Webstat Free Counter Tracker His Little Lambs
His Little Lambs
July 25, 2007

We've Officially Started School!

This is a silly little blog just to say i am LOVIN' IT!

Since Julia was a tiny babe Joe and I have both wanted to hometeach our children. Just seems to make sense that as the military life brings such constant change in thier lives, the fact that school is always with mom no matter where we move would be nice to have. Plus, i just love teaching my kids. I think every parent does this instinctually since the birth of thier baby. You read to them. You sing to them. You answer thier questions and ask them questions back, "yes, that is a carrot. they are vegetables and keep our bodies healthy...do you know what color it is?" plus i really really love watching thier faces light up with they "get it", and watching them bloom with self confidence and reassurance that comes with learning is just an extra boost as well! it is awesome...but it is also a huge responsibility. to be honest, although i have known the last 5 years we wanted to try hometeaching, and that i myself was hometaught my elementary years, IT IS STILL SCARY!

i have been really really really nervous! It is such a big responsibility, and what if i don't do it right? what if i do it wrong and handicap thier learning more than helping them? what if i miss something, or don't do a certain subject right? what curricullums do i use and what if we run into stumbling blocks??

yeah, nervous to say the least.

but still God's peace would remain. He'd lead me to different websites with resources that seemed to "fit" our family...and to different other homeschooling families to encourage us...i think one of the biggest peices of reassurement I heard was that we don't have to decide here at kindergarden if we are going to homeschool all the way through highschool. but rather, and probably better, to take it year by year, child by child to the Throne of Grace and ask for God's guidance....

Because I don't know what next year or 4 years from now may hold for Julia, or for Megan, or for Joey. I don't know if there may come a time that a public or private school may be exactly where they need to be for that year...but my good Father does know. He knows all circumstances, where their hearts will be, their strengths and weaknesses for each of those years for each child, He knows!! He knows the right curriculums for each subject for each child for each year, and has all the resources I need to teach His children. He is there, and as long as I remain open, as long as I remain honest within myself and submitted to Him in each step, I can't go wrong. I seriously can't go wrong!

So Busy Bees Montessorie school (where the girls went 2 hours a day twice a week last year) finally ended this last week. Joe would like to keep Megan in at the same schedule for next year, but since Julia is now 5, she has "graduated" and would either attend DoDs schools on base, A british Primary school, or be full time hometaught next year. As thier "school year" at Busy Bees grew to a close, my knees seemed to shake just a bit more...

so I have 6 weeks before school starts again and decided to try some "dry runs" to see how we'd do. I pulled out some "3-5 years preschooler" level workbooks i'd had for ages, blew the dust off and introduced them to the girls...don't you know they took to it like fish to water?!

THEY LOVE IT!

i have never been so surprised and proud and pleased and excited and relieved all at once!

So we do "school" everyday now. at my home! on my kitchen table, and we love it! In my pj's, in thier pj's, it doesn't matter! I let them work at thier own pace and we stop when one of us gets tired...(although it has yet to be them first! i usually am the one calling for break first lol!) Just yesterday Julia did 18 pages nonstop! and would have kept going if my eyes hadn't started to go crosseyed lol. We went out to dinner with joe and they wanted to bring the book with us, so I did, and they together did another 6 pages while we waited for our meal...

and I am just amazed at how easy it is..

and how much they love it,

and how capable they are already...

Next time i am out i need to pick up a "kindergarden/1st grade" book as Julia is just flying through this one.

and at the end of the day, the goal is being accomplished....They are becoming self learners, they are learning to LOVE learning and that is is fun and easy and school is something to look forward to, not to dread! and that's all I want to do...is teach them they can do it, teach them how to research when they have questions and that nothing is out of thier grasp or too difficult for them.

the nervousness has gone and peace has replaced it...and not just peace, but a true sense of excitement.

We're really doing this...! and i am really loving it.

Comments (3) Post A Comment! Permanent Link


July 16, 2007

Update on Julia and Joey's Doctors Appointments in Cambridge

 


Hey everyone! I originally typed this out into an email to my mother, so please excuse the typos and understand it was written for an audience of 1 at the time. *grins* ..this is the follow up for Julia's Pediactric Endocrinology appointment and Joey's Pediactric Neurology appointment, both at Addenbrooks hospital in Cambridge.~K

 

hi! i have been gone all morning. julia had her endrocrinologist appt today in cambridge. it went really well. a good friend came with us to stay with the children in the waiting room. another friend had mentioned to me that if i was concerned about Julia overhearing "concerns" about her growth and not wanting to worry Julia or anything, then to ask someone to come with us and when they were done with the examination to have Julia go into the waiting room while the doctor spoke with us. i was ALL for that!
 
When we got there they measured her standing height, as well as her height when sitting, from her rump to the top of her head. they also took her weight. asked us some basic questions, birth weight, full term, any delivery complications etc (4 lbs, 11 oz, yes full term, no complications normal birth) they also took my height, my birth weight, and joe's height as well. then we waited more in the waiting room (which was awesome. i totally wish i could transform my house into their waiting room! it was so kid friendly and had tons of activities for them to do. they didn't want to leave 2 hours later!!)
 
Finally the "Proffessor" called us back, took a look as Julia, went over the notes his nurse had taken, asked some of the same questions. we talked a lot about family history as well. he made an offhand comment about how nice it would be if we had information from the parents childhood, notes records..etc. i told him we had looked for them but couldn't find them, but i did show him the photograph you sent of me at 5 and Israel at 2 1/2 and how we were so close to the same size. he chuckled at it and said it was very helpful and thanked me for it. (SO glad you thought to send it!)
 
i thought it was very interesting how they did both her standing and sitting height to get a comparision on her total body proportion. we learned that her leg length is completely normal and that she "falls short" on her upper torso...the length from her head to her bottom is considerbly smaller on the chart. so he studied her spine, made sure there was no curvage to rule out short height by scoliosis. asked about her bowels to rule out diseases such as celiac disease (which is when you have trouble absorbing nutrients because your body lacks a certain chemical to break down certain things...basically gluten. it is fixed with a change in diet. but her bowels are fine so that is ruled out) asked about the tests they did for chromosomes and that had been ruled out as well as a thyriod levels or a growth hormone difienciency. so..all those things ruled out he wanted to order a xray of her back just to make sure her vertebre are growing as it should as that seems to be the area that is smaller than normal. he also wanted to repeat the bonescan on her hand for a bone age as their machines are a bit more hightech for such tests than the base's.
 
both joe and i felt a real peace with this doctor. he was very relaxed, yet doesn't want to just "Assume" that genetics is the answer. he said he is leaning towards that way and just wants to confirm it for us through a process of elimation on non-invasive tests. he doesn't believe we need to put Julia through the ringer,which SO relieved me. neither joe nor i wanted to do a whole swarm of tests on our little girl just to say, yep she's small like mom, like grandma, like her great aunts and second cousins and great grandmother..go figure! but at the same time there are little easy tests we CAN do to make sure we dont miss anything either. i feel so much more comfortiable with this guy than i did with the initial gal onbase. i dunno..maybe it is because she seems to have this sense of urgency, whereas he doesn't. he wants to be thorough, but only as much as what is truly needed...if there isn't a NEED, then let's not push it. (my sentiments EXACTLY!)
 
i did NOT realize though that the Brits do not push growth hormones for cosmetic reasons, whereas in the states they do! in the UK they only prescribe them when there is a TRUE natural deficiency from the Pituitary Gland and you are just giving the body what it is naturally lacking. joe and i completley agree with this. we want Julia's body to work as God would have intended in the Garden of Eden before Sin and sickness came and took it away...we DO NOT want to alter her system if it is working correctly, in order to try to cosmetically maintain her peers height when her peers parents are 5 1/2 and 6 foot tall and Julia's parents are 5 foot and 5 foot 9 inchs tall! (btw, they also asked what your height and what dad's height is, as well as Joe's parents height too...i loved that. i loved that they are considering all factors from both sides of the families)...It was just alarming to me that The States would deem cosmetic reasons as valid enough to push hormones on a child!  i cant remember the exact words he said, but something about "growth hormones becoming more readily used for cosmetic reasons in the USA, but they don't do that in the UK" my mouth dropped and i asked him to repeat himself since i was not aware of that, as though "short stature" is some dreaded disease needing a cure!!? then i laughed and said, "i'm rather insulted. i like being short!" this makes more sense though....why the doctor on base was so adamant about "seeing if Julia qualifies"...."qualifies"?? who uses a word like "qualifies" with growth hormones? "qualifies" like as for a car loan? *groans*
 
so... anyway, julia got "pictures" taken of her back and her hand today. 6 months from now we will return for check on her height both standing and sitting again to compare. he said at this age kids typically grow 5-6 centimeters per year. so in January if Julia grows around 2-3 centimeters then she is just normal healthy Julia and we needn't worry. If she hasn't grown any we will repeat the xrays to compare and possibly talk about doing a growth hormone test.
 
with this test they insert a small heplock like catheter thingy and draw out a bit of blood. then they will give her something which should make her own growth hormone in her body react. after abit of time they will take another sample of blood to see measure the growth hormone levels and compare to the first sample. it seemed like a similar test to the glucose screening they do in pregnancy, take your blood, make you drink something to make your own body react by secreting insulin..etc, take another sample of bkood to compare your sugar levels...except instead of measuring your glucose/insulin levels, they are measuring growth hormone production. IF this test showed julia's body is lacking in the growth hormone levels, they would do a subsequent MRI to take a screening of her Pituitary Gland, is it small in size? is it developed normal? is there anything i n her brain that is possibly keeping it from developing..etc? this would just be to confirm and access what has caused her body to not produce the needed hormone. IF she truly lacks growth hormone, it is a "simple" injection..once again, similar to insulin injections for the diabetic....BUT he doesn't think growth hormone is really something to be concerned about with her. he said typically in such cases there are other factors that contribute to a hormone defiencency and Julia doesn't exhibit any of those. She is anormal, healthy, active child. (really he only went into details about these test beucase joe and i kept questioning about "next steps"...we were very open with him that we do not want to be more invasive than what is necessary and we are NOT interested in doing growth hormones just to make a short person tall if there was no true defienciency. cosmetic reasons are not good enough for us. he completley agreed, i LOVED that this doctor is on the same page with us.) i truly feel at peace with him and that God has truly answered our prayers with this doctor. i know, whatever turns out in time, truth will come of it. that we aren't pressing for something that isn't truly there in hopes of some cure of the dreaded "disease" of short stature (God forbid! *rolls eyes*) and i truly feel at a peace that if we find "something" it will be because it needs true treatment, and if nothing is found abnormal in these beginning tests then we won't be pressing on with more invasive things that are not needed because obviously nothing is "wrong!"
  
anyway, i'll stop before i have to pull out my soapbox lol. so all in all it went very well. both joe and i feel a peace about seeing this Professor Hughes. He reminds me a bit of my old OB in the states..With enough experience to know when to not worry about things, he can sift through what is normal and what is really a red flag, and also have enough knowledge to not be arrogant or naive either. there is a balance between these which is so important. i dont want a doctor freaking out believing everything is an emergency of somesort or everything needs medication of some sort, but i also don't want a doctor too arrogant to look for things or research or check things out when it is needed either.
 
so that's the scoop on Julia. her next appt for a recheck on height and possibly another round of xrays is January 8th, 2008.
 
as for Joey's appointment with his Pediatric Neurologist last thursday, it went fine. he was deemed "completely healthy, active, infant boy". the nuero was fantastic. went over him with a fine toothed comb and listened well to us as we recounted his shaking spells..etc. She kind of said the same thing the ER doc and his pediatrician said, not quite sure what it was, but wasn't siezure related and he shows no red flags or signs for other neurological conditions. it was more reassuring coming from a specialist trained to easily pick out concerning symptoms in children and knowing that she found none in joey.
 
he is doing fantastic by the way. scooting and pulls up to crawling stance on knees and hands, rocks back and forth but doesn't know how to move his knees and balance his weight yet, so no crawling yet. and he got his second tooth this last Sunday at 7 months, 1 week old. he is following closely behind megan...she got her first tooth at 7 1/2 months if i remember right.
 
so anyway, that is our update! thanks for all your prayers on the doctors. i believe they have truly been answered. :)
 
Comments (2) Post A Comment! Permanent Link


June 14, 2007

Spring/Summer 2007 Update!


 

Spring/Summer 2007 Update!

 

Sorry this has taken so long to update! It seems to be increasingly harder for me to get a good block at the computer to sit, and think (and type!) Anyway, let’s see what all I can update you with while I can….

 

 ~Julia~

In October 2006 her pediatrician became concerned about her short stature and wanted to run a whole gamut of tests to rule out any chromosomal abnormalities (Including Turner’s Syndrome) and possiblky try to put her on growth hormones. As most of you know, I seriously bucked against this. I was 9 months pregnant at the time and have just grown tired in MY own 26 years of living of hearing “how small” I am (and how small Julia is in her 4 years of life) as though it is a disease needing a cure, or as though I am with holding food from my child resulting in her not growing to her “peers” (nevermind that mom is barely 5 foot tall and dad is 5 foot 10, and was a small child when he was growing up too!) Anyway….we recently went ahead with the blood tests and can officially say, guess what?! Julia is a normal healthy happy newly-turned-5-year old little girl! (This is where I slap my head and say “I told you SO!” but it does feel good to have medical science to back up what my intuition was telling me all along)

Her growth hormone levels are normal, No turner’s syndrome or any other chromosomal abnormalities, her thyroid is normal, all of her “levels” are NORMAL! But still..if you can believe this, the doc put in a referral to send her to an off base endocrinologist to see “if she qualifies” for growth hormones….I truly don’t understand why this doc thinks being short is such a terrible thing. The projection of Julia’s height from now until she us 18 puts her at 5 foot tall, surprise, just like me! So I really don’t understand all the “concern” of that being “avoidable if possible”…at any rate Joe and I have decided to go speak to this endocrinologist just to get a specialist take on it. The way we see it is this, Julia does not need growth hormones. God made her this way for a special reason and who are we to try to “fix” it as though it is a mistake? But it will feel nice to have a specialist say “you know, she is just small like her mom” so anyone else that says “MY! She is so small!” can just plant a nice big smackeroo on the back of my knee…no really, we’ll be polite. We are both interested in what they may have to say….we just have no desire whatsoever to put our child on medication simply because it is optional and not seriously needed for the wellbeing of her overall health.... and HELLO?! Genetics anyone??

Otherwise Julia is doing fantastic! She recently had her 5 year well baby check up and is 36 inches tall and weighs 27 pounds. She is wearing size 3T to 4T shirts and 2T pants. She plays imaginary games with her sister and bounces around the house constantly. The “why?” game has started (oh yippie) and her writing is continuing. She is so involved in discovering her world and trying to make sense of it. She can not take anything just as it is…she continues to question the” why, how, when, where” aspects of everything! A simple discovery to the joy of Earthworms can easily lead to a weeks worth of study and materials pulled off the internet (I love homeschooling! Really all it is, is indulging my child’s natural curiosity and encouraging her desire to learn myself, and not leaving it to an outside influence! *grins*) not to mention the rest of that night alone was spent, you guessed it, pure earthworm talk! Lol! She has also become very interested in the way things grow. I have 3 anonymous seeds that she randomly found on the ground sitting in a cup of water on the table lol!

 

~Megan~

She is doing very well! She will be 4 years old in just a couple weeks! I can’t believe it! She has really been developing in the artistic area. She is our little diva. She sings songs she makes up, hums while twirling in the mirror, and loves imaginary play with dolls, cars, and stuffed animals.

(Here she is with her friend Aidan. I have no idea what pose she is doing lol. Isn't he so cute?! His mom took this picture and she said when he saw it he said, "Look mom! There's my gurlfriend"...look at his expression, it's just too cute. They are church buddies and can occaionsally be spotteed holding hands inbetween playing with dinosaures and matchbox cars.)

For her birthday we have a wooden dollhouse to give her to encourage her natural love of pretend play and mimicking family. She also is really loving books right now. I lose count to how many books she has me read to her a day. (and you know I really don’t mind! I LOVE that she is enjoying reading so much and pray this instills a love of books in her) Her favorite “character” right now is Maisy Mouse. We have ordered a few Maisy books for her and hope to make a Maisy cake for her birthday.

Her party will be on her actual birthday of July 2nd and we’re doing an “art” themed party like we did for Julia’s second birthday. With Megan’s natural artsy-fartsy mind this suits her perfectly. Julia is very analytical. She explores to make sense of her world. (for instance she loves writing people’s names and making pretend mail to send. She can write her name, “mom” “dad” and “Megan”) Megan just celebrates life in general. Her art constantly amazes me because of how her brain works. Last week she drew a “chinchilla” for me!!!! It even looks like one lol! Cat? Dog? Those I expect, but a CHINCHILLA?!

The next day she found my bingo stamper and made me a page “full of balloons.”

Her creativity is just abounding! 3 weeks ago I bought them some toddler scissors to work on their fine motor coordination and also because I just knew they’d love cutting things. Two days later I had TONS of random pieces of construction paper littering my house, so they made their first collage. It is hanging in their play room now. They loved it and are currently cutting more paper for another one! (*mental note, mommy needs more glue!*)

I will post pictures of her birthday when it comes!

 

~Joey~

He is growing like crazy! At his 6 month check he weighed 15 ½ pounds and is 26 inches long. He smiles, coos, giggles, squeals, babbles “dada, mama, gaga, blah blah” and everything in between…he is sitting 5-10 minutes unsupported and is a scooting madman! He is officially mobile…nothing in my house is safe and I am really having to step up on vacuuming lol. He constantly explores. Where Julia inspects her world (my future scientist?) and Megan celebrates life (our artist), so far Joey must conquer….explore and conquer, explore and conquer! We’ve had to be careful not to drop him on several occasions as he will push himself completely out of your arms just to face outward. His hands are constantly out reaching, grasping, and pulling. Everything is in his mouth! He is the most adorable little caterpillar, inching his way across our living room! He started on baby foods around 5 months old and is now on oatmeal with a fruit or veggie twice a day. His sleeping is getting better. No longer is he up every 1-2 hours a night, but a more consistent 3 hours. No teeth yet, although he has had several bouts of teething pain. Those first ones are always the hardest the get in, it seems.

He did have a bout of shaking spells around 5 months of age that scared us for abit. We now know they were not seizures, but perhaps something along the lines called “shuddering”. Shuddering has no found cause, seems very common in baby’s 4-6 months old, happens as they are falling asleep or upon waking, needs no medication, does no apparent physical harm, and seems to be something the babies outgrow. It is also more common in breastfed infants. Two “spells” happened while he was nursing where his arm, then his head, then his whole upper body began to rhythmically shake for about 5-6 seconds (although it felt much longer!) I called his name and held his arm still against my chest and the shaking subsided. He then curled his body around me and nursed vigorously for a few more seconds, then finished eating and went to sleep as usual. He woke up fine. No fever. No nothing. He was seen by the ER and had a follow-up appointment at the peds office. Everyone has the same ruling “pretty sure it is not seizure activity, although we’re not too sure what it was.” He has an appointment for July 5th to be seen by a pediatric neurologist in Cambridge. He only had those two episodes and hasn’t had any sense then. I am not worried, more curious than anything about what the specialist will say. With all the online research I have done, I am content with the Shuddering possibility as it best describes what I witnessed as in the type of shaking he had…I don’t think it was a seizure either.

(Sleeping with my baby blanket handmade by my grandmother 27 years ago!)

Other news on the home front:

Britain is FINALLY warming. Seems June/July is the time frame to finally break out the shorts and leave the jackets at home. The kids and I have truly been enjoying getting outside more and see some sun for a change! Two weeks ago we took a small cartrip to Petite’s Animal and Adventure park…basically a very small amusement park designed for toddlers to have rides their own size! The kids had a blast and I have a few pictures to include here:

 (Daddy with his girls)

("Look Ma! I can drive!")

("Choo! Choo!" Julia and Megan ride the train)

(Dumbo has nothing on us! Wave Megan!!)

Our new van should be here in the next two weeks. Feels like we have been waiting and waiting and waiting. We keep putting off any further road trips until we can drive a more dependable vehicle. All is well anyway as we are trying to save as much as possible for a small visit back to Oklahoma. I miss my family and friends. I miss good AMERICAN food, I miss paying for things in dollars and not pounds and pence. I just miss home. Flying commercial would cost near 4 grand which we do not have, so right now we are checking out taking military hops, then renting a car and driving down. We’d probably stay 1 week to ten days with no other plans than to eat, eat, eat and visit the people we’ve missed so much the last 2 ½ years. Right now more than anything we are waiting on Joey’s passport. It will take 2 months to come in, and his Visa requires a trip to London and 500 pounds (equals 1000.00 American dollars...it is reimbursable, but none the less that is quite a chunk of cash!)…so we need time to get the passport/visa in and money to do it all. It will probably be this fall before we’ll be able to come…so just be praying everything comes together and it is a safe, unstressful trip.  Well, that’s all I have for now.

 (Are you SURE that's it mom?...)

I’ll just post a few extra pictures and check back later when we have an appt date for Julia’s Endocrinologist and after Joey’s neuro appt.

 (....Nope, just one more pic! Megan giving Joey kisses, of course)

 

Comments (2) Post A Comment! Permanent Link


April 11, 2007

Our trip to visit Orford Castle

Well, as promised on my other blog, Here is our trip to Orford Castle we took about 3 weeks ago.

Orford Castle sits on the furthest eastern coast of England. It has two marble spiral staircases (flashbacks of Pisa kept hounding me lol) and was built in 1165 AD. It remains in excellent condition to this day! Here are the girls exploring the castle canons on the grounds outside:

It was a really beauitful day, although very windy which made it feel colder than it was. The Castle overlooks the north sea, so wind off the water chilled everything quite a bit. This picture is of the girls and I walking up the steps to the front door. For those that have wondered, this is how i look with 3 kiddos lol. I had Joey tucked inside my coat in a ababy carrier so I could at least have my hands free to help the girls up...the steps went up pretty high before you were inside and they were worn and chipped in some places.

 

Inside the castle they had a giant illustrated book of how it would have looked in it's prime day, and how life was lived. it was very interesting, although I had to watch the girls closely as they almost managed to tear the pages several times. This page is showing the different ways people may have tried to overtake the great castle walls and you can see megan doing her usual "song and dance vanna routine" lol. she gets so excited. it is so funny to watch!

Here is what used to be the Chapel of the Castle. this room was very interesting. they had a place for a "Sink", a few cubby nooks in the stones served as storage for goblets or other things they may have used at that time. Here are the girls and i sitting upon the "alter"...i know, this is probably so wrong, but i couldn't help the picture opportunity lol! I told the girls to pretend they were drinking from the goblets. I can't help but think that Julia is looking at megan thinkinkg, "NOT in the mouth megan! eeeeew!" okay, maybe that is just what I was thinking lol.

And here is a modern day picture of the town of Orford itself. The church was also built around the same time.  It was a cute little village. not much parking though...but alot of walking potential lol.

So that was our lasttest castle adventure! Joe and I want to take a trip to see Warwick Castle and that will probably be our last one. I think this had been the 5th or 6th castle we've seen and they are starting to all "look the same." Warwick is a 3 hour drive from us one way though, so that will be saved for when our more dependable vehical arrrives. Until then, here is an awesome site and history about Orford Castle! it has some great photographs and illustrations of how it would have looked in it's prime and with it's curtain wall! 
Comments (2) Post A Comment! Permanent Link


April 11, 2007

Kitty, I mean erm, Julia Learns a new lesson

Poor baby! I am referring to both Julia, and her little cat. An orange stuffed tabby that her Aunt Terra gave her 2 years ago. This kitty has been everywhere with us. Even to Spain when we went in '05. Well tonight was a lesson in "tough love", for both kitty and Julia.

 

Joe and I were in the living room last night and Julia comes running in in hysterics. Big fat tears running down her face and talking so fast we couldn't understand her 4 year old words. She just kept saying, "kitty hurt! by the fire! Kitty hurt!" of course, the word "Fire" sent both Joe and I running, asking Julia (much like we would Lassie) "where's the fire, girl?" She takes us to the candle i had burning by the sink in the bathroom, then tearfully points at kitty's now burnt nose. Apparantly Julia was "showing" her kitty the fire and letting kitty smell the pretty scent of the candle, and 2 whiskers and part of kitty's nose got singed.

It was a hard lesson to learn. Julia kept asking for us to "make it white again" and hugging kitty with a death grip. she was still crying profusely...she really really REALLY felt her kitty was hurting and  in pain and was so upset she had put her cat through it. it broke my little mommy-heart!! Me being emotionally based wanted to immediatly put her out of that emotional pain and let her know that kitty was not in any pain. Joe, (the logical thinker of the family and who is gifted seeing the bigger picture than just things at hand) gave me the "look" to let him go first and began reafiirming exactly what happened to kitty, why the fire did as it did, and why it is so important to treat it respectfully. It was a hard balance of a lesson to teach, this is why fire is so dangerous, yet kitty is absolutly fine, but don't you do it because you wouldn't be fine, but yes kitty isn't in pain, but you would be if you did it....not in such words, but you know, it was hard not to be contradictory.  

 

After the little talk Julia and I put a band aid over kittys "owie" singed brown nose, and then spent another 10 minutes talking in depth about scars and how they don't hurt, but they serve as reminders. poor Julia. it was a hard lesson for her to learn...and let me tell you, she has been babying that kitty just as much as i would had one of my own real baby's been injured. She is such a compassionate child.

Comments (0) Post A Comment! Permanent Link


About Me

A friendly blog from a humble heart of a young Christian mom whom refuses to be invunerable. My greatest fear in life would be to look back and see hurting souls whom might have reached out if they'd only known they weren't the only ones suffering. Here are my struggles and my joys, plain and simple. No false fronts, no brave faces, just a common ragamuffin human being learning more and more of the Savior whom sees through the mud and still loves. How else can He be shown as Great, without me being shown as weak? ..."It is not I, but Christ through me..."

On our hearts

• Please click here to read our friend Emily's story as she fights cancer

• Praying for Molly's 2 year old son Israel as he fights the rare Kawasaki Disease

Music Pick

• Nothing but the Blood
Jadon Lavik

Links

Home
View my profile
Archives
2006
March 2006
February 2006
January 2006

2005
December 2005
Email Me
Our Flickr Site
Our Homepage
My Blog's RSS
My pregnancy Journal: "TinyToes"

Friends

DMalament

deedeeuk
dogalways524
thegirls

christywhisty
tinytoes

Barbara Curtis
Choosing Home
Joe's MySpace
The Falling Star
Bible Gateway
Page 1 of 9
Last Page | Next Page