The elevator to success is out of order. You'll have to use the stairs...one step at a time. ~Joe Girard

Spreading Awareness

My purpose in writing this blog is to spread awareness and provide support to parents of children with and without special needs. I have one child with a Learning Disability, more specifically, a Visual Processing Disorder including Dysgraphia and another child with a disease called Eosinophilic Esophagitis, an allergic white blood cell disease that attacks the esophagus.

Tuesday, October 12, 2010

Eosinophilic Esophagitis is in Remission (FINALLY) on Elemental Diet and Flovent - Now Bring on Food Trials!

Finally...Andrew is in remission!  The scope he had on Thursday September, 29 confirmed it.   The elemental diet of EO28 Splash plus swallowed flovent has done the trick.  It's taken a while to figure out the right combinitation, but thankfully we have. 

Andrew had been anticipating this scope for quite a while.  He knew that if it was clear he would be able to begin food trials.  As we waited for his procedure to begin he chatted with the nurse about normal 8 year old boy stuff, as at ease as if he was talking to a friend's mom.  It still amazes me how unconcerned and comfortable he is while he is at the hospital.  I, on the other hand, feel sick to my stomach each time he has a scheduled procedure.  Then the conversation turned to food and what food he wants to be able to eat if he has a clear scope - a reminder of the reason we were there, although to Andrew it was still a matter of fact conversation.  Although I am glad that he does not get nervous or upset about going to the hospital, there is still something unsettling about knowing that your child has had so many procedures that he is actually comfortable, at ease, and the staff knows him by name.

After the prep time was over and I signed all the papers, basically signing my baby's life away, he was rolled back to the OR where we met the anesthesiologist, the GI and the rest of the team.  They answered any questions Andrew, my husband or I had and then they put the mask on his face and he started to fall asleep.  I absolutely hate that feeling-watching my baby go under.  I gave him one last kiss, told him I love him, and my husband and I went to the waiting room until Andrew was brought into recovery.

About  half an hour later a receptionist came for us and brought us to recovery.  Andrew was still partially asleep, in that drugged state.  Dr. Caicedo walked in shortly after.  I could tell by the look on his face that he had good news for us.  It was the best looking scope to date.  He said there were no visible white spots.  The only other time that has happened was when Andrew was in remission on systemic steroids.  After he said that, there was this little drugged voice from the bed, "Does that mean I get to have food?!"  My heart almost broke.  Even though he was still drugged, he knew enough to understand what was being said.  Dr. Caicedo was optimistic, as were we, but we had to wait for the biopsy results.

Fast forward 5 days:  A nurse calls to let us know that Andrew is definitely in remission, which meant that Andrew could begin his first food trial.  I needed to speak with the doctor about the particular food that Andrew wanted to eat (bison) before allowing him begin, which took another 2 days.  After waiting so long to eat, I was not going to do anything to jeopardize it by not speaking with the doctor before we began.  So a week after the scope we got the green light from the doctor.  On Friday we purchased some ground bison and on Saturday, 282 days since the last time he had food, Andrew was able to eat a bison burger.

What a wonderful lunch we had.  We were all able to sit down and actually eat food as a family for the first time in over 9 months.  Watching Andrew eat his bison burger brought so much joy to our family.  He ate it so slowly, savoring each bite.  He enjoyed his meal thoroughly.  Madison was so happy for him.  She grabbed her camera before lunch started and continued to take pictures of him throughout lunch. 

When Andrew started his elemental diet he was told it would be for 6 weeks.  It has been 282 days.  Can you imagine not being able to chew food for 9 months? How would you feel knowing your family is eating meals and you can't each day for 282 days?   Watching your friends at school eat lunch, celebrate birthdays with cupcakes, use candy for lessons for 38 weeks and not participating?  The list goes on and on.  But my Andrew did this with maturity, grace, and so little complaints.  I know the challenges have just begun, introducing foods can bring on issues of their own, but I am so grateful that God has given Andrew the strength to deal with curve balls that are thrown his way.  I know that as a family we will be able to handle the challenges of food trials if we follow Andrew's lead.

The next step?  Andrew will continue eating bison for 2 weeks.  If he has no symptoms, he will reintroduce a food every 2 weeks.  If symptoms occur we will stop that food and he will be scoped.  If no symptoms occur, then he will be scoped after every 5 foods , or every 10 weeks.  There is a systematic way to introduce foods based on a scale of the least allergenic foods.  It usually starts with vegetables, fruits, and moves on from there.  We are deviating some from the protocol by allowing Andrew to start with bison, however, it is on the bottom of allergenic scale for meats.  Now it is just wait and see....Wish us luck!

5 comments:

  1. This comes on the heels of Canadian Thanksgiving here which was yesterday! What wonderful news. I am convinced I have EE related to my seasonal allergies. I have a slew of food allergies however the EE seems very tied to the seasons. Your blog has been very informative!

    ReplyDelete
  2. What wonderful, wonderful, wonderful news. Tears of joy are running down my face as I read about eating his bison burger. I wish you all the best of luck and pray that all continues to go well in the reintroduction diet.

    Allergy Mum
    http://allergymum.blogspot.com/

    ReplyDelete
  3. Thank you both for your comments and well wishes. It truly is wonderful news.

    Lan, EE can definitely be related to seasonal allergies. There are many doctors that will not scope at certain times of the year for that exact reason. I hope you are able to keep your symptoms under control. I'm glad my blog has been a source of information to you. Please feel free to contact me at any time.

    ReplyDelete
  4. I'm curious about your sons treatment. My husband and boys also have EE. All three of them have a huge list of foods they don't eat. However, they don't have outward signs on all of those foods. Only internal ones. They each have maybe 3 or 4 foods that we actually see hives or worse. So our game plan is to elemenate all the positive testing foods and wait for the clear biopsy. Then we slowly reintroduce the foods least positive first. Scoping every 3 months to make sure EE hasn't gone up in numbers again. Our doctor didn't want to make the treatment worse than the disease. That is why she doesn't put them on the elemental diet only. My youngest (2) recently tested 0 and has started foods back in his diet (wheat and corn). He was diagnosed in Jan of this year. My oldest son (4) was diagnosed in May and my husband in June. They all three will be scoped again in December so we're hoping our oldest son will be at 0 as well. My husband will probably never actually get back to zero and has a lot of scar tissue. With him we'll just keep an eye on it and when he feels more swollen he'll eliminate certain foods. They said he's had it since he was a baby. He's a whole other story. Somedays I think trying to figure out 3 meals a day for 3 different diets is tough but if I had to tell any of them here's your meal and hand them a drink it would be much harder. I can't imagine what you've gone through dealing with that. Cheers to you mom!

    ReplyDelete
  5. Somehow I must have missed this comment. Thank you for your kind words. It is difficult telling your child that he can not eat and feeding him only liquids...however, what is the alternative? No one really knows on a definitive basis. The damage that eos are causing, even if they are not making him symptomatic, may be irreparable, thus making his future of eating rather grim. In theory, if he continues to eat, with the way his esophagus looks now and the numbers he has now, may cause him difficulty swallowing, food impaction, continual stomach pain, etc. with the likelyhood of esophageal surgeries. If we can do something now to prevent that for him in the future, as hard as it is for him (and for me), I'm going to do it. Believe me, it was not an easy decision. My husband and I agonized over it for a long time before we decided to put him on the elemental diet. We also discussed it with Andrew. And as difficult as the first few weeks were, after they passed, he realized he FELT better and decided drinking with little to no pain, was better than eating with pain.

    Each child, family and case is different. So are the doctors that treat us. We just need to take the information that we have, look at our children as individuals and make the best decisions we can. Being parents of EE children is not an easy task, but we are strong and they are well worth the effort!

    ReplyDelete