Re: HRT and LD

[Guest guest]

Hi ,

That's a terrible ordeal that you went through. You can't trust doctor's to

figure things out for you. I found that Bart lowered my hormones, but may-be

the opposite can happen too.

When I got LD my first symptoms were hormonal imbalances and fatigue, so I went

to doctors for that and got on Armour Thyroid and more estrogen. I didn't know

I had Lyme. I thought I was feeling bad because of the hormonal imbalance. When

that supposedly was corrected my hot flashes and other symptoms disappeared, but

I was still feeling bad, so I thought Adrenal fatigue, but that was not either.

Now I am on progesterone as well. I had a hysterectomy too. I haven't noticed

any difference in the Bart symptoms because of the increase in hormones that I

take, but mine were minimal. I would guess that your body might be very

sensitive now after your horrific ordeal with hormone overload for such a long

time. I would be very curious how this turns out for you. How did you do

without HRT? If your hormone levels were ok and you didn't have any hormonal

symptoms, why change? It is safer to be on both estrogen and progesterone even

if you have had a hysterectomy, as you have to think about your breasts as well.

Let me know what happens. What a roller coaster ride!! Love and Light, Maud

On Sep 11, 2010, at 1:52 AM, MG wrote:

>

> Hi Again

>

> So I had a total hysterectomy in 2001 for stage 1 ovarian cancer and

Endometriosis. Then I had what I thought was a hard time with bioidentical HRT,

but now know it was the LD. I then had a doctor who gave me the up and coming

" pellets " of hormones implanted in my hip. He never 1 time in 5 years took my

hormone levels even though I kept asking. He said he didnt need to because they

would only release as much as my body needed. I had no money and no insurance to

go elsewhere so I trusted he knew what he was doing. The pellets were supposed

to last 4-6 months but I went in every month with what I though were menopause

symptoms. I now know they were Bart symptoms. He kept giving me more pellets

every month.

>

> When I started having low thyroid symptoms and adrenal issues I begged him to

please draw all the specialty thyroid tests. He did and I was Hypo with reverse

T3 syndrome. Armed with this diagnosis I found a specialist and spent my life

saving seeing them for 3 years. They are the ones who missed the lyme diagnosis

even though they also see Lyme patients as Endocrinologists who specialize in

Bio Hormones/Endocrine and Auto Immune diseases. When they drew my hormone

levels my estrogen was 2,487 and normal range is 70-200. It took me 11 months to

crash off of all that estrogen and testosterone.

>

> I was then terrified to take any hormones because when i did my head would

hurt and I felt like poison was running through my veins (It was the LD reacting

to it). So fast forward to today since my LD diagnosis. My LLND wanted me to

take a very small dose to help my body be more stable going thorugh this. So I

got the creams and I tried the tiny bit night before last and my Bart symptoms

flared real bad and I was terrified. Does anyone know if this might settle down

as my body adjusts to the chemical change? Will it make more bugs? I hear such

conflicting reports as to weather we need them or not. I had been HRT free for

18 months before this. Sorry so long I am just a little confused. Thank you for

any advice.

>

> Blessings

>

>

>

[Guest guest]

hi Maud,

 

thanky ou for your posts Having a hard day today after the epinephrine in the

dental shot for my 5 fillings. i also have had to be off my herbs for 3 days

because of doing a stool culture and saliva tests. I don't have any mood swings

or hot flashes due to menopause at all. On good lyme days I even have a libido.I

have not been on HRT for 18 months now and maintain a very strict diet, rest and

mild excercise while supporting my adrenals. the ND told me that maybe adding

the hormones would help my sleep etc. but upon taking them Thursday night my

heart was racing, I vomited 3 times, my breasts hurt real bad and I was tossing

and turning all night. They are both tiny little doses and I know there is an

adjustment period, but I just felt so very horrible. Im wondering if I should

try it again for 2 consecutive days, but I don't know. I am just really confused

right now and a little down(Im assuming because I have not taken my herbs in a

few days). I read

all over the place that post menopausal women without proper hormone ratios

have a harder time with lyme and treatment which is why I agreed to do them. I

am going to get a massage now and meditate hoping it helps. Thank you so very

much for all of your help.

 

Love and Light

> 

> Hi Again

> 

> So I had a total hysterectomy in 2001 for stage 1 ovarian cancer and

Endometriosis. Then I had what I thought was a hard time with bioidentical HRT,

but now know it was the LD. I then had a doctor who gave me the up and coming

" pellets " of hormones implanted in my hip. He never 1 time in 5 years took my

hormone levels even though I kept asking. He said he didnt need to because they

would only release as much as my body needed. I had no money and no insurance to

go elsewhere so I trusted he knew what he was doing. The pellets were supposed

to last 4-6 months but I went in every month with what I though were menopause

symptoms. I now know they were Bart symptoms. He kept giving me more pellets

every month.

> 

> When I started having low thyroid symptoms and adrenal issues I begged him to

please draw all the specialty thyroid tests. He did and I was Hypo with reverse

T3 syndrome. Armed with this diagnosis I found a specialist and spent my life

saving seeing them for 3 years. They are the ones who missed the lyme diagnosis

even though they also see Lyme patients as Endocrinologists who specialize in

Bio Hormones/Endocrine and Auto Immune diseases. When they drew my hormone

levels my estrogen was 2,487 and normal range is 70-200. It took me 11 months to

crash off of all that estrogen and testosterone.

> 

> I was then terrified to take any hormones because when i did my head would

hurt and I felt like poison was running through my veins (It was the LD reacting

to it). So fast forward to today since my LD diagnosis. My LLND wanted me to

take a very small dose to help my body be more stable going thorugh this. So I

got the creams and I tried the tiny bit night before last and my Bart symptoms

flared real bad and I was terrified. Does anyone know if this might settle down

as my body adjusts to the chemical change? Will it make more bugs? I hear such

conflicting reports as to weather we need them or not. I had been HRT free for

18 months before this. Sorry so long I am just a little confused. Thank you for

any advice.

> 

> Blessings

>

>

>

[Guest guest]

- I hope today is better. I do take the bio-identicals and for me,

they help hugely. sleep...mood. and the rage I believe. Talk to the doc

about taking them at different times. Do you use melatonin at night? I have

had to Sun-TH and Sunday nights I have to drug myself to sleep or I will

stress out and stay awake.

Like we talked about, you do what you have to to live and put a roof over

our heads.

I have never heard of hormones making on vomit. Do you easily vomit? Could

it be something else that upset you? Keep that log and look for patterns.

That seems to help me. First I feel like I'm doing something and secondly

some patterns start to show up - the analytical side of me!

_____

From:

[mailto: ] On Behalf Of MG

Sent: Saturday, September 11, 2010 12:44 PM

Subject: Re: [ ] HRT and LD

hi Maud,

thanky ou for your posts Having a hard day today after the epinephrine in

the dental shot for my 5 fillings. i also have had to be off my herbs for 3

days because of doing a stool culture and saliva tests. I don't have any

mood swings or hot flashes due to menopause at all. On good lyme days I even

have a libido.I have not been on HRT for 18 months now and maintain a very

strict diet, rest and mild excercise while supporting my adrenals. the ND

told me that maybe adding the hormones would help my sleep etc. but upon

taking them Thursday night my heart was racing, I vomited 3 times, my

breasts hurt real bad and I was tossing and turning all night. They are both

tiny little doses and I know there is an adjustment period, but I just felt

so very horrible. Im wondering if I should try it again for 2 consecutive

days, but I don't know. I am just really confused right now and a little

down(Im assuming because I have not taken my herbs in a few days). I read

all over the place that post menopausal women without proper hormone ratios

have a harder time with lyme and treatment which is why I agreed to do them.

I am going to get a massage now and meditate hoping it helps. Thank you so

very much for all of your help.

Love and Light

>

> Hi Again

>

> So I had a total hysterectomy in 2001 for stage 1 ovarian cancer and

Endometriosis. Then I had what I thought was a hard time with bioidentical

HRT, but now know it was the LD. I then had a doctor who gave me the up and

coming " pellets " of hormones implanted in my hip. He never 1 time in 5 years

took my hormone levels even though I kept asking. He said he didnt need to

because they would only release as much as my body needed. I had no money

and no insurance to go elsewhere so I trusted he knew what he was doing. The

pellets were supposed to last 4-6 months but I went in every month with what

I though were menopause symptoms. I now know they were Bart symptoms. He

kept giving me more pellets every month.

>

> When I started having low thyroid symptoms and adrenal issues I begged him

to please draw all the specialty thyroid tests. He did and I was Hypo with

reverse T3 syndrome. Armed with this diagnosis I found a specialist and

spent my life saving seeing them for 3 years. They are the ones who missed

the lyme diagnosis even though they also see Lyme patients as

Endocrinologists who specialize in Bio Hormones/Endocrine and Auto Immune

diseases. When they drew my hormone levels my estrogen was 2,487 and normal

range is 70-200. It took me 11 months to crash off of all that estrogen and

testosterone.

>

> I was then terrified to take any hormones because when i did my head would

hurt and I felt like poison was running through my veins (It was the LD

reacting to it). So fast forward to today since my LD diagnosis. My LLND

wanted me to take a very small dose to help my body be more stable going

thorugh this. So I got the creams and I tried the tiny bit night before last

and my Bart symptoms flared real bad and I was terrified. Does anyone know

if this might settle down as my body adjusts to the chemical change? Will it

make more bugs? I hear such conflicting reports as to weather we need them

or not. I had been HRT free for 18 months before this. Sorry so long I am

just a little confused. Thank you for any advice.

>

> Blessings

>

>

>

[Guest guest]

nancy,

 

having a hard time with dental work friday and then being off my herbs for 3

days for stool/saliva tests. Then tonight part of my tooth thye worked on broke

off and im in pain...will it ever end? UGH. Below is what Dr. Lee Cowden said

about HRT in my case because I have been off them for 18 months and to start

them now would set my reocvery back as the flutuations until stable would cause

the bug to go nuts....hugs

 

" Borrelia & co-infections can slow hormone metabolism by the liver & can alter

hormone receptor function. It's probably best to not add HRT back in until the

bugs are under better control (that usually happens around day 78 of the

Condensed Program). The best way to deal with Herx is to take 8 drops of Burbur

or 8 drops of Parsley Detox in 1/2 cup of water every 10-15 minutes for 1-2

hours. Dr. Cowden "

>

> Hi Again

>

> So I had a total hysterectomy in 2001 for stage 1 ovarian cancer and

Endometriosis. Then I had what I thought was a hard time with bioidentical

HRT, but now know it was the LD. I then had a doctor who gave me the up and

coming " pellets " of hormones implanted in my hip. He never 1 time in 5 years

took my hormone levels even though I kept asking. He said he didnt need to

because they would only release as much as my body needed. I had no money

and no insurance to go elsewhere so I trusted he knew what he was doing. The

pellets were supposed to last 4-6 months but I went in every month with what

I though were menopause symptoms. I now know they were Bart symptoms. He

kept giving me more pellets every month.

>

> When I started having low thyroid symptoms and adrenal issues I begged him

to please draw all the specialty thyroid tests. He did and I was Hypo with

reverse T3 syndrome. Armed with this diagnosis I found a specialist and

spent my life saving seeing them for 3 years. They are the ones who missed

the lyme diagnosis even though they also see Lyme patients as

Endocrinologists who specialize in Bio Hormones/Endocrine and Auto Immune

diseases. When they drew my hormone levels my estrogen was 2,487 and normal

range is 70-200. It took me 11 months to crash off of all that estrogen and

testosterone.

>

> I was then terrified to take any hormones because when i did my head would

hurt and I felt like poison was running through my veins (It was the LD

reacting to it). So fast forward to today since my LD diagnosis. My LLND

wanted me to take a very small dose to help my body be more stable going

thorugh this. So I got the creams and I tried the tiny bit night before last

and my Bart symptoms flared real bad and I was terrified. Does anyone know

if this might settle down as my body adjusts to the chemical change? Will it

make more bugs? I hear such conflicting reports as to weather we need them

or not. I had been HRT free for 18 months before this. Sorry so long I am

just a little confused. Thank you for any advice.

>

> Blessings

>

>

>

[Guest guest]

I have read that some people are allergic to hormones even their own. I know

there is a way around it, but I don't know what it is.

Connie

Re: [ ] HRT and LD

hi Maud,

thanky ou for your posts Having a hard day today after the epinephrine in the

dental shot for my 5 fillings. i also have had to be off my herbs for 3 days

because of doing a stool culture and saliva tests. I don't have any mood swings

or hot flashes due to menopause at all. On good lyme days I even have a libido.I

have not been on HRT for 18 months now and maintain a very strict diet, rest and

mild excercise while supporting my adrenals. the ND told me that maybe adding

the hormones would help my sleep etc. but upon taking them Thursday night my

heart was racing, I vomited 3 times, my breasts hurt real bad and I was tossing

and turning all night. They are both tiny little doses and I know there is an

adjustment period, but I just felt so very horrible. Im wondering if I should

try it again for 2 consecutive days, but I don't know. I am just really confused

right now and a little down(Im assuming because I have not taken my herbs in a

few days). I read

all over the place that post menopausal women without proper hormone ratios have

a harder time with lyme and treatment which is why I agreed to do them. I am

going to get a massage now and meditate hoping it helps. Thank you so very much

for all of your help.

Love and Light

[Guest guest]

Hi ,

The doctor told me that if you have any amalgams or mercury in your system that

you will not be able to get rid of Lyme. I don't know if it is true. I got rid

of all my amalgams and lowered my level of mercury in my blood to almost

undetectable amounts and they still wanted to do IV detox with DMPS, which is

very dangerous. I refused to go that route, but getting rid of amalgams is a

good idea, I think. Good luck with having all that dental work done. I never

knew you could have all these problems with Novocaine and Epinephrine. So sorry

that you had to go through that. Love and light. Maud

On Sep 13, 2010, at 7:09 PM, Connie Blaze wrote:

> I have read that some people are allergic to hormones even their own. I know

there is a way around it, but I don't know what it is.

>

> Connie

>

> Re: [ ] HRT and LD

>

> hi Maud,

>

> thanky ou for your posts Having a hard day today after the epinephrine in

the dental shot for my 5 fillings. i also have had to be off my herbs for 3 days

because of doing a stool culture and saliva tests. I don't have any mood swings

or hot flashes due to menopause at all. On good lyme days I even have a libido.I

have not been on HRT for 18 months now and maintain a very strict diet, rest and

mild excercise while supporting my adrenals. the ND told me that maybe adding

the hormones would help my sleep etc. but upon taking them Thursday night my

heart was racing, I vomited 3 times, my breasts hurt real bad and I was tossing

and turning all night. They are both tiny little doses and I know there is an

adjustment period, but I just felt so very horrible. Im wondering if I should

try it again for 2 consecutive days, but I don't know. I am just really confused

right now and a little down(Im assuming because I have not taken my herbs in a

few days). I read

> all over the place that post menopausal women without proper hormone ratios

have a harder time with lyme and treatment which is why I agreed to do them. I

am going to get a massage now and meditate hoping it helps. Thank you so very

much for all of your help.

>

> Love and Light

>

>

>

[Guest guest]

>

> Hi ,

>

> The doctor told me that if you have any amalgams or mercury in your system

that you will not be able to get rid of Lyme. I don't know if it is true.

of course it is not true, it would be quite obvious if there was such a

difference in lyme disease recovery between people with or without amalgams.

I agree that amalgams are a potential health concern, but it can't be so

dangerous as many ND's in the US are suggesting. There are plenty of people with

amalgams and perfect health (and very ill people with no amalgams at all).

Just last week I read a new article about dangerous chemicals leaking out of new

composite fillings. Everything unnatural that is put in your mouth is a health

risk, especially if it has chemical properties that help it 'resist the bugs'.

[Guest guest]

Hi and

I am mostly lurking (sorry) but did want to mention that in my recent

research on Porphyria...which I believe is complicating the Lyme recovery

for some....I have learned that hormone replacement is not for everyone.

Hormone replacement can push a person with Porphyria into an acute stage and

nausea is one of the many symptoms of Porphyria. There are 8 different forms

of Porphyria and some are inherited, some are caused by the infections and

/or mercury and some are triggered by prescription medications including

hormone replacement. There are many lists of drugs contraindicated by those

with Porphyria which you can pull up on a search.

Just in case,

On Sun, Sep 12, 2010 at 8:30 PM, <wilson33@...> wrote:

>

>

> - I hope today is better. I do take the bio-identicals and for me,

> they help hugely. sleep...mood. and the rage I believe. Talk to the doc

> about taking them at different times. Do you use melatonin at night? I have

> had to Sun-TH and Sunday nights I have to drug myself to sleep or I will

> stress out and stay awake.

>

> Like we talked about, you do what you have to to live and put a roof over

> our heads.

>

> I have never heard of hormones making on vomit. Do you easily vomit? Could

> it be something else that upset you? Keep that log and look for patterns.

> That seems to help me. First I feel like I'm doing something and secondly

> some patterns start to show up - the analytical side of me!

>

>

>

> _____

>

> From: < %40>

> [mailto: < %40>]

> On Behalf Of MG

> Sent: Saturday, September 11, 2010 12:44 PM

> < %40>

> Subject: Re: [ ] HRT and LD

>

> hi Maud,

>

> thanky ou for your posts Having a hard day today after the epinephrine

> in

> the dental shot for my 5 fillings. i also have had to be off my herbs for 3

> days because of doing a stool culture and saliva tests. I don't have any

> mood swings or hot flashes due to menopause at all. On good lyme days I

> even

> have a libido.I have not been on HRT for 18 months now and maintain a very

> strict diet, rest and mild excercise while supporting my adrenals. the ND

> told me that maybe adding the hormones would help my sleep etc. but upon

> taking them Thursday night my heart was racing, I vomited 3 times, my

> breasts hurt real bad and I was tossing and turning all night. They are

> both

> tiny little doses and I know there is an adjustment period, but I just felt

> so very horrible. Im wondering if I should try it again for 2 consecutive

> days, but I don't know. I am just really confused right now and a little

> down(Im assuming because I have not taken my herbs in a few days). I read

> all over the place that post menopausal women without proper hormone ratios

> have a harder time with lyme and treatment which is why I agreed to do

> them.

> I am going to get a massage now and meditate hoping it helps. Thank you so

> very much for all of your help.

>

> Love and Light

>

>

>

>

> >

> > Hi Again

> >

> > So I had a total hysterectomy in 2001 for stage 1 ovarian cancer and

> Endometriosis. Then I had what I thought was a hard time with bioidentical

> HRT, but now know it was the LD. I then had a doctor who gave me the up and

> coming " pellets " of hormones implanted in my hip. He never 1 time in 5

> years

> took my hormone levels even though I kept asking. He said he didnt need to

> because they would only release as much as my body needed. I had no money

> and no insurance to go elsewhere so I trusted he knew what he was doing.

> The

> pellets were supposed to last 4-6 months but I went in every month with

> what

> I though were menopause symptoms. I now know they were Bart symptoms. He

> kept giving me more pellets every month.

> >

> > When I started having low thyroid symptoms and adrenal issues I begged

> him

> to please draw all the specialty thyroid tests. He did and I was Hypo with

> reverse T3 syndrome. Armed with this diagnosis I found a specialist and

> spent my life saving seeing them for 3 years. They are the ones who missed

> the lyme diagnosis even though they also see Lyme patients as

> Endocrinologists who specialize in Bio Hormones/Endocrine and Auto Immune

> diseases. When they drew my hormone levels my estrogen was 2,487 and normal

> range is 70-200. It took me 11 months to crash off of all that estrogen and

> testosterone.

> >

> > I was then terrified to take any hormones because when i did my head

> would

> hurt and I felt like poison was running through my veins (It was the LD

> reacting to it). So fast forward to today since my LD diagnosis. My LLND

> wanted me to take a very small dose to help my body be more stable going

> thorugh this. So I got the creams and I tried the tiny bit night before

> last

> and my Bart symptoms flared real bad and I was terrified. Does anyone know

> if this might settle down as my body adjusts to the chemical change? Will

> it

> make more bugs? I hear such conflicting reports as to weather we need them

> or not. I had been HRT free for 18 months before this. Sorry so long I am

> just a little confused. Thank you for any advice.

> >

> > Blessings

> >

> >

> >

[Guest guest]

Here's what I found on porphyria

Porphyrias are a group of genetic disorders caused by problems with how your

body makes a substance called heme. Heme is found throughout the body,

especially in your blood and bone marrow, where it carries oxygen.

Porphyrias affect the skin or the nervous system. People with the skin type

develop blisters, itching, and swelling of their skin when it is exposed to

sunlight. The nervous system type is called acute porphyria. Symptoms

include pain in the chest or abdomen, vomiting, and diarrhea or

constipation. During an attack, symptoms can include muscle numbness,

tingling, paralysis, cramping, and personality or mental changes. Certain

triggers can cause an attack, including some medicines, smoking, drinking

alcohol, infections, stress and sun exposure. Attacks develop over hours or

days. They can last for days or weeks.

Porphyria can be hard to diagnose. It requires blood, urine and stool tests.

Each type has a different treatment. It usually involves medicine, treatment

with heme or drawing blood.

For me - not having estrogen makes me not a nice person to be

around...:-)...therfore, in the interest of society, I am taking my

bio-identicals. but I can see using something like horse urine, one's body

might not be happy.

W

Re: [ ] HRT and LD

Hi and

I am mostly lurking (sorry) but did want to mention that in my recent

research on Porphyria...which I believe is complicating the Lyme recovery

for some....I have learned that hormone replacement is not for everyone.

Hormone replacement can push a person with Porphyria into an acute stage and

nausea is one of the many symptoms of Porphyria. There are 8 different forms

of Porphyria and some are inherited, some are caused by the infections and

/or mercury and some are triggered by prescription medications including

hormone replacement. There are many lists of drugs contraindicated by those

with Porphyria which you can pull up on a search.

Just in case,

On Sun, Sep 12, 2010 at 8:30 PM, <wilson33@...> wrote:

>

>

> - I hope today is better. I do take the bio-identicals and for

> me, they help hugely. sleep...mood. and the rage I believe. Talk to

> the doc about taking them at different times. Do you use melatonin at

> night? I have had to Sun-TH and Sunday nights I have to drug myself to

> sleep or I will stress out and stay awake.

>

> Like we talked about, you do what you have to to live and put a roof

> over our heads.

>

> I have never heard of hormones making on vomit. Do you easily vomit?

> Could it be something else that upset you? Keep that log and look for

patterns.

> That seems to help me. First I feel like I'm doing something and

> secondly some patterns start to show up - the analytical side of me!

>

>

[Guest guest]

Yes I agree unless you had Porphyria and then it would be

contraindicated....if you are feeling better...I would doubt you need to

worry but it was the nausea which caused me to mention it ,

On Thu, Sep 16, 2010 at 8:39 AM, <wilson33@...> wrote:

>

>

> Here's what I found on porphyria

>

> Porphyrias are a group of genetic disorders caused by problems with how

> your

> body makes a substance called heme. Heme is found throughout the body,

> especially in your blood and bone marrow, where it carries oxygen.

>

> Porphyrias affect the skin or the nervous system. People with the skin type

> develop blisters, itching, and swelling of their skin when it is exposed to

> sunlight. The nervous system type is called acute porphyria. Symptoms

> include pain in the chest or abdomen, vomiting, and diarrhea or

> constipation. During an attack, symptoms can include muscle numbness,

> tingling, paralysis, cramping, and personality or mental changes. Certain

> triggers can cause an attack, including some medicines, smoking, drinking

> alcohol, infections, stress and sun exposure. Attacks develop over hours or

> days. They can last for days or weeks.

>

> Porphyria can be hard to diagnose. It requires blood, urine and stool

> tests.

> Each type has a different treatment. It usually involves medicine,

> treatment

> with heme or drawing blood.

>

> For me - not having estrogen makes me not a nice person to be

> around...:-)...therfore, in the interest of society, I am taking my

> bio-identicals. but I can see using something like horse urine, one's body

> might not be happy.

>

> W

>

>

> Re: [ ] HRT and LD

>

> Hi and

>

> I am mostly lurking (sorry) but did want to mention that in my recent

> research on Porphyria...which I believe is complicating the Lyme recovery

> for some....I have learned that hormone replacement is not for everyone.

> Hormone replacement can push a person with Porphyria into an acute stage

> and

> nausea is one of the many symptoms of Porphyria. There are 8 different

> forms

> of Porphyria and some are inherited, some are caused by the infections and

> /or mercury and some are triggered by prescription medications including

> hormone replacement. There are many lists of drugs contraindicated by those

> with Porphyria which you can pull up on a search.

>

> Just in case,

>

>

>

> On Sun, Sep 12, 2010 at 8:30 PM,

<wilson33@...<wilson33%40sonic.net>>

> wrote:

>

> >

> >

> > - I hope today is better. I do take the bio-identicals and for

> > me, they help hugely. sleep...mood. and the rage I believe. Talk to

> > the doc about taking them at different times. Do you use melatonin at

> > night? I have had to Sun-TH and Sunday nights I have to drug myself to

> > sleep or I will stress out and stay awake.

> >

> > Like we talked about, you do what you have to to live and put a roof

> > over our heads.

> >

> > I have never heard of hormones making on vomit. Do you easily vomit?

> > Could it be something else that upset you? Keep that log and look for

> patterns.

> > That seems to help me. First I feel like I'm doing something and

> > secondly some patterns start to show up - the analytical side of me!

> >

> >

>

>