Welcome Everyone!
Morrises, Brileys, Piazzas, Ybarras, Fausts, Messers, Vaughns, Rogerses, Christensens, Caughrons, Fullertons, Andersons, Sanfords, Lassanskes, Johnsons, Pritchetts, Lewises, Spahns, Rogalskis, Montgomerys!
And to all Limbs, Branches, and Twigs of each Family Tree ~ Welcome!
Friday, August 29, 2008
Our Darling Janie
Thank you so much for all of the support, prayers and well-wishes. I can't believe she's finally here! I could go on and on about her, but the pictures say it all. Love, Laura
Monday, August 25, 2008
Meet Jane Cara Vaughn
Thursday, August 21, 2008
Arnold and Mary Bell (Lawton) Widmer
Arnold and Viola (Kellicut) Widmer
Sunday, August 17, 2008
Widmer Photo
Lawton Family Photo
More Pictures and Hello!
Hello - I'm Joe Rogalski, son of John and Mary Rogalski. My mother gave me the information about this site months ago and I'm finally getting around to posting.
I'm 31 yrs old, living in Madison Wisconsin. Have fond memories of growing up and trying to teach the Texans how to say "root" beer correctly.
Anyway here are some family photos that I've scanned/cropped/enhanced. Enjoy!
Scan of the original Pretty Lake photo in 1984
"Kid Photo" from 1984 in Pretty Lake
Tomah, WI 1995
I'm 31 yrs old, living in Madison Wisconsin. Have fond memories of growing up and trying to teach the Texans how to say "root" beer correctly.
Anyway here are some family photos that I've scanned/cropped/enhanced. Enjoy!
Scan of the original Pretty Lake photo in 1984
"Kid Photo" from 1984 in Pretty Lake
Tomah, WI 1995
Happy Birthday, Clint - Aug. 17th
Friday, August 15, 2008
Widmers
Wednesday, August 13, 2008
Look-alikes
Nicole Morris Fullerton and Ruth Widmer Sanford
Most of the family thinks Nicole looks like her Great Grandma
Heather Morris Caughron and Mary Ann Sanford Morris
Many of us think Heather favors her Grandma.
Kim brought it up in one of her comments, so I thought I'd post the evidence. See what you think! ~Nancy~
Tuesday, August 12, 2008
Clint, Liz & Baby
We had another dr. appointment today to check the the probability of the baby having down's syndrome. We got to look at the sonogram for a very long time, since the technician was trying to get the baby to move for good measurements. The baby wasn't cooperating.
Everything seems to be normal so far. Liz is finally starting to get over the morning sickness. She is 13 weeks now.
See ya in November...
~Clint
Anyway, thought I'd share a few photos from today.
Everything seems to be normal so far. Liz is finally starting to get over the morning sickness. She is 13 weeks now.
See ya in November...
~Clint
Ruth and Geneva
Ruth (second from left) and Geneva (second from right). I'm guessing this would be the Kickapoo River, don't know the date--
SO I AM IMPLORING EVERYONE TO DATE AND NAME PICTURES NOW, before no one knows who anyone is!! :) (But I'm sure you all do that, right?) It's starting to get hard to identify baby pictures, especially.----Mary
SO I AM IMPLORING EVERYONE TO DATE AND NAME PICTURES NOW, before no one knows who anyone is!! :) (But I'm sure you all do that, right?) It's starting to get hard to identify baby pictures, especially.----Mary
Monday, August 11, 2008
More Old Photos
Sunday, August 10, 2008
Widmers and Sanfords
Thursday, August 7, 2008
New Morris addition
There is a new member to the Morris family - a precious four-legged black and white cat! :) I found him last week in my apartment courtyard and couldn't resist seeking him out every day since to see how he was doing. I'd bring him in for a few hours to cool off and give him some food (chicken - since I didn't have any official cat food on hand). I've decided to adopt him, for now anyway. We'll see how my allergies hold up. He has the sweetest disposition and a squeak for a meow. Gave him a bath, and he didn't put up much of a fuss. I can carry him around anywhere, and he just goes right along. He's a real trooper. :) I nicknamed him Bookends because of his coloring. Don't know if that'll stick, but it's all I can think of right now. Any suggestions? ~Kim
Tuesday, August 5, 2008
Four Weeks to Go!
Still waiting for Janie! I know it's a terrible picture, but it's really the only exciting event I have going on in my life right now, and I hardly ever have anything to post. It's hard to believe that this time next month I will probably finally have my hands on her. I feel great- just the expected aches and discomforts. It's been a really great pregnancy, thank God. Her due date is September 9, but at this point, I hope she comes a week or two early. My biggest fear is my maternity leave from teaching at the beginning of the year, but people tell me that I'll care a lot less once she's here. I'm sure that's true. We also have a lot of work to do on her nursery yet, but I'm sure it will get done soon. We don't have a middle name for her yet; her daddy is giving it to her and taking great care to make it a good one. Loose ends keep you going, I guess. C'mon, Janie! - Laura
Monday, August 4, 2008
Kristin's Home!
Hello everyone! Kristin and I came home from the hospital yesterday afternoon. It is so good to be home! She is doing well right now, eating cheese and playing with her brother and sister. She started a new seizure medicine at the hospital which seems to be reducing the amount of seizures she has. We will start treatment in 2 weeks called the Ketogenic Diet, so we'll be back in the hospital for 5 days. The doctor believes that Kristin will respond well to the diet which has a 50% chance of preventing all her seizures. That would be amazing! For those of you who have not heard her diagnosis, here goes:
Kristin was diagnosed with cerebral palsy when she was 18 months old and with generalized Epilepsy last August. She experienced "absence" and "myoclonic" type seizures regularly throughout the day. She was on 3 types of anti-seizure meds, and we were still making changes to dosages/combinations to reduce her seizures even more. (Before starting her medication last August, she was having 12-15 seizures a minute.) Her CP is highly functional -- she is able to walk with leg braces, feed herself and speak 2-3 word phrases.
When she got really sick 3 weeks ago with vomiting, dehydration and high fever, something triggered in her brain, and she began experiencing an increased amount of seizures as well as new types of seizures. The brain MRI told us that she has a condition called Polymicrogyria (PMG.) It is a rare congenital brain defect most likely resulting from the twin-to-twin-transfusion syndrome. It can not be fixed, and it will not get worse, although the seizures caused by the PMG may damage her brain further if we can not control them. Further brain damage will worsen her cerebral palsy, making it more difficult to walk and eat and control her movements. She could also go into "status epilepticus" which is a state of being in a constant seizure and will stop her breathing.
That's pretty much what we are working with now. Controlling her seizures is top priority, and I think we have a good plan with a good doctor.
Thank you so much for keeping Kristin in your thoughts and prayers these last 3 weeks. We still have a long way to go, but with God's grace, we will get through this as well. Kristin seems to be the expert at overcoming "rare" conditions! We love you all!
Sarah
Friday, August 1, 2008
A Slight Delay
Kristin will go home on Sunday. They decided to introduce a new seizure medication through an IV and wanted to keep her a couple of days to see how she does. She is so precious and good about everything. Please pray this medication will lessen the seizure occurrences.
~Nancy~
~Nancy~
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