1/15/18

Staying Strong After The Devastating Diagnosis.....

March 25, 2015 we were told that our sweet newborn baby who was only 5 days old had a terminal diagnosis. The world stopped, the tears were uncountable, you could hear our hearts breaking. How long did we have with her, how would we tell her sister, what will our lives be like, will she ever leave the hospital, how can we do this, and will we make the right decisions. These are all the things plus a million more that went through our minds as the Drs. enter the room with so much unknown information. Emma is pretty rare (1 in 100,000) there are not many Drs. that know about her diagnosis. Reading the info given to us from 1995 (she was born in 2015) was so limited and heartbreaking at the same time. What was Emma's life going to be like, will she even have one. We were told to take her home and love her because she might not be with us very long.

When I look back on diagnosis day I think about how uneducated every one in that room was. We all thought (including Drs) that Emma would just be a vegetable from the information that was given to us. What we didn't think about was all the unknowns, no one knows everything and definitely no one can write someone else's story. Only Emma can write her own story.

I know that nothing can take away the pain from your child receiving a terminal diagnosis like lissencephaly. But these quotes help me everyday to refocus when I am down. I wanted to share them in hopes I can help someone else who is struggling with the heartbreak of your child receiving a devastating diagnosis. Please help us to reach others by sharing this blog post, sharing Emma's facebook page and/or instagram page.
Facebook: https://www.facebook.com/Embracelifeemma/
Instagram: embrace_life_emma


Staying positive and strong after such a heartbreaking diagnosis, like lissencephaly is very hard. Here are some inspirational quotes and stories that have helped me to see our life in a different light. We are blessed that we were given Emma and we will never see it as sadness or a pity party. Yes, we are sad she has to go through what she does but we will never be sad she was given to us.


I always worried they wouldn't have a connection and boy was I wrong. Ava is an incredible person because of Emma and we are so thankful for that.
Emma had a rough year last year and I never thought she would regain her strength but slowly she is and I felt so helpless. But again she is showing us she will Defy the odds the best that she can.

She is a fighter all of our children are.......

It's ok to cry and it's ok to be sad but wake up everyday smarter and stronger than yesterday. As the job of a special needs parent is not an easy one. 

Emma is the best tour guide ever!

I never thought I could care for a child with special needs....I wasn't strong enough but Emma gave me that strength

Our family has grown and learned so much over the last 2 (almost 3) years


Creating awareness for Lissencephaly in hopes we can help other families that find themselves in our same position

yes this is hard but we have gained more than what has been taken away from us

Everyday we learn something new and we have to find a "new normal" to fit with our new situations. Embrace the change and learn it will happen more than you think. Finding "new normals" is actually what becomes normal.

LOVE THIS

New Normals are okay 

It's ok to be sad.......

Emma's life is unknown...really all of our lives are unknown. So let's not worry about the end of the staircase and just enjoy every step of the way. Embrace it, and cherish it!

Breathe

We were told Emma would never smile, laugh or show any emotion but as you can see from the pictures on this blog she made that miracle happen. So we believe in Miracles, life is a miracle

To: Ava
Love: Emma
Here are two more short stories that I love to read from time to time.......

Welcome To Holland
By: Emily Perl Kingsley
I am often asked to describe the experience of raising a child with a disability – to try to help people who have not shared that unique experience to understand it, to imagine how it would feel. It’s like this…
When you’re going to have a baby, it’s like planning a fabulous vacation trip – to Italy. You buy a bunch of guidebooks and make wonderful plans. The Coliseum. The Michelangelo David. The gondolas in Venice. You may learn some handy phrases in Italian. It’s all very exciting.
After months of eager anticipation, the day finally arrives. You pack your bags and off you go. Several hours later, the plane lands. The stewardess comes in and says, “Welcome to Holland.” “Holland?!?” you say. “What do you mean Holland?? I signed up for Italy! I’m supposed to be in Italy. All my life I’ve dreamed of going to Italy.”
But there’s been a change in the flight plan. They’ve landed in Holland and there you must stay. The important thing is they haven’t taken you to a horrible, disgusting, filthy place full of pestilence, famine and disease. It’s just a different place.
So you must go out and buy new guidebooks. And you must learn a whole new language. And you will meet a whole new group of people you never would have met. It’s just a different place. It’s slower-paced than Italy, less flashy than Italy. But after you’ve been there for a while and you catch your breath, you look around…and you begin to notice Holland has windmills…and Holland has tulips. Holland even has Rembrandts.
But everyone you know is busy coming and going from Italy…and they’re all bragging about what a wonderful time they had there. And for the rest of your life, you will say, “Yes, that’s where I was supposed to go. That’s what I had planned.”
And the pain of that will never, ever, ever, ever go away…because the loss of that dream is a very, very significant loss.
But…if you spend your life mourning the fact that you didn’t get to go to Italy, you may never be free to enjoy the very special, the very lovely things…about Holland.


The Brave Little Soul
"Not too long ago in Heaven there was a little soul who took wonder in observing the world. She especially enjoyed the love she saw there and often expressed this joy with God. One day however the little soul was sad, for on this day she saw suffering in the world. She approached God and sadly asked "Why do bad things happen; why is there suffering in the world?" God paused for a moment and replied, "Little soul, do not be sad, for the suffering you see, unlocks the love in people's hearts." The little soul was confused. "What do you mean?" She asked. God replied, "Have you not noticed the goodness and love that is the offspring of that suffering? Look at how people come together, drop their differences and they become motivated by love alone."
The little soul began to understand and listened attentively as God continued. "The suffering soul unlocks the love in people's hearts much like the sun and rain unlock the flower within the seed. I created everyone with endless love in their heart, but unfortunately most people keep it locked up and hardly share it with anyone. They are afraid to let their love shine freely, because they are afraid of being hurt. But a suffering soul unlocks that love. I tell you this- it is the greatest miracle of all. Many souls have bravely chosen to go into the world and suffer- to unlock this love- to create this miracle for the good of all humanity."
Just then the little soul got a wonderful idea and could hardly contain herself. With her wings fluttering, bouncing up and down, the little soul excitedly replied, "I am brave; let me go! I would like to go into the world and suffer so that I can unlock the goodness and love in people's harts! I want to create that miracle!"
God smiled and said, "You are a brave soul I know, and thus I will grant your request. But even though you are very brave you will not be able to do this alone. I have known since the beginning of time that you would ask for this and so I have carefully selected many souls to care for you on your journey. Those souls will help you create your miracle; however they will also share in your suffering. Two of these souls are most special and will care for you, help you and suffer along with you, far beyond the others. They have already chosen a name for you."
God and the brave soul shared a smile, and then embraced. In parting, God said, "Do not forget little soul that I will be with you always. Although you have agreed to bear the pain, you will do so through my strength. And if the time should come when you feel that you have suffered enough, just say the word, think the thought, and you will be healed."
Thus at that moment the brave soul was born into the world, and through his suffering and God's strength, she unlocked the goodness and love in people's hearts. For so many people dropped their differences and come together to show their love. Priorities became properly aligned. People gave from their hearts. Those that were always too busy found time. Many began new spiritual journeys, and some regained lost faith- many came back to God. Parents hugged their children tighter. Friends and family grew closer. Old friends got together and new friendships were made. Distant family reunited, and every family spent more time together. Everyone prayed. Peace and love reigned. Lives changed forever. It was good. The world was a better place.
The miracle had happened.
God was pleased."
–by John Alessi



EMBRACE LIFE

1/8/18

2017 = Decisions, Heartache, Seizures, and..........

Feeling Blessed?????

As I reflect on the last year my heart hurts from all the decisions we have had to make for Emma. Some wrong, some right and some that we will NEVER think about again. Decisions from medications, treatment options, diets, doctors, equipment, and seizures. But with all of the decisions and heartache, between thousands of seizures, we feel blessed. 

Blessed??? you ask how can you feel blessed, you are watching your daughter suffer through multiple seizures a day, watching medications and treatments not work, and you are constantly tired. Well I would have to say yes to all those things, but here are some other things you may not see that help us to see our blessings......

*Teamwork between two parents who love their girls more than anything

*Amazing family who calls and checks in everyday

*Drs and therapists who call, email and check in ALL THE TIME just to make sure not only Emma is ok but we are ok as a family

*Drs and therapists who support your fundraisers, Help get you a Make-A-Wish (and rush it), and attend important moments

*Drs and therapists who research to find the best treatment and actually listen to our concerns and/or opinions

*Our Lissencephaly family who are always there to help; answer questions, suggest ideas and most importantly there to listen

*Amazing Foundations who help us to have family time (Mascot Miracles, Angels Hands Foundation & Embrace Life Foundation), make our lives easier (donating us a van Angels Hands Foundation), and helping us purchase supplies our insurance wont cover (Embrace Life Foundation).

*Brandon and I also have great jobs with bosses who understand and are willing to work with us when things come up so that we can both be there for Emma.

*Having such an amazing 6 year old who loves her sister so much. Does incredible at school, dance and recently won an award in Reflections contest in photography. This girl continues to impress me everyday. 

*Lastly and most importantly is that Emma is still here with us and will be 3 in March! This year was really heartbreaking for our Lissencephaly community. We lost a lot of warriors this year, some I only knew from a few posts here or there on facebook, some I created a a real friendship with their mom and talked with them weekly if not daily, and then one I actually met and held in my arms. Losing a child is something that should never happen, as I watch these families lose their precious children my heart hurts for them as they are living my biggest fear. Attending a funeral of a child who has passed and has the same diagnosis as your daughter is......well lets just say tears for days (and still now as I type this). I just hold Emma and cry praying she will not be next and that we can defy the odds and live a long and happy life. Reality can be hard but so can living in fear, so we choose to live in the now. Don't get me wring sometimes that "now" can be sitting on the couch crying but it can also be cherishing every moment and creating incredible memories.  

Through all the ups and downs this year I have to say we ended on an UP!
Dec 6-12 we were able to take the trip of a lifetime to DisneyWorld and stay at Give Kids The World thanks to Make-A-Wish Utah. we had the most incredible time. Emma's seizures started to get controlled about 2 weeks prior to this trip the timing couldn't have worked out any better. 

Praying for less seizures in 2018!














8/7/17

Let Me Tell You 'Bout My Best Friend(s)...........

I Hope as you read the title you kinda sang it too.....LOL 

As a mom I have found that I have a few "FAVORITES" that help me tremendously with motherhood. As my life of motherhood has changed since Emma was born 2 years ago my "FAVORITES" have changed along with that. Being a special needs mom has made me realize how much I count on other special needs parents to help me when Drs can't. With Emma's diagnosis being so rare, 1 in 100,000, I am constantly turning to other amazing parents for help. Well, today I am going to try and help some other mothers and not just special needs mothers by letting you in on my  "FAVORITE" things that as a mother I have come to realize I can not live without......



#1: OWLET BABY MONITOR:  
This favorite actually gets me a little emotional for a couple reasons....first of all I truly believe this monitor has saved Emma's life on more than one occasion. Second it gives me piece of mind knowing that it's ok for me to fall asleep at night because I know she is being monitored and if something goes wrong with her breathing I will know immediately. Lastly, this company and their customer service has been more than amazing to me. Below I am going to go into detail on how it has saved her and how customer service has treated us. 



my first post about the Owlet 2015
*Emma started wearing this monitor immediately after we returned home from the hospital at about 2 weeks old (after receiving the news of her rare diagnosis of Lissencephaly which is 1 in 100, 000 as mentioned above). Emma was diagnosed at 5 days old after experiencing over 20 seizures at 4 days old. This monitor was a shot in the dark, hoping to help us better monitor Emma while she was at home because her oxygen would drop after seizures and if she has one in the night we wanted to make sure her oxygen would return to normal range in a fast amount of time. Honestly, the first year of Emma's life we didn't have a lot of notifications but it helped so much with the transition to her own room. At around 2 years old Emma's monitor became even more important to us because her seizures returned and were very, very powerful up to 20 a day again. We started new meds and even started a new diet. During this time her monitor started to go off nightly and not after a seizure just randomly at night. We would pick her up, rub her chest and whatever else we could do to stimulate her breathing again. We mentioned this to our pediatrician who said lets double check with an at home oxygen test. Which showed results exactly like what the Owlet was showing us. Emma was below a safe range of oxygen at night for over 2 hours and 35 mins. For a typical person the limit to be safe is about 5 mins. This pointed Emma right to a pulmologist who started her on some meds for her lungs (which are severely damaged due to aspiration, from the increased saliva from her new medication for her seizures), scheduled a sleep study, and put her on oxygen while she is sleeping. We would have never known that Emma was having these breathing issues without the Owlet. I fear the day that her feet actually grow lol the owlet typically only goes to 18 months 24 if you're luckily. But Emma's feet are incredibly small she is currently in a size 3 sock and we have a size 4 left (only style sock wish they had it in the new style, staying hopeful they will before she gets to a size 4). I am not paid by Owlet nor do I get any perks by sharing this story with you. I am just truly a huge fan of Owlet and I owe my daughters life to them. So thank you Owlet. I pray this story makes it to you and your employees. 

IT ARRIVED!!!!
*Which now leads me to employees and customer service........When we first received our Owlet we were struggling to get it hooked up to our internet. We tried to 2 days before I decided to chat in on the app and ask for help. Which directed me to one of the head people of the company who offered to come out to my house and help set it up (luckily we got it figured out over the phone) but seriously it warmed my heart to know they cared enough to help us get is set up ASAP that they would drive to out house (Owlet is a Utah based company about a 40 min drive from our house).  A while later I noticed that the monitor would no longer connect to the base station for some reason it wouldn't even turn on. I chatted in and within 5 min they trouble shooted with me and decided we just needed a new part, which was then shipped, overnighted and on my porch in hours. Our Owlet was one of the firsts to be sold they actually went on backorder for a while so ours is the first version and still working out some kinks and stuff. Which leads me to July 26, 2017 at 11:00 PM as I am leaning against my bed holding the owlet monitor and sock in hand (that I had been working with for 2 hours) as tears stream down my face because I can not get it to charge. I would plug it in and it would say completely  charged but then I would put it on Emma and it would say battery low less than 20%. What was I going to do I need this monitor, I wont sleep without it I can't. So again I decided to chat in and talked with someone named A (yes slight humor for those Pretty Little Liar fans LOL),  who was amazing to help me and we were able to get it to work that night. But when we ended the conversation she said if you have any other issues chat in and ask for me. I felt comforted knowing if I needed help again I wouldn't have to explain it all again. I received my email of my chat transcript (which I love because it helps me to remember our conversation and keep important info etc.) Over the next week I fought nightly to get the Owlet to charge most nights it would go off at 2-3 AM saying it had 20% left but it was fully charged (supposedly) when I put her to bed. I was getting frustrated so another night as I stressed about Emma being monitored Brandon said just chat in again on the app and talk with A again. So I did and she was so helpful making it easy to get it replaced as it was under warranty and she overnighted it! So today when it was delivered to my porch it was like Christmas Morning knowing my sweet angel will once again be watched over and I can hopefully get some sleep again. So thank you Owlet and Thank you A! I am sure at this point you are wondering how you can get one so I will make it easy for you just simply click HERE!
Post from January 2017: She can sleep in her own room
#2 iBaby Video Monitor:  https://ibabylabs.com/
This video monitor has also been a huge part of us getting Emma to sleep in her own bed. We are able to watch her right from our cell phones. We can see the temperature in the room as well as the humidity in the room. But most importantly it records motion. We have been able to capture some seizure activity on the monitor and send it to her Neurologist, I am also able to go back through the videos to check if i missed one through out the night . We have also caught some pretty sweet moments between sisters who love each other more than you could even imagine. Here are some videos and pictures that we have captured using the iBaby video Monitor. Warning the video is a seizure video if you don't want to watch then I suggest you skip the video and enjoy the pictures instead. 

SEIZURE WARNING

SISTERS <3

Sleep tight love bug

These items help me sleep at night
(this picture of the owlet sock is the old version see the new toeless version above, it's amazing)

I hope that you have enjoyed reading about my favorite must haves as a mom and a special needs mom. I also hope that you too are able to experience the amazing benefits that I have by using these 2 products. I would also like to mention that both of these companies also donated their product for us to place under our tree at the Utah Festival of Trees 2016, which helps to raise money for Primary Children's Hospital and they were very happy to be able to donate. I felt blessed knowing that I loved the product but that the company behind the product is just as amazing as the product itself.

Hope you are all EMBRACING LIFE TO THE FULLEST!



7/26/17

Healing One Day At A Time And Then Some More......

When Emma was diagnosed every dream we once had for our newborn baby (and Ava's little sister) was violently ripped away from our thoughts and was replaced with... how long will we have with our sweet innocent newborn? What will we tell her sister? Will they have a relationship? Will she ever know how much we love her????? The questions will never end even as time goes by more and more questions come into our minds as Emma's parents, but one thing we try to remember is that no one knows the answers to the questions that fill our minds with anger, worry, sadness, even guilt at times.

Sometimes I blog/write to help remind me of our goals, our goals which consist of living in the moment and not the what ifs, or what could have beens. It is not always easy to live with that mindset, but we really try. When we go out and see family and/or friends who have little ones around Emma's age, yes, I wonder and wish and honestly I don't believe it will ever stop, but I do know that it gets easier. Yes, jealous moments happen when I wish it was Emma that Ava was playing with and holding hands with, as they run around the grass. But, then I realize Ava wouldn't be who she is and we wouldn't be who we are without Emma. We are better people and we have learned to not take anything for granted. Every moment we have is a miracle and we are so lucky to every second together that we are given.

Some days are just plain HARD, like hard like you never imagined hard. Sitting there feeling helpless as you watch your baby have countless seizures and praying she will breathe when it's over. The honest brutal truth is I awake up multiple times throughout the night either due to seizures and if not seizures just to make sure she is still breathing. Every morning I pray she is still alive. I worry every night that I will miss a seizure, one that she really needed me for.  It's hard to manage meds, feedings, therapy, Dr appts, work, and other duties of just being a mom....dance, breakfast, lunch, dinner, homework, bedtime etc. the day is completely exhausting and hard..... don't get me wrong, I am saying HARD, but NOT impossible. Some ask how do I do it?.....Well she's my child wouldn't you do anything for your child too??? My child may just need a little more and if your child needed more I promise you would find it in yourself to make it happen.


I titled this blog post... Healing one day at a time and then some more..., I did this because one day I feel like I am doing great and then BAM something happens and I could cry all day. But then something else can happen and I am on cloud nine feeling like anything is possible. Things may get easier to live with but I don't think I will ever not cry or be completely sad about Emma and what she has to endure in this life. I try everyday to make it the best it can be and do it with a smile, but I also know a good cry is always ok too. Living with so much unknown is hard but when you really think about it what is known? NOTHING...nothing is guaranteed for any of us. Sadly, anything can happen any day to any of us, but we know that and realize that much more with Emma than we would without her. The quote below says it all.....

Healing will be a constant in my life it is like an open wound that I will keep trying to heal and cover up,  but it never really ever goes away. But we try and we fight and we will never give up. I in no way ever feel sorry for us as parents and I never want any one to pity us or our family. Because we are blessed, Emma is a shining light in our family. The only thing I ever am sorry for is what she has to go through it can be painful to watch and understand. The second part that I feel sorry for is Ava and what she tries to understand about her sister at such a young age (6). For example a few nights ago she asked if we could all say a family prayer. So we all held hands and she prayed....she prayed to please help Emma's seizures get better because she misses her sleeping in her bedroom with her...she continued to pray and at the end she says again...please please help Emma I can't live without her....my heart broke, tears flooded my eyes and came rushing down my face knowing that one day that would be her reality. She finished the prayer and we all immediately held onto each other just crying. Later as I tucked her into bed we talked and I told her that we are always here for her if she ever needed to talk to us about Emma or had questions. I told her that sometimes when mom and dad are having a hard time we talk to each other and it helps us, so please come talk to us if you need us ok.... she replied ok... as we hugged goodnight she whispered in my ear mom you can come talk to me to if you need to when dads not home. SERIOUSLY you guys she's 6! How in the world could we have been blessed with 2 amazing little girls. I don't know but in those moments I heal a little knowing that we all have each other and that will never change.  

Healing happens at moments you wouldn't have expected...like this weekend even tho my niece who is only 6 months old and Emma is 2 years old, my niece played with and looked at Emma as a "typical" child. It made my heart burst to know that they too can have a special relationship. Even my nephew this weekend is opening his heart and mind to children that are different. He was so curious about Emma's feeding tube and seizures and I was so happy to talk to him and help him to try and understand Emma a little more. The next day he started asking, "Aunt Jaclyn how many seizures was that for today?' I would reply and he would say "o man thats too many" This heals me, this makes me smile that even tho Emma is 2, she is making a huge impact on so many around us. It makes my heart full knowing she's doing her job here on earth, educating us and showing us what life is all about.....LOVE!

In moments like this my heart heals a thousand times over. Seeing her happy and knowing she is loved means the world to me. For a moment she is "typical" and healing happens. 

SO FOR NOW WE WILL KEEP EMBRACING LIFE AND LOOKING FOR THOSE MOMENTS THAT BRING US PEACE AND A LITTLE BIT OF HEALING 

6/28/17

Ketogenic Update, Questions, Foundation Info and Brainwave

Ketogenic Diet:
As I sit here and comb my fingers through Emma's hair my heart is literally breaking because she is so tired from all these seizures. Her body is just quivering from all the seizures no matter how much I wrap her up and snuggle her she still just shivers like she is freezing. I believe this is from her muscles just being exhausted because it's like a full work out every time she seizes. She is also battling the side effects of the diet which make her tired and weak as her body adjusts to this new ratio, no carbs and no sugars (her poor body).  Read more about how the diet works here:
 https://www.facebook.com/Embracelifeemma/photos/a.979834438818643.1073741830.628304373971653/989405147861572/?type=3&theater


Labs are no fun but Emma is a fighter
We got word today that her labs are looking great from adjusting to the 4:1 ratio which she has been on for one week as of today. We also got great news that her labs were great and we are able to start weaning the Onfi medication she is on. This is a med that can be very hard to get off of so we didn't want her on it for a long period of time especially when it's not working for her. This med also has caused us to put a hold on increasing her CBD oil as much as we would like to since they interact with each other. So our plan is to wean this med and then hopefully have room to play with the oil to increase it. We pray that the diet will work and we can do CBD oil and the ketogenic diet. Our Drs say that the diet is in no way a fail just yet, they want her to at least be on it for up to 5 months. After that if we see no improvement we can consider it a fail. But even little improvement would give us hope to go for longer trial period, because overall Emma's body is handling the diet wonderfully.


Questions From You:

*How do you access CBD oil and what was the process to get it in the state of Utah?
We order Emma's CBD oil from a company called Charlotte's Web (cwhemp). They are located in Colorado and they ship her oil directly to our house. They have various strengths of the oil and she takes the Everyday Advanced (highest amount cannabinoids). CBD oil has a very very low amount of THC (less than .03%). THC is actually also very beneficial for kiddos like Emma due to muscle tone (painful) and seizures. Some kids need THC in addition to CBD to get the full seizure control. Sadly, we don't legally have access to THC to help her to the fullest extent but if we can create awareness to show people how important this plant is maybe we can get a law passed to legalize Medical Cannabis (currently working on it here in Utah).

*How has Emma's diagnosis affected Ava (big sister) in both good and bad ways?


When Emma was diagnosed my heart dropped for us as parents but mostly for Ava. Before Emma was born all Ava would talk about it how much fun they were going to have playing together. How was I going to turn and tell our 4 year old that her little sister might die and soon. We decided to be as honest as possible to Ava when explaining Emma's Diagnosis, but didn't want to discuss life expectancy with her because honestly who knows.....NO ONE KNOWS! Ava grew up really, really fast and went from 4 years old to 12 years old overnight. She is very, very compassionate towards others and has learned everyone is different and that's ok. As far as affecting her in a bad way...I am sad she had to grow up so fast. I am also sad that she has a false sense of what it's like to have a sibling or to be a big sister. She thinks being a big sister is helping with therapy, comforting her little sister through a seizure, and hooking up a G-tube feeding. All these things are normal for her and that hurts my heart. Here is another example....My sister had a baby in January and a month ago Ava came up to me and said that her new cousin, Brynlee was freaking her out, I asked why and she replied because she already has head control. I had to explain to her that yes that is a normal age to learn to hold your head up. She also asked when Brynlee would start having seizures. This kind of stuff breaks my heart because she thinks this is how life is, not that our life is bad we are just different. She also has a hard time that Emma has been sleeping in our room lately due to seizures so it hurts her feelings which I can't blame her, so daddy has been being a good sport and having sleep overs with her. She has more worry than a 6 year old should have but man does she handle it well.

*How does Emma have Lissencephaly but not Ava if its genetic?
They believe that Emma's partial deletion on chromosome 17 happened by a random mutation. So they don't think it had anything to do with our genetic make-up and that it was just random. Lissencephaly occurs 1 in 100,000


*What do we do for fun with Emma, What is her favorite things to do?
see light up sticks in her hands :)
This question is kinda a two part question....so what we like to do as a family with Emma is anything outside Emma absolutely loves being outside. So swimming, park, just laying on the grass, and Lagoon amusement park (even the water park). As far as some of Emma's favorite things to do besides being outside is her balloons, Emma has a love for Mylar balloons we should take up stock in balloons LOL. She also loves her light up toy sticks (see pic), one more toy she loves is her beads (see pic) sadly her interest to these toys have kinda been put on hold since the seizure outbreak but we have faith she will get it all back. But in all honesty Emma is happiest when playing with her sister.
Hanging outside with the family

Emma Loving her Balloon
More Beads
most favorite is just being together with her sister


*How many seizures does she have in a 24 hour period?
Currently Emma is having between 10-20 seizures. Sometimes her seizures come in clusters so even though we count it as one she sometimes has a cluster of 3 just seconds apart but only lasting about 10 seconds each, occasionally she will have seizures that last longer than that.



*What do Emma's Seizures look like?
Sadly I hate to post seizure videos but I think they help teach people about epilepsy so I have posted some below if you do not want to watch them I understand they are not easy to watch. Emma has exhibited many seizure types and they all look different. I don't have recordings of them all but here are a couple of them.....

WARNING GRAPHIC CONTENT NOT EASY TO WATCH!




Embrace Life Foundation:
I am so excited to share this with you all. So back in January when we started to look into intense physical therapy and learned it was $6,000 and our insurance wouldn't cover it, well it really made my brother upset. He was frustrated and heartbroken so he reached out to me and said lets do something this is not ok Emma needs this. In the next week or so he called and said let's make a foundation in honor of Emma so her legacy will always live on. He wants to help Utah Lissencephaly families and others with brain disorders to be able to reach these unreachable things that our children need but can't due to insurance coverage. This foundation is hoping to help with therapy, medical supplies, medical devices, anything to help make life easier for our children. The foundation will be having their first fundraiser to help families on Aug 18th. If you live in Utah please come out and meet some adorable lissencephaly kiddos (5 of them that I know of)  as they have all been invited to attend. We want you to see the faces you will help by attending and donating to these families. If you do not live here in Utah or can't make it but would still like to donate here is a link paypal.me/Embracelifefoundatio
Follow the Foundations Facebook Page for more updates on this fundraiser event and many more. Here is a link to the page https://www.facebook.com/Embrace-Life-Foundation-827189144098414/


Family Pictures June 2017:
We have been wanting family pictures since the girls birthdays in March but Emma was hardly awake and so we didn't want her to be sleeping. Well Flash forward to June 19 at about 8:30 PM when I see a post on The Angels Hands Foundation page asking if there is a family that could go for family pictures the next night at 5:30 PM. I ran to Brandon begging please please this is our perfect opportunity Emma is awake more now and we really need them done. So in less than 24 hours we threw stuff together for family picture and let me tell you they turned out better than I could have ever imagined! Thank you Fotofly and AHF for this much needed photo shoot for our family <3 



RIDE The Brainwave 2017: 
Team Embrace Life Emma
The Brainwave is a fundraiser put on by Children and The Earth. Emma's team is made up of 5k walkers and motorcycle riders. This year her team was better than last year and we hope next year it's even bigger. We want to thank all of you that participated this year whether it be in person or virtually.  We had so much fun getting out with family and friends to support Emma and other children with life changing illness/diagnosis. Remember how I told you Emma's Drs are amazing well I have to give a shout out to her pediatrician, Dr Richard Greenberg, he and his family came out to support Emma and walked the 5k with us. Emma also had the support from her Occupational Therapist Katie, we are truly blessed. Here is a little video to show you the fun we had at the Brainwave. Check out Emma's facebook page too for some of the live video feeds we did....SO FUN!