Your Child Medicine and School

Medical Conditions and School

I was devastated when my son was diagnosed with type 1 diabetes. It was a huge relief to discover why he had been feeling so poorly but nothing prepares you for hearing those words. It changed our lives forever and has presented a whole new dynamic to how we approach going back to school. What do you do when your child needs medicine to be administered during the school day? Who administers the medicine? How do you ensure the staff has been informed of your child’s condition?

First and foremost don’t panic. You need to put in place a plan of action to ensure that your child will be getting all the support that they need. The last thing I wanted to do was make my son feel awkward and centered out but at the same time I needed to know that the entire staff was aware of his condition and that steps were in place to ensure his safety.

I am not going to lie it was a chore to get everyone on the same page and we did encounter some road blocks but I stuck to my guns and made sure that the school got on board.


The first thing I did was go to our physician. I wanted to pick up flyers explaining the signs of a diabetic high and low. I made a list of what symptoms my son usually displays when he is experiencing a high or low because they can vary greatly.

In my sons case he got very, very moody and even rude when his blood sugar was too high and this is easily mistaken for being drunk or disrespectful. He becomes unresponsive and although he is conversing he will not remember anything that transpires once his blood sugar is returned to normal which can only be done with insulin.

If his blood sugar gets too low he gets very lethargic and sleepy and he requires a juice or carbohydrate immediately to bring him back to normal.


I made arrangements to go in and speak to all his classes regarding his requirements and to educate them on what to expect. I also spoke to his teachers individually. I met with the principal to make sure plans were in place to educate any substitute teachers. I provided the school with a diabetes poster and attached a picture of him to be kept in the office.  This whole process took several weeks and was an uphill battle.


ptpa post2

My son requires insulin in order to eat as well as snacks throughout the day. He also needs to test his blood sugars before eating or when he is feeling either high or low. The problem was the school considered his lancet (the device he uses to poke his skin to produce blood for testing) to be a weapon. The same held true for this pen needle for injecting his insulin. I was in shock when I heard this. They tried to insist that both of these be kept in the office and that he go there each time he needed to test and to give himself insulin. That was not going to happen and the battle began.

My son was old enough to test and administer his own insulin. When my son feels off he needs to test immediately. They wanted him to travel to the office, request his device and then test. This was unacceptable to me. The time it would take for him to travel there while experiencing a high or low could mean the difference between averting a crisis and preventing a trip to the hospital. I wanted his diabetic kit on him at all times. He had a special pack that he wore that holds everything including snacks. They also wanted him to travel to the office to take his insulin. My demands were simple. My son would keep his kit with him at all times, could test in class when necessary and have a snack during class. He also need to go have access to the closest bathroom on each floor. In this case it was the teachers bathroom. A newly diagnosed diabetic has to urinate frequently and they are unable to hold it. In his one school the children s washroom was on the first floor while his classes were on the second. I needed to ensure that he could get up and go immediately and not have to worry about raising his hand to ask for permission or travel two flights of stairs. Sadly some teachers are bullies and when your child is young they can be intimidated.


Does your child need medication to be administered during the school day? Where will the medicine be kept? Who will administer it? Who is the backup person should the regular person be unavailable.

One teacher said to my son “I am sure you can hold it for a few more minutes”. The last thing your child wants is to cause a scene or stand out. By the time he got out of class it was too late and he did not make it. He left school and came directly home. You can imagine my shock when he showed up upset and humiliated. They had no clue he was gone. Needless to say the teacher and I had words and I also reported them to the board of education.

My son was given access to the teachers bathroom on each floor and permission to leave class when necessary without obstruction.

DO NOT TAKE NO FOR AN ANSWER. I actually had to threaten legal action at one point.

The school did drop the ball on a few occasions especially in regards to substitute teachers. One teacher tried to prevent him from having a snack while another told him to go to the bathroom to test. Luckily I had educated his entire class and they promptly informed the teacher that my son had special privileges.


I did this after each break to refresh everyone. As my son got older he was able to speak up for himself. When they are younger I found that many teachers tried to intimidate him. I also repeated the entire education process at the beginning of each school year.


I was actually shocked to learn that each school had their own set of rules. I use the term “rules” loosely because there was nothing written down. It was simply the way they did things.

As my son got older and more independent I wanted him to have a cell phone on him at all times. When he entered high school a whole new set of problems arose. The schools policy forbid any student from using a cell phone while inside the school walls.

On one occasion my son started to feel badly. He was in between classes and pulled out his phone to call me and request that I come pick him up. A teacher saw him and made him go outside. My son tried to explain he had special permission but the teacher was unrelenting and since my son was experiencing a low he was not in a position to continue to argue. By the time he got outside he was barely coherent. When I answered the phone I could barely make out what he was saying. I jumped in the car and off I went. I kept him on the phone and rushed to the office. The search was on to find him. He was eventually located wandering the school grounds. You can imagine my fury. I demanded to know what teacher did this but they would not come forward. I was able to locate the teacher who made my son go outside only because a student came forward. He had witnessed the entire thing. The student was not aware of my sons condition and thus did not speak up. I had some choice words for the school and for the teacher in question. They were reprimanded and I know I could of handled it better but mom mode kicked in. This teacher went out of his way to make my sons life difficult. He accused my son of acting rude and suspended him for 3 days. I learned there is no recourse for this. Once the suspension is in place they are not permitted on school grounds. You cannot appeal it and when you try they tell you that it does not go on their permanent record and there is nothing they can do.

I told the school when he gets low or high one of the symptoms is a moody and abrupt behavior. My son was in fact having a low. Teenage years and puberty wreak havoc on a their systems. It is even worse when they have medical condition as their insulin dosages change continuously. Our battle with this particular teacher continued throughout the year and it took me til years end to convince the school that the suspensions (3) were not warranted and the teacher was acting out of malice. I spent weeks on the phone with the school board and made several visits to them. That teacher did not return in the fall.

Another situation arose when the school tried to restrict my sons access to his testing kit. They wanted him to keep his kit in his locker.  Once again they were  insisting that the lancet and needle were weapons and posed a threat to other students.


diabetic lancet and pen needle
The idea that my son would pull out his lancet and brandish it as a weapon was ridiculous. It became apparent that the school had no idea what these devices looked like and were simply putting their own needs first. The needle on the lancet is 1 mm long and the pen needle is 4 mm long hardly a threat to anyone. Regardless of their policy my son was going to have his kit on him come hell or high water.

This was a huge battle with the school but I stuck to my guns and we worked it out.

My son experienced many medical emergencies during grade 9 and 10. He was taken to the hospital on several occasions. I battled the school insisting that they call me first and then call the ambulance but I was only partially successful. If my son was able to call me and alert me he was feeling poorly then I could get to the school within 4 minutes. An ambulance could take up to 10.


If they do have procedures make sure you get them in writing and feel free to make alterations based on your child’s needs. Our kids are our first priority and each situation is unique.


I actually pulled my son out of school on two occasions until I was confident his needs would be met. We did not know it at the time but my son was also suffering from Addison’s Disease, a very rare auto immune disorder. The symptoms mimic a diabetic low and went diagnosed for almost two years. He was unable to continue in school and we began home schooling.

I am not saying you will experience all of these problems but it is important to be aware that you could. I hope that by sharing my experiences I can give other parents a heads up and maybe steer them in the right direction.

Comments (9)

  • Wow – I am so sorry for all the troubles you went through just trying to make sure he was okay at school! We had problems with our son’s ventolin. They also wanted to keep it in the office which I refused to allow them to do. He was fully capable of using it by the age of four (from so much experience!) and he knew when to use it. Had to insist it be left on him at all times. This is so important for parents to know especially if their child is entering JK. Thanks for sharing!

  • I am sorry to hear you also had problems but I am so glad you stuck to it and got what was right for your son’s needs. You are very welcome

    Jo-Anne Pfoh
  • I’m sorry to hear about your son’s diagnosis Jo-Anne. I’ve been a type 1 diabetic since the age of 4 and I know everything he’s having to deal with. It’s definitely a challenge as a child to have a disease that needs constant management. Kid’s shouldn’t have to worry about what & when they eat or if they ate before exercising! I love all the steps you took to inform the school staff of his condition and I couldn’t agree with you more! Great post and information/tips

  • Thank you Jason for those kind words. I am sorry that you have also been living with this disease for so many years. I hope ech and every day for a cure or an easier way to test and administer the insulin. I agree that no child should have to constantly worry about everything as you and my son do. It is sad that the school system makes it so very difficult.

    Jo-Anne Pfoh
  • Medic Alert has a wonderful free program for school age children. Have a look

    Jo-Anne Pfoh
  • Great article Jo-Anne. My son has been a Type 1 Diabetic since he was two, he is now 9. I must admit that I felt so nervous sending him off to school after being used to taking care of him 24/7 but our school was wonderful, the nurse is excellent, and we have had no major issues or roadblocks (thanks to the school being so willing to do everything they can). We even had a lock-down last year where the kids had to stay in the school until 6:30 in the evening ( I was worried but the nurse called and we discussed our plan of action).

    I also lucked out with the fact that none of my child’s classmates seem to really think of his as that different. They have always known that he is Diabetic so it’s great to have a bunch of extra sets of eyes to make sure he is ok : )

  • It is so nice to hear that the school worked with you. We don’t have school nurses here

    Jo-Anne Pfoh
  • My daughter was diagnosed almost 3 years ago. It hasn’t been easy sending her to school with her disease. Learned quite a bit, like you! Hope to stay connected!

  • I am sorry that you received so much road block with your son’s school. It is a good thing you are doing as only you are your child’s best advocate as his parent. Although, I do agree that in most cases a child should be allowed to self-administer glucose testing or dosing of insulin, it is something that should be thoroughly planned out as you are doing. I applaud you for that. I wish all parents and schools could partner in this way and therefore “educate” the schools on diabetic management. I say “most” cases because some children are not responsible or capable to self-administer. I see in your blog that your son is very capable. My daughter had the misfortunate accident of getting stuck by a diabetic lancet belonging to another student. This student is in the 7th grade. My daughter is in the 8th grade. She found his lancet on the ground. She did not know what it was thinking it was a black marker. She inadvertently set it off and pricked her finger. Apparently, there was no such diabetic plan for this student. It has come out in his own testimony that sometimes he would forget it on the lunch tables where he would self-test. Again, I am in 100% agreement with you and your case, but, I wish that more parents would be as dedicated as you in ensuring the safety of all and not just her own child. Only the parent knows best what her child is capable of. Now, my daughter has to endure several months of hepatitis testing.

    Lisa Murdoch

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