Forbidden Food for G6PD Cases
88In our family, there has been a rising trend in G6PD diagnosed cases in my 2 nephews and my niece. G6PD is Glucose-6-Phosphate Dehydrogenase Deficiency. It is a condition inherited and passed on through the X chromosome and is said to be a common deficiency of human enzyme. This deficiency causes red blood cells not to function normally. It may result to hemolytic anemia if the person is exposed to certain medicines, food or even infections.
When we got our first (diagnosed) case of G6PD in the family, it seemed so unreal. Since we didn’t have prior experience of this deficiency, we didn’t know how to react. What made it worse was that our first case was classified as “severe”, that is, exposure to the prohibited medicines and food may cause death to the child. So we started educating ourselves about this deficiency. We found out which medicines were not allowed on the child, and even which vitamins should not be taken in excess. Most of all, we found out which food was not allowed for the G6PD child. Our research has led us to the following food generally not allowed for them:
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Fava Beans. This is the number one “no-no” food for the child and has been proven to trigger the symptoms. This is so related to the deficiency that G6PD may be sometimes referred to as “favism” in reference to this food.
Legumes. Beans, black beans, etc., this is another group of foods that must be avoided by children / adults with G6PD.
Soya or Soy. This is an additive to some common food that we eat, including ice cream, burgers, pizzas, chocolate, doughnuts and other food products. It may go by different names but it is definitely one of those food or food additives that should be avoided if one has G6PD.
Peanuts. Peanuts (in particular) and legumes (in general) are found everywhere, including peanut butter, cereals, sauces and salad dressings. Legumes are vegetables and are, supposed to be, in general, good for ones’ health. Peanuts are known as “brain food” and are becoming more popular with recently-discovered antioxidant qualities. But for G6PD cases, avoiding these foods is highly recommended.
Menthol-Flavored Candies and Food. People with G6PD are not advised to not only eat menthol-flavored candies and food, they are not allowed to inhale this substance as well! Menthol can be found in various candies, in mouthwashes, toothpaste and gums. For children with G6PD, it is doubly hard to avoid menthol-flavored candies but avoiding these is not a matter of choice for them but a matter of survival.
Note There are times when these food can be found as ingredients in certain processed foods. Like peanuts in chocolates or soy added as meat extenders or in butter. The key here is to read the ingredients carefully to check for these food. When you see them, avoid these food at all cost. Better to be safe than sorry.
- G6PD (Glucose-6-Phosphate Dehydrogenase) Deficiency
Detailed information on g6pd deficiency, including cause, diagnosis, and treatment - Newborn Screening Reference Center
Some frequently asked questions about G6PD. - Home - G6PD Deficiency Association
The homepage for G6PD information, facts, how to's, etc.
The above are the food my nephews and niece are not allowed to eat. They are a lot fewer than the medications not allowed for people with G6PD (the list of medications is almost one page long while the above is like only a half page) but they are no less dangerous. Knowing this has made us more conscious in terms of reading food labels and checking the ingredients. The children are also taught at a very young age to choose the food that they eat (my two and a half year old niece already knows that she cannot eat peanuts!). Lastly, their parents made sure that the people around them (especially their doctors, teachers and classmates) were advised that these children need to avoid certain foods. This is to ensure that we gain their cooperation. Children with G6PD may grow up to live healthy, normal lives and this is what we hope for them (my nephews and niece) as they grow older and more adept in handling their deficiency.
Note: The facts I wrote here are all based on consultations with my niece / nephew's pediatrician and the websites I have provided links to on the right side of my hub. Although the Internet is a great place to look for information on G6PD, my advice is still to consult your child's doctor. G6PD may be relatively unknown for people outside the medicine profession but I have found that, in general, doctors are very well aware of this condition.
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Comments
Yes, it's kind of hard to have this deficiency. Fortunately, a lot of people are becoming more aware of it so it's getting easier to get information. Just hard sometimes to explain to the child why he / she can't eat a certain type of food, especially peanuts, which is my favorite too. Thanks for the comment, dohn.
I am always learning something new in here. G6PD can be extremely serious if not diagnosed on time. It is amasing how we take things for granted and hardly ever think about the ingredients on the things we are eating or feeding our children with.
Thanks for such an informative hub and a big hug to your niece and nephews.
Thanks for the comment and the hug Princessa. Actually, my husband and I are the ones taking care of my niece and I'm proud to say that we have already taught her which foods she cannot eat. Having her with us certainly increased our awareness of this deficiency as well as the contents of some food that we eat.
I have never heard of this disease. What symptoms would make you suspect you might have it? Is the peanut allergy we hear so much about part of this? Just curious.
I don't think there is any symptoms. The disease is diagnosed during the tests done right after a baby is born (which was how we found out about my nephews and niece). Anemia is the most likely result when the child with G6PD eats food or takes in medicine that are not allowed for such cases. As to peanut allergy, I'm not really sure if this is related to G6PD. Will try to look that up.
i have G6PD an i eat most of the food above such as peanuts and beans but nothing happen. The only thing i garentee that is true is fava and mothballs
Ian, are you a mild or severe case? Mild cases can risk it and eat these foods. Severe cases, dare they risk it? My nephews and niece also eat some peanuts but we try to steer them clear from these things. Better be safe than sorry.
my son was diagnosed with g6pd. so, how am i going to know if he has a mild or severe type of this disorder? do you have a complete lists of foods and medicines that he's not allowed to take or eat? please e-mail me at this address papilit_z02@yahoo.com..please and thank you!
Hi jonas erick. Please check your email. Thanks.
is there a possible cure for g6pd?
As far as I know, none.
my son was diagnosed to have a severe case of g6pd deficienty... he's 5 months old now and i'm afraid to start giving him solid foods since i don't know which ones to give my baby... i hope u can help me on this.
Hi sally. I'm not an expert by any means but I'll try to help. First, you can check out the sites I have listed above. These are sites where you can see what your son can or cannot eat. Second, please get a good doctor who knows g6pd very well. They should give you a brochure or a listing of the do's and don'ts for your son. Third, solid foods are okay but please be conscious about the ingredients. We got into the habit of always looking at the list of ingredients for any indication that the food contains peanuts or soya or beans and stuff and as much as possible we don't give the food to the child. Most foods are okay (suggest you prepare them yourself so that you're sure what they contain), you just need to have a long, serious talk with your doctor so that you'll feel confident about your approach. Hope this helps.
ths is really very helpful for me. i just receive the NB screeining result of my son ad foundout that he is positive in g6pd.. i cant sleep since then so i started researching about this disease. thanks for the info.
hi,
pls email allm important details about g6pd. i wold really appreciate if you could help me regarding my sons condition.. my email add is. maezon21@yahoo.com
What are fava beans called in marathi /hindi
my email : umeshdalvi123@rediffmail.com
i wanted to know if any one had a list of food and/or medicines that my son can not have if please e-mail me @ patience_dozier87@yahoo.com P.S my son just turn two and he has been drinking SOY MILK since he was about four or five months will that hurt him PLEASE HELP ME UNDERSTAND G6PD













dohn121 says:
3 months ago
This was great information. Fortunate enough, members of my family do not have any known allergies to foods. Many of the foods that you mentioned are among my favorites. Thanks, emievil!