"The Lord himself goes before you and will be with you; he will never leave you nor forsake you.
   Do not be afraid; do not be discouraged.”
Deuteronomy 31:8

Friday, December 16, 2016

Luella's Flight to the North Pole

Luella got to take part in a very special experience on Wednesday. Make-A-Wish Minnesota sent Luella an invitation to take part in Sun Country Airlines "Flight to the North Pole". She's been invited every year since her Wish trip but we just haven't been able to make it work. This year I wanted to make sure to make it and fortunately the weather cooperated and Luella and I made the drive up to Minneapolis on Wednesday. It was a LONG day - driving up to the cities, taking a little time to shop at Ikea (that part was for me), then on to park and get on the bus to head to the airport!

We got off the bus and headed to ticketing to get our tickets to the "North Pole". Luella knows we didn't really go to the North Pole, but it was fun no matter what! Everywhere we went we were greeted by "elves" and so much festivity! We got our tickets and headed to the gate. Up at the gate area there were of course more elves but also lots of team mascots and fun! Soon it was time to board. The plane was all decked out and the flight attendants were dressed as elves too. The kids shut their window shades and the plane "took off"! The pilot revved the engines and taxied around while everyone was served supper on the plane. When we "arrived" we had to wait a bit for Santa to signal that he was ready for the kids. Then it was time to get off the plane and visit Santa!

We got off the plane a few gates down from where we boarded. They had transformed the area into a fun place to meet with Santa. Luella was so excited to meet Santa and tell him what she wanted for Christmas. Santa took a few minutes to meet with each of the almost 70 kids there. When it was Luella's turn she made sure to tell Santa she wanted a scooter for Christmas. Then Santa gave her a little early gift to take home - a little stuffed Cambri toy and a Sun Country airport playset! Luella also got a special Rudolph balloon hat! Luella wasn't sure if this was going to be the "real" Santa but after he greeted her with a "Ho, Ho, Ho" she told me she knew it was the real Santa!

There wasn't a "return" trip from the North Pole so I was glad Luella understood it was a pretend trip. I heard a few kids say "but don't we need to fly home?" ;-) Soon it was time to get back on the bus to head back to the parking garage! We stopped for gas and Luella changed into PJs for the ride home. It was about 9:15 when we got on the road! Thankfully Luella was out within about 30 minutes... despite all the cookies and candy they filled her up with! I was thankful for good driving conditions and a list of podcasts to keep me awake for the drive home. Luella slept the entire way home and we pulled in the driveway at 12:30!

It was such a fun and magical night for Luella. I'm so glad we had this opportunity. Make-A-Wish Minnesota and Sun Country Airlines did an amazing job making sure all the kids had a terrific time!

You'll have to view the video slideshow to see all the fun!! https://youtu.be/pqLAZZ3es8g

Tuesday, November 29, 2016

Giving Tuesday

Today is Giving Tuesday - a movement to create an international day of giving at the beginning of the Christmas and holiday season. We are passionate about raising funds for the Dravet Syndrome Foundation and their work to find a cure. If you are wondering where to share your gift today please consider DSF. You can donate here: https://app.etapestry.com/onlineforms/DravetSyndromeFoundation/onlinecontributions.html

I'm sure you are all aware of all Luella has been through but here's a little reminder. This short video represents only a handful of the experiences we've had with Dravet syndrome. And this would be only a small fraction of what some kids have to deal with. Through it all we consider ourselves quite fortunate but we just don't know what Luella's future holds. We need a cure. So many others need a cure. Thanks for taking a minute to read this, watch the video and consider a donation. God bless you!

Sunday, November 13, 2016

Purple November ... and many updates.

How did I let it get to be November 13th before I wrote about Epilepsy Awareness Month?! By now you should all know the drill.... November is Epilepsy Awareness Month and purple is the color. We love to see everyone wearing purple during the month and supporting 65 million people around the world who are living with epilepsy, especially one exceptionally cute little one living with us! If you do wear purple sometime this month - send me a picture! And thanks for the support!

In other news Luella is currently at 72 days seizure free!! Praising God for all those wonderful days and fun times had without seizures! Luella's leg continues to heal well. She had a follow up with her orthopedic doctor and everything looks great. We are officially done with the wheelchair and walker! Luella was so glad to finally ride her bike again and super excited to get to ride the bus for the first time this school year!


We also just recently had an appointment with Luella's neurologist in St. Paul. Dr. Wical was SO thrilled with how well Luella is doing. Luella is for sure beating the Dravet odds and we are so thankful and pray that she will continue on this path! We were sad to find out that Luella's beloved doctor will not be seeing patients anymore. Dr. Wical has helped us during some of Luella's most troubling times and we will miss her so much! We were lucky to snap a quick picture of Luella with Dr. Wical before we said our good-byes. We got some great referral options from Dr. Wical and we will continue to take Luella to Gillette Children's.

Luella and Dr. Wical
While at Gillette Children's we also checked in with a pediatric orthopedic doctor that Luella saw about three years ago. Children with Dravet syndrome often times develop gait issues and sometimes are wheelchair bound. We knew from our earlier consult with this doctor that Luella already had the extremely loose joints common in Dravet. We wanted to check in with him again after the growth plate fracture and also to check out Luella's knees which look to be more "knock knee'd" lately. He did verify that yes, her legs and hips are extremely flexible - much like how we are born. Over time as kids get older those ligaments tighten and we aren't as flexible. Luella is still very loose like a newborn and she has a bigger range of motion in her knees and hips. Right now there isn't much we can do. Just keep an eye on things and make sure she remains active - not a problem there!! We'll see him again in two years. 

Look at that cute little missing tooth spot!! 
One last SUPER EXCITING bit of news from our visit to St. Paul was that Luella LITERALLY lost her first tooth!! I was talking with her after supper and there was a gap in her bottom teeth!! We have no idea where that tooth ended up!! I didn't even know it was loose!! When I checked it out I was surprised to see that she had a permanent tooth already coming in just behind where that tooth was! AND the tooth next to it was very loose too!! I guess I need to pay more attention to her teeth!

Luella worked on that 2nd loose tooth all night. The next morning it was SO loose. I told her she needed to pull it out before we LOST that one too. I gave it a little tug but she didn't like that so I told her to try really hard. She grabbed a kleenex and pulled and says, "Here's my tooth!" She was so proud! When we got home on Wednesday night she couldn't wait to get her little tooth pouch - never used before, and carefully tuck her tooth inside. That sweet Tooth Fairy left her TWO golden dollar coins to make up for the other tooth that was lost. 

There are TWO missing tooth spots!! ... and a cute little Rainbow Dash hoodie PJ wearing girl!! 

Don't forget to wear some purple this month!!

Sunday, October 23, 2016

She's SEVEN !

We just wrapped up an amazing week celebrating our amazing Little Luella! It's hard to believe she is SEVEN!! She's actually not so "little" anymore! <sniff, sniff>

On Sunday - October 16th, Luella celebrated her birthday with her friends and a fun swimming party! The girls made a special beaded bracelet with a pretty silver sea charm to take home. We had strawberry cake with cream cheese frosting at the request of the birthday girl! Luella got many fun gifts. It was a super fun party topped off with about an hour of swimming! (Seizure-FREE swimming!!) Luella also got to bring a special treat to school on Wednesday (since there wasn't school Thurs or Fri). Then a trip to the farm to celebrate on Thursday and finally on Friday, October 21st - her ACTUAL birthday... supper at Pizza Ranch and then off to see the firemen's movie "The BFG"! Oh and the firemen let her climb up and honk the horn on the fire truck too!! It was an amazing week celebrating our amazing Luella!!

Luella has been on a roll again with seizure-free days.... we are currently counting at 52 days!! She is also doing great and walking all over the place without even using a walker anymore! We'll be checking in with her orthopedic doctor on Monday but we anticipate hearing that everything is healing up great. Hopefully getting to ride the bus to/from school again will be on the agenda this week too!!

I'll leave you with a few birthday week pictures... More pictures can be seen online here: https://goo.gl/photos/8rimWY1M5fvDF38H9

The little mermaid herself!

Having fun swimming!

A cozy mermaid blanket from mommy and daddy!

A birthday funfetti donut for breakfast!

She's SEVEN!!

Thursday, September 29, 2016

Luella: The Speech and OT Graduate

We had Luella's IEP meeting on Tuesday and it went SO well!! Luella graduated from Speech and OT!! There's just no need to continue with the therapies since she is doing it all!! Another big highlight is that she will not be visiting her special education teacher as much. She was going 3 times a week for 20 minutes and that has been cut back to one 20 minute session a MONTH! Luella is getting all her work done in the classroom right along side her peers so there just wasn't a need to have that extra time to work on things. We couldn't be more thrilled with all the progress Luella has made. She is doing amazing things and we pray that she can continue on down this path.

The team at school said that if at anytime we feel like she needs some extra help again... they are just right there, willing to step in! We are so fortunate to be in such an amazing school district. I've said it before, but so many parents dread those IEP meetings, feeling they need to fight for the things their child needs, but we have never been in that situation. Everyone cares so deeply about Luella and her success! Blessed!!

It was party day for Luella today!! Celebrating the end of Speech and OT! Awesome Job Luella!!

Wednesday, September 21, 2016

That Cast is OFF!! Wheelchair / Walker will be sticking around...

Luella was SOOO excited to get her cast OFF today!! She tolerated that cast much better than I would have these last 5 weeks! It was great that she only had to have it for 5 weeks and not the 6-8 they originally told us. Unfortunately riding bike and running around with friends will still have to wait another month or so. She'll continue to use her wheelchair and walker as she gradually transitions to bearing weight on that leg. She did not need to have a brace or anything on her leg! Her doctor said that kids typically heal much faster than adults and, while her leg isn't completely healed, having more range of movement and gradually bearing weight will allow her to heal up over the next several weeks. Her x-rays today looked great! She will go back to the doctor on October 24th for follow-up x-rays and we hope she will be walking completely on her own by then!

Luella's cast was so beautifully decorated. She did some doodling (as did I) and when school started she brought a baggie of permanent markers for her friends to draw pictures or write their name. We had to take some pictures of her cast this morning to remember all those fun doodlings!

Getting her cast off was a breeze! The lady that took her cast off said she's had 12 year olds crying while getting it cut off, but Luella was super brave and did great!!

Ear protection from the loud saw... actually it wasn't that loud... I think more so the kids don't get worried. Maybe I should have been the one wearing them!! I was WAY more nervous than Luella was!

Starting to cut.

Working through the layers.


Luella is looking forward to a nice long bath tonight!!! :-)

Saturday, September 3, 2016

Bedtime Seizure

As you tuck your little one into bed you shouldn't have to worry about a seizure gripping their little body and taking their breath away. You shouldn't have to listen to that same little one moments earlier praying to God to keep her safe and to take her seizures away. We are not guaranteed a perfect life in this lifetime... free from the pains of the world. Only when we are with our Father in Heaven can we be free of these worries and fears and all we can do in the meantime is just trust that God's will be done.

Therefore do not throw away your confidence, which has a great reward. For you have need of endurance, so that when you have done the WILL OF GOD you may receive what is promised. 

                                                             Hebrews 10:35-36

Last night literally just minutes after I left Luella's room, a nasty seizure gripped her and took her breath away. I prayed and just rubbed and rubbed her chest and back to stimulate a breath. Thankfully she did take a breath but she was struggling and the seizure wasn't stopping. We put the oxygen on her and after 2 doses of midazolam the seizure finally did stop. After several more minutes her breathing returned to normal and she slept the rest of the night peacefully.

This morning Jim got Luella up and ready for the day while I got ready. I asked him if he told her about the seizure. He hadn't. She was perky, happy, and anxious for the day. She didn't know about the scary seizure. We decided not to tell her. She has already started worrying about seizures herself... sometimes wanting us to be with her while she's brushing her teeth or just a room away... saying "but what if I have a seizure?" We assure her that we are always close enough to hear her and are still keeping a close eye on her. We don't want her to fear going to sleep at night. Some kids are scared of the dark, Luella isn't. No kid should have to be scared of a seizure after falling asleep.

It's been just over 2 weeks since her last seizure - the night she got her cast. We are praying this pattern won't continue and we can once again enjoy longer seizure-free stretches, especially as school is starting in just a couple days. This little lady is going to be in 1st grade!! Please pray for a great year of school and fewer seizures. Love and thanks to you all!

Friday, August 19, 2016

Full Leg Cast and a Seizure to Boot

What a week!! The kids and I had fun on Tuesday night "camping" in our backyard in a tent. They all get a kick out of "roughing" it and that's about as much camping as I can do! We stayed up late and watched Toy Story and woke up early to the sounds of the birds chirping! The kids all had fun on Wednesday playing outside and enjoying the nice weather. I was doing some work in the garage in the afternoon when I heard Luella start crying. She was on the trampoline with Ashlyn and Ryker and she was wailing. It's not uncommon for her to exaggerate an injury. I came out of the garage and told the kids to come in so I could figure out what happened. Luella didn't want to move so I went to get her. I carried her in the house and set her down on the bench in the kitchen and once I got a look at her knee/leg I knew something wasn't quite right. She was in a lot of pain so I called the clinic and got her right in to the on-call doctor. After a series of excruciating x-rays it was determined she had a growth plate fracture and needed to be seen by an orthopedic doctor in Sioux Falls right away. They splinted her leg to immobilize it and got her ready to go.

Jim and I opted to drive her there ourselves vs. the ambulance. The experience in Sioux Falls was a bit frustrating with lots of waiting only to be sent home to return the next morning to see the orthopedic doctor and have surgery. Sleeping on Wednesday night was a little challenging but Luella did okay and we got on our way Thursday morning.

We finally got to meet with the orthopedic surgeon and get more details as to what happened and what they could do to fix it. Basically Luella had a fracture to the growth plate above the tibia in her left leg. He was going to try to do a closed reduction (no incision) to put things back in place and then they would cast her leg. If he wasn't able to move things into the right place he would need to open up the leg and then there was the possibility of needing pins or wires to hold things in place.

I was able to walk back with her until they had her asleep. This mama was a little weepy leaving my baby back in the OR but she did great! Thankfully a closed reduction worked and they were able to get the cast on right away. And boy does she have a cast! That pink cast goes from the very top of her leg all the way down to her toes! She handled the anesthesia fine and we were able to see her after an hour or so.

After recovering awhile, meeting with home medical and getting a little walker and wheel chair we were able to be on our way. Luella impressed everyone in the hospital with her walker skills! She caught on right away! And we now have visible tracks around the house from the wheel chair! :-)

Unfortunately Luella is dealing with a fair amount of pain, especially when it's getting close to her next dose of pain meds. She was able to fall right to sleep last night and was up around 12:30 to use the bathroom (which is a MAJOR challenge). She got right back to sleep but at 3:30 woke up in a lot of pain. We gave her more pain meds then but it was taking awhile for those to kick in so I laid with her to snuggle and try to distract her from the pain. Around 4:30 she was finally settling down and I slipped out of her bed to let her sleep..... 10 minutes later she had a seizure. :-( She was really convulsing and her poor little leg was jerking so much. I was about to give her rescue meds but thankfully the seizure stopped. She slept well then until about 8:00 this morning. When she got up though she was so sore and it took awhile to move.

She's been in great spirits despite all she's been through. She did ask at bedtime last night if it was time to take off the cast!! I don't think she understands just how long she has to have it... but maybe that's a good thing! She will be in the cast for at least 6 weeks and then maybe a brace for another 2 weeks. She can not bear any weight on that leg so it'll be a long 2 months!!

Unfortunately we had to cancel our vacation plans to Duluth. We were supposed to be leaving tomorrow. That vacation involved a LOT of walking. We'll have to see if we can find something else to do instead.

Thanks for your thoughts and prayers. Just another bump in the road but we are so thankful to be dealing with this at the end of summer and not the beginning!

Luella in recovery... not wanting her picture taken!

Luella in her wheelchair with the little walker beside her.

Trying to get comfy in bed!

Tuesday, July 5, 2016

Day 122 was "The Day"

Well, tonight (Tuesday) was the end of our longest seizure-free run ever - Luella made it 122 days. Shortly after falling asleep tonight Luella had a seizure. We had a bunch of family visiting this week for Jim's parents' 50th anniversary celebration. We had several people here and we're visiting in the living room. At 9:22 her alarm began to ring and it kept going. I listened in the monitor and I could her her gasping. I'm running up the stairs praying I'm not hearing what I am hearing. Then I turn her lights on and pull her blankets back to see her eyes wide open, fixed. Gasping. Seizing. Sadness hits me as I know I will have to tell her tomorrow that we stop counting and start over again. I'm thankful that she won't remember this. She won't know that I had to give her two doses of her rescue med to stop the seizure. I wonder if she will feel any different in the morning? If her body will somehow let her know that it did happen? This was hard on me tonight. I didn't want to see this. I wanted to pretend she was healed. That it was done. That Dravet wasn't a part of our lives.... but it is and it will be. This is why we fund raise. This is why we work hard for a cure. Thank you again to everyone who helped make our "a cake 4 a cure" fundraiser a success. We appreciate all the support and more than anything we appreciate your prayers. Luella's prayer at bedtime was "to have a fun day tomorrow without any seizures." I pray that will be the case and we can once again strive to beat a record!

Friday, June 24, 2016

2016 a cake 4 a cure Winner!!

I couldn't wait to see who the winner was this year!! I had a lofty goal of $1,500 this year. Things started out slow but WOW you guys rallied and put me over the top!!

We ended up raising $1,630!!! 

All of that money will be sent to the Dravet Syndrome Foundation to help find a CURE!! Thank you so much to everyone that contributed!! You are all amazing!! To see what DSF has been working on you can see some of the current research here - http://www.dravetfoundation.org/research/dsf-funded-research.

Time for the BIG announcement!!

The winner is..... Vicki Murra!!!! 
I'm so excited to make you a special cake Vicki!!! YAY!!!

I took a video of me doing the drawing so you'd know it was done far and square!! :-) So many friends and family are included in the drawing and I didn't want anyone to think I was playing favorites!! :-)

Here's a video of the drawing...

Thanks again everyone for all your support!! We are SO BLESSED to have such an amazing network of friends and family to support Luella!!


Monday, June 20, 2016

Wear Your Purple on Thursday

Thursday is the 3rd Annual Dravet Syndrome Awareness Day - June 23rd! Please wear something purple and share a picture with me. We LOVE to see all the purple people out there!! Also Thursday will be the LAST day to get a chance to win a cake in my "a cake 4 a cure" fundraiser / raffle. I'm super excited to announce the winner on Friday!! Thank you to everyone who has donated!!

Wear your purple!! 

More details on a cake 4 a cure can be found on this blog post - http://littleluella.blogspot.com/2016/05/third-annual-cake-4-cure-fundraiser.html.

You can donate online herehttps://www.youcaring.com/acake4acure

Luella - 2 years ago on the 1st Dravet Day! June 24, 2014

Friday, June 17, 2016

Luella got her cake... do you want one?

Well, on Monday we celebrated Luella's 100 Days of Seizure Freedom (and we are still counting!!)!!! She of course wanted to celebrate with a cake. I decided to do a watercolor buttercream cake. She LOVED it!! And now your chance to win a fun cake made by me is winding down. Only SEVEN DAYS LEFT to get your donation in for the Dravet Syndrome Foundation and earn one entry for every $5 you donate! Sadly, I'm still far from my goal of $1,500. All the money goes directly to the Dravet Syndrome Foundation in honor of Luella to help find a CURE!! Help us celebrate her with a donation!!

More details on a cake 4 a cure can be found on this blog post - http://littleluella.blogspot.com/2016/05/third-annual-cake-4-cure-fundraiser.html.

You can donate online herehttps://www.youcaring.com/acake4acure

Luella's fun cake to celebrate 100 DAYS!!

Monday, June 13, 2016

100 Days Hooray!!

Luella is 100 DAYS SEIZURE FREE!! Luella surpassed her all time longest seizure free run of 90 days on June 3rd and we were just waiting to see if she could make it to 100 and share the exciting news with all of you!! She is excited to be celebrating today... we are honoring many of her special requests... including chicken strips and macaroni and cheese for supper tonight!! Oh... and maybe a cake too! ;-)

We are amazed and blessed at all she continues to do! Thank you so much for all your continued prayers and support!!

We are celebrating!!

Monday, May 23, 2016

THIRD ANNUAL a cake 4 a cure Fundraiser

Dravet Syndrome Awareness DayThe third annual Dravet Syndrome Awareness Day is coming up in just ONE month - on June 23rd! That means my third annual "a cake 4 a cure" raffle / fundraiser is kicking off too!! Please visit the fundraising website to make a donation. I will keep track of all donations and entries into the drawing.
The donation site will close on June 23rd and a winner will be announced on June 24th! 

ALL money will be donated to the Dravet Syndrome Foundation in honor of Luella and to help find a cure! In the past 2 years we've sent over $2,500 to the Dravet Syndrome Foundation!!

Last year's winner was Angie Fick. She choose to have a cake made to help her parents celebrate their 50th wedding anniversary. I really enjoyed making this special cake!

So, how does this raffle work? Each entry into the cake drawing is $5. If you donate $50 - you will get 10 entries into the drawing. This is basically a LOCAL raffle since I will not ship a cake. I WILL deliver to the Luverne, Sioux Falls or Estelline areas OR you may pick up the cake in Luverne. If you live outside these areas and do not plan to pick up the cake, you may still donate but you will not be eligible to win the cake.

Please visit the fundraiser website to make a donation!! 

**Now for the fine print... 

1. I will only deliver to Luverne MN, Sioux Falls SD or Estelline SD areas or areas in between OR you may pick up the cake in Luverne. NOTE – If you live outside these areas, you may still donate but you will NOT be included in the raffle. If you are outside these areas and plan to pick up the cake yourself, please let me know so I can include you in the drawing.

2. The cake will be a 10" round cake (or equivalent). This would be a great sized cake for a birthday with 20-25 guests! 

3. The cake will not exceed 12 hours to make – this eliminates some of my more extravagant cakes. 

4. Cake must be “ordered” at least 4 weeks in advance. I will try to be available, although please understand that we get busy at times and may have travel planned. I would ask that you be flexible and maybe have another occasion in mind. 

If you'd like to follow Luella's Blog please visit: http://littleluella.blogspot.com/

If you'd like to learn more about Dravet Syndrome or the Dravet Syndrome Foundation, please visit: http://www.dravetfoundation.org/

To read more about Dravet Syndrome Awareness Day please visit: 

To find out more about my little cake biz, check out Embellished Sugar ! http://www.embellishedsugar.com/ 

Thank you!!! I can't wait to announce this year's winner!!

Please share!!

Luella on the first Dravet Syndrome Awareness Day in 2014. June 23rd is all about her!

Get your purple ready for June 23rd!

Friday, May 20, 2016

Blessings! (warning... you may shed a tear!)

We are just amazed at what God is doing in Luella's life! We are SO blessed. Can you believe Luella is currently 76 days seizure-free?? This is her 2nd longest run EVER!! We are closing in on 11 weeks without a seizure!! How are we doing this...? Faith and prayer! God is giving Luella the opportunity to do SO many things. I have to admit we've been nervous about letting her do some of the things she's gotten to do these last 10 weeks... things like going to swimming birthday parties, another party at a big trampoline park and jumping for ONE HOUR, getting her ears pierced - YES! Her ears pierced!! She didn't even cry!! Playing at a children's museum for several hours. She's upgraded her very small 12" bicycle with a bigger 18" bike and is still doing great without training wheels! She completed the Cardinal Dash run at school and had a full afternoon of Kindergarten track and field. She went on a class field trip to city park where she got to play for 3 hours!! She also managed to stay healthy during 2 bouts of strep throat at our house!! Each one of these events may have caused me to hold my breath for a second but I exhale and pray. Pray for protection. Pray for no seizures. God is good and has answered our prayers in the most amazing way.

So far this year - since January 1st - Luella has only had THREE seizures!! Thank you all for continuing to keep Luella in your prayers! I couldn't even get through writing this post without crying some tears of joy... especially after looking at all the pictures of the fun Luella has enjoyed these last 10 weeks. These are all pure blessings!! I'll leave you with a few pictures of some of the precious moments Luella has had these last 10 weeks.... Enjoy them as I have and see a little girl that getting to live the most amazing life!

She got her ears pierced!

Butterfly earrings!

Jumping at SkyZone with a friend!

LOTS of jumping!

Flying a KITE!

Children's Museum Fun

Cashier Luella

In the clouds with Burke.

Ball toss at track and field day.

She can hurdle!!

And long jump!

Holding a baby chick.

New bike!!

One happy, and blessed, little girl!! 

Sunday, March 20, 2016

She's an International Star

I'm happy to be writing a blog NOT about a seizure! Actually, Luella is just over 2 weeks seizure free and we hope to add several more weeks to that!

I wanted to share a special little spotlight that Luella had bestowed on her back in February. The International Bureau for Epilepsy held a photo competition with the theme 'Yes, I Can' to demonstrate achievement in overcoming obstacles. They wanted to showcase the best entries for International Epilepsy Day on February 9th. A select few were exhibited in the European Parliament in Strasbourg, France from February 1st through 5th. Luella's photo did not win the competition, but I knew I had a good one to enter and the judges thought so too. Her photo was one selected and displayed in the European Parliament!! It would have been fun to be there to see it in person. I got to see several pictures of how the photos were displayed. It was a special honor to have Luella and her story included!

This was Luella's piece of one of the posters that was displayed.

You can see Luella peeking out behind this lady! These posters were BIG!!

This is the hall in the European Parliament in Strasbourg, France where the photos were displayed. 

All the photo entries can be viewed here: http://epilepsy.org/gallery/

Your next opportunity to wear purple and bring some awareness to epilepsy is March 26th which happens to be Saturday! It is Purple Day for Epilepsy Awareness! If you have a chance to wear purple and tell people WHY you are wearing purple... that would be AWESOME!! Share a picture with me if you want to be included in my yearly purple video AND Luella always loves seeing her supporters wearing purple!! Thanks everyone!!