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FDA give 10 Tips for Medicine and Sick Kids



As a father of two school aged kids that are always getting sick with whatever sickness is going around the school I am always concerned about medications for the kids. The FDA came out with a top 10 list of things to think about when giving meds to kids.

10 Tips for Medicine and Sick Kids

When it comes to taking medicines, kids aren’t just small adults. When using nonprescription medicines, here are 10 ways to be sure you’re giving your children the right medicine and the right amount.

  1. Read and follow the label directions every time. Pay special attention to usage directions and warnings. If you notice any new symptoms or unexpected side effects in your child or the medicine doesn’t appear to be working, talk to your doctor or pharmacist immediately.
  2. Know how much medicine to give and when. Read and follow the label.
  3. Know the abbreviations for tablespoon (tbsp.) and teaspoon (tsp.). You should also know: milligram (mg.), milliliter (mL.), and ounce (oz.).
  4. Use the correct dosing device. If the label says two teaspoons and you’re using a dosing cup with ounces only, don’t guess – get the proper measuring device. Don’t substitute another item, such as a kitchen spoon.
  5. Never play doctor. Twice the recommended dose is not appropriate just because your child seems twice as sick as last time. When in doubt about your child’s condition, call your doctor.
  6. Talk to your doctor, pharmacist, or other health care professional before giving two medicines at the same time to avoid a possible overdose or an unwanted interaction.
  7. Follow age and weight limit recommendations. If the label says don’t give to children under a certain age or weight, don’t do it. Call your doctor.
  8. Always use the child-resistant cap and re-lock the cap after each use. Be especially careful with iron-containing vitamins or supplements, which have been a source of accidental poisoning deaths in children under three.
  9. Follow the “KEEP OUT OF REACH” warning. Today’s medicines are often flavored to mask the taste of the medicine, which is all the more reason to keep all drugs out of the sight and reach of children.
  10. Always check the package and the medicine itself for signs of tampering. Don’t buy or use any medicine from a package that shows cuts, tears, slices, or other imperfections. Report anything suspicious to the pharmacist or store manager.

I know that most of this list is obvious but there are other things to think about as well and that is taste (as listed above) and drug interactions (Ibuprofen, Aspirin, Acetaminophen)

Aspirin – Never give aspirin to kids as it can cause problems like Reyes syndrome. Baby aspirin as we have all heard of is not actually for babies but is actually just a small aspirin for adults.

Acetaminophen – is fine for kids to treat pain or a fever but is not good for too long. Make sure that you are dosing right as it can be hard on the kids liver if you give them too much.

Ibuprofen – is fine also for kids although again watch the dosing as it can be a problem as well if you exceed the dose

Finally it is critical not to mix the Acetaminophen and Ibuprofen with kids, or even with adults for that matter as these pain relievers can cause serious health problems when mixed together.

I think mostly for kids when they are sick the most important thing is to make sure that they sleep, have a warm bath if they are cold and a cold compress on their head or neck and a cool bath if they are hot. And always make sure they take in lots of liquids. Although kids are really good at letting you know how they feel (mine are anyway) they usually get over colds and the flu pretty quickly and easily.

 

 

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Weight Loss Exercise

This months Diet is next months body



This is a great picture. We really have to remember that whatever we start today will have an impact tomorrow. This means not only the dessert today but the exercise and good eating today as well.

Make great decisions today:)

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This months Diet is next months body, 5.0 out of 5 based on 1 rating

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My Daughters Kidney Disease


You may have noticed that I have not been as active this year as I usually am on the blog and there is one pretty big reason. My daughter is sick with Chronic Kidney Disease and I think I am finally ready to write about it, come out and talk about it. This is the first time that I am writing about my daughter and her Kidney disease and what is going on within our family as we struggle and work through this.

Early last year my daughter Taylor, who is now twelve, went for a normal annual physical and her blood testing came back with higher than normal levels of Creatinine. This was not too much of a worry to our family doctor as she was just slightly out of range but he still sent my wife and daughter to a pediatrician and some more testing. While time went by and we waited for the appointment a few weeks later I did a little Googling around and found that this could be a sign of some kind of kidney issue but it was really vague to us at the time.

My wife and daughter went to the pediatrician a couple of times and then got sent to a specialist and then finally to our children’s hospital for more testing and everyone was very indecisive about what was happening.

Getting the Diagnosis

Finally at one meeting last November that just Taylor and my wife Michelle went and had more testing and the doctor let them know that Taylor has Nephronophthisis and would have her kidneys fail and need to have a kidney transplant. Not good news and I still feel bad that I was not at the doctors appointment.

Nephronophthisis is a genetic condition so Michelle and I are both carriers of a bad gene and because of this there was a 1 in 4 chance that either of our kids would inherit the two bad gene halves. Taylor did, we think Jaiden or son did not. This form of kidney disease affects kids between the ages of 8 and 14 and the odds are really low, about 2 kids out of 100,000 would get this, and of course you don’t catch it, you are born with it and it just shows as you get older.

How Our Family is Dealing with Kidney Disease

Happy TaylorSo since last November we have been learning a lot and had a lot of hard times with Taylor’s kidney disease. Taylor is a bit scared of course like any 12 year old should be. My wife Michelle is always looking far ahead and nervous about what the future holds, and I am day to day. Every day that Taylor feels well I am happy and every day that she is feeling unwell I feel terrible for her.

So far since the Nephronophthisis diagnosis Taylor’s kidney function has dropped from about 45% to 28.6% and as we watch the kidney function drop we get more and more nervous but the doctors stay level headed and are keeping us informed on the next steps for us and Taylor and meeting with us on a monthly basis. Here in Calgary Alberta we have a Nepherology clinic at the Alberta Children’s Hospital and so each monthly meeting there we meet with a psychologist, a dietician, a pharmacist, and the kidney doctor. They are fantastic and I feel like we are in great hands.

So far we have not had to change Taylor’s diet at all (no sodium restriction), and she has to take a few vitamins and on Sunday nights she get the good fortune of having me give her an Eprex shot. Also Taylor has to drink a ton of water as her kidneys do not keep her water level where it needs to be and she dehydrates easily, so easily in fact that we have had to take her to hospital three times in the last few months for dehydration.

Next Step – Kidney Transplant

So now we are getting close to our next step. Taylor will need a new kidney sooner rather than later. As the kidney function drops Taylor’s kidneys will not clean blood, regulate vitamin D or calcium very well until finally none of this would happen and she would need to go on dialysis. So the first step was for my wife and I to get ready tested as transplant donors. We went for blood testing and the living donor clinic (independent or our doctor or us) have decided to start testing me to donate a kidney. I have a 24 hour heart rate monitor on right now as I type and then there will be a full day of testing in a few weeks to test me and see if I am a good match.

As for kidney transplant itself, a transplanted kidney will last for 10 to 15 years and then Taylor will be shopping for another one. The surgery seems to be common and the doctor that we spoke to earlier this week say that they do about 50 kidney transplants every year with only about 5 being done for kids. If all goes according to plan I will donate the kidney, Taylor will get the kidney put into her body and hooked up, and we will be out of the hospital within a few days. People live completely normal lives with just one kidney and the only suggestion that our transplant doctor gave me was to not eat protein powder because of the pressure it puts on the kidney. Diet and exercise should be the same.

So as you can imagine this as been a really trying time for our whole family. We are worried for Taylor and hoping that everything is done before she would have to go on dialysis but for now we are day to day with this thing struggling, praying, hoping, and just living through it.

I know that I may have missed a lot in this post, in fact I expect to write a few posts on the subject as we are becoming pretty well versed in kidney issues and health of kidneys. Fire away any questions that you want and Michelle and I will answer them for you.

My Daughters Kidney Disease, 5.0 out of 5 based on 1 rating

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