JollyRoger's blog

Things have changed a little bit. I just received a call that they are going to admit Megan on the 12th, which is next Tuesday. Before they go in and do anything to her they plan on doing other things first, basically to make sure it is going to be ok for her to be put under. Please pray for our sweet little Megan. Pray they will be able to find some resolution for her so she can comfortably tolerate her feeds and absorb her food better and maybe ease some of her pain. As of right now though we are not going to be able to have any visitors when we go into the hospital.

Things have changed a little bit. I just received a call that they are going to admit Megan on the 12th, which is next Tuesday. Before they go in and do anything to her they plan on doing other things first, basically to make sure it is going to be ok for her to be put under. Please pray for our sweet little Megan. Pray they will be able to find some resolution for her so she can comfortably tolerate her feeds and absorb her food better and maybe ease some of her pain. As of right now though we are not going to be able to have any visitors when we go into the hospital.

For Stacy's blog, and from her heart:

For Stacy's blog, and from her heart:

First up, Halo. I won't try and explain. Simply read. :)

Here's the article:

First up, Halo. I won't try and explain. Simply read. :)

Here's the article:

Not much to post, but Megan is scheduled to have surgery the week of August 25th. We are waiting on more details. They expect they might have to remove the J-tube as it is hurting her intestines but she will also have her biopsy done and other things. Her GI doc and her mitochondrial doc are going to be there to help decide what is next for Megan. Please pray.

Not much to post, but Megan is scheduled to have surgery the week of August 25th. We are waiting on more details. They expect they might have to remove the J-tube as it is hurting her intestines but she will also have her biopsy done and other things. Her GI doc and her mitochondrial doc are going to be there to help decide what is next for Megan. Please pray.

For some reason I have the hardest time trying to write updates lately. Most of you that know me, know that it is very unlike me to not have words, but whatever. Anyways, we talked at length with Megan's doctor yesterday. They have determined that Megan needs to have another biopsy done on her small bowels. She had one done in 2007 and they found lots of inflammation and irritable spots. It could be getting worse which is why she is having so much pain lately tolerating her feeds and her medicine.

For some reason I have the hardest time trying to write updates lately. Most of you that know me, know that it is very unlike me to not have words, but whatever. Anyways, we talked at length with Megan's doctor yesterday. They have determined that Megan needs to have another biopsy done on her small bowels. She had one done in 2007 and they found lots of inflammation and irritable spots. It could be getting worse which is why she is having so much pain lately tolerating her feeds and her medicine.