Showing posts with label epipen. Show all posts
Showing posts with label epipen. Show all posts

Saturday, April 9, 2011

Always the same.

Finally beautiful weather to take the little guy to the park today. I was not the only parent with that idea. The park was buzzing with kids today and it felt so good. Our guy had a great time.

As usual I had his epipen on me. I didn't bring a bag so it was sticking out of my pocket a little. I think any mom with a child who suffers from food allergies can spot and epipen a mile away. That's what happened today and I'm glad.

This very nice mom to a beautiful little boy came up to me and asked if Mac had food allergies? I of course said yes and then laughed because I remember the epipen sticking out of my pocket. She said I have mine in my bag. We got to talking and comparing allergies.

Whenever I meet someone who has a child with food allergies they all same the same two things:
1. How it is such a life changing diagnosis.
2. How alone they felt when hearing those works your child has a life threatening allergy to...

The second one always make me so sad. Why is it that we feel so alone? There are over 12 million people estimated to have food allergies. I am meeting people all the time now who have to deal with them in their families or just know someone.

I am reminded once again that more research, education and awareness is needed. I told her about the support group Helen and I are starting and she was excited to hear about it. I hope she comes. This is the exact reason I wanted to do this. We need to be there for each other, and learn from each other. Most importantly we need to know we are not the only ones.

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Thursday, March 3, 2011

Do you know your expiration dates?

Yesterday on Facebook I said I forgot what I wanted to write about. Well I remembered! I was dropping the little man off at the sitter/good friends house. Since earlier in the week we signed the kids (Cormac and her daughter), up for a class together that she will be bringing them too. That with spring hopefully on the way means she will be taking them out more.

So I just wanted to have the EpiPEn reminder talk. It's time to have it with everyone. We don't talk about it every time we see her or even monthly so I thought it would be a good idea to start refreshing people's memories.

I just stated the 2 simple rules that we have.

1. It MUST go everywhere with him. The park, library, a play date, everywhere. No exceptions.

2. Never leave it in the car. Temperatures can damage the medicine and make it less effective. Plus you never know when you may need it.

His sitter (and also good friend), is on top of this! I know she knows and does this, but it still needs to be said to anyone who takes care of our little man. A little reminder never hurts. Mom and Dad your next!

This EpiPen talk lead me to remember that both sets of EpiPen's are expiring soon. One set next week, and the other next month. How I remembered with my baby brain is beyond me! Let me say this is an accomplishment for me. I have the worst memory when it comes to dates. I can't remember the exact date of my best friends birthday and we've been friends for over 20 years. You would think that the husband couldn't remember the wedding anniversary. Nope it's me. I get it wrong all the time! When people ask I just wait for him to answer. Of course I get the look from him every time. I even mess up his and Cormac's birthday. I just have a hard time with numbers.

However I guess when it comes to my son's life, dates are not a problem. I can tell you when his EpiPens and car seats expire. So the really important stuff is in there. If you get a chance, go and check you emergency meds and epi's. If you can't remember when they expire, you can always register you EpiPen's here and they will send you a free e-mail reminder. They also have a app for your iPhone. I don't have it yet, but may try it out. I think it's a good idea for care takers to have. If you don't wan to register, you can also put it on your calendar at home, computer or phone. If you use an electronic calendar, have a reminder set at least a week in advance so you have time to call the Dr. to get a new Rx.

I just have to remember to call the Dr. and get the Rx. Oh baby brain how I hate you! I also have to go find out why ducky is in the naughty chair.

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Thursday, December 16, 2010

Two Reminders

Epi Pens

With the cold weather settling in remember that your epi pens are affected by the temperature. Remember do not leave them in the car in the cold or hot weather. It can damage them and they may not be as effective as you need them to be. We have the Epi Pen Jr and there is a little window to check and see if it's still good. Make sure to check them and their expiration dates.

We finally went and got our Christmas tree last week. We didn't need to bring his diaper bag so we left it in the car. The chances of him having an ana reaction while getting a tree are slim but we always carry it with us. I put it in the inside pocket of my jacket to keep it from getting too cold. So remember that when sledding or just playing outside keep it with you where it won't get too cold.

Read it before you eat it!

Another reminder is this. With the holidays almost here we are getting busier and busier. It was the week between Thanksgiving and Cormac's birthday. I was at Costco getting things for his party and was stressing out. They have really yummy premade meals that just need to be heated up. I LOVE their chicken and past alfredo. I scooped it up and was all set for dinner.

We got home and the leaf truck was on our street. We just have to rake our leaves to the curb and the truck sucks them up. So I bundled Cormac up and in a mad rush tried to finish the raking I started the day before. The calvary arrived! My parents pulled up at that moment and even 2 of our neighbors jumped in to help get the yard done. With their help the front got done just as they stared to pick up out leaves.

Well, still without checking I asked my mom to put in the chicken dinner. She did and it smelled so yummy. Then my mom came running out of the house. She was looking at the directions and by chance saw that is was process on the same equipment as peanut and tree nuts. I felt so horrible. In my rush to get a bunch of things done I didn't do the easiest and most important thing done. I didn't read the label! I was just going to give it to him. It really would have been all my fault. My mom thought I checked it so she didn't. We were lucky that she caught it. I beat myself up over it for days.

So my point is, don't let all the craziness get to you so bad you get careless like me. Remember to always check labels and ask people who made dishes what's in them.

And check those EpiPens and other meds, and beware of the cold temperatures.


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Friday, July 16, 2010

Food Allergy Action Plan

What is a food allergy action plan (or FAAP), and do you have one? Well a FAAP is basically a set of instructions of what medicine to administer, when to give it, how much, how often, emergency contact names and numbers and any other important information someone may need to help and treat you or your loved one in case of an allergic reaction. It can also give directions for using your epipen. If you google Food Allergy Action Plan, a number of links with plans you can fill out and use will come up. Here is just one I found http://www.foodallergy.org/files/FAAP.pdf. Ask your Dr too. They probably have one for you.

I've been meaning to do this, but haven't just yet. We're actually waiting to talk with the allergist next week and have her help us with it. I'm still not 100% clear when Cormac will get the epipen vs only Benadryl. It's a bit overwhelming so I suggest talking with your Dr. to make sure you get it right.

Ok, so what do you do with it? I plan on keeping a copy on the fridge and copies with his epipens at home, and epipens that go everywhere with us. When it's time for school the teacher, school nurse, and bus driver will have one. Since my husband and I can't be with him 24/7, I will show the FAAP to who will be watching him.

Right now we explain how to use the epipens, and how to administer any other medication he needs. I will feel better if they have directions as well. Explaining this over and over again gets tiring and frustrating but it's a must now. Trusting people with out little man is so difficult for us. At the same time it also can be overwhelming for them too. Watching someones child is hard enough, but one with a life threading allergy or other condition is just pain scary. As the parents of the kids with allergies, we have to remember that too.

I urge you to talk with your Dr. about your own FAAP. It could help keep you or your loved one safe.

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