Tuesday, November 18, 2008

The skinny on Porter...




Well, we were kinda keeping it under wraps, but I got about 17 phone calls yesterday about Porter. I thought I would BLOG this little journey we have embarked on... not for your sympathy, but to keep people... who want to know... updated. Here's how it all went down.

We were sitting at my sister's house after Sunday dinner when I asked my mom and my dad and my sisters... pretty much everyone there... what they thought about the bump near Porter's eye. You can't see this bump, but you can definitely feel it. They thought it was strange and told me to go get it checked out.

Monday morning, I made an appointment with Porter's doctor. He examined it... and decided that since it's so close to the eye that I should take him to an eye doctor. The nurse made the appointment for me and took me across the hall to Dr Bowman's office. He examined Porter's eye and decided that he'd like his colleague to check it out.

Unfortunately, his colleague was out of town until Thursday.... so we came back then. Porter got the whole eye doctor routine... as much as a 2 year old can handle. It was determined that Porter can see great, his eye moves properly, and everything eye-related was perfect... except that darn bump.


Well, the two doctors told me that they think Porter's bump is probably a tumor. They suspect that it's the kind or tumor that is made of good cells... they're just in the wrong place. Tumors like this are known to have teeth in them, or hair, or skin. (SICK!!) They just formed in the wrong place. I asked if it would be easily removed... they said it was "a little bit of procedure". I guess that means that it's not quick and simple, but it's not re-attaching a limb or open-heart surgery.


At this point, we don't KNOW it's that toothy tumor at all... we don't know how big it is... we don't know if it's attached to anything. We really don't know much... that is the scary part. They set up an appointment for a CT scan so we could have a better idea what we're dealing with. That was yesterday...


We went to the Hospital early yesterday morning. We waited in the first waiting room, then went down to patient check-in... got all squared away with wristbands, insurance and paper work... waited in waiting-room #2... then followed a nurse to waiting room #3. Then it was Porter's turn. We took him in, laid him on the bed and tried to coax him to hold still for the first picture... the practice before they do imaging with contrast. (that's just fancy-talk for injecting him with DYE and taking pictures of it.)


Porter would have NONE of that. He was ticked! So the nurse... doctor... tech... whoever he was, decided to give him his I.V. and strap him down. (side-note... the IV was not to sedate Porter, it was to inject dye throughout his body in 40 seconds...amazing.) That is exactly what he did. They popped that sucker in... then tied his arms under his body... strapped him to the bed.... taped his head to a head-rest-thingy... then pushed the bed into the huge donut-shaped CT scanner. Porter couldn't move, but he could scream! He kept saying, " No want to!" It was so sad... broke my heart to see that little guy so scared.


The good part is it was quick. It was also quite amazing. Spence got to wear the led apron thing and stay by Porter's side while I went behind the window to watch. I was checking out the computer and watched images of Porter's brain flash all over the screen. In 10 seconds, about 400 pictures were taken... I only know that because the x-ray guys told me. It was truly amazing.



It was over quick, so we unstrapped him... and loved him... and gauzed his IV wound... and took him home. He was pretty ticked the rest of the day. I don't blame him.

I made him get a few pictures... I'm sure one day he'll want to remember it.


Now is the hard part... WAITING. We won't know the results from the CT Scan until Thursday morning. I can tell you, Porter is not in pain, he's acting normal, he doesn't even KNOW why he has to go to all these doctors. I think that's a good thing. As for the bump... small and it hasn't grown. I feels like a ball of some kind. I really don't know how long he has had it... I just noticed it a couple weeks ago. And what's more of a mystery, I don't know how I ever found it!


Our spirits are high... we are just putting all our faith in Heavenly Father... he can fix this for us! We love you all and appreciate all the concerned phone calls and your prayers... we are blessed to have such great friends and family.

11 comments:

sarahhicken said...

I am so grateful for doctors and medical science that can do so much. But it still breaks a mother's heart to hear those screams.

Jessica Potter said...

Poor little guy! That makes me sooo sad! I hope all turns out okay!

Glazier Family Blog said...

Sweet little Porter...we will keep you guys in our prayers.

Julie said...

We'll be thinking of you and praying for the little guy. Let me know if you need anything, I would even take Jackson for the day if it would help! (Can you imagine the trouble he and BElla could cause?)

Lilian said...

He's such a cutie! I have been keeping him in my prayers and will continue to do so.

Jacci Halliday said...

God Bless you and sweet Porter. I pray for good results on thursday!

Michelle Woj said...

Oh gosh! My heart goes out to you! I can't imagine how it would be to watch your kid go through a CT with contrast! Yikes! You're a good mommy.

Mandy said...

Holy cow! Keep us posted! Maybe you'll get lucky and he just swallowed a bouncy ball or a whole gumball or something and it got stuck! :) Good luck! We'll be thinking of you guys!

Lisa said...

Wow. What an experience. We will be praying for you all. Keep us posted.

Brook said...

Poor little guy. I don't know who its harder on though, him or the parents. Hope all is well, I'm sure it will be. We'll keep him in our prayers!

Gardner said...

Okay now I am crying. Honey you guys are in my prayers. i will be thinking of you often. Love you tons. I know that you guys will get through this trail.