Hanks Place

Hanks Place Please follow Henry's journey. He was diagnosed at 6 months old with EOE- Eosinophilic esophagitis. Henry is my five month old son, born October 23, 2012. Panick.

At two weeks old he developed a cough that has yet to go away. At seven weeks old Henry was diagnosed with Flu-A. We were sent home from the doctor that day and told that there was nothing they
could give him. He rode out the symptoms with us and when they didnt go away we took him to the doctor. That day, a friday, he was diagnosed with bronchiolitis. Sent home with nothing much they could do for him but albuterol treatments through a nebulizer. By sunday he was having seizure like symptoms from the albuterol and we stopped them at the doctors orders. Sunday evening he stopped eating. Monday morning he stopped output. That afternoon he was admitted into Texas CHildrens hospital. The triage nurse though his coloration was a little suspect due to the fact that his
heart -rate was 80 beats per every 20 seconds. His heart could stop. Turns out my son is simply see-through. Casper-like. Thanks to his mic daddy. :)
He was well enough to go home the next day. THrough-out these ordeals we kept telling the doctor that he was spitting up an awful lot. Mind you- I have three children, I know whats normal spit-up. This was not normal
So here Henry was. Barely three months old. On Zantac and Albuterol. When the symptoms of wheezing would just not go away I took him to the doctor yet again. Breathing treatment in office stat. Go to the hospital again, Stat. Not this time, I said. Give me an alternative. She complied. Chest x-ray and Pediatric Pulmonologist in the Medical Center, Downtown. I get to leave the x-ray center with the images. I Peeked. Clouds and spots. Pulmonologist was amazing! Diagnosed with G.E.R.D. Gastroesophogeal Reflux Disease. With Asthma stemming from it. A week later I want a second opinion. I jump through hoops to get an urgent care referal. He needs a pediatric GI
Monday March 25, a well baby check-up! Finally! He is "well" enough for vaccinations! we leave that day defeated. Henry has lost weight
Since Henry was weighed at 2 months old he has only gained 2 pounds. Henry is now 5 months old. We also leave that day with an urgent refereal to be tested for Cystic Fibrosis. Monday April 1, 2013. Maybe we can get some answers. Henry cant keep his food down. Henry cant gain weight
Henry chokes
Henry aspirates on his acid
Henry cant breath without a wheeze. Ever. Please keep Hank in your prayers. I am not the kind of mom to do this. To put this all out for public viewing. But, there is a power in prayer that just cannot be denied. Please pray hard to whoever you pray to. I pray to the Lord
and my belief teaches me that where one or more gather there HE will be. Please gather here. Pray here. UPDATE: Henry is now 9! We have narrowed down his issues to eosinophilic esophagitis, eosinophilic colitis and a small hole between two chambers in his big heart!

Now that Henry’s “out” of the main part of the Regeneron study, the meds get delivered to us monthly! He’s starting to g...
05/10/2023

Now that Henry’s “out” of the main part of the Regeneron study, the meds get delivered to us monthly! He’s starting to gain a little weight and has been seeing a neurologist for some small side affects but all in all we’re so grateful for this!

Today henry is having his last Endoscopy as part of the dupixant trial! 52 weeks flew by! While we’ve seen some improvem...
12/19/2022

Today henry is having his last Endoscopy as part of the dupixant trial! 52 weeks flew by! While we’ve seen some improvement with symptoms, overall it hasn’t been the vast improvement we hoped for last year. However, Regeneron has agree to keep Henry in the study for another 106 weeks! 💙💙

Welp!! We’re halfway through the dupixant trial!! Today was the halfway scope and biopsy! This also marked Henrys 12th p...
04/13/2022

Welp!! We’re halfway through the dupixant trial!! Today was the halfway scope and biopsy! This also marked Henrys 12th procedure at 9 years old! They don’t even go through the formalities anymore … just “any questions? Nope- great! See ya on the other side buddy!” 😂 got a decent view of his little tissue samples today too! Off they go to Cincinnati 😳!! He had a rough recovery with a sore throat this time and the doc did show us some areas of concern with “crepe paper” tissue in the upper esophagus that has never shown up before. This time around we won’t be told his “numbers” or eosinophil count due to double blind but that’s ok! He’s home resting now and being spoiled with Gatorade and ramen 🍜 💙💙

02/01/2022
Today was at home injection day!! We will do every other injection in the home from her on out (I believe).  Today his b...
01/28/2022

Today was at home injection day!! We will do every other injection in the home from her on out (I believe). Today his big brother Connor offered to assist! It takes a village to calm him down before each injection. I wish I could say I’m getting good at these but today didn’t go so great. A bit of a reaction at the injection site so now we’re just monitoring him. He is cozy in mom and dads bed with a movie!! 💙💙

Injection three in the books!! Henry has had a couple very weird side affects (we think) since his first injection. The ...
01/15/2022

Injection three in the books!!
Henry has had a couple very weird side affects (we think) since his first injection. The main one has been spitting-a lot! He seems to think there is a “hair” in his mouth and he must get it out! This has gone on since injection one to this day… so we just got a call from our sponsor saying they’d like Henry to start seeing an ENT as well to rule some things out and a therapist for some major anxiety this kid has.
All in all we’re trucking along, taking the advice as it comes and continue to monitor his weight! Which , even through covid, has increased by 1 pound! 🙌 to small miracles!!

In an effort to document all of Henrys journey with eoe and subsequently , dupixent, we have had a doosey of a couple of...
01/05/2022

In an effort to document all of Henrys journey with eoe and subsequently , dupixent, we have had a doosey of a couple of weeks since injection one! There was a bit of a scare with his bloodwork that came back from the first injection, so we quickly went to the lab to recheck some things! Then, just as we were given the all clear to proceed with injection two, on January 4, covid struck our home! Our quick thinking, over achieving (🥰) team at Texas children’s got permission from the sponsor to have the second injection couriered to our home! It arrived late this afternoon and we quickly removed it from its special refrigerated box (thanked our courier profusely) and waited for it to cool down to room temp! With a little help from FaceTime, our Nurse prac and pickles the pug: Henry is officially on to injection three!!

Today was the day!! Henry had his first dupixent injection. As part of a double blind trial there were lots of condition...
12/16/2021

Today was the day!! Henry had his first dupixent injection. As part of a double blind trial there were lots of conditions, consents and moving parts to this but it went well! Henry has been a part of the EOE clinic with Dr Davis (pictured below) since he was six months old. She came in today and said “what a journey we’ve been on henry, nine years” and what a brave boy he is to be in this trial to help other kids his age with eoe feel better. Henry told her that kids with disabilities are like superheroes - because they have something no one else has. What a great way to start this next journey. The injection itself didn’t hurt, but the push of meds did. Henry has expressed he doesn’t like the term “drug” so we’ll be calling this “medicine” from here on 😂. He immediately had no reaction but throughout the day started showing major fatigue, which we fully expected, and now a sore injection site, also expected. So! We carry on! Next injection January 4th!

HE’S IN!!!  Just got the call from the study manager at Texas Children’s - Henrys scope showed high enough levels of eos...
11/22/2021

HE’S IN!!! Just got the call from the study manager at Texas Children’s - Henrys scope showed high enough levels of eosinophils in at least two places and he is in the dupixent trial!! Thank you all so much for your thoughts, vibes and prayers for our son !!💙☮️

He’s out! And parts of my baby are on their way to Cincinnati Children’s Hospital!  🤞
11/17/2021

He’s out! And parts of my baby are on their way to Cincinnati Children’s Hospital! 🤞

Here we are nine years later… after hearing things like “incurable,untreatable”, “new disease, not a lot of research,” “...
11/17/2021

Here we are nine years later… after hearing things like “incurable,untreatable”, “new disease, not a lot of research,” “in its infancy,” “may be the youngest we’ve seen with this yet,” amd my favorite- “well, let’s try this and this for a while…”
Today we’re on the verge of an ACTUAL TREATMENT! One that has had significant findings in children 12 and up. Henry is in his final phase of possibly being approved for the 12 and under study. He’s just been taken back for what will be his most intrusive biopsy but one with, hopefully, the most impactful results.

This is such a great article (quick read) about the double blind trial we’re in ! Henry goes for his endoscopy on Nov 17...
10/26/2021

This is such a great article (quick read) about the double blind trial we’re in ! Henry goes for his endoscopy on Nov 17 to determine if he has a high enough level of eos in two places of his esophagus. Henry will be in the first group for his age group (under 12). If so, he’s in!! This article also does a quick rundown of his disease and what he has dealt with his whole life .. 💙

TARRYTOWN, N.Y. and PARIS , Oct. 25, 2021 /PRNewswire/ -- Dupixent 300 mg weekly significantly improved the ability to swallow and reduced eosinophils in the esophagus compared to placebo, reinforcing positive results from first Phase 3 trial Eosinophilic esophagitis is a progressive disease that

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