Fructose Malabsorption
I'd like to start a discussion on fructose malabsorption, how to control it, what to eat and not eat, etc. . Is anybody interested?
Interested in more discussions like this? Go to the Digestive Health Support Group.
I'd like to start a discussion on fructose malabsorption, how to control it, what to eat and not eat, etc. . Is anybody interested?
Interested in more discussions like this? Go to the Digestive Health Support Group.
I don't have diabetes but someone who is diabetic can eat tons of sugar compared with what I can eat.
They are told they can, they shouldn't eat fruit, sugars or carbs but even Mayo gave me a diabetic diet full of it!!
Yes I would like to work on that. Presently can only eat chicken, fish, turkey, eggs and 2 cooked vegetables.
I too can't eat potatoes. I read on the "Smithsonian" magazine that they are members of the Deadly Nighshade family and that about 25% of the population cannot tolerate them. Plus they are starch which I cannot eat.
Are you still checking this? I would love to chat more about this.
I have been struggling with sugar for 2 years. You are the first person I've learned about with a diet similar to mine. If I ear more than 2 grams of simple sugar at a time, I get a head rush, feel dizzy, and oftentimes have uncontrollable emotions (excess crying, anger, etc). If I eat over 25 g of complex carbs, I fall asleep 1 hour 45 minutes after eating them. I sleep for 2 hours and wake up like nothing happened. I have been tested for every possible endocrine issue and everything is fine there. I also do get very gassy when I eat anything with even a little sugar.
I have not yet seen a GI. Do you have any more insights since you posted this?
I have recently been diagnosed with exocrine pancreatic deficiency (EPI), Sucrase-Isomaltase Difficiency (CSID), and Collagenous Colitis (CC) and have been told the cause is autoimmune problems. I'm over 60 and I may have to accept the auto immune cause, but am looking for other causes. Any ideas?
Hello, my son has been diagnosed with collagenous gastritis, not colitis. He gets stomach aches. I wonder if you have any ideas about the origin of this inflamation and how to relieve the symptoms.
I also have pain but not tremendous. No one seems to know much about causes...just the mysterious "auto-immune" cause. How does your son get relief?
Yes please👏