.
(2) pray that her system will return to its normal motility and function.
(3) pray for her momma, Ryan Elizabeth... this has been a long and grueling ordeal for Ryan. She is very tired and wants to take EKM home.
(4) pray for Conner, he's tired of not having his parents at home.
- MFM
Friday, April 7, 2006
April 7, 2006
What we've learned up to this point is that something is wrong with Ellie Kate's small intestine. The word that is used to describe what is wrong is "ileus"... meaning intestinal obstruction. We don't know if this is an intermittent obstruction, partial obstruction or (as one doctor has hypothesized) a showing of poor muscle tone related to NKH. The last possibility is something that I dispute, based on no literature that I've found to support it but he is a doctor and might be smarter than me.... might.
Anyway, the treatment regime is consisting of TPN, reglan, and 1-2 ozs of milk every 3 hours. We'll try this approach to see if it (A) stimulates her small intestine and (B) the reglan helps the ileus. If this doesn't work we will probably transport EKM to another facility... possibly back to Houston.
Pray that Ellie Kate's small intestine will start to clear up and function properly again. We'll keep you updated once we receive updates.
- MFM
Anyway, the treatment regime is consisting of TPN, reglan, and 1-2 ozs of milk every 3 hours. We'll try this approach to see if it (A) stimulates her small intestine and (B) the reglan helps the ileus. If this doesn't work we will probably transport EKM to another facility... possibly back to Houston.
Pray that Ellie Kate's small intestine will start to clear up and function properly again. We'll keep you updated once we receive updates.
- MFM
Wednesday, April 5, 2006
April 5, 2006
Ellie Kate has endured a battery of testing during this hospital stay... and it looks like we may be getting closer to knowing what is causing all the GI problems. Yesterday, a "lower GI" was performed and with no signs or evidence of an obstruction. This morning, an "upper GI" was administered. This test took much longer to perform, for reasons not germane to this post (ask your doctor about the diffrence between and betwixt the two.)
From the upper GI, the preliminary feedback is that something is not right. This created a melancholy reaction from Ryan and I because we don't want anything to be wrong with EKM. But, since something is wrong with her, we want to know what it is.
After we get a definitive answer to what it is, we should then learn what treatments and remedies are at our disposal. Tomorrow has promise. Promise in that we are one step closer to relieving EKM's pain and discomfort and one step closer to her and her mommy sleeping in beds under my roof and not Integris's roof.
Thank you for the prayers, emails, phone calls, carrier pigeons and the like. In all seriousness, I enjoy reading this website because of the uplifting nature of your thoughts and prayers. You are evidence that God is real and working in my life and the lives of my family.
Thank you and Good Night Now.
- MFM
From the upper GI, the preliminary feedback is that something is not right. This created a melancholy reaction from Ryan and I because we don't want anything to be wrong with EKM. But, since something is wrong with her, we want to know what it is.
After we get a definitive answer to what it is, we should then learn what treatments and remedies are at our disposal. Tomorrow has promise. Promise in that we are one step closer to relieving EKM's pain and discomfort and one step closer to her and her mommy sleeping in beds under my roof and not Integris's roof.
Thank you for the prayers, emails, phone calls, carrier pigeons and the like. In all seriousness, I enjoy reading this website because of the uplifting nature of your thoughts and prayers. You are evidence that God is real and working in my life and the lives of my family.
Thank you and Good Night Now.
- MFM
Tuesday, April 4, 2006
April 4, 2006
A lot has happened since the past update. The cliff notes version is that Ellie Kate is and will be undergoing some GastroIntestinal (GI) testing. They performed a lower GI tonight that the GI specialist will look at in the morning. The preliminary analysis of it is that she does not have any blockage in her large intestine. Ellie Kate should undergo an upper GI tomorrow at some point.
The bad news is that she had her first seizure this morning. We have her in the PICU (our home away from home)... she has not had any since the morning, but she has resummed her myclonic jerks. They have lessened in intensity and frequency as the sun moved along the sky. Though she is in the PICU she is stable. She is not on the ventilator or any other life sustaining device.
Tomorrow we should know more than we know right now so we will update this site as soon as we can. Thank you for your prayers and offering of support. Once we stop going 100 mph we will return all the calls and make time for our friends.
- MFM
The bad news is that she had her first seizure this morning. We have her in the PICU (our home away from home)... she has not had any since the morning, but she has resummed her myclonic jerks. They have lessened in intensity and frequency as the sun moved along the sky. Though she is in the PICU she is stable. She is not on the ventilator or any other life sustaining device.
Tomorrow we should know more than we know right now so we will update this site as soon as we can. Thank you for your prayers and offering of support. Once we stop going 100 mph we will return all the calls and make time for our friends.
- MFM
Monday, April 3, 2006
April 3, 2006
Well, its becoming routine that whenever we need to take Ellie Kate to the Hospital... its on the weekend. This past weekend (March 31-April 2) Ellie Kate started throwing up and her stomach became distended. We later learned that she had "an incredible amount" of air in her intestines creating gas and extreme discomfort.
All that to say, Ellie Kate is back in Baptist Hospital undergoing testing and evaluation. The good news is that she is not in the PICU and is not critical or life-threatening. She will undergo some GI tests today. They have taken away her medicine and food and that has helped the problem. They will re-introduce her food and medicine slowly to see if she can handle them. We will post an update when we know more.
The short-version: EKM is in the hospital with a GI problem and will undergo some testing.
- MFM
All that to say, Ellie Kate is back in Baptist Hospital undergoing testing and evaluation. The good news is that she is not in the PICU and is not critical or life-threatening. She will undergo some GI tests today. They have taken away her medicine and food and that has helped the problem. They will re-introduce her food and medicine slowly to see if she can handle them. We will post an update when we know more.
The short-version: EKM is in the hospital with a GI problem and will undergo some testing.
- MFM
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