Jump to content
RemedySpot.com
Sign in to follow this  
Guest guest

Re: Keratosis pilaris--- or similiar what the biomed take on this?

Rate this topic

Recommended Posts

Guest guest

i do not know the answer,but one thing you can check.

people and children with thyroid problem do not convert beta carotene to vit

A.

they have often yellow palms of the hand and yellow bootom of the feet.

you must check good what sort of vit A it is.retinol is ok

On Mon, Nov 29, 2010 at 2:00 PM, Ellen wrote:

>

>

> HI all you wonderful people! My dauhgter has developed Keratosis pilaris,

> oe something similiar on the backs of her arms. They are whiteheads that are

> hard and will not pop, and when we tried to ( with her permission and

> particiaption) we just got a hard pearl of stuff out of it.

> I looked it up and seems it is more of the same.... aggravated by food

> allergies, lack of vit a, need more omega 3's, more fruits and veges, more

> water. Any other suggestions?? Thanks in advance.

> Emma is very strictly SCD with many restrictions, eats super healthy, I

> supplement with omega three's. The one thing I did do is stop Vit a, because

> of it's adverse reaction wiht vit d levels... of which my daughter's are

> very hard to keep up.. we are currently doing 8000 iu a day and still only

> at a 66, with 80 being ideal.

> Anywhoo, any ideas would be welcome.

> Starting the extra vegeatable, water, and .. and and....

>

> Ellen

> Mom to Emma, age 7

>

>

>

Share this post


Link to post
Share on other sites
Guest guest

It was mentioned at the DAN conference in Long Beach in the general session that

it is very common in kids on the spectrum.

I've also heard moms on the GFCFkids yahoo group say that their kids get it when

they have a gluten infraction.

My 2.5 year old son has it on/off. I figure it's not the pretty but, it's not

causing him any harm. So I've not worried about it.

-Eileen

>

> HI all you wonderful people! My dauhgter has developed Keratosis pilaris, oe

something similiar on the backs of her arms. They are whiteheads that are hard

and will not pop, and when we tried to ( with her permission and particiaption)

we just got a hard pearl of stuff out of it.

> I looked it up and seems it is more of the same.... aggravated by food

allergies, lack of vit a, need more omega 3's, more fruits and veges, more

water. Any other suggestions?? Thanks in advance.

> Emma is very strictly SCD with many restrictions, eats super healthy, I

supplement with omega three's. The one thing I did do is stop Vit a, because

of it's adverse reaction wiht vit d levels... of which my daughter's are very

hard to keep up.. we are currently doing 8000 iu a day and still only at a 66,

with 80 being ideal.

> Anywhoo, any ideas would be welcome.

> Starting the extra vegeatable, water, and .. and and....

>

> Ellen

> Mom to Emma, age 7

>

Share this post


Link to post
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
Sign in to follow this  

×
×
  • Create New...