Showing posts with label GracieGirl. Show all posts
Showing posts with label GracieGirl. Show all posts

Tuesday, June 26, 2012

Allergies and More Allergies!

It's common for E to frantically run to me, crying about his eyes or ears itching. He gets so worked up that it's often difficult to tell if it's real or imagined.

I get a cold compress for his eyes, rub his ears for him, and try to calm him down. I also give B-dryl if I think he needs it.

Last week, when he ran in, I did all of those things, and he eventually calmed down, only to return a couple of minutes later. This is what he looked like when he returned:



Nick took this a couple of hours after the initial reaction.
E had calmed down a lot, but the side of his face had not.
I still don't know what he ate or touched. He'd had a bite of GracieGirl's GF pizza, that he was really nervous about eating. He asked three times if it was okay. It was a leftover slice from a frozen pizza that Nick had bought, so I hadn't actually seen the ingredients. Nick's really good about checking, but it was just strange that E was so worried about it. He didn't want any more after the first bite.
He also touched a latex balloon. He's been around balloons before, so I don't think that he's allergic to latex, but he'd had a really severe asthma attack after playing with these particular balloons, so I'd put them away, just to be safe. One of the kids found them and got them out, and E touched one.
I didn't know it, but I found out that he'd gone downstairs and pet one of the cats. He goes down there occasionally, but I always make him wash up thoroughly afterwards. Since I didn't know that he'd gone down there, I hadn't made him wash his hands.
So, I don't know what it was, but his meds didn't touch it. His eye stayed swollen for the next 24 or so hours, and then graduated to looking like this:
The swelling is finally gone now, but he has a nice scar under his eye.


The next day, GracieGirl had a reaction to something, and itched from head to toe. A bath usually helps, but not this time. She just got more upset and wanted to get out. B-dryl didn't seem to do much, so I just smoothed the body butter I make all over her, and tried to calm her down.

Jay was next. He gets this strange, painful rash that only happens when we travel, usually to the beach. His dermatologist thought it might be an allergy to the sun, but he's not sure. This time, he got it while we were at the Chesapeake. It was unbearably hot for a couple of days, and he was outside a lot (in his long-sleeved shirts and jeans, of course). He went right from the Chesapeake to the beach, and now his entire face, except for his eyelids, is covered, as is most of the rest of his body. I haven't found anything that helps, and his dermatologist doesn't seem to be able to help him.

I dream of a life without any allergies!


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Monday, April 16, 2012

Allergy Season!

It's allergy season. Jay gets two allergy injections every week, and he's had some bad reactions, so he's taking additional meds prior to the shots. The shots aren't helping with his symptoms yet, and he, along with E, got hit a few weeks ago. As of this past weekend, Nate and GracieGirl are ready to rip their eyes out, too. I didn't even think about it, but E's PCA was here today, and she said that the trampoline is covered with pollen. What a way to kick it up, by jumping on it! No wonder the kids started hurting yesterday!

E just screams because his eyes are so swollen and itchy. He rubbed them so hard that he actually broke the skin and has scabs under his eye. He's had a number of asthma flares, and he also broke out in an itchy rash on his wrists. He wakes up crying and screaming during the night, and I know he's exhausted.

Spring was always my favorite season, but it's hard to enjoy it when I have to watch all four of my kiddos suffer. I'd love to open the windows, but that's out of the question. So, we have the a/c running in April. Even so, Jay just took five ice packs up to bed because he's so hot. Of course, he won't change out of his ever-present long sleeves and jeans. There's no point in arguing with him, so I just hope that he falls asleep soon!

Sunday, February 12, 2012

Another (Gluten-Free) Birthday Party!


Yesterday, in the final day of celebration
for GracieGirl's birthday,
we had a family party at our house.

GracieGirl loved this dress from her aunt,
especially because it came with a
matching dress for her baby doll.
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GracieGirl was actually tired of cupcakes
after having them several times this week,
so we opted for gluten-free brownies.
We cheated and used Betty Crocker Gluten-Free
Brownie Mix
. Everyone thought that they were
really good and couldn't tell that they were gluten-free.

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I don't have a picture, but we also had
Food by George's Brownies, which are a
longstanding favorite. They're premade,
so we try to keep them in the freezer
for emergencies. They are also soy and
corn-free, unlike the Betty Crocker's.
They are, however, processed with products
containing tree nuts, so they're not safe for E.

We tried Let's Do Gluten-Free
Ice Cream Cones
for the first time,
and even the picky eaters ate them!
They are also soy-free.

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One of GracieGirl's newest loves
is Lego Friends. She got several
sets for her birthday, and I was amazed
at how she built every one without
any help at all. This was the largest set,
almost 200 tiny pieces. She was very
proud of her accomplishment!
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She loved her new dress so much that she
wore it to church today with a sweater.
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As crazy as it's been with all of the celebrations, it was so worth it because GracieGirl is so sweet and appreciative. Every little thing made her happy, and I loved seeing her face light up at each show of attention. Birthdays haven't always been easy in our house, so we didn't take any of this for granted!

Now I'm ready for a quiet week...except that tomorrow is the 100th Day of School party, and Tuesday is the Valentine's Party and GracieGirl's Gotcha Day!

I should know better than to expect a quiet week! :)


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Friday, February 3, 2012

Bribery Week

We've learned that the key to successful parenting is bribery.

Some people may judge, but for us, it's all about survival. :)

Monday was the allergist for Jay and GracieGirl. Jay's dust mite allergy is off the charts. I haven't found a free housekeeper yet and allergy meds aren't cutting it, so the good doctor (he's one of the few that I actually like, even if we don't always agree) once again suggested allergy shots. I'd told him before that we will never again attempt anything involving a needle unless general anesthesia is involved. However, with the use of bribery, Jay actually had a "test run" shot in the office, and agreed to weekly allergy shots. Unbelievable.

Next was GracieGirl. The doctor is now thinking wheat allergy rather than celiac disease. He ordered another blood test, and then wants to do skin tests again. Bribery will be involved because GracieGirl has had both tests before and knows what she's in for!

E didn't have an appointment but he went along for the ride, and the allergist was very happy that he was in such good shape, just a week after being so sick.

Tuesday morning was E's fasting blood draw morning. He remembered the lab and wanted no part of it. There were tears but no screaming, so it could have (and has been) worse. Thank you, bribery.

Tuesday afternoon was Jay's appointment with his autism doctor. There have been many issues recently, but the doctor didn't get to witness any of them. Why? Because Jay knew that, after this appointment, he was getting his reward for surviving the allergy shot the day before!

One of the behavior therapists is here every Tuesday evening for Jay and E, and last week, she pushed Jay a little bit too hard for his liking. So he was not at all cooperative with her this week (understatement). She appreciates bribery and my guess is that she'll need to start using it again with him!

Wednesday was reading support and then the chiropractor for Jay, but he actually tolerates those two, so it was all good. He also had reading support on Monday and again yesterday. He's doing amazingly well, and even though he doesn't love going there (his teacher stopped giving him chocolate after each lesson!), I know that he's proud of his accomplishments.

Right now, Nate and Jay are seeing the orthodontist. Nate's appointment won't be fun, but this will be a particularly tough appointment for Jay. I had to figure out that fine line between telling him enough so that he's prepared without telling him so much that he's riddled with anxiety. He took two doses of a sedative prior to the appointment, so I'm just praying that it works.

Nick gets Father of the Year Award for taking the kids to every single one of these appointments (I was conference called in for a few of them), in addition to social skills classes, a school board meeting, two homeschool classes, youth groups, kids' groups, and soccer!

Finally, I have the quote of the week. I'm going to keep it anonymous, although most people who know my kids could easily guess who said it. It was said at an appointment to one of the doctors who loves to inquire about bowel issues. Every single time, the response has been that there are no problems. This response: "Well, yesterday I had a poop that was the size of a wedding cake!"

All I can say is that if we ever lose our sense of humor, we're in trouble!

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Saturday, December 3, 2011

Going Gluten-free...Again!

GracieGirl and E went bowling on a school field trip yesterday. Before they left, the school secretary called me to see if it was okay for E to have a soft pretzel. Well, when they got home, GracieGirl lifted her shirt, saying, "Look what happened after *I* ate the soft pretzel!"

Her tummy was covered with itchy, red bumps! I gave her some B-dryl, and before long, the bumps were gone.

I'm spending the day today making lots of gluten-free foods for her. Since timing is everything, I'll add that just last week, we went through our huge tote full of different GF flours and threw away at least 50 pounds of flour after discovering lovely weevils in them! I thought that they would be safe in zip-locks inside of the tote, but apparently not. Ugh.

Nick got new flour yesterday and I'm ready to start cooking. GracieGirl isn't too happy about this, and she already has food issues, but I'm going to do my best to have a lot of options for her so she doesn't feel deprived in the beginning.

Also, when we got E his Allerbling allergy alert bracelet, it came with two bracelets. Since E isn't allergic to wheat, we gave the extra bracelet with the wheat charm to GracieGirl.

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Let the fun begin! :)


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Friday, December 2, 2011

Adventures in Cookie-Making

I continue to hang on to Normal Rockwell imagines, especially when it comes to the holidays. One would think that I would have given up on that years ago.

We decided to make Christmas cookies. Roll-out cookies, to be precise. I pictured candles burning, Christmas music playing, the family gathered around the table, laughing and making cookies together.

It was originally Jay's idea to make cookies, and he'd searched online for a recipe. He found one and printed it out, and was later devastated to learn that it was a regular sugar cookies recipe, not a roll-out recipe. (Totally not his fault; the recipe pictured roll-out cookies!)

Meltdown #1.

That was a couple of days ago. We made them anyway, with the promise that we'd also make roll-out cookies.

It took me two days (recovering from making the first batch) to make the roll-out cookies. Jay and I made the recipe, and then we all sat down to roll out the cookies. Within minutes, I noticed that GracieGirl became agitated. Then, she started flipping out, scratching at her arms, crying because they itched so badly. It was driving her crazy, and we quickly gave her medicine and took her upstairs for a bath.

As a baby, GracieGirl couldn't handle gluten. She didn't have gluten for several years, and then we reintroduced wheat. It wasn't a conscious effort, really, more just laziness on my part. She seemed to do fine with it, but slowly started having some symptoms again. The allergist was sure that she had Celiac Disease, and he ordered a blood test. He was very surprised when she tested negative.

In the past week, she's had some symptoms again, although we hadn't associated them with gluten. One day, she came in with a huge hive on her face. I gave her medicine and it went away. The same thing happened the following day, again, just one hive. Another time, she started crying because she said that she itched all over. Again, we gave her medicine and a bath, and she seemed to be okay. The backs of both of her legs are covered with eczema, which comes and goes but is currently back with a vengeance. She's also had a lot of GI issues.

This latest incident just kind of firmed up that it must be the wheat. She was fine until she started rolling out the cookies, using wheat flour to roll them out.

She's feeling better now. I made some Monkey Munch for her, so she wasn't too sad about not having the Christmas cookies.

Time to go pull out my GF cookies recipes!


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Tuesday, July 19, 2011

More Allergies and More Prayer

So, after listening to Jay screaming at the top of his lungs, and having to hold him down to prevent him from bolting from the room (and this was with the sedative that J had taken before leaving the house!), Nick learned that Jay is allergic to shellfish, trees, weeds, cats, and dogs. But, dust mites are by far his worst allergy.

The night before he went in for testing, I was reading about how most kids with eczema are allergic to dust. So now I'm praying that we can get the dust in this house under control so that we can get his allergies and eczema under control!

I spent hours cleaning and dusting the bedroom, and Nick went in and vacuumed thoroughly. The allergist said that we really have to take up the carpeting, put in floors, replace the blinds, and cover the mattresses and pillows with allergy covers. I'm just praying about all of that because I have no idea how we're going to come up with the funds to do it.

Meanwhile, I've been up since 3:30 this morning because GracieGirl now has eczema on her back and legs, and she was going crazy with the itching. I gave her medicine and then held her for an hour until she stopped whimpering and went back to sleep. I'd started cleaning out her room, because she is also allergic to dust. We need to get the rug out of her room, too, and get her mattresses and pillows covered.

Now I know what my mom went through with me when I was little because I'm allergic to dust. I don't know how she found the time to clean my room each day, but that's what I need to do with our bedrooms. The problem is that I can't vacuum or do a lot of the other cleaning, and Nick's already up to his eyeballs doing all of the other things I can't do! All I know is that five out of six of us are allergic to dust, and we need to find a way to keep on top of the cleaning.

So, I'm praying for flooring, allergy covers, and someone to come clean our house! :)


Oh, and they want Jay to start weekly allergy shots immediately. I'd better pray about that one, too!


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Monday, May 23, 2011

Allergies and Asthma and Eczema...oh My!

I took GracieGirl and E to the allergist today. We borrowed a van from a friend (thank you!!) so that Nick could pick Jay up from his autism class, while I took the kids. I was a little bit nervous about E getting out of control, so I pulled Nate away from his friends to come along and help. He was not thrilled.

I love our allergist, and he always keeps the kids entertained and in line. He pretended to hypnotize E with his stethoscope, and I told him that if he pulled that off, that stethoscope was coming home with me! He said that of course E couldn't sleep; he has too much energy to sleep!

He was happy with GracieGirl, except for the eczema that covers the backs of both of her legs. He wasn't happy with E at all, saying that we need to get his asthma under better control. He started him on a new med and wants to see him in three months. He also wants to do another blood test and then possibly another egg challenge, depending on the results of the blood test.

I came home with a whoppin' 14 scripts! Fourteen meds for two little kids! Unbelievable.

E was good, for the most part. He did tell the doctor that he didn't look like a doctor; he looked like he married a man. Huh?? I finally figured out that he meant that the doctor looked like a man who was getting married because he was wearing a tie! Apparently, he didn't look like a doctor because he doesn't wear a lab coat!

E did run out of the office as I was scheduling his next appointment, and then tore out of the building as we left. Couldn't have done it without Nate...

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Monday, May 17, 2010

Weekend Sleep and Test Results

Nick and I have had a much-needed relaxing weekend. I knew I needed a break when I went to call my in-laws and couldn't remember their last name! Thankfully, my son reminded me that I share a last name with them, so I was able to call them. :) They picked up the children on Friday and took them to their house for a long weekend. I'd forgotten what it was like to sleep all night long, without being woken up by screams in the night or being kicked in the side or hit in the face while sleeping. Amazing how much better I feel after a good night's sleep...

We did some crazy things like order Vietnamese takeout, which meant that we ate PEANUTS in the house!!! Honestly, I felt like we were doing something illegal! We also worked on the business, visited my mom in the hospital, and cleaned up/organized the house. Nothing exciting, but I'm happy!

We did get some test results last week. The allergist called and said that E's blood tests showed the same thing as the skin tests: he's extremely allergic to peanuts, all tree nuts (sadly, even almonds), and sesame seeds. Eggs were also high, but he wants to do a cooked egg challenge in his office. He said that I have to make angel food cake, making sure to bring in enough for the entire staff. (He's so funny!) He assured me that he would have any needed meds right there, and he'd start by touching the cake to E's lips and then waiting to see if there's a reaction. Then he'll touch it to his tongue and wait again. Next, E will actually eat a little bit of it. Not only will this determine if E can handle cooked eggs, it may also help him outgrow his egg allergy sooner. So, we'll see what happens. My gut tells me that he'll be able to handle cooked eggs, but that may just be wishful thinking, especially since our grocery store just stopped carrying Egg Replacer!

GracieGirl's Celiac test came back a few days later. Negative. I was really surprised. So was her allergist. She's going back to see him this week, so we'll find out what to do next. I, of course, started researching online and came across this info on NCGS (Non-Celiac Gluten Sensitivity). The logical solution seems to be to take her off of all gluten again but I want to get as much medical information as I can before doing so.

I'm thankful that we continue to get answers, even when they're not always the answers we'd like to hear! :)

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Friday, May 7, 2010

Catching Up


Our business, Truly Pure & Natural is finally up and running. We've had a good time working on it, even though Nick has done the vast majority of the work. Some people have asked if it's a Multi-Level Marketing company, such as Shaklee or Arbonne, and it definitely is not! It's simply an eclectic collection of natural products that we use and that work for us. We're slowly adding new products that we want to share with others.

GracieGirl and E both had to have bloodwork at the beginning of the week. I dreaded it because last time, E's screams could be heard three counties away! So, I did the wise thing this time...and stayed in the car while Nick took him in. :) Amazingly, he didn't struggle or cry. Nick brought him out to the car and took GracieGirl in. Same result, not even a whimper. I want to get that tech's name and ask for her every time!

E was having blood tests to confirm the skin tests for his allergies. I was hoping and praying that he wouldn't be allergic to almonds because I'd love to be able to use almond flour as an alternative to wheat and other grains. No such luck. The doctor will call us on Monday but the nurse said that he is highly allergic to all tree nuts and eggs. Unfortunately, in E's head, the doctor said he won't die if he eats nuts! So, I've been working on convincing him that the doctor most definitely did not say that. He's been really good about asking before eating anything, and I want him to continue doing that!

GracieGirl's Celiac test didn't come back yet. I'm hoping to hear something on Monday. She's been complaining of a hurt tummy for the past few days, so I'm just praying that the test shows whether or not it's Celiac.

Jay got his sleep study results and he does not have sleep apnea and his adenoids do not need to come out. So...back to the drawing board. I'm still waiting to hear back from the sleep specialist, and he sees his autism doctor in a few days, so we continue trying to find some answers!

I don't even know what to say about E. His behavior continues to worsen. I asked Nick if it was me, thinking that maybe I'm just getting too old and burnt out for all of this. He said that it definitely was not me! (I knew that, but I just had to confirm it!) The good news is that I'm getting support, which means so much. People have suggested things like bi-polar, RAD, and ODD. Hard to hear at first, but now I just want answers. I filled out a 15-page request for evaluation and sent that off. It's just hard because he has such a wonderful side, so I keep thinking that I must have been exaggerating his other behavior, and it really wasn't that bad. But then he gets violent, often without warning, and I'm reminded that things really are bad. I'm just praying that we can find the right help for him because there's a side of him that really is so sweet.

Besides being busy, the other reason that I don't generally blog during the day is that I pay for it afterwards. This time, GracieGirl and E have gotten into the crafts box. Judging by the creative mess they've made so far, I really should be focused on them, rather than on this blog! Off to survey the rest of the damage... ;)

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Monday, April 26, 2010

Allergy Update

I've become accustomed to the boys' large medical files. Well, Nate's is large; Jay's and E's are downright huge! In-between, hidden in the file cabinet, is GracieGirl's file. I think it has two sheets of paper in it. She's been the healthy one.

Today, she and Jay had appointments with the allergist. We never took her before because, although she had problems as a baby, a friend suggested that we take her off of wheat. Problems solved! I told her doctor what we'd done, and he didn't see the need in having her tested.

Late last summer, we reintroduced wheat into her diet, and she seemed to tolerate it well, so we assumed she'd outgrown any allergy or sensitivity she may have had to it. Then, in the fall, her nose started running...all the time. She started having lots of problems with gas, and we wondered if she had reflux.

She was tested this morning, and the allergist said that she isn't just allergic to all trees, all grasses, and all weeds, she's severely allergic to every last one of them! Animals were okay, except for mice. Foods were okay; she didn't test positive to any of the top allergens. She's allergic to one mold and to dust. Ugh.

The allergist suspects Celiac Disease, so we have to get a blood test for that.

So much for my healthy little girl. I'm just thankful that we have some answers and can start working towards helping her!

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Sunday, April 25, 2010

Doctors and More Doctors!

We've been in full swing with doctor's appointments again. We'd switched allergists, thinking that it would be easier to have all of the children's doctors at Children's Hospital, but we decided to go back to our old allergist. Nate and E went this week and GracieGirl and J are going tomorrow. The allergist said that Nate's asthma is under control but his allergies are bothering him. E's report wasn't as good, and the poor little guy came home with a stack of prescriptions!

Jay saw the dermatologist again, too, and she thinks that some of his problems with nighttime scratching may be behavioral. I'm not sure why she would think that, since the majority of his body is covered with eczema, and I'd kind of think that that's why he's scratching! She wants us to make an appointment with a behavioral specialist through Jay's developmental pediatrician at the autism center. We'll try anything that might help; I just to get to it on my To Do list yet!

Jay had a sleep study a few nights ago. He had some trouble dealing with all of the wires, but he loved the room...the bed with a sleep number mattress, the big, comfy quilt, the large flat screen TV, and lots of snacks. Once he was settled in, he lay back and said, "Yep, I could definitely get used to this!" He paused for a second and added, "It's not because of the TV or even the snacks; it's because there's a bed in here for you, too!" He's so sweet...

He brought his sleeping bag with him because he practically lives in it at home, so that helped comfort him a bit.

J
Jay in his favorite sleeping bag. I don't know how he does it,
but he walks in it and goes up and down stairs in it!


So, I was selfishly thinking that I might get a decent night's sleep, being away from the nighttime drama here at home. I went to bed at around 11:00pm, got comfy, closed my eyes...and Jay's monitor started going off! The tech came in and turned it off, and once again, I settled in. Three minutes later, it went off again! This time, both techs came in, turned on the lights, started replacing parts on the machine, and finally left. I don't know what the problem was, but this went on most of the night! I was feeling far from refreshed when they woke us up at 6:00am! I'd begged asked for late checkout, just as I'd done during my sleep study, and once again, I was turned down! ;)

I was feeling sad this weekend because, for the first time ever, we missed Sesame Place with the Variety Club. E is really struggling with his asthma, so he couldn't go. He's had a few rough days (and nights!) between the asthma, allergies, hives all over his arm one night, and the little, itchy bumps that are covering his entire back! The allergist ordered blood work for him to check on some of his allergies. Nick thought that these symptoms were perhaps linked to the Cyclic Neutropenia, which makes his white count low every three weeks. If this is the low period, maybe his little body just can't handle everything. I don't know, but I sure would like to help him feel better!

Now we're just continuing to pray that E stays out of the hospital. The treatments aren't helping much, and tonight his breathing was really labored. I still don't feel confident about knowing exactly when he needs to go to the hospital, but Nick is confident that he knows. Prayers greatly appreciated for our little guy!

E
E decided that the only way to feed the birds is to dump the seed
all over the place, roll in it, pull up leaves and sticks,
and then sit and call the birds to come eat!


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Saturday, May 16, 2009

Living with Food Allergies

As Food Allergy Awareness Week wraps up, I thought I'd share, as others have done, a bit about how food allergies affect our life. Most days, we just go with the flow, but there are times when I stop and think about how much easier our lives would be if there was a cure for food allergies.

I was allergic to hundreds of things when I was growing up, but anaphylaxis wasn't part of the picture, so I had no idea what living with life-threatening food allergies was like.

In our house, Jay is allergic to wheat and gluten (rye, barley, and most oats) and dairy. The nutritionist also has him off of soy, refined sugars, and most carbs. GracieGirl is allergic to wheat and gluten. E is allergic to peanuts and tree nuts (anaphylactic), eggs, and dairy. Nate was tested as a toddler and no foods showed up, but I suspect a dairy allergy or intolerance.

Jay has severe eczema, E has eczema and asthma, and Nate has asthma.

We make almost all of our food from scratch. There are some prepared foods we can buy but they're expensive and often don't taste as good as homemade.

Baking is an adventure. We have a cabinet and freezer full of different flours. We can't use just one flour when we bake; we have to combine several flours, such as rice, sorghum, tapioca, and potato starch. We use xanthan gum to keep baked goods from becoming a crumbly mess, and powdered egg replacer as a binder. We use olive or coconut oil instead of butter and rice milk instead of cows' milk.

We never have peanuts or tree nuts in the house. We do have eggs, and it's a bit stressful keeping E away from them. E doesn't have anaphylaxis to eggs, but he did have an immediate reaction after eating them, so we don't know what a second reaction might be like. It's sometimes challenging, especially when we're rushing, to remember who eats what. GracieGirl can't have the Ezekiel Bread; she has to have the brown rice rolls. E can't have the rolls because they have egg whites in them. Jay doesn't like meats or most vegetables and that's all he's supposed to be eating right now. Nate can't stand rice milk or gluten-free bread.

On the rare occasions that we find a meal, or even a single food, that everyone likes and can eat, it's cause for celebration!

We always plan ahead. When we leave the house, we pack food and drinks for everyone. We don't have the option of stopping to pick something up if we run late and get hungry.

We read labels, read labels, and just when we think we've read enough, we read more labels! Product ingredients change, so, just because we bought something that was safe one time doesn't mean it will be safe the next time we go to buy it. We also avoid products that were processed in facilities or on equipment that processes peanuts or tree nuts. Studies have shown that a full 10% of foods manufactured on shared equipment will actually have nuts in them.

We avoid some homeschool events, especially those centered around a meal or where a lot of snacks will be served. We opt for more of the outdoor events and field trips.

Family get-togethers are difficult. Jay has a tough time watching his cousin eat pizza and chicken nuggets and desserts that he loves but can't have. When possible, we bring our own substitutions so that he doesn't feel as left out, but it's not always possible and it usually doesn't look as good to him as the stuff his cousin is eating!

Baseball games and flying are two other things that we avoid because of nut allergies. We always carry wipes, and when we go shopping, we wipe down the cart before putting E in it, in case the child before him was eating nuts. E is at that age when he puts everything in his mouth and I worry that he'll pick up a piece of discarded candy at the park that has nuts in it. He also believes that all cups and water bottles must be his, and I worry that he'll grab one that may belong to someone who was eating nuts before drinking from it.

I'm also concerned about people not taking the children's allergies seriously, and/or thinking that we're overreacting or being overprotective. With Jay and GracieGirl, they'll get sick if they eat foods they're allergic to, but with E, he could die from eating nuts or peanuts. He doesn't have to eat a Reece's Cup; he could react from getting a kiss from someone who had eaten peanuts or from eating food that had been served with a spoon that had just a trace of nuts on it.

E can never be without his EpiPen. Thankfully, we have never had to use it. It scares me to think of using it on him, but I'm confident that I would do what I had to do if he was having an anaphylactic reaction. We have EpiPens in a bag by the door, along with a bottle of Benadryl. There are EpiPens and Benadryl in the kitchen and upstairs in our bathroom. We always have them on hand, in their designated spots, and we always make sure they're in date.

E is rarely away from us, and I wonder about sending him to friends' houses when he gets older. It's hard enough for us to keep on top of reading labels all the time; can we expect others to do it vigilantly? What if his friend gives him something, without the friend's mother knowing?

Jay, who is almost nine, knows what he can and cannot eat, and he's good at telling people that he can't eat something. GracieGirl is good, too; she knows that she can't eat bread or pasta or cookies or pizza at people's houses, but I sure can't expect her to know about all of the hidden sources of wheat. All of the kids are very protective of E and will quickly tell family or friends not to feed him certain things or eat nuts near him.

I don't worry about E all the time, but I do have concerns when he suddenly develops hives and I have no idea what caused them. When his eczema or his asthma flares, I wonder if a food allergy is involved. Recently, his eyes have been swelling and he screams and rubs them frantically. He's also been sneezing a lot, after which he also screams and holds his ears. I'm also concerned about other allergies to foods he hasn't been tested for. We haven't given him fish or sesame seeds, for instance, because they're highly allergenic foods, and we don't know if he'll react.

Maybe this is sounding whiny, but I'm not complaining about it. We do what we have to do. Yes, it's a pain, and yes, if I had a choice, I'd certainly prefer that the kids not have food allergies.

On my Fantasy Food Allergy Wish List, if I couldn't get a cure for food allergies, my next requests would be a freezer full of allergy-safe, delicious convenience foods that all of the kids loved, and a healthy, allergy-free fast food restaurant in every town.

I can dream, can't I?? :)
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