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Eosinophilic Esophagitis

Entertainment Over Eating (EoE)

This is a narrative written by big sister, Madisyn.

Almost every family in America sits around the dinner table and has a conversation about their day. Some of us look forward to it and some of us do not. Being with my family is one of my favorite things, and getting to sit down and listen to each other’s day was something I looked forward to each evening. Some of my best memories were made just sitting around the table as a family. Laughs were shared, water was spit across the table, forks were dropped on the floor, and we just had a good time, but one day that all changed.

My family consists of four people. We have my mom, my dad, and my little sister, Lyndsee. Lyndsee and I are twenty-one months apart, so we were born to be lifelong best friends. She is one of the funniest and spunkiest people I know, and I love her with all my heart. One day we were getting ready for Super Bowl L. The M&M company was kind enough to send us a gigantic bag of Panthers M&M’s because our family loves the candy, and the tasty treat was the perfect way to root for our home team. While Lyndsee was eating an M&M, she felt like it was stuck in her esophagus. My mom and she rushed to the emergency room, and Lyndsee was crying as anxiety overwhelmed her body. Lyndsee was taken back quickly and given a liquid solution that would allow the M&M to go down the esophagus, but ultimately had to have emergency surgery to have her esophagus stretched with a balloon device.

We continued having our family dinners like usual, but Lyndsee started eating less and food impactions were happening more frequently. None of us knew what was going on, so we went from doctor to doctor with no definite answers.  Finally, after two months of going through tests, a doctor at Brenner’s Children’s Hospital told us Lyndsee has a rare disease called Eosinophilic Esophagitis (EoE). This diagnosis changed our family dynamic forever.

EoE is a disease where the body thinks food is a parasite. This description basically means she is allergic to every food on the planet. Everything over the last few years started making sense at this point. We figured out why Lyndsee was not eating as she used too, and why she was always complaining about food impactions. Approximately 150,000 people have been diagnosed with EoE in the past twenty years, so it is really difficult to find a doctor that knows exactly how to treat Lyndsee or EoE in general.

This diagnosis has made my family and I realize that our entire livelihood revolves around food. When you go to a birthday party you expect to see pizza, cake, and ice cream. While visiting new places most of us enjoy finding unique restaurants with good food. Even just walking around on the streets, many are holding something to eat or sipping on a beverage. Just imagine if you walked around and smelled all this mouthwatering food, or heard the sizzling of grills cooking delicious hot dogs and hamburgers, but your body cannot have any of it because it will cause harm to not only your esophagus but other parts of your body.

Family dinners are no longer something we do because we do not want Lyndsee just staring at her family eating food. We do not get that aspect of laughing and sharing the funny moments at the dinner table as you see in all the movies and TV shows. We do not have the good and deep discussions like we used to before Lyndsee’s diagnosis. Next time you are dreading a family dinner, please think of all the laughs and good conversations you will have with your family that you will later share with your own kids. One day those moments could all be gone in the blink of an eye.

Horse (Equine) Therapy Brings a Smile to L’s Face!

Do you see that smile on our L’s face? That smile is priceless! We are coming up on the three-year mark of L’s diagnosis of eosinophilic esophagitis. The last three years of living on formula only and failed food trials have caused great anxiety to L. This past Spring, she was diagnosed with sensory processing disorder. Our sweet girl’s body is going through so much. Before her diagnosis, horse therapy was not even on my radar. If you do a quick google search, you will see horse therapy has been around for ages. The therapy works for patients dealing with chronic illnesses, autism, sensory processing disorder, cerebral palsy, down syndrome, and the list continues onward.

The progress in L is amazing. She is learning how to deal with her anxiety and sensory issues. The doctors hope that by getting these two things under control, she will be able to tackle food trials better and not be scared to move forward with trying new foods. When I came home from work this evening, L greeted me at the door and talked non-stop about her therapy session. The joy in her voice proves how much the therapy is working. Also, her therapist has created a great bond with L which was huge for us. L does not let her guard down often but we see how she beams with the therapist.

Most insurances will cover this type of therapy under occupational therapy. Start a conversation with your child’s medical professional and then talk to your insurance. We will continue to update about progress, but at this moment, I am a very happy mom to see my daughter smiling so much again. Feel free to reach out with any questions.

We continue to pray each night in our family prayers that L will see a cure soon!

 

Cincinnati Trip – Denied!

Can you imagine our heartbreak? L and I are supposed to be at Cincinnati Children’s right now. I received a phone call last Wednesday that even though we received prior approval and insurance approved L to go to Cincinnati, they are now denying.

Even though we received the discouraging news and both of us shed tears, we are trying to stay positive and keep the faith. Plans change for a reason! My husband and M couldn’t go since it was M’s last week of school and she had exams. I wonder if God didn’t want L and I driving by ourselves. I’m not sure but there is a reason for everything.

We were not promised an easy life, but God did promise He would never forsake us. Our family has been through a lot but we continue to believe and keep the faith. God has a plan. L had a full week of evaluations scheduled to better treat her Eosinophilic Esophagitis. This amazing young lady has lived off of prescription formula Neocate Splash for 2.5 years. She only has one safe food, pears! Could you imagine?

There is no doubt, L is the strongest person I know as food is all around her, but she keeps her head held high. I’m currently fighting insurance in hopes we can reschedule the trip. Friends, please never stop fighting for your loved ones. It’s sad that we have to fight for our family’s healthcare but I will not stop advocating for the best care for our girl.

L, you are my hero! I love you to the moon and back. We need a cure!

Costco Has Paleo Pancake Mix (Non-GMO)

Food ingredients is a hot topic in our household. L cannot eat food and then I have a dairy and gluten allergies. Ever since L was diagnosed with eosinophilic esophagitis, we all changed the way we eat. We try very hard to only eat all natural foods. I was so excited to find this paleo pancake mix at Costco.

The best part? You only have to add water! I did add fresh blueberries because I love blueberry pancakes. This mix is non-GMO, no added sugar, and of course gluten, dairy, and grain free!

My husband is my worst critic when it comes to new foods. As I flipped the pancakes into his plate, I silently was hoping he would enjoy them.

May I get a drumroll? My husband loved them and asked for seconds. It was M’s turn to try them and she thought they were delicious. Finally, it was my turn. Friends, they were not dry. Score! It’s hard sometimes with gluten-free recipes. I enjoyed every bite and I believe the fresh blueberries made the pancakes even more delicious.

I highly recommend putting this good for you food in your tummy.

By the way – this is not a sponsored post.

 

Life Update {Is it really May?}

Friends! We are alive. Praise the Lord.

When I wrote this post five months ago, I had no idea what our future held, but I knew God was giving us strength. As I mentioned, L was going in for a scope, and Scott was stable. Life changes fast.

This is our strong girl. She didn’t know in this picture but soon found out that she failed sweet potatoes. Her scope showed the most eosinophils she has ever had in any scope. The doctor could not believe the biopsy results, so had the lab recount. Sure enough, the results were correct. L had to give up sweet potatoes. She did it in such a graceful manner. She knew how much they were making her sick, so that is why she knew it was the right decision. In two weeks, L and I make the trek up to Cincinnati Children’s for a week stay to meet with the leading doctors in the EoE world. She will have a scope while we are there to see if the eosinophils are gone from her esophagus. Currently, she stays alive by continuing to drink her prescription formula and pears. Could you imagine life without food? L is going on 2.5 years without food.

Two weeks after L received discouraging news, Scott had another heart incident. He was hospitalized once again. Thank goodness my sister-in-law gifted us the Kardia Mobile so we could do EKGs at home. This device saved Scott’s life that night. Scott told me he wasn’t feeling well that night in February, we did the EKG and realized we needed to get him to the ER fast. I drove him there, showed the front desk the Kardia and she took him straight back in a wheelchair. Doctors swarmed around us so fast hooking Scott up to machines and IVs. He was at high risk of having a stroke.

After this hospitalization, I realized that we didn’t have time to waste. I got in touch with Duke to get his care transferred. During this time, Scott wore a heart monitor for two weeks. During the two weeks, the monitor picked up 26 episodes. We had to keep him calm and not doing much while Duke reviewed his records to accept his case. Finally came the time to have our first meeting with Duke. I prepared Scott’s notebook with all of his medical records, EKGs, and test results. The electrophysiologist viewed Scott’s records and said he needed surgery ASAP as he could go into cardiac arrest at any time. He said there was something wrong with the left atrium of his heart causing his heart to misfire. He believed Scott was born with an extra electrical pathway, but would not know for sure until he was able to get inside of Scott’s heart. A week later, Scott was scheduled for surgery.

My husband was nervous, but relieved his heart would be fixed! We knew God was in control and led us to Duke for a reason. We both stayed very optimistic for a successful surgery. The length of surgery could take anywhere from 3 to 6 hours. After a little longer than 2.5 hours, I received a call that the doctor needed to meet with me outside of the operating room. The first words were Scott was doing well, but when the Doctor hit a certain pulmonary vein, Scott’s heart stopped. The doctor knew at that moment that he hit the trouble part of Scott’s heart. They were prepared and knew exactly what to do. Again, we give God the glory for a successful surgery. God is so good! I broke down in tears in the waiting room and the girls hugged me. We are a strong and tight family. Tomorrow is three weeks from surgery, and Scott is doing amazing. His blood pressure is phenomenal and his pulse is now in the 70s and 80s instead of 40s and 50s. Praise the Lord!

In the midst of all of this going on, I needed to finish my last semester of college. I had 21 hours this semester and it was intense! Oh yeah, all the while working a full-time job. I am proud to say that I made all A’s, except one B. Yes, one B 🙁 – but I graduated last weekend with a Bachelor’s in Communication Studies with a Minor in Business. Now, I have three Associate Degrees and one Bachelor’s Degree. You better believe I was smiling ear to ear on graduation day. Knowing my family was right by my side cheering me on – was priceless!

Friends, I do not say that previous paragraph to brag. I shared because even though life can be hard, God is always there to give us strength and direction. He tells us in His word that he will never forsake us.

“Be strong and of a good courage, fear not, nor be afraid of them: for the LORD thy God, he it is that doth go with thee; he will not fail thee, nor forsake thee.” Deuteronomy 31:6

The last five months were a whirlwind, but here we are alive and well! I’m excited to start blogging again and sharing our faith. I want to show how our family has grown stronger in our faith, and share how to navigate the hard medical system. We have to fight for our family’s medical care. It’s not easy, but can be done. I will help you.

I look forward to writing and sharing with you all!

P.S. M has a big summer coming up. She is doing amazing and I can’t wait to share more about her adventures.

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Hello! I'm Jen and my family is my world. My hope is One Moms World will give you ideas for family travel and/or give you great consumer product suggestions that will be useful for your family. Remember to spread joy today!

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