Jump to content
RemedySpot.com

Re: since scd helps autism can it be messing with my temp control in my brain???

Rate this topic


Guest guest

Recommended Posts

It certainly could be die off but if it persists please check with

your doctor Eileen.

> i mentioned before if I get a bit warm then blood rushes to my hands

> bulging veins etc but i'm also having hot flashes dizziness here and

> there- is this die-off or body correcting itself from being a

> hypoglycemic low blood pressured cold person all these years while not

> absorbing properly?

> make any sense???

> thanks

> eileen scd 4 weeks

>

>

>

>

Carol F.

Celiac, SCD 8 years,MCS, Latex Allergy

http://www.celiac.com/authors/143/Carol-Frilegh

http://www.talkaboutcuringautism.org/gfcf-diet/sc-diet.htm

Link to comment
Share on other sites

i used to get something very similar to this.. just it would alternate

between feet, hands, neck. never saw veins bulge too much.. but i

would feel like that part of my body wanted to explode.

i think it had to do with dehydration, malabsorption, anemia, low

blood pressure. i must say all of those feelings have mostly gone

since about 2.5 months into scd. there were days i couldnt really get

out of bed because of this.

i still get the headaches, blood rushing but it is so much better and

it doesnt stop me from being able to get out of bed and i dont feel

like it will explose or that i want to puke.

i hope this helps..

i'm looking forward to when all of this is gone!

jodi

crohn's/colitis 10 yrs sick for 17

scd 4 months

>

> i mentioned before if I get a bit warm then blood rushes to my hands

> bulging veins etc but i'm also having hot flashes dizziness here and

> there- is this die-off or body correcting itself from being a

> hypoglycemic low blood pressured cold person all these years while not

> absorbing properly?

> make any sense???

> thanks

> eileen scd 4 weeks

>

Link to comment
Share on other sites

what type of doc do you think???

eileen

>

> > i mentioned before if I get a bit warm then blood rushes to my

hands

> > bulging veins etc but i'm also having hot flashes dizziness here

and

> > there- is this die-off or body correcting itself from being a

> > hypoglycemic low blood pressured cold person all these years

while not

> > absorbing properly?

> > make any sense???

> > thanks

> > eileen scd 4 weeks

> >

> >

> >

> >

>

> Carol F.

> Celiac, SCD 8 years,MCS, Latex Allergy

> http://www.celiac.com/authors/143/Carol-Frilegh

> http://www.talkaboutcuringautism.org/gfcf-diet/sc-diet.htm

>

Link to comment
Share on other sites

thanks it's nice to know someone else has felt this - freaking me

out - as all this has for months! but you - 17 years wow!! but if I'm

improving why is it showing up now??? any thoughts?

> >

> > i mentioned before if I get a bit warm then blood rushes to my

hands

> > bulging veins etc but i'm also having hot flashes dizziness here

and

> > there- is this die-off or body correcting itself from being a

> > hypoglycemic low blood pressured cold person all these years

while not

> > absorbing properly?

> > make any sense???

> > thanks

> > eileen scd 4 weeks

> >

>

Link to comment
Share on other sites

Your family doctor for starters but I saw that Marilyn made some

suggestions for you.

> what type of doc do you think???

> eileen

>

>

>

>

>>

>>> i mentioned before if I get a bit warm then blood rushes to my

> hands

>>> bulging veins etc but i'm also having hot flashes dizziness here

> and

>>> there- is this die-off or body correcting itself from being a

>>> hypoglycemic low blood pressured cold person all these years

> while not

>>> absorbing properly?

>>> make any sense???

>>> thanks

>>> eileen scd 4 weeks

>>>

>>>

>>>

>>>

>>

>> Carol F.

Celiac, SCD 8 years,MCS, Latex Allergy

http://www.celiac.com/authors/143/Carol-Frilegh

http://www.talkaboutcuringautism.org/gfcf-diet/sc-diet.htm

Link to comment
Share on other sites

I'm not sure. Never had the veins bulging, just the exploding

feeling. As I said it took a while for it to get better (like over 2

months on SCD) and I still experience a little of it here and there.

But, maybe your experience is different than mine!

On different occasions (specifically for a time when I was totally

over medicated and underweight) I also experienced very intense fluid

shifting in my body- my PCP said it was the cerebral spinal fluid

rapidly moving (I should read about this) This was totally

debilitating and it would happen during my sleep or when I pushed too

much on the toilet! I would feel a hot wave come over me and then I

would feel my head/chest explode and want to vomit. Sometimes I would

scream out of my sleep. This is a long shot but maybe you experience

intense fluid shifts too?

I have to say over the years during these episodes I always went to my

doctor because it always scared the hell out of me!

Jodi

>

> thanks it's nice to know someone else has felt this - freaking me

> out - as all this has for months! but you - 17 years wow!! but if I'm

> improving why is it showing up now??? any thoughts?

>

Link to comment
Share on other sites

thanks i'll call a doc just to clarify

eileen

> >

> > thanks it's nice to know someone else has felt this - freaking me

> > out - as all this has for months! but you - 17 years wow!! but if

I'm

> > improving why is it showing up now??? any thoughts?

> >

>

Link to comment
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...
×
×
  • Create New...