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>

>

> ----- Original Message -----

> From: mmc2315

>

> Wait..., are you saying the trouble coincided with the dose

increase of ALA?

>

> <<

> The thing I don't understand is on the Ala she is complaining

regularly that her head feels weird (right frontal lobe) and making

this movement and the minute we stop the Ala and just give the Dmsa

she is fine and she's always fine the very next day.

,

I don't know if this will be useful to you, but the " head feels

weird " is something I'm very familiar with, so I'll just share

my experience.

I have had lots of " weird head " feelings on chelation. (Very

similar to the feelings I get from killing yeast, actually.)

At the worst, it evolves to become a type of dizziness.

I had some of these feelings for years before chelating, but it

got a lot worse when I started chelation. Part of the problem

was not taking chelators often enough. When I took DMSA often

enough the problem went away, but it came back worse than ever

when I started ALA.

The only thing that has helped since starting ALA is GABA. I

started it for anxiety, and did not expect it to help the

weird-headed feelings. A pleasant surprise, though, and made it

possible to (finally) raise my ALA dose.

My experience is the same - when I drop the ALA and continue

DMSA, the weird head feelings go away promptly. I had never

localized it before, but now you mention it, mine can be frontal

or at the crown of my head.

I get some jerky muscle movements at times, too, but these are

not necessarily tied to the weird-headed feelings. Somewhat

controllable, but not entirely voluntary. And I certainly get

hyper moods, anxiety, panicky stuff. GABA has been a big help

with a lot of these symptoms. Now that I think about it, this

has all been better when my adrenals have been doing better, and

makes me think now I am not on enough support. Interesting.

I'm glad you posted about this, and glad Andy replied.

I am in the process of pursuing some investigation of these

problems, but to date I have not had an EEG. I did have a neuro

exam that was normal (I think). I'd be interested to hear what

happens with her situation - hopefully all will clear up quickly

for her.

-- (formerly a PA girl and born in OH :)

> in Ohio, yeah for the Midwest

>

> in Illinois

>

>

>

>

>

>

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----- Original Message -----

From:

>

,

I don't know if this will be useful to you, but the " head feels

weird " is something I'm very familiar with, so I'll just share

my experience.

I have had lots of " weird head " feelings on chelation. (Very

similar to the feelings I get from killing yeast, actually.)

At the worst, it evolves to become a type of dizziness.

I had some of these feelings for years before chelating, but it

got a lot worse when I started chelation. Part of the problem

was not taking chelators often enough. When I took DMSA often

enough the problem went away, but it came back worse than ever

when I started ALA.

<<

>>>>>>>>>>>>>

The only thing that has helped since starting ALA is GABA. I

started it for anxiety, and did not expect it to help the

weird-headed feelings. A pleasant surprise, though, and made it

possible to (finally) raise my ALA dose.

<<<

>>>>>>

My experience is the same - when I drop the ALA and continue

DMSA, the weird head feelings go away promptly. I had never

localized it before, but now you mention it, mine can be frontal

or at the crown of my head.

I get some jerky muscle movements at times, too, but these are

not necessarily tied to the weird-headed feelings. Somewhat

controllable, but not entirely voluntary. And I certainly get

hyper moods, anxiety, panicky stuff. GABA has been a big help

with a lot of these symptoms. Now that I think about it, this

has all been better when my adrenals have been doing better, and

makes me think now I am not on enough support. Interesting.

I'm glad you posted about this, and glad Andy replied.

<<

>>>

Thanks , forgive the rambling, I sometimes get my best ideas when I

am wandering aimlessly, cognitive-wise.

(whose mother lives in Nevada, and says that Ohio is a great place to

be FROM

-- (formerly a PA girl and born in OH :)

> in Ohio, yeah for the Midwest

>

> in Illinois

>

>

>

>

>

>

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>

> (whose mother lives in Nevada, and says that Ohio is a great place

to be FROM

>

> -- (formerly a PA girl and born in OH :)

>

> > in Ohio, yeah for the Midwest

> >

> > in Illinois

You girls are killin' me. ;)

, is Ohio really considered Midwest?

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> ----- Original Message -----

> From:

> was not taking chelators often enough. When I took DMSA often

> enough the problem went away, but it came back worse than ever

> when I started ALA.

>

> <<

Also, did you get the " weird head " feeling with Ala from the

beginning?

Yes, I did. I commented on her set of similar symptoms because I

haven't seen any adults report a set of symptoms so similar to mine.

Even though hers are more in the nature of an exacerbation and mine

are more long-standing, I thought it interesting.

I just think it's odd that we have used Ala for over 2

years and this is the first time we are hearing complaints, although

Dean reports this same phenomena after a year, why? This sudden

complaint made me question if the Ala pathway was somehow blocked

previously and through some developmental stage is now open. Highly

speculative here as I am hopelessly clueless about a lot of aspects of

physiology and it's not for lack of trying.

It sounds like you noticed effects with ALA in the past, so I doubt

that an " ALA pathway " is suddenly open that wasn't before. What I

was thinking was more that the brain has changed (anatomically?

physiologically?) so that metals can come out from some location they

could not before, or come out faster, or something... Don't know,

just a thought.

It would be possible that she needs to take ALA more often, possibly

just temporarily (maybe her liver is detoxing?).

> We did one round of just Ala, round 30, when she was 4. She was

happy, euphoric even and spacey as heck. We tried another just Ala

round at round 50 and got nothing, couldn't even tell we were giving

her the Ala, continued for 10 rounds, and she actually lost a little

ground there (could have been the stall period) so we put her back on

the dmsa/ala combo and she continued to progress.

>

> And, yes, when asked where her head hurts/feels funny she will

point to her right frontal lobe near the hairline to aout 2 inches

down her forehead.>>>>>>>>>>>>>>

Sounds pretty tightly localized. Mine is rarely so localized.

Maybe a totally different thing.

> The only thing that has helped since starting ALA is GABA. I

> started it for anxiety, and did not expect it to help the

> weird-headed feelings. A pleasant surprise, though, and made it

> possible to (finally) raise my ALA dose.

>

> <<<

>>>>>>

I hope it helps.

> <<

>>>

In any case, it would make sense to use what you have done in the

past, the adrenal cortex extract and the frequent C/B5.

> Thanks , forgive the rambling, I sometimes get my best

ideas when I am wandering aimlessly, cognitive-wise.

Me too. Thanks for letting me.

--

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>

> ----- Original Message -----

> From:

> was not taking chelators often enough. When I took DMSA often

> enough the problem went away, but it came back worse than ever

> when I started ALA.

>

> <<

Also, did you get the " weird head " feeling with Ala from the

beginning?

Yes, I did. I commented on her set of similar symptoms because I

haven't seen any adults report a set of symptoms so similar to mine.

Even though hers are more in the nature of an exacerbation and mine

are more long-standing, I thought it interesting.

I just think it's odd that we have used Ala for over 2

years and this is the first time we are hearing complaints, although

Dean reports this same phenomena after a year, why? This sudden

complaint made me question if the Ala pathway was somehow blocked

previously and through some developmental stage is now open. Highly

speculative here as I am hopelessly clueless about a lot of aspects of

physiology and it's not for lack of trying.

It sounds like you noticed effects with ALA in the past, so I doubt

that an " ALA pathway " is suddenly open that wasn't before. What I

was thinking was more that the brain has changed (anatomically?

physiologically?) so that metals can come out from some location they

could not before, or come out faster, or something... Don't know,

just a thought.

It would be possible that she needs to take ALA more often, possibly

just temporarily (maybe her liver is detoxing?).

> We did one round of just Ala, round 30, when she was 4. She was

happy, euphoric even and spacey as heck. We tried another just Ala

round at round 50 and got nothing, couldn't even tell we were giving

her the Ala, continued for 10 rounds, and she actually lost a little

ground there (could have been the stall period) so we put her back on

the dmsa/ala combo and she continued to progress.

>

> And, yes, when asked where her head hurts/feels funny she will

point to her right frontal lobe near the hairline to aout 2 inches

down her forehead.>>>>>>>>>>>>>>

Sounds pretty tightly localized. Mine is rarely so localized.

Maybe a totally different thing.

> The only thing that has helped since starting ALA is GABA. I

> started it for anxiety, and did not expect it to help the

> weird-headed feelings. A pleasant surprise, though, and made it

> possible to (finally) raise my ALA dose.

>

> <<<

>>>>>>

I hope it helps.

> <<

>>>

In any case, it would make sense to use what you have done in the

past, the adrenal cortex extract and the frequent C/B5.

> Thanks , forgive the rambling, I sometimes get my best

ideas when I am wandering aimlessly, cognitive-wise.

Me too. Thanks for letting me.

--

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