Monday, June 2, 2014

Freiberg's Infraction

Yet another word that I learned today that I would not have cared if I had never learned it...ever!

Camille has had some pretty bad toe pain since at least December.  We saw our pediatrician about it once and talked to physical therapist about it while in treatment.  Both said that there is nothing to do for a broken or stubbed toe and to just wait it out and the pain should go away...  Well, several months later, the pain is still there and often worse than the week before.

I made another appointment to see our pediatrician last week and saw the Physicians Assistant there that we love.  She said that this has lasted long enough that it suggested an x-ray.  X-ray was taken Thursday and Friday morning they called and said they had already set up and appointment with a specialist.  When I asked if it was broken she said "Well, no, but there is something there that definitely needs attention from a podiatrist.  We got you an appointment for Monday morning"  YIKES!  That was quick is it serious?  And then she sprung the new word on me that I researched this weekend.  

Freiberg's Infraction.


We went and saw Dr. Hewitt this morning and he stated that this is a common issue found in dancers, which Camille is not.  Its also more found in females between the ages of 12 and 14, but its apparently rare enough that people often don't find it until its to late.  As a matter of fact, the x-ray was read as "normal" at the hospital, it was only when the specialist peeked at it they found the Freiberg disease. Camille's issue was advanced enough that she needed treatment, or if left untreated, she would need surgery in 2 - 3 years..  SOOOOOOO


Camille is starting the summer out like no 12 year old pre-teen wants to.  With a "medical boot" that she has to wear for at least the next six weeks... No activity, no pressure on the foot, no skating, no jumping on trampoline, no SWIMMING??!!!!! (can only sit on pool edge or in water but no bouncing or swimming)  Bummer Camille... but it beats the alternative of surgery in a few years.  Chin up girly, at least we can decorate it with colorful stickers or something ;)


Sunday, April 27, 2014

Wake Up Mom!

6:15am:        I have something dropped on my pillow right beside my head...startled I jump up to see what it is and it's Isaac with his iPad.  Then I hear the iPad say "WAKE UP MOM!".... he really is getting it, I am so elated that we are getting this kind of communication.  Best.Day.Ever!!!

Thursday, April 24, 2014

S-l-o-w progress.... but PROGRESS is happening with the iPad

Our family has been blessed beyond words with help getting both boys an iPad for communication purposes. Being a larger family that always seems to have something "pop up" that uses unbudgeted money and yet still trying to find that "extra money" to purchase two iPads was not something that was about to happen easily or quickly. We were thankful that the Lord provided for us in other ways.

Caleb received his iPad from his shopping spree via Make A Wish and Isaac was awarded one through an amazing organization called Shane and Wyatt Down Syndrome Foundation.  This foundation makes it a point to provide iPads to children with Down Syndrome who are having severe communication issues.  Isaac was chosen as their first recipient, how cool is that!?  You can click here to read our blog post about receiving it.



Caleb and Isaac have now had the iPads now for a little better than two years.  I must admit I have been getting discouraged with their progress using it.  I just KNEW it was going to be our answer to better communication with the twins. They are both whizzes navigating the iPhone for apps and games and YouTube videos they want to watch.  They really are impressive!  We have chosen to use the Proloquo2Go app to try to facilitate conversation.   I had high hopes reading reviews of the software that this is the right match for the twins to use.  After downloading it and going through kindergarten with it I began to have doubts that we, the family, and the school were properly trained to teach the boys to use it.  For the past two school years the iPads have just stayed at the school each and every day and during the summer months the iPad was sent home for us to use with them.  Honestly, we didn't know how to use them.  We didn't know how the school had been using them, so how were we to replicate that and keep the boys active with it?  It didn't happen.  I was frustrated, mostly with myself for not knowing how to use them to help my boys.



We started this school year with a few tweeks to the IEP in hopes for the iPad to be our answer again for communicating with the twins.  About 3/4th the school year has passed and I still am not seeing or feeling the iPads are 100% properly being utilized.  Not that the school isn't trying with them, just that I was expecting and hoping for m-o-r-e.  So about two weeks ago I sent a letter to the teacher requesting that the iPads be sent home with them each day after school.  One concern with this is the possibility of breaking it in transit.... that would be bad!  Another concern is that we would use them differently at home than the school uses them there and perhaps confuse the boys.   The only way to find out how to use the iPad was to take the plunge and request it be brought home and use them.

This past week I have seen two different instances that are worth sharing and to get excited about.  Easter weekend was a great time to give them some alone iPad time.  Just to hammer out buttons and let them explore the different folders and talking options.  To be honest they like to push the same button over and over and over and over and over and over....get my point?  Then they laugh hysterically when they push the talk button and the iPad says the same word 25 times in a row.  Its quite comical to watch them.  BUT in doing this they are navigating their way through the program and finding new funny words to repeat over and over and over and over again. This is learning the device in my opinion, so we let them do it.  At school they really refrain from allowing them to push the button more than once as it really is a time waster and a distraction to the rest of the classroom, so this was fun for them.

Saturday afternoon Isaac was browsing around different subject and pushing random buttons all over the place.  Not really making any sense of anything but just having fun saying different words... THEN, he found the dessert button.  He pushed dessert 20 times and out of no where formed a complete sentence.  "I want ice cream sandwich dessert.... and signed Please!!!" Whaaat??  He had the biggest smile on his face and brought the iPad directly to me and said the sentence again.  "I want ice cream sandwich dessert...and signed Please".  You better believe we ran right into town to get that boy an ice cream sandwich and he was very happy that he was clearly understood with what he wanted.

Then last night we gave him his nighttime meds to make him sleepy and  gave him his iPad to pass some time and hopefully learn more of the folders and words within them.  I can already tell he is very smoothly getting around and realizing where to push to talk about family stuff or school stuff or feelings or food.. This is VERY EXCITING to watch.. THEN after about 20 minutes of playing around he found the feelings folder.  He pushed "tired" and "sleep" buttons.  He looked at me and signed sleep, put down the iPad and laid down for bedtime.... What??!!!! This may seem like a tiny progress note but to me its a big big step.

Looking back over the past eight years I can honestly say I have been discouraged with a lot of things. Thinking that this might not happen or that might not happen.  Perhaps feeling like we should give up trying a certain thing with the boys only to find when we are about at the end of our ropes trying desperately to make it work something they "get it".  It took us signing words to them for almost 10 months before we got one sign back from them.  The first word signed back to us was Cracker.. Caleb wanted a cracker.  When that happened we were all so thrilled and emotional.  Now that I am seeing some actual progress with the iPad I am having the very same emotions.  They are GETTING IT.... They are GETTING IT!!!!

By far the hardest thing about parenting children with special needs is for me to be patient and allow Caleb and Isaac to do their thing when "they" are ready, not when "I" am ready or when I know the other kids have done something by time wise.


I'm not giving up on you boys!!! Mama wants to talk with you and get to know even more than I already do.

Thursday, March 20, 2014

Being a parent... to kids with Down Syndrome

Tomorrow, March 21st, is World Down Syndrome Day.  The reason behind this particular date is that individuals with Down Syndrome have 3 - 21'st chromosomes.  Thus 3/21 has be designated World Down Syndrome day in their honor and to spread awareness of this disability.  Over the past eight years I have learned a whole lot about Down Syndrome (DS), not only by living with it in my identical twin boys both with DS but from online research, meeting other families and reading several books on the topic.  I would consider myself very knowledgeable but certainly still in the learning stages.

I remember when my husband and I were informed that baby B, Caleb, was confirmed to have Down Syndrome.  I was more afraid of not knowing what to do with him than I was about having a child with something wrong with him.  Long story short, twins came 9 weeks prematurely, one at 3# 3 oz and other at 2# 10oz.  We had no idea that they had DS.  Baby A (Isaac) was reason for emergency c-section as he was literally born with head trauma from being stuck in my ribs.  Due to this head trauma they were not able to identify DS in him but saw features right away in Caleb and took some blood to confirm.  I was told that having twins both with DS was very unlikely and certainly very uncommon so they would wait until Isaac (2#10oz) was bigger to draw blood to test for DS.  Two weeks later Isaac developed NEC and was taken to Children's Hospital in Pittsburgh to have surgery on his small intestine, at which time they removed enough blood to confirm that he did indeed also have DS.  In our opinion, as mom and dad, we were grateful that both boys had it versus one with and one without.



Down Syndrome is most certainly scary to brand new parents. Down Syndrome is most certainly scary to experienced parents who have children growing up into adults.  Down Syndrome is most certainly scary to think to far ahead in the future about.  Down Syndrome shapes and molds a families lifestyle differently than those without a family member with Down Syndrome.  Down Syndrome is filled with uncertainties, no doubt.




BUT.... I am going to removed the words Down Syndrome from the above statements and fill it in with the word Parenting:

Parenting is most certainly scary to brand new parents.  Parenting is most certainly scary to experienced parents who have children growing up into adults.  Parenting is most certainly scary when you think to far ahead into the future.  Parenting shapes and molds families lifestyles differently than those who have no children. Parenting is filled with  uncertainties, no doubt.




Looking back on the past eight years am I going to say that raising children with Down Syndrome is as easy as raising children without... NO WAY (I have three typical children)!!! Would I say that raising children with Down Syndrome feels fair all the time... NO WAY.  Honestly, I selfishly get sad and down sometimes when I see other families who can just pick up and go to the drive in movie theater or have fun together at an amusement park, or even just go for a walk in the woods together.  Things like going to a ball game or swimming pool are just easy fun things to do.  But my circumstances are different than those raising children with just Down Syndrome.  My twins are non-verbal and also have Autism.  Autism is a whole different story that I won't go into on this post.




What can I say that I have learned the most about raising children with Down Syndrome?  I have learned that I was (and still am in many ways) very selfish.  I did what I wanted when I wanted with my other children and I cannot do that with my twins.  I have learned that unconditional love trumps selfishness.  I have learned that people with Down Syndrome just want the same thing that you and I want.... someone to LOVE them and NOT GIVE UP on them.  I have learned that the saying "Children with Special Needs does not take a special family to raise them, it MAKES a special family" is so very true in more ways than I can mention.  I have learned that people with Down Syndrome are beautiful people who just want others to take a minute to see them for who they are and accept that they are a little different but amazing in their own way. I have learned that I will never stop learning what I means to put others needs in front of your own.  The Lord works in mysterious and wonderful ways when it comes to something one might consider a trial in life, only to come to realize that it is in fact a blessing!!

My three older children have learned a valuable lesson that I can honestly say I did not know as a youngster. My boys have opened all of our eyes to sympathy, empathy and compassion.  These boys have changed my world and might I say for the better.  I pray that what I've explained here today does not make it seem as though raising my children is a burden but in reality a true blessing.   Some days are easy, some days are hard... but WAIT, isn't that the same thing I could say about my three older children without Down Syndrome?  You betcha.



When people say to me "I don't know how do you do what you do?", I can simply just say in love and truth, because they are my beautiful children and you would certainly do the same if they were yours.  Down Syndrome is not something that scares me, people who don't take the time to understand and enjoy people with Down Syndrome does.  Through all its ups and downs, parenting a child with Down Syndrome is a gift and I find it a privilege to be Caleb and Isaac's mom.

Happy World Down Syndrome Day 2014!


Thursday, February 27, 2014

Throw Back Thursday - taking my blog back!!!!!!!!!!



Today as I searched Google for something Down Syndrome related I came across these beautiful twin boys when I searched images.  These are MY beautiful twin boys!!!  As I stared at this photo I became so sad that I have let my blog go.  The idea of sharing their beautiful faces and personalities with the world to perhaps create a sense of awareness and acceptance has been swept under the proverbial carpet.  Life has gotten in the way.

I am NOT the same person or even mom as I was 8 months ago when I last blogged.  So much has changed and yet so much has stayed the same.  Its time I start cracking my knuckles and diving back into my blog.

See ya soon!!!

Monday, August 5, 2013

Its' been a Simple Blackberry Jam Kinda Day

I have been gone from blogging for quite some time now.  My days have been so busy, heck my life has been so busy.  About a month ago I really felt that God has put something so strongly on my heart that I could not deny it any longer.  He led me to a decision that I had been putting of for a few years but could not bring myself to do.  I resigned from a job that I truly loved working as the Executive Director of our local Arc chapter.  I enjoyed getting to know so many people and gaining a better understanding of the needs in our community for people with disabilities.

What I came to realize was that I had a very important need in my own household.  Raising five children and trying to keep it all together is not something that one can do lightly, I WAS NEEDED!!  I was needed to stay home and be the best mom and wife that I could possibly be.  And thus I begin the stay at home mom routine again.  The income loss will hurt but I have faith that God has a better plan for us and He will see us through.  Already I have had more time to tend to my garden and keep the weeds from overtaking everything like it usually does by this time of year.  Already I am working hard with the kiddos to simplify things in our home.  I have said several times, I don't know if I'm losing my mind or if I'm getting smarter, but we currently have NO FURNITURE in our living room... thats right!! We have a rickety ole glider rocker that I bought when I got pregnant with Tristin (16 years ago) and an Amish wooden rocker that is not the most comfortable to sit in for a long period of time.  So a rocker for mama and a rocker for dada.  The kids can sit on the floor....and they do!!  The kids had spilled things on the furniture, jumped on it until fabric was torn, the twins had pee'd on it a few times and the odor would not fade, the dog used it more than I did and I just plum got tired of having something like that in my house... so I paid someone to come and haul it away to burn.  Honestly, felt great!!!

We are downsizing the bazillion pieces of clothing that my children have, and don't take care of.  I will wash laundry only to have them throw it on their floor and declare it dirty again and end up back in the wash before its even worn... no more!  What does not end up in the dresser goes away in some fashion or another.

Yesterday my darling husband informed me that the blackberries were ripe and huge.  He spent about an hour or so pickin for me last night.




 I didn't want to see that beautiful harvest end up as just a snack so today I took some time and made some blackberry jam.  I have made strawberry jam, I have made blueberry jam, I have made peach jam, I have even made tomato jam, but never have I had a chance to make blackberry jam... I have to boast and let you know it turned out delicious!!! Can't wait to spread it out on pancakes or eat it ontop of ice cream and enjoy it for breakfast ontop of my toast.. YUM!!



So as I start my new journey of being a stay at home mom again, I see wonderful things in my future.  I see canning, I see baking, I see crafting, I see home improvements, I see landscaping.... BOY oh BOY I guess I really was needed right here ;)

Recipe for blackberry jam:

9 cups of fresh blackberries
5 cups of sugar
1 1/2 cups of apple juice
1 box pectin

mash blackberries, add apple juice and bring to a boil adding sugar slowly.  When boiling add package of pectin and boil until thickened.  HELPFUL HINT: I always take a spoonful out and set it on some ice cubes for a minute to see if its the thickness I desire when finished.  Ladle into jelly jars, top with sterilized lid and hot pack for 10 minutes.  This recipe makes about 9 jelly jars full, with a little extra to enjoy ASAP!!

Wednesday, July 24, 2013

Elijah hits double digits


10 Years!! 10 Years Old!!!  

My first born boy, Elijah, has hit double digits   His beautiful brown eyes still melt my heart every single day and his personality keeps me on my toes from day to day.  Some days he's a comedian, some days he's an inventor, some days he tries to see who he can irritate the most, some days he's a big ole snuggle bug.  Elijah has really grown this year and he sure loves to play baseball.  His birthday present is, of course, a ball game with dad and papa on Friday.  They are going to State College Spikes because 1. its a ball game and 2. Mountain Man from Duck Dynasty will be there and that's equally exciting for the guys ;)

Love Ya Buddy!!!  Enjoy #10 and looking forward to seeing what the next 10 years bring!!