Sunday, December 7, 2008

Not me! Monday

Hey guys! Welcome to Not me! Monday. I love this little blog fun started at http://www.mycharmingkids.net/ So check it out, join in the fun, and have fun finding out how "perfect" we really are.



I did not carry Evan upstairs last night to get him ready for bed and put him down on the changing table to find my whole arm wet. I did not proceed to find the biggest blow out of poop in my lifetime. It was not completely up Evan's back and out the sides of his diaper. I did not have to call Andy in for reinforcements because I did not have poop everywhere it could possibly go. Evan was not competely smiling through the whole ordeal like he didn't have a care in the world. Nope! not me

I did not let my kids eat way too much candy and junk this weekend. What kind of mom would do that? Nope! not me.

I did not eat too much candy and junk myself this weekend. For crying out loud I am not a fitness instructor and I am not supposed to set a good example. Nope! not me.

I have not forgotten to hide Jack, our elf on the shelf, at least three times this week. I have not gotten up in a panic to race downstairs before the kiddos and hide him before they could realize he was in the same spot as the day before.

I do not have more Christmas shopping to do. I am supposed to not be finished already, right!

and last but not least...
I do not have leftovers still in my fridge from Thanksgiving. That would be kind of gross, so Nope! not me

Have a great rest of your Monday




Posted by at
Labels:

4 comments:

Amy said...

Ginger,
You crack me up! If it makes you feel any better, we just cleaned out Thanksgiving leftovers a few days ago and we are not even big leftover eaters!

Love,
Amy

December 8, 2008 at 9:50 AM
Kelley said...

See your not alone... I just dumped some very nice sweet potatoes with marshmellows on top. At least I think they were marshmellows. LOL

December 8, 2008 at 5:14 PM
Megan @ Hold it Up to the Light said...

I am so with you on the Elf thing, and we have NOT had the same thing happen at least 3 times this week! Caden did NOT also come with a VERY annoying CD this year....whatever you do, DON'T buy the activity book that goes with the Elf on the Shelf!

Love the SARS story, btw! Made me LOL! So happy I have someone to empathize with!!!

Love Ya!

December 8, 2008 at 9:12 PM
Dee said...

LOL! Dont you just love those blow outs!

December 9, 2008 at 9:03 AM

Post a Comment

Subscribe to: Post Comments (Atom)

Ty's birthmark

Ty's birthmark
Ty before laser treatments

Tyler's Birthmark

A port wine stain (PWS) is a congenital birthmark that affects approximately 3 out of every 1,000 people. They are most commonly found on the face and neck, but they can be found elsewhere. The underlying dilated blood vessels cause the red/pink color of the PWS. When Ty gets upset or hot the blood flow to his face increases causing the birthmark to appear redder. When Ty is colder and the blood flows away from his face the PWS can appear invisible. If left untreated, the vessels may become enlarged and elevate the skin causing the surface to take on a cobble appearance. Sometimes the PWS can also develop into a deep purple color. Occassionally, the vessels can create overgrowth causing the area where the PWS is to become larger than normal.
PWS are present at birth and usually clearly visible. PWS grow with the person and never regress. The problems of PWS can now be treated by laser.
With different wavelengths a laser beam can be made to react upon materials of only certain colors and densities. The laser is tuned to only affect the darker more dense blood vessels deep in the skin that cause the birthmark, leaving the lighter less dense outer skin with minimal damage.Unfortunately, at this time, most people do not see complete removal of their birthmark by laser treatments. 10%-15% of those treated see 75%-100% fading, 70%-80% see 25%-75% fading, and 10%-15% see 0%-25% fading.
Treatments have a better chance of being effective when a person is still young. The skin is thinner and the mark is smaller. The skin has also not been exposed to the sun as much on a young infant or child. The sun thickens the skin and makes it darker, which in turn keeps the laser from penetrating the skin and hitting the vessels. Ty has had 15 treatments so far, beginning when he was 2 ½ months old. He will be 5 years old in Sept. 2008. He has had 80%-90% lightening in most areas, and almost complete clearing of the pws on his neck. The hardest areas to treat are the mask area around the eyes, and his lip area. Ty’s laser doctor is Dr. Roy Geronemus. He is the director of the Laser and Skin Surgery Center in New York, Ny. Ty goes to New York’s Eye and Ear Infirmiry for his laser treatments and eye surgeries/appointments for treatment under anesthesia. The healing time varies for Ty’s laser treatments. It is usually between 10-15 days, but we may see fading for up to a few months. There's no definitive number of treatments that Ty will need. So far we have always seen some improvement so we continue to get them. He will always need to maintain treatment in order to keep the PWS from getting darker again.
A PWS may also be a marker for associated syndromes such as Sturge Weber. Sturge-Weber Syndrome (encephelotrigeminal angiomatosis) is a congenital, non-familial disorder of unknown incidence and cause. It is characterized by a congenital facial birthmark and neurological abnormalities. Other symptoms associated with Sturge-Weber can include eye and internal organ irregularities. Each case of Sturge-Weber Syndrome is unique and exhibits the characterizing findings to varying degrees.
Ty has had three MRIs to check if the vessels were involved in his brain. Brain involvement is one of the symptoms of SWS, and it can cause seizures. All MRIs were clean for vessels in the brain. Ty does have a malformation behind his eye in the area called the chrodial area, which is another marker for SWS. Since his birthmark covers his eyes, the blood vessels are causing the intraocular pressure in his eyes to elevate. Therefore, he has been diagnosed with glaucoma in both eyes. This malformation, along with his glaucoma, attribute to Ty’s diagnosis of SWS. One reason why his eyes stay so squinty and red all of the time is due to his glaucoma. Glaucoma can cause light sensitivity and watering of the eyes. It can also cause loss of vision and enlarged corneas. Ty has had 9 surgeries to control his glaucoma. Unfortunately, it can not be cured only controlled. He takes three different types of drops two times every day. He will most likely have frequent surgeries on his eyes for the rest of his life, or until a cure for glaucoma is found. In May of 2007, Ty developed a severe bacterial infection in his left eye. He was in the hospital for a week getting his eye injected with antibiotics. The result of this infection coupled with his severe glaucoma has left him blind in his left eye. This is also the reason for the droopiness and the physical appearance of his eye. He has since been able to see an ocularist. She formed a new partial prosthetic eye for him. You can not even tell that it isn't real. It is so cool. We are still learning day by day about PWS/SWS/Glaucoma. The hardest part about Ty's condition is not knowing what the future holds for him. We just take it day by day and rely on our faith in the Lord Jesus Christ to help us through.

Thank you for taking the time to learn a little about Ty and his condition. For more information, please visit the sources of the above information at http://www.sturge-weber.com/, http://www.birthmarks.com/, and http://www.laserskinsurgery.com/

What Ty's skin looks like after having a laser treatment

Tyler after 15 laser treatments

Sturge-Weber Syndrome Awareness