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a

I don't know the answers but I'm having a similar problem.

Although, the last u/s day after O showed a lining of 5mm for me.

It wasn't done as a fertility measure but more for pelvic pain. It was beginning

to feel as if something was pushing on

my bladder.

All is well now, with no explanation, but my AF is diminishing also.

Last month I had a temp drop and period-like cramps. I didn't start bleeding

until 24 hours later. That is not like me at

all. I did have an AF for 2 1/2 days but after day 1, the bleeding didn't even

reach the pad. I have an appt. with an A-list

doc next month. I never had any other followup, but was told my AS was very mild

and my uterus looked normal after

removal of the adhesions.

I'm hoping it is the thin lining and not scarring that is causing my periods to

be so light.

It sounds like there is help for that and it is promising. I don't think your

lining is " thick " but it does sound ok.

I will keep you updated and hope you can do the same.

BTW, when I got pg the first time, I also had light periods, but I did get pg.

> Hello everyone,

>

> I have just had an U/S here in UK and my cavity still looks open which

> is great news. Further more my lining is 6.7mm which sounds very

> promising. I am also ovulating with no problems. However I still can't

> understand why my periods are diminishing by the month. I asked about

> checking blood flow to the uterus but my consultant thought that was

> unnecessary. He is confident that with time things should improve and I

> should ttc for the next three months. He did mention having another hsg

> and I wish I had pushed for this as I'm not sure how good an U/S is as a

> diagnostic source. I know other members are also having similar problems

> with their periods but I think some of their linings were certainly

> thinner than mine. If it's not to do with thickness of lining what else

> can it be - unless my uterus is beginning to scar over again like it did

> following my previous surgeries. Can anyone shed any light on this or is

> there anyone else with a 'thick' lining whose periods are getting

> lighter by the month?

>

> Thanks for reading,

>

> a

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a

I don't know the answers but I'm having a similar problem.

Although, the last u/s day after O showed a lining of 5mm for me.

It wasn't done as a fertility measure but more for pelvic pain. It was beginning

to feel as if something was pushing on

my bladder.

All is well now, with no explanation, but my AF is diminishing also.

Last month I had a temp drop and period-like cramps. I didn't start bleeding

until 24 hours later. That is not like me at

all. I did have an AF for 2 1/2 days but after day 1, the bleeding didn't even

reach the pad. I have an appt. with an A-list

doc next month. I never had any other followup, but was told my AS was very mild

and my uterus looked normal after

removal of the adhesions.

I'm hoping it is the thin lining and not scarring that is causing my periods to

be so light.

It sounds like there is help for that and it is promising. I don't think your

lining is " thick " but it does sound ok.

I will keep you updated and hope you can do the same.

BTW, when I got pg the first time, I also had light periods, but I did get pg.

> Hello everyone,

>

> I have just had an U/S here in UK and my cavity still looks open which

> is great news. Further more my lining is 6.7mm which sounds very

> promising. I am also ovulating with no problems. However I still can't

> understand why my periods are diminishing by the month. I asked about

> checking blood flow to the uterus but my consultant thought that was

> unnecessary. He is confident that with time things should improve and I

> should ttc for the next three months. He did mention having another hsg

> and I wish I had pushed for this as I'm not sure how good an U/S is as a

> diagnostic source. I know other members are also having similar problems

> with their periods but I think some of their linings were certainly

> thinner than mine. If it's not to do with thickness of lining what else

> can it be - unless my uterus is beginning to scar over again like it did

> following my previous surgeries. Can anyone shed any light on this or is

> there anyone else with a 'thick' lining whose periods are getting

> lighter by the month?

>

> Thanks for reading,

>

> a

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a

I don't know the answers but I'm having a similar problem.

Although, the last u/s day after O showed a lining of 5mm for me.

It wasn't done as a fertility measure but more for pelvic pain. It was beginning

to feel as if something was pushing on

my bladder.

All is well now, with no explanation, but my AF is diminishing also.

Last month I had a temp drop and period-like cramps. I didn't start bleeding

until 24 hours later. That is not like me at

all. I did have an AF for 2 1/2 days but after day 1, the bleeding didn't even

reach the pad. I have an appt. with an A-list

doc next month. I never had any other followup, but was told my AS was very mild

and my uterus looked normal after

removal of the adhesions.

I'm hoping it is the thin lining and not scarring that is causing my periods to

be so light.

It sounds like there is help for that and it is promising. I don't think your

lining is " thick " but it does sound ok.

I will keep you updated and hope you can do the same.

BTW, when I got pg the first time, I also had light periods, but I did get pg.

> Hello everyone,

>

> I have just had an U/S here in UK and my cavity still looks open which

> is great news. Further more my lining is 6.7mm which sounds very

> promising. I am also ovulating with no problems. However I still can't

> understand why my periods are diminishing by the month. I asked about

> checking blood flow to the uterus but my consultant thought that was

> unnecessary. He is confident that with time things should improve and I

> should ttc for the next three months. He did mention having another hsg

> and I wish I had pushed for this as I'm not sure how good an U/S is as a

> diagnostic source. I know other members are also having similar problems

> with their periods but I think some of their linings were certainly

> thinner than mine. If it's not to do with thickness of lining what else

> can it be - unless my uterus is beginning to scar over again like it did

> following my previous surgeries. Can anyone shed any light on this or is

> there anyone else with a 'thick' lining whose periods are getting

> lighter by the month?

>

> Thanks for reading,

>

> a

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,

Thanks for responding to my dilemma. It's really interesting to hear

from other people with the same problem, particularly as there doesn't

seem to be a reasonable explanation. Have you had a hyst. to open your

cavity? I wonder if the ultra sound just isn't detecting the AS - this

has certainly been the case in the past. It's just that my consultant

seems very confident that my cavity is still open.

Thanks again for your story. I would be really interested to hear how

you get on with the A list doc. It's also encouraging to hear that you

managed to get pg with light periods - it shows it is possible and maybe

I should just persevere!

a

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,

Thanks for responding to my dilemma. It's really interesting to hear

from other people with the same problem, particularly as there doesn't

seem to be a reasonable explanation. Have you had a hyst. to open your

cavity? I wonder if the ultra sound just isn't detecting the AS - this

has certainly been the case in the past. It's just that my consultant

seems very confident that my cavity is still open.

Thanks again for your story. I would be really interested to hear how

you get on with the A list doc. It's also encouraging to hear that you

managed to get pg with light periods - it shows it is possible and maybe

I should just persevere!

a

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,

Thanks for responding to my dilemma. It's really interesting to hear

from other people with the same problem, particularly as there doesn't

seem to be a reasonable explanation. Have you had a hyst. to open your

cavity? I wonder if the ultra sound just isn't detecting the AS - this

has certainly been the case in the past. It's just that my consultant

seems very confident that my cavity is still open.

Thanks again for your story. I would be really interested to hear how

you get on with the A list doc. It's also encouraging to hear that you

managed to get pg with light periods - it shows it is possible and maybe

I should just persevere!

a

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  • 2 years later...

Have the told you what is causing you to be hyper?

The radiation you received, was it as part of a scan or did they use it to kill off part of your gland?

Do you have copies of your labs, with ranges, for us to see? That way we can see what they've already been testing and what the results are....

Topper ()Yahoo IM: toppertwoSkype: topperlinda

On Tue, 17 Jan 2006 20:24:59 -0000 "rose4253508" writes:

Hi all, I have been all over trying to get info on my condition. I was told by my doctor that I have hyperthyroidism. i went for the radiation treatment, but i am one of those rare cases that had a bad reaction to the treatment. my neck swelled up really bad and iwas in severe pain. the doc put me on steroids for 2weeks. i have a nodule that is very big that you cn see with the naked eye juust looking at my throat. the dr. has put me on 80mg of propanol and30mg of methimazole. within a day i developed an eye infection and was put on attbiotict. i have insomnia, i am always cold, my throat hurts all yhe time, i have severe stomach pains, i have no appetite,the only thing i can stomach is bannanas,i've been very moody,my eye sight has been blurry,i have bad headaches all the time and the newest is my bones are always feeling heavy and weak. is this all normal? I am feeling really alone and scared. My father passed away from throat cancer. it started as a large thyroid.

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Have the told you what is causing you to be hyper?

The radiation you received, was it as part of a scan or did they use it to kill off part of your gland?

Do you have copies of your labs, with ranges, for us to see? That way we can see what they've already been testing and what the results are....

Topper ()Yahoo IM: toppertwoSkype: topperlinda

On Tue, 17 Jan 2006 20:24:59 -0000 "rose4253508" writes:

Hi all, I have been all over trying to get info on my condition. I was told by my doctor that I have hyperthyroidism. i went for the radiation treatment, but i am one of those rare cases that had a bad reaction to the treatment. my neck swelled up really bad and iwas in severe pain. the doc put me on steroids for 2weeks. i have a nodule that is very big that you cn see with the naked eye juust looking at my throat. the dr. has put me on 80mg of propanol and30mg of methimazole. within a day i developed an eye infection and was put on attbiotict. i have insomnia, i am always cold, my throat hurts all yhe time, i have severe stomach pains, i have no appetite,the only thing i can stomach is bannanas,i've been very moody,my eye sight has been blurry,i have bad headaches all the time and the newest is my bones are always feeling heavy and weak. is this all normal? I am feeling really alone and scared. My father passed away from throat cancer. it started as a large thyroid.

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Have the told you what is causing you to be hyper?

The radiation you received, was it as part of a scan or did they use it to kill off part of your gland?

Do you have copies of your labs, with ranges, for us to see? That way we can see what they've already been testing and what the results are....

Topper ()Yahoo IM: toppertwoSkype: topperlinda

On Tue, 17 Jan 2006 20:24:59 -0000 "rose4253508" writes:

Hi all, I have been all over trying to get info on my condition. I was told by my doctor that I have hyperthyroidism. i went for the radiation treatment, but i am one of those rare cases that had a bad reaction to the treatment. my neck swelled up really bad and iwas in severe pain. the doc put me on steroids for 2weeks. i have a nodule that is very big that you cn see with the naked eye juust looking at my throat. the dr. has put me on 80mg of propanol and30mg of methimazole. within a day i developed an eye infection and was put on attbiotict. i have insomnia, i am always cold, my throat hurts all yhe time, i have severe stomach pains, i have no appetite,the only thing i can stomach is bannanas,i've been very moody,my eye sight has been blurry,i have bad headaches all the time and the newest is my bones are always feeling heavy and weak. is this all normal? I am feeling really alone and scared. My father passed away from throat cancer. it started as a large thyroid.

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  • 4 weeks later...

Opinions needed please. Hope all of you are doing well this fine Sunday.

Ok, after the 1st mamo, they sent the doctor a " normal " report. The 1st

sono showed a fluid filled cyst, the radiologist

reported nothing appeared to be abnormal, no masses. When

the surgeon aspirated the cyst, she was so sure that it was

only a benign cyst, not to worry. Aspirated 20cc's of tan fluid.

Then 2 days later the path report from the aspirate said

" atypical cells highly suspicious for malignancy " , and

" biopsy recommended " . Ok. To me highly suspicious still

didn't mean I had breast cancer.

Three days later DH and I go to surgeon's office, and she

is shocked about the path report. DH asked her if this

means I have BC, and she said I am afraid so, but we won't

know anything else until after the biopsy " .

So, the same day I have another mamo and sono. These

reports both concluded " The findings are highly suspicious

for malignancy, particularly given the hx of malignant

cells within the aspirated fluid " . " Recommend lumpectomy " .

So I had a lumpectomy on Thurs, but she didn't test any

lymph nodes. She said she took out the 5 X 7 cm mass (not cyst), and

plenty of surrounding tissue. Sent to pathology and margins

came back clean. Which means they didn't see any cancer

cells in the margins. She called me Fri and said that there were no malignant

cells in the

margins, that the final path report should be back by Fri..

So I went to the ER, where I am an RN, and printed out the report. The

conclusion was

" Intraductal hyperplasia with atypia. Definitive malignancy is not found in the

current

sections " . Good news? I hope so. Do I need a 2nd opinion? I have been reading

this list

since 1/14/06 when all this started. There are many intelligent women here, and

I trust

that ya'll will give me your opinions.

I can talk to the surgeon tomorrow, but feel the need for some feedback today.

Thank you

so much.

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Lynn,

Veing an RN give you an advantage over us. If you are not comfortable with the report then I would get a second opinion. Some insurance companies prefer second opinions.

Did she say why she didn't take any nodes? I know back when I had my surgery, in 1990, they didn't have sentinel node biopsies yet so I had 23 removed and one was malignant. I will keep you in my prayers. Please keep us posted.

Hugs

nne

Breast Cancer Patients Soul Mates for Lifehttp://www.geocities.com/chucky5741/breastcancerpatients.html

Check out my breast cancer ornaments at:http://www.geocities.com/chucky5741/bcornament.htmlalso check out my other ornaments and lots of nice gifts at:http://www.cancerclub.com

Confused

Opinions needed please. Hope all of you are doing well this fine Sunday. Ok, after the 1st mamo, they sent the doctor a "normal" report. The 1stsono showed a fluid filled cyst, the radiologistreported nothing appeared to be abnormal, no masses. Whenthe surgeon aspirated the cyst, she was so sure that it wasonly a benign cyst, not to worry. Aspirated 20cc's of tan fluid.Then 2 days later the path report from the aspirate said"atypical cells highly suspicious for malignancy", and"biopsy recommended". Ok. To me highly suspicious stilldidn't mean I had breast cancer. Three days later DH and I go to surgeon's office, and sheis shocked about the path report. DH asked her if thismeans I have BC, and she said I am afraid so, but we won'tknow anything else until after the biopsy". So, the same day I have another mamo and sono. Thesereports both concluded "The findings are highly suspiciousfor malignancy, particularly given the hx of malignantcells within the aspirated fluid". "Recommend lumpectomy".So I had a lumpectomy on Thurs, but she didn't test anylymph nodes. She said she took out the 5 X 7 cm mass (not cyst), andplenty of surrounding tissue. Sent to pathology and marginscame back clean. Which means they didn't see any cancercells in the margins. She called me Fri and said that there were no malignant cells in the margins, that the final path report should be back by Fri..So I went to the ER, where I am an RN, and printed out the report. The conclusion was "Intraductal hyperplasia with atypia. Definitive malignancy is not found in the current sections". Good news? I hope so. Do I need a 2nd opinion? I have been reading this list since 1/14/06 when all this started. There are many intelligent women here, and I trust that ya'll will give me your opinions.I can talk to the surgeon tomorrow, but feel the need for some feedback today. Thank you so much.

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lynn, if after you see your surgeon you are not happy with the results or you just don't feel right and have any doubts what so ever, I would seek out a 2nd opion or more until you get the answers you are seeking...

prayers and hugs from carol in michigan

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Yhank you Carol. After talking with the surgeon, she encourared me to get a 2nd

opinion. I

just don't feel comfortable with the way things are. God bless you.

>

> lynn, if after you see your surgeon you are not happy with the results or you

just don't feel

right and have any doubts what so ever, I would seek out a 2nd opion or more

until you get

the answers you are seeking...

> prayers and hugs from carol in michigan

>

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I talked to my surgeon this am, and she encouraged a second opinion. She acted

as if she

were not comfortable with the report. Thank you so much for your reply. Being an

ER RN

gives me no advantage, believe me! I will now become an expert and educate my

pts about

mamo's, etc...

>

> Lynn,

> Veing an RN give you an advantage over us. If you are not comfortable with the

report

then I would get a second opinion. Some insurance companies prefer second

opinions.

>

> Did she say why she didn't take any nodes? I know back when I had my surgery,

in 1990,

they didn't have sentinel node biopsies yet so I had 23 removed and one was

malignant. I

will keep you in my prayers. Please keep us posted.

> Hugs

> nne

> Breast Cancer Patients Soul Mates for Life

> http://www.geocities.com/chucky5741/breastcancerpatients.html

>

> Check out my breast cancer ornaments at:

> http://www.geocities.com/chucky5741/bcornament.html

> also check out my other ornaments and lots of nice gifts at:

> http://www.cancerclub.com

> Confused

>

>

> Opinions needed please. Hope all of you are doing well this fine Sunday.

>

> Ok, after the 1st mamo, they sent the doctor a " normal " report. The 1st

> sono showed a fluid filled cyst, the radiologist

> reported nothing appeared to be abnormal, no masses. When

> the surgeon aspirated the cyst, she was so sure that it was

> only a benign cyst, not to worry. Aspirated 20cc's of tan fluid.

>

> Then 2 days later the path report from the aspirate said

> " atypical cells highly suspicious for malignancy " , and

> " biopsy recommended " . Ok. To me highly suspicious still

> didn't mean I had breast cancer.

>

> Three days later DH and I go to surgeon's office, and she

> is shocked about the path report. DH asked her if this

> means I have BC, and she said I am afraid so, but we won't

> know anything else until after the biopsy " .

>

> So, the same day I have another mamo and sono. These

> reports both concluded " The findings are highly suspicious

> for malignancy, particularly given the hx of malignant

> cells within the aspirated fluid " . " Recommend lumpectomy " .

>

> So I had a lumpectomy on Thurs, but she didn't test any

> lymph nodes. She said she took out the 5 X 7 cm mass (not cyst), and

> plenty of surrounding tissue. Sent to pathology and margins

> came back clean. Which means they didn't see any cancer

> cells in the margins. She called me Fri and said that there were no

malignant cells in

the

> margins, that the final path report should be back by Fri..

>

> So I went to the ER, where I am an RN, and printed out the report. The

conclusion was

> " Intraductal hyperplasia with atypia. Definitive malignancy is not found in

the current

> sections " . Good news? I hope so. Do I need a 2nd opinion? I have been

reading this list

> since 1/14/06 when all this started. There are many intelligent women here,

and I trust

> that ya'll will give me your opinions.

>

> I can talk to the surgeon tomorrow, but feel the need for some feedback

today. Thank

you

> so much.

>

>

>

>

>

>

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Thanks Ruth, very helpful.

> >

> > Opinions needed please. Hope all of you are doing well this fine

> Sunday.

> >

> > Ok, after the 1st mamo, they sent the doctor a " normal " report. The 1st

> > sono showed a fluid filled cyst, the radiologist

> > reported nothing appeared to be abnormal, no masses. When

> > the surgeon aspirated the cyst, she was so sure that it was

> > only a benign cyst, not to worry. Aspirated 20cc's of tan fluid.

> >

> > Then 2 days later the path report from the aspirate said

> > " atypical cells highly suspicious for malignancy " , and

> > " biopsy recommended " . Ok. To me highly suspicious still

> > didn't mean I had breast cancer.

> >

> > Three days later DH and I go to surgeon's office, and she

> > is shocked about the path report. DH asked her if this

> > means I have BC, and she said I am afraid so, but we won't

> > know anything else until after the biopsy " .

> >

> > So, the same day I have another mamo and sono. These

> > reports both concluded " The findings are highly suspicious

> > for malignancy, particularly given the hx of malignant

> > cells within the aspirated fluid " . " Recommend lumpectomy " .

> >

> > So I had a lumpectomy on Thurs, but she didn't test any

> > lymph nodes. She said she took out the 5 X 7 cm mass (not cyst), and

> > plenty of surrounding tissue. Sent to pathology and margins

> > came back clean. Which means they didn't see any cancer

> > cells in the margins. She called me Fri and said that there were no

> malignant cells in the

> > margins, that the final path report should be back by Fri..

> >

> > So I went to the ER, where I am an RN, and printed out the report.

> The conclusion was

> > " Intraductal hyperplasia with atypia. Definitive malignancy is not

> found in the current

> > sections " . Good news? I hope so. Do I need a 2nd opinion? I have

> been reading this list

> > since 1/14/06 when all this started. There are many intelligent

> women here, and I trust

> > that ya'll will give me your opinions.

> >

> > I can talk to the surgeon tomorrow, but feel the need for some

> feedback today. Thank you

> > so much.

> >

>

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  • 3 years later...

>I'm now taking 150 mcg of Cynomel but my pulse averages 100 bpm. I tried

taking some HC to see if it would help with my pulse (salt doesn't help). It

lowers it a little but also lowers my temps. My temps stay at 98.1 or 98.2. My

temps are higher without the HC but so is my pulse.

>

>I'm not sure what this means and am confused by it. Any insight is much

appreciated!

How much HC did you take??

if you take too little you can end up lowering the circulating levels,

the " feedback loop " in the body shuts your own production down too

much.

A high pulse that does not respond to salt together with a low

temperature says to me adrenaline being produced instead of cortisol.

Supplement enough HC and then the T3 will get through, at that point

temperature will come up and losing weight becomes possible.

The HC won't cause the weight gain, the hypo will, and without enough

HC you can't clear the hypo.

Have you graphed average temperatures lately?? my guess is they will

be unstable

If you do decide to try a higher dose of HC then back off on the T3

for a day in case it's pooling, if that's happening then adding enough

HC could send you hyper briefly as the pooled T3 gets through to the

cells suddenly.

Good luck

Nick

--

for more information on RT3 and Thyroid Resistance go to

www.thyroid-rt3.com

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