Vit E deficient-induced Neuro-sensory issues

fkewatson

New member
Hi - my first post here. My 4 year old son had a postive fecal fat (sudan stain) test indicating malabsorption, a negative sweat test but has a heterozygous deltaF508 mutation. We are waiting on the Ambry amplified results to see if there is another.

His only GI symptoms have been foul-smelling, floating stools (not necessarily bulky) and reflux. He has gained weight appropriately (although he is very lean) and is very tall for his age (42 inches). He usually stands a head above his peers. He has never had any respiratory issues other than seasonal allergies.

His most serious issues, however, are severe verbal apraxia and sensory integration dysfunction. It's a long story, but we learned about 9 months ago that the symptoms of Vitamin E deficiency mimics my son's issues. From the first dose of 200IUs d-alpha tocopherol and 200mg d-gamma, his major sensory issues vanished as long as he was continually supplemented (we are at much higher doses now). It seems to "wear off", even though I know Vit E is supposed to be stored. It apparently isn't in him. The apraxia (my son is non-verbal. Apraxia is a motor planning problem - like that of a stroke victim that loses the ability to speak. He knows the word in his head, he just cannot make the message get from his brain to his mouth). Motor planning is highly connected to essential fatty acid metabolism, so he is likely suffering from a deficiency in that as well. There is nothing wrong with him cognitively.

I've found a body of scientific CF literature that deals with not only malabsorption but also oxidative stress that inhibits the bodies' ability to properly metabolize Vitamin E and essential fatty acids.

FINALLY, MY QUESTIONS: Is anyone familiar with another case like my son's, where Vitamin E-induced neuro-sensory issues played a major role in their CF? Is anyone familiar with the research on Vit E and essential fatty acids I referenced above? And one more - is anyone familiar with a metabolic or CF specialist that could possibly help us (it doesn't matter where they are located). I know that sometimes message boards have a "hero" doctor that is often referenced.

Any and all help is appreciated. Thanks!
 

fkewatson

New member
Hi - my first post here. My 4 year old son had a postive fecal fat (sudan stain) test indicating malabsorption, a negative sweat test but has a heterozygous deltaF508 mutation. We are waiting on the Ambry amplified results to see if there is another.

His only GI symptoms have been foul-smelling, floating stools (not necessarily bulky) and reflux. He has gained weight appropriately (although he is very lean) and is very tall for his age (42 inches). He usually stands a head above his peers. He has never had any respiratory issues other than seasonal allergies.

His most serious issues, however, are severe verbal apraxia and sensory integration dysfunction. It's a long story, but we learned about 9 months ago that the symptoms of Vitamin E deficiency mimics my son's issues. From the first dose of 200IUs d-alpha tocopherol and 200mg d-gamma, his major sensory issues vanished as long as he was continually supplemented (we are at much higher doses now). It seems to "wear off", even though I know Vit E is supposed to be stored. It apparently isn't in him. The apraxia (my son is non-verbal. Apraxia is a motor planning problem - like that of a stroke victim that loses the ability to speak. He knows the word in his head, he just cannot make the message get from his brain to his mouth). Motor planning is highly connected to essential fatty acid metabolism, so he is likely suffering from a deficiency in that as well. There is nothing wrong with him cognitively.

I've found a body of scientific CF literature that deals with not only malabsorption but also oxidative stress that inhibits the bodies' ability to properly metabolize Vitamin E and essential fatty acids.

FINALLY, MY QUESTIONS: Is anyone familiar with another case like my son's, where Vitamin E-induced neuro-sensory issues played a major role in their CF? Is anyone familiar with the research on Vit E and essential fatty acids I referenced above? And one more - is anyone familiar with a metabolic or CF specialist that could possibly help us (it doesn't matter where they are located). I know that sometimes message boards have a "hero" doctor that is often referenced.

Any and all help is appreciated. Thanks!
 

fkewatson

New member
Hi - my first post here. My 4 year old son had a postive fecal fat (sudan stain) test indicating malabsorption, a negative sweat test but has a heterozygous deltaF508 mutation. We are waiting on the Ambry amplified results to see if there is another.

His only GI symptoms have been foul-smelling, floating stools (not necessarily bulky) and reflux. He has gained weight appropriately (although he is very lean) and is very tall for his age (42 inches). He usually stands a head above his peers. He has never had any respiratory issues other than seasonal allergies.

His most serious issues, however, are severe verbal apraxia and sensory integration dysfunction. It's a long story, but we learned about 9 months ago that the symptoms of Vitamin E deficiency mimics my son's issues. From the first dose of 200IUs d-alpha tocopherol and 200mg d-gamma, his major sensory issues vanished as long as he was continually supplemented (we are at much higher doses now). It seems to "wear off", even though I know Vit E is supposed to be stored. It apparently isn't in him. The apraxia (my son is non-verbal. Apraxia is a motor planning problem - like that of a stroke victim that loses the ability to speak. He knows the word in his head, he just cannot make the message get from his brain to his mouth). Motor planning is highly connected to essential fatty acid metabolism, so he is likely suffering from a deficiency in that as well. There is nothing wrong with him cognitively.

I've found a body of scientific CF literature that deals with not only malabsorption but also oxidative stress that inhibits the bodies' ability to properly metabolize Vitamin E and essential fatty acids.

FINALLY, MY QUESTIONS: Is anyone familiar with another case like my son's, where Vitamin E-induced neuro-sensory issues played a major role in their CF? Is anyone familiar with the research on Vit E and essential fatty acids I referenced above? And one more - is anyone familiar with a metabolic or CF specialist that could possibly help us (it doesn't matter where they are located). I know that sometimes message boards have a "hero" doctor that is often referenced.

Any and all help is appreciated. Thanks!
 

fkewatson

New member
Hi - my first post here. My 4 year old son had a postive fecal fat (sudan stain) test indicating malabsorption, a negative sweat test but has a heterozygous deltaF508 mutation. We are waiting on the Ambry amplified results to see if there is another.

His only GI symptoms have been foul-smelling, floating stools (not necessarily bulky) and reflux. He has gained weight appropriately (although he is very lean) and is very tall for his age (42 inches). He usually stands a head above his peers. He has never had any respiratory issues other than seasonal allergies.

His most serious issues, however, are severe verbal apraxia and sensory integration dysfunction. It's a long story, but we learned about 9 months ago that the symptoms of Vitamin E deficiency mimics my son's issues. From the first dose of 200IUs d-alpha tocopherol and 200mg d-gamma, his major sensory issues vanished as long as he was continually supplemented (we are at much higher doses now). It seems to "wear off", even though I know Vit E is supposed to be stored. It apparently isn't in him. The apraxia (my son is non-verbal. Apraxia is a motor planning problem - like that of a stroke victim that loses the ability to speak. He knows the word in his head, he just cannot make the message get from his brain to his mouth). Motor planning is highly connected to essential fatty acid metabolism, so he is likely suffering from a deficiency in that as well. There is nothing wrong with him cognitively.

I've found a body of scientific CF literature that deals with not only malabsorption but also oxidative stress that inhibits the bodies' ability to properly metabolize Vitamin E and essential fatty acids.

FINALLY, MY QUESTIONS: Is anyone familiar with another case like my son's, where Vitamin E-induced neuro-sensory issues played a major role in their CF? Is anyone familiar with the research on Vit E and essential fatty acids I referenced above? And one more - is anyone familiar with a metabolic or CF specialist that could possibly help us (it doesn't matter where they are located). I know that sometimes message boards have a "hero" doctor that is often referenced.

Any and all help is appreciated. Thanks!
 

fkewatson

New member
Hi - my first post here. My 4 year old son had a postive fecal fat (sudan stain) test indicating malabsorption, a negative sweat test but has a heterozygous deltaF508 mutation. We are waiting on the Ambry amplified results to see if there is another.

His only GI symptoms have been foul-smelling, floating stools (not necessarily bulky) and reflux. He has gained weight appropriately (although he is very lean) and is very tall for his age (42 inches). He usually stands a head above his peers. He has never had any respiratory issues other than seasonal allergies.

His most serious issues, however, are severe verbal apraxia and sensory integration dysfunction. It's a long story, but we learned about 9 months ago that the symptoms of Vitamin E deficiency mimics my son's issues. From the first dose of 200IUs d-alpha tocopherol and 200mg d-gamma, his major sensory issues vanished as long as he was continually supplemented (we are at much higher doses now). It seems to "wear off", even though I know Vit E is supposed to be stored. It apparently isn't in him. The apraxia (my son is non-verbal. Apraxia is a motor planning problem - like that of a stroke victim that loses the ability to speak. He knows the word in his head, he just cannot make the message get from his brain to his mouth). Motor planning is highly connected to essential fatty acid metabolism, so he is likely suffering from a deficiency in that as well. There is nothing wrong with him cognitively.

I've found a body of scientific CF literature that deals with not only malabsorption but also oxidative stress that inhibits the bodies' ability to properly metabolize Vitamin E and essential fatty acids.

FINALLY, MY QUESTIONS: Is anyone familiar with another case like my son's, where Vitamin E-induced neuro-sensory issues played a major role in their CF? Is anyone familiar with the research on Vit E and essential fatty acids I referenced above? And one more - is anyone familiar with a metabolic or CF specialist that could possibly help us (it doesn't matter where they are located). I know that sometimes message boards have a "hero" doctor that is often referenced.

Any and all help is appreciated. Thanks!
 

fkewatson

New member
Hi - my first post here. My 4 year old son had a postive fecal fat (sudan stain) test indicating malabsorption, a negative sweat test but has a heterozygous deltaF508 mutation. We are waiting on the Ambry amplified results to see if there is another.

His only GI symptoms have been foul-smelling, floating stools (not necessarily bulky) and reflux. He has gained weight appropriately (although he is very lean) and is very tall for his age (42 inches). He usually stands a head above his peers. He has never had any respiratory issues other than seasonal allergies.

His most serious issues, however, are severe verbal apraxia and sensory integration dysfunction. It's a long story, but we learned about 9 months ago that the symptoms of Vitamin E deficiency mimics my son's issues. From the first dose of 200IUs d-alpha tocopherol and 200mg d-gamma, his major sensory issues vanished as long as he was continually supplemented (we are at much higher doses now). It seems to "wear off", even though I know Vit E is supposed to be stored. It apparently isn't in him. The apraxia (my son is non-verbal. Apraxia is a motor planning problem - like that of a stroke victim that loses the ability to speak. He knows the word in his head, he just cannot make the message get from his brain to his mouth). Motor planning is highly connected to essential fatty acid metabolism, so he is likely suffering from a deficiency in that as well. There is nothing wrong with him cognitively.

I've found a body of scientific CF literature that deals with not only malabsorption but also oxidative stress that inhibits the bodies' ability to properly metabolize Vitamin E and essential fatty acids.

FINALLY, MY QUESTIONS: Is anyone familiar with another case like my son's, where Vitamin E-induced neuro-sensory issues played a major role in their CF? Is anyone familiar with the research on Vit E and essential fatty acids I referenced above? And one more - is anyone familiar with a metabolic or CF specialist that could possibly help us (it doesn't matter where they are located). I know that sometimes message boards have a "hero" doctor that is often referenced.

Any and all help is appreciated. Thanks!
 

Rebjane

Super Moderator
Hi there, I don't know specifically the answers to your questions but you may want to post this on the adult or family section as it seems to get more views there. I know that people with CF have trouble absorbing the "fat-soluable" vitamins, ADEK. Most people with Cf take special vitamins everyday because of their malabsorption of fats and vitamins. People with Cf get their blood drawn yearly to make sure they are not deficient in their vitamin levels. HTH
 

Rebjane

Super Moderator
Hi there, I don't know specifically the answers to your questions but you may want to post this on the adult or family section as it seems to get more views there. I know that people with CF have trouble absorbing the "fat-soluable" vitamins, ADEK. Most people with Cf take special vitamins everyday because of their malabsorption of fats and vitamins. People with Cf get their blood drawn yearly to make sure they are not deficient in their vitamin levels. HTH
 

Rebjane

Super Moderator
Hi there, I don't know specifically the answers to your questions but you may want to post this on the adult or family section as it seems to get more views there. I know that people with CF have trouble absorbing the "fat-soluable" vitamins, ADEK. Most people with Cf take special vitamins everyday because of their malabsorption of fats and vitamins. People with Cf get their blood drawn yearly to make sure they are not deficient in their vitamin levels. HTH
 

Rebjane

Super Moderator
Hi there, I don't know specifically the answers to your questions but you may want to post this on the adult or family section as it seems to get more views there. I know that people with CF have trouble absorbing the "fat-soluable" vitamins, ADEK. Most people with Cf take special vitamins everyday because of their malabsorption of fats and vitamins. People with Cf get their blood drawn yearly to make sure they are not deficient in their vitamin levels. HTH
 

Rebjane

Super Moderator
Hi there, I don't know specifically the answers to your questions but you may want to post this on the adult or family section as it seems to get more views there. I know that people with CF have trouble absorbing the "fat-soluable" vitamins, ADEK. Most people with Cf take special vitamins everyday because of their malabsorption of fats and vitamins. People with Cf get their blood drawn yearly to make sure they are not deficient in their vitamin levels. HTH
 

Rebjane

Super Moderator
Hi there, I don't know specifically the answers to your questions but you may want to post this on the adult or family section as it seems to get more views there. I know that people with CF have trouble absorbing the "fat-soluable" vitamins, ADEK. Most people with Cf take special vitamins everyday because of their malabsorption of fats and vitamins. People with Cf get their blood drawn yearly to make sure they are not deficient in their vitamin levels. HTH
 

fkewatson

New member
Thank you, I will do that.

We just learned last week of the one CF mutation. When the GI doc ordered the test based on the positive malabsorption results I just thought he was covering all the basis. We had no idea there could be a CF link to my son's issues - just came out of the blue for us. And then to find CF literature that discusses the same theories on malabsorption and oxidative stress that we were exploring for the apraxia and sensory issues - that hit home. I'm praying they don't find another mutation.
 

fkewatson

New member
Thank you, I will do that.

We just learned last week of the one CF mutation. When the GI doc ordered the test based on the positive malabsorption results I just thought he was covering all the basis. We had no idea there could be a CF link to my son's issues - just came out of the blue for us. And then to find CF literature that discusses the same theories on malabsorption and oxidative stress that we were exploring for the apraxia and sensory issues - that hit home. I'm praying they don't find another mutation.
 

fkewatson

New member
Thank you, I will do that.

We just learned last week of the one CF mutation. When the GI doc ordered the test based on the positive malabsorption results I just thought he was covering all the basis. We had no idea there could be a CF link to my son's issues - just came out of the blue for us. And then to find CF literature that discusses the same theories on malabsorption and oxidative stress that we were exploring for the apraxia and sensory issues - that hit home. I'm praying they don't find another mutation.
 

fkewatson

New member
Thank you, I will do that.

We just learned last week of the one CF mutation. When the GI doc ordered the test based on the positive malabsorption results I just thought he was covering all the basis. We had no idea there could be a CF link to my son's issues - just came out of the blue for us. And then to find CF literature that discusses the same theories on malabsorption and oxidative stress that we were exploring for the apraxia and sensory issues - that hit home. I'm praying they don't find another mutation.
 

fkewatson

New member
Thank you, I will do that.

We just learned last week of the one CF mutation. When the GI doc ordered the test based on the positive malabsorption results I just thought he was covering all the basis. We had no idea there could be a CF link to my son's issues - just came out of the blue for us. And then to find CF literature that discusses the same theories on malabsorption and oxidative stress that we were exploring for the apraxia and sensory issues - that hit home. I'm praying they don't find another mutation.
 

fkewatson

New member
Thank you, I will do that.

We just learned last week of the one CF mutation. When the GI doc ordered the test based on the positive malabsorption results I just thought he was covering all the basis. We had no idea there could be a CF link to my son's issues - just came out of the blue for us. And then to find CF literature that discusses the same theories on malabsorption and oxidative stress that we were exploring for the apraxia and sensory issues - that hit home. I'm praying they don't find another mutation.
 
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