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  • 1 year later...

Hi Marie, *wavs*

Welcome and glad you joined the group! There are so many wonderful

people here full of ideas, great advice, and most of all, support. You

are not in it alone! I'm rather new myself, and have already found this

group to be extremely caring, upbeat, informative and fun!

I do hope you talk to a professional about your binging. I won't offer

advice about that because I really know nothing about it. I'm glad you

know it's a definite problem and hope you find the cause of it and learn

to control it.

By the way, I'm 36, 5'7 1/2 " and currently 227 lbs., with a goal weight

of around 147. Please jump in and start posting and see how great this

group is!

Autumn :)

On Sat, 23 Aug 2003 18:15:41 -0000 " feb_showers16 "

writes:

Hello, my name is Marie. I'm new.

I've struggled with my weight all my life and am sick of dieting. I

want to learn how to live healthfully and exercize for my health and

not my looks... because I am getting nowhere.

I am a compulsive binge eater. It's always been a real problem with

me. I will eat and eat to the point of vomiting and still eat more.

It's ridiculous, and dangerous considering I'm a type 1 diabetic. I

keep my sugars real good with insulin, but the more I eat, the more

insulin I need.

I could really use some support, and I think I could be good support

for others as well.

It's nice to meet you all.

Marie

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  • 4 weeks later...

Just wanted to say hello and let everyone know that I am a new member

as well. I look forward to getting to know some new people and

hearing from you! Good luck!

> Just wanted to say hello, and that I am new here. I am struggling

> to lose weight and have a thyroid disorder. If you want to chat

> sometime, you can reach me online via email, and then maybe we can

> chat on messenger too. I look forward to chatting w/ you all.

When

> is the best time to catch people in the chat room area?

>

> Thanks, Dison

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  • 3 months later...

I first discovered I had 2 uterine fibroids when I was pregnant with

my first child in 2001 (I was 37 at the time). My doctor said that

after I delivered the baby the fibroids would most likely shrink, but

I continued to look very pregnant after my daughter was born. I

conceived again when my first daughter was only 9 months old, and

with my second pregnancy they said I had 5 fibroids. I ended up

needing an emergency C section and they counted 13 fibroids. The

doctor performing the C section said that I should have something

done about them. I have Kaiser in Oakland, CA and I went to a UAE

class they have which was very helpful. They said I should wait

until I was finished breastfeeding before doing anything about my

fibroids, and that UAE generally only reduces the uterus size by

50%. I have some relatively minor pressure symptoms (occasional

constipation, somewhat frequent urination, a little lower back pain),

and moderately heavy bleeding during the beginning of my period.

I've weaned my second daughter now, and I'm ready to do something

about my fibroids. I was sold on UAE, but because I still look so

pregnant, I really just want them all to be completely gone. So now

I'm leaning toward myomectomy, although I'd hate to go through

surgery just to have them grow right back again. I have an

appointment at the end of the month, and I'll be getting an

ultrasound soon. I guess the type, size and location will be factors

in deciding which procedure is best. I was considering hysterectomy,

since we don't want to have any more children, but I've decided

against it after looking into it. I'm just worried that the doctors

won't always recommend the best course of action after researching

what's going on in the medical field with regard to fibroids, so I

want to have as much knowledge as possible before I go for the

appointment. Any suggestions?

Carolyn

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I have NO specialists and my GP knows next to nothing about it. i

have had NO luck with any doctors to do with EDS and have even seen 2

useless geneticists. The periodontal stuff is said to go with (it is

either type 7 or type 8)now known as Periodontal EDS and there is a

possibility that my family has Hypermobility type (old type III) with

periodontal crossovers (it seems VERY common here to have symptoms of

more than one type. Barbara has a great explaination of how they

decide which type you are.

Yeah my shoulder is pretty bad this time and I am waiting to see

about getting a MRI or ultrasound etc doen to see what soft tissue

damage I have done.

My shoulder OS is away overseas until Monday and even then I doubt if

I will be ablet o get in for at least a month but more likely a few

months.

Good luck in finding an EDS knowledgable doc (Jill has a great list

of EDS doc's around the place) and she can probably give you the name

or names of some doc's in your area.

Sharon

Australia

> Thanks Sharon,

> Sorry to hear about your most recent shoulder issue, Sounds really

bad. Last year I dislocated left shoulder twice in same week. That

was no fun especially since when I can't get it back in lately, the

muscle spasms start and it is very painful...didn't used to be as

painful, just scary. You mentioned periodontal stuff in your family.

I thought the periodontal stuff went with one of the other EDS

types, not type III. I am beginning to think there are not such clear

distinctions between types and that there can be overlaps in types.

The literature I've read says otherwise, but I don't know. Wonder if

others feel the same way?

>

> I live in Naperville, Illinois, USA. I'm about 25 miles west of

Chicago. Out in the suburbs.

> It is hard to believe, being this close to Chicago, which as you

probably know is a very large metropolitan city, but so far I have

been unable to locate a physician who is familiar with EDS and

willing to supervise treatment. I did have one who was familiar with

it in children but he has retired and was unable to refer me to

anyone else. Do you find it any easier to find specialists in

Australia?

> Robin

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Hi Jen,

Yeah, thank goodness, there is no evidence of fibroid (when my Dr did

the Ablation 14 months back it was confirmed that indeed no fibroids,

but there were polyps which were removed thorugh the procedure.

You are further correct about the sucess rates: Nationally it is 85%

with my Dr claiming 91% locally, it simply seems my body has either

regrown the entire or at least a portion of the endometrium, or they

perhaps did not remove enough of it (deep enough through the laser

removal). With the failure rate of 15% nationally, statistics show

that these women have at least 1-2 more ablations before facing

hysterectomy.

My children are grown and my helath is otherwise excellant so I guess

that leaves me in the position to ponder whether it is worth having

this procedure done every 14 months (taking time off work the

insurance issues etc... and STILL face possibly having the uterus

removed, or simply " fast forward " and be done with things.

Thanks for listenning and responding,

Suzanne

> Are you sure you don't have a fibroid? Endometrial ablation is

> not effective if there are fibroids. Otherwise, it's supposed to

> be very effective

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  • 10 months later...

> Hello everyone.

> I have just joined this group and have read several back posts

from the

> board and would like to introduce myself and ask a few questions

(though I

> know you must feel as though you are repeating yourselves

constantly to new

> members).

> I have a long family history of low thyroid in my family mom,

mom's mom,

> sister). I am almost certain I have has symptoms on and off of

this for

> several years....I had a doc take some blood (on a better day) and

all I got

> back from them was the secretary called and said the tests were in

the

> normal range....... I am not convinced...esp after reading some

posts on

> this and another loop......The thread on unexplained pain just

clinched it

> for me......oh, I am not crazy...or just lazy!

> I just recently had a rough miscarriage and I will wager that it

had a lot

> to do with dipping thyroid levels....bouts with very cold spells,

etc.(which

> I was having at the onset of miscarriage).

> Anyway, I really, really want to do what I can naturally for

this...however

> I may be stuck with meds no matter what I do and I would like to

know how I

> can find a doctor that knows something about this condition (in

the way you

> are all educated).....

Hi I am sort of a newbie myself. I love this group. I was hypo and

my doctor said my tests were NORMAL. Even though I mentioned all the

symptoms I was having. Would not give me any meds. So, I just had to

start self-medicating. I feel so good.!!!

> I simply can not go on like this as I know you all feel the

same....I have 6

> children which I homeschool and there is little room for mommy is

too tired,

> etc. and we are always getting behind on everything as I wake up

tired....go

> to bed tired, have achy flu like symptoms....etc.etc......all

known to you

> all....

> If anyone would be willing to do an overview of how you treat this

problem

> naturally, I would be surely thankful for your time and efforts!

> Thank you so kindly,

> Kim in Tn

>

>

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  • 2 weeks later...

Hi Kathy,

I¹m more of a lurker, than poster, but I do have a few ideas that may help

you.

I too, have a job where I don¹t get home until 6 or later at night, and I

need something easy to make for dinners. I should mention that I also have

2 teenagers who often don¹t want to wait for mom, and they will cook

something easy for dinner.

On the weekends, I usually make some type of casserole that I divide up into

1 cup servings and put in the freezer. I also make myself porridge oats,

and put that in the freezer for morning breakfasts on the go. (I have a

microwave at work) I keep homemade ³egg & cheese² rolls on hand for a quick

bite as I¹m dashing out the door. I use Egg Beaters, and a slice of ff

cheese on a small deli roll, assemble them, and put them in freezer baggies.

Keeping boneless, skinless chicken breasts on hand is easy- just toss Å’em in

a pan with some garlic, turn the oven on to 350, and let them cook.

But my total saving grace is my slow cooker! Take those same chicken

breasts, put Å’em in the cooker with a can of Diet Cola, your choice of

brands, about a 1/4 cup of ketchup, some onion or garlic, and let it cook.

When you come home at night, you will have a great BBQ chicken waiting for

you! On the weekends, I chop and prepare fresh veggies for the week¹s

dinners, so it saves me time in the prep work. I¹d really like to try the

BIG cooking on the weekends, so I don¹t have to cook during the week, but

I¹m just not there yet. :-)

Hope that helps a little bit,

Holly

> scarlettquilts wrote:

> Hi, I'm Kathy, I just joined this group because I really really

> really need to change my life! And, I need help.

>

> My main problem: quick healthy meals I can make within 1/2 hour, or

> freeze ahead meals I can put together on the weekend. I work M-F, 8-

> 5--but usually end up having to stay late if a patient isn't done (I

> am a chemo infusion nurse). Last Wed. I didn't get out until 8pm!

> I used to get the Menu-Mailer but don't have the time to put those

> meals together at night.

>

> I haven't weighed myself today, but failed the jeans test--I no

> longer fit in my 16's. That was depressing enough.

>

> Please give me advice and assist. Tomorrow am is the first day of

> the rest of my life -- I am back on the program.

>

> Kathy G.

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  • 1 year later...

Hi ,

Thank you so much for your reply!!! I didn't think of using tape to hold

the actual hearing aids to his head as opposed to the mold in the

ear...wonderful! Where might I purchase " wig tape " ...a wig shop?

Thanks again for your experienced advice!

Peace, Love & Harmony to you

~Carolyn

> Carolyn,

> I've been browsing through messages and recently found your

> posting. & nbsp; My son is now 3 years-old and has been wearing his aids

> since 3 months. & nbsp; I remember those early days of hearing aids. & nbsp;

> The first day he wore aids also corresponds with the first time he

> really laughed outloud. & nbsp; It was almost immediately after the

> audiologist put the aids in. & nbsp; What a joyful day!

>

> Anyways, we struggled with taking his hearing aids out

> constantly at first, and then again around 8 months old. & nbsp; The worst

> was when he put them in his mouth or would throw them in his

> food. & nbsp; I remember being so frustrated I ended up using about 50

> pieces of scotch tape to adhere the aids to his head. & nbsp; It was an

> interesting fashion statement but that too did not last. & nbsp; I don't

> remember doing anything significant to make his aids stay on, but he

> eventually got used to them and relied on them (except again for about

> a month-long period of protest at 8 months old). & nbsp; I do use little

> strips of wig tape that I cut to fit his hearing aids. & nbsp; This helps

> to hold them to his head so they aren't flopping around when he's being

> active. & nbsp; I also found it reduces feedback.

>

> E-mail me if you have any questions about this.

>

> Take care,

> Walden

> 's mom

> & gt;

> & gt; Hello All, & gt; & gt;I'm new to the group as of today. I recently

> joined the LVAS (enlarged vestibular aqueduct syndrome) list serve. A

> mother on the group recommended I take a look at the Listen Up

> website. I was so excited to see that it was a site for parents only!

> & gt; & gt; & gt; & gt;I am a first time mom to the world's most beautiful

> happy precocious 4 month old baby boy (sorry all of you other moms he's

> taken the title…in my eyes of course) *smile* Wow, who knew that

> your heart could be so overwhelmed with love, joy, and protection until

> you're a parent! & gt; & gt; & gt; & gt;So along with freaking out about being

> a first time mom, Ozzie (my son) was diagnosed with LVAS when he was 3

> months old. The result is moderate to severe hearing loss (sorta

> flat lined) in both ears. He began wearing his first pair of hearing

> aids on 12/21/05. Technology is amazing. The hearing molds were so

> tiny. He's growing so quickly we're already on our 2nd pair of molds

> with the third set of impressions made yesterday. Ozzie is a big

> boy...measuring and weighing in at around 6 months as opposed to his 4

> months. Our audiologist says this is the first time that she has made 3

> impressions in 30 days. & gt; & gt; & gt; & gt;This is an entirely new world

> for my husband and I, as we are not hearing impaired. As far as we know

> there aren't any relatives with hearing difficulties either. Of course

> I had to quiz my husband since he has & quot;selective hearing & quot;

> *smile.* I'm going to saunter my way through the archives for

> tidbits of applicable knowledge. I look forward to everyone's

> experiences and & quot;been there done that…now do this & quot; stories. I

> welcome any and all advice, suggestions, and directions especially from

> parents with kids in hearing aids as infants. You won't offend me!

> & gt; & gt; & gt; & gt;I am so happy to have been guided your way!

> & gt; & gt;Peace, Love & amp; Harmony & gt; & gt;~Carolyn & gt; & gt; & gt; & gt; & gt;

> & gt;

> & gt;

> & gt;

> & gt;

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I bought toupee tape at a Sally's Beauty Supply store. The little packet was

about $5, and had enough tape (when cut into little lengths to fit tiny ears)

for a lifetime!

Edith

Re: Re: New Member

Hi ,

Thank you so much for your reply!!! I didn't think of using tape to hold

the actual hearing aids to his head as opposed to the mold in the

ear...wonderful! Where might I purchase " wig tape " ...a wig shop?

Thanks again for your experienced advice!

Peace, Love & Harmony to you

~Carolyn

> Carolyn,

> I've been browsing through messages and recently found your

> posting. & nbsp; My son is now 3 years-old and has been wearing his aids

> since 3 months. & nbsp; I remember those early days of hearing aids. & nbsp;

> The first day he wore aids also corresponds with the first time he

> really laughed outloud. & nbsp; It was almost immediately after the

> audiologist put the aids in. & nbsp; What a joyful day!

>

> Anyways, we struggled with taking his hearing aids out

> constantly at first, and then again around 8 months old. & nbsp; The worst

> was when he put them in his mouth or would throw them in his

> food. & nbsp; I remember being so frustrated I ended up using about 50

> pieces of scotch tape to adhere the aids to his head. & nbsp; It was an

> interesting fashion statement but that too did not last. & nbsp; I don't

> remember doing anything significant to make his aids stay on, but he

> eventually got used to them and relied on them (except again for about

> a month-long period of protest at 8 months old). & nbsp; I do use little

> strips of wig tape that I cut to fit his hearing aids. & nbsp; This helps

> to hold them to his head so they aren't flopping around when he's being

> active. & nbsp; I also found it reduces feedback.

>

> E-mail me if you have any questions about this.

>

> Take care,

> Walden

> 's mom

> & gt;

> & gt; Hello All, & gt; & gt;I'm new to the group as of today. I recently

> joined the LVAS (enlarged vestibular aqueduct syndrome) list serve. A

> mother on the group recommended I take a look at the Listen Up

> website. I was so excited to see that it was a site for parents only!

> & gt; & gt; & gt; & gt;I am a first time mom to the world's most beautiful

> happy precocious 4 month old baby boy (sorry all of you other moms he's

> taken the title.in my eyes of course) *smile* Wow, who knew that

> your heart could be so overwhelmed with love, joy, and protection until

> you're a parent! & gt; & gt; & gt; & gt;So along with freaking out about being

> a first time mom, Ozzie (my son) was diagnosed with LVAS when he was 3

> months old. The result is moderate to severe hearing loss (sorta

> flat lined) in both ears. He began wearing his first pair of hearing

> aids on 12/21/05. Technology is amazing. The hearing molds were so

> tiny. He's growing so quickly we're already on our 2nd pair of molds

> with the third set of impressions made yesterday. Ozzie is a big

> boy...measuring and weighing in at around 6 months as opposed to his 4

> months. Our audiologist says this is the first time that she has made 3

> impressions in 30 days. & gt; & gt; & gt; & gt;This is an entirely new world

> for my husband and I, as we are not hearing impaired. As far as we know

> there aren't any relatives with hearing difficulties either. Of course

> I had to quiz my husband since he has & quot;selective hearing & quot;

> *smile.* I'm going to saunter my way through the archives for

> tidbits of applicable knowledge. I look forward to everyone's

> experiences and & quot;been there done that.now do this & quot; stories. I

> welcome any and all advice, suggestions, and directions especially from

> parents with kids in hearing aids as infants. You won't offend me!

> & gt; & gt; & gt; & gt;I am so happy to have been guided your way!

> & gt; & gt;Peace, Love & amp; Harmony & gt; & gt;~Carolyn & gt; & gt; & gt; & gt; & gt;

> & gt;

> & gt;

> & gt;

> & gt;

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  • 5 months later...
Guest guest

Thanks for the warm welcome! The last part of the email here REALLY rang a bell for me! I've had allergy problems since I was 4, that's why nothing prescribed works for me more than once. And when it does work the one time I have to take 3 times the dose for it to do so. But I didn't know that allergies and thyroid are combined!!! That opens up a whole new field for me! My thyroid just stopped the summer I was 6, between kdgn and 1st grd. I puffed up like a little marshmallow and I was in my terrible 2's again. My mom said I would cry at the drop of a hat. I was put on what I only remember as a little white pill and was told I'd have to take it for the rest of my life. I was on it a year, then I didn't have to take it anymore. I don't remember any tests to that effect tho. My allergies were really bad until the summer I was 19. I was born and raised on a ranch and allergic to every animal on it, especially cats. But that summer I was milking

cows for a neighbor, helping out on their dairy and it was really really hot that year. I drank a gallon of water a day easily, and didn't even have to use the bathroom. ( I was out fixing fence for quite a bit of the time too, no bathroom out there...lol ) I'd heard alot about sweat baths helping people and I just turned my nose up at it. But drinking that much water and sweating that much for about 2 months seemed to really help. I went with one guy to chuck out some hay to some heifers and I thought, well, this is it, my face is gonna puff up like a toad and I won't be able to breathe. But I only sneezed twice and that was it! ( Since then I've not had any real reactions to hay, and I've proved that to myself again this year by being able to bale hay for my cousin and not get even a sniffle. For those of you that know, baling hay is like being bathed in it ). I found out after a few months I was able to lose weight, had alot of energy ( I was working out, breaking

horses and working at a newspaper in the mailroom where the paper is put together ). I was all over the place. Now, I'm 38 and it seems that my thyroid is starting to pull its crap all over again. I'm only really allergic to chicken ( eating them and cleaning the shed ) and turkeys, also eggs and still cats. I think the fowl ( foul? LOL ) allergies are due to the crap they feed those poor birds, really. I had some chickens the past few years and ate some of the eggs and I never got sick. Course I never ate that many either. But mine were free range and never had any chemicals. I live right in my cousin's hay field and the hay no longer bothers me, in fact, when he cuts it, the smell of fresh cut hay puts me to sleep. I'm not taking any medication, natural or otherwise for this right now. I finally put 2 and 2 together and realized that it's probly my thyroid and not having a problem with being lazy. I'm kinda tough on myself that way. If I'm not doing

something all the time then I think of myself as lazy and I'm trying to reason w/ myself that it's not lazy it's something wrong. I've got a lot of reading to do to catch up with you all, there's alot of posts! I'm trying to find the first ones now. Thanks much! Spiffdawn prince wrote: Hi Spiff,Welcome and hope you find what you are looking for, all we do is share the knowledge that we have learned from our years of dealing with thyroid problems. Take what you read and see which

will apply to what you are going through. We offer a listening ear at all times and feel free to express how you feel, venting is allowed, we all have big shoulders when you need one to lean, or cry on. Largely it will depend on which country that you live in as to what you can get. But to my thinking you really do need to know where your starting point is and whether you are in need of meds or not. There are places in the USA where you can get testing done that may be cheaper than what you have been quoted. I live in Canada and I have to have a scrip to get anything to help. Naturopaths will give iodine which does not help when the thyroid is not or only partially working. Not sure if you can get it in UK or Aus I'll let those girls inform there. Have you been on meds or is it something that you have just lived with? If you are on meds what are they and how much. Natural remedies may work for allergies but the

thyroid issue is not quite the same, as it means that a vital gland of the body is not working as it should and allergies are the body's response to something that it doesn't like. Thyroid irregularities are the cause of our problems and dust, pollen etc are the cause of allergies.Dawn>> Hey everybody!> I'm a new member to the group, just signed on. I've had thyroid > problems since I was 6, and now it's rearing its ugly head once again. > I made an appt with the dr to find out what's going on, get tested and > all. $100 up front. I DON'T THINK SO! I can't even afford that. I've > been using natural remedies for my allergies and have had tremendous > success with that. I'd like to hear what you all have

to say about > natural remedies for thyroid. |> I look forward to hearing any and all theories!> Thanks!> mzspiff ( aka spiff )>

Talk is cheap. Use Yahoo! Messenger to make PC-to-Phone calls. Great rates starting at 1¢/min.

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  • 1 month later...

Hey... Deana... I just noticed that you are with Charter.... we have a Charter in my area, don't know how wide spread they are.. it could be the cover a large area.. but now I'm curious... you aren't in Minnesota, are you???

Topper ()

Deana Brown > skip < @charter.net> wrote:

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  • 2 weeks later...

>

> Hello. My name is Colleen and I don't know, after reading a lot of

> the posted messages, if it is appropriate that I be a member of

this

> group, but I got accepted, so here goes. I am 51 years old,

> peri-menopausal, with a high risk of breast cancer. My eldest

sister

> got it at 33, and fought it, and eventually died at 43 (1987). My

> mother got it in her 70's, and had a mastectomy, but had had

> Alzheimer's, which is what she died from at age 75 in 1997. I

thought

> my elder sister and I would go through our lives unscathed, but no

go.

> She, at 58, was diagnosed last year, and just finished up all the

> chemo and radiation. So, here I am, the only female in my

immediate

> family to not yet have breast cancer. I have high deductible

health

> insurance, with a company that requests and usually gets, nearly

> annual rate hikes. I joined this group just after hearing about

their

> latest request on the news. I guess I was upset. I have fears, but

> they are nothing compared to any of you guys. I want to stay

> healthy. In case you are wondering, I get annual mammograms (my

> living sister had skipped two), and do self exams (although how I

will

> know when I find something is beyond me). I keep myself healthy

with

> good food, and exercise. So, I guess I am here to " listen " and

learn.

>

Colleen, eating health is sure the best place to start plus getting

those mammograms. But with the history of your family you need to

be vigliant in keeping your seld checked. I didn't have any history

in my family but got it any way. I will be finishing my chemo this

comeing Tuesday. THe last one I had has been the worse so

far,,,they all have been bad but this one I haven;t been without

pain.I ususaly have at lest 3 to 4 good days but not this last

treatment, So I am dreading my next one even though it is my final

one!!!Amen MY body is just warn out from the treatments,,,I have no

muscles left my skin sags from losing so much weight and of course

bald as a cue ball....lol I can't wait to finally start feeling

better when ever that might be!!!! I start my rads the 16th and will

be finished with them the end of NOV. THen they put me on

arimidex,for 5 yrs. But if I get muscule and joint pains with it I

will stop taking it. I am so tired of being in pain.!!!!

Steph

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> > Hello. My name is Colleen and I don't know, after reading a lot of

> > the posted messages, if it is appropriate that I be a member of this

> > group, but I got accepted, so here goes. I am 51 years old,

> > peri-menopausal, with a high risk of breast cancer. My eldest sister

> > got it at 33, and fought it, and eventually died at 43 (1987). My

> Welcome to the group! I believe you are very welcome here as

you've

> been effected by breast cancer. Information is the best weapon against

> this disease and you've come to the right place to get this info.

> I'm sorry to hear about all your female relatives having breast

> cancer. I know you didn't ask for advice, but I think if I were in

your

> shoes I might at least look into a prophylactic bilateral mastectomy.

> Presently I have a large tumor in one breast (likely stage III) and HAD

> a Stage I in the other (chemotherapy has made it such that the Stage I

> cannot even be detected by an MRI, which was the only thing that found

> that one. Yes, I'm having chemo first which, while accepted, is not

> standard most places.). Even though the Stage I is gone and there

is no

> " lump " to be removed in a lumpectomy, I am having a bilateral

> mastectomy. I already know that there are cells in both breasts that

> " can't play nice, " so decided to go the " better safer than sorry "

(there

> is no such thing as " safe " with cancer).

> This is a great group of ladies and a few WONDERFUL men who love

> their ladies very much and want to care for them the best way they know

> how. You'll learn about more than just breast cancer. You'll learn

> about relationships, eating right, and heaven knows what else. :-)

> Again, welcome.

> -Frances

> --

> -Frances Bartels *** ki0dz@... (((#))) ^ ^

> http://www.qsl.net/ki0dz Central Ohio | ^ - ^

> Watkins Products www.watkinsonline.com #092389 ------- (o o)

> Internet ONLY $9.99/mo. **Free accelerator** |ooOoo| >{ | }<

> http://continue.to/internet ------- RRR)*

>

Thank you for your welcome and your information. I know someone who

did just that - prophylactice bilateral mastectomy - because she

has/had a stronger risk than I. The females in her family with the

disease extended beyond her immediate family. But, I will certainly

keep your information in my " file. " I pray that you yourself have a

positive outcome. Colleen

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Hello, . My doctor says I have a " cancer family " which is very

comforting (haha). My father died of the nastier of the lung cancers

(he was a cigarette smoker who had quit and then went back to it).

Beyond my immediate family, there was just my paternal grandmother

who, I think, had cervical cancer. Just like you, however, this is

scary for me, as the last woman in my immediate family to not yet have

breast cancer. Thank you for sharing with me. Colleen

>

> Hello Collen!! my name is and I am almost 49. and I have

two reasons to be here, My twin aunts of 65, currently fighting BC,

my maternal Grandmother died of vaginal cancer, her sister died of

stomach cancer, one of my moms cousin died at 18, stomach cancer, and

at least two more close relatives on my maternal side have died of

cancer. as you would guess, this is very scary for me.

>

>

>

> ---------------------------------

>

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Hello, Jen and thanks! I am here to listen and learn. Colleen

>

> Hi Colleen and welcome! You will find this to be a friendly and

> highly informed bunch of folks : ) Happy to have you (smile)

>

> - Jen

>

> On Fri, 29 Sep 2006 00:14:59 -0500 (CDT) Ramos

> writes:

> > Hello Collen!! my name is and I am almost 49. and I have

> > two reasons to be here, My twin aunts of 65, currently fighting BC,

> > my maternal Grandmother died of vaginal cancer, her sister died

> > of stomach cancer, one of my moms cousin died at 18, stomach cancer,

> > and at least two more close relatives on my maternal side have died

> > of cancer. as you would guess, this is very scary for me.

> >

> >

> >

> > ---------------------------------

> >

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> >

> > Hello. My name is Colleen and I don't know, after reading a lot of

> > the posted messages, if it is appropriate that I be a member of

> this

> > group, but I got accepted, so here goes. I am 51 years old,

> > peri-menopausal, with a high risk of breast cancer. My eldest

> sister

> > got it at 33, and fought it, and eventually died at 43 (1987). My

> > mother got it in her 70's, and had a mastectomy, but had had

> > Alzheimer's, which is what she died from at age 75 in 1997. I

> thought

> > my elder sister and I would go through our lives unscathed, but no

> go.

> > She, at 58, was diagnosed last year, and just finished up all the

> > chemo and radiation. So, here I am, the only female in my

> immediate

> > family to not yet have breast cancer. I have high deductible

> health

> > insurance, with a company that requests and usually gets, nearly

> > annual rate hikes. I joined this group just after hearing about

> their

> > latest request on the news. I guess I was upset. I have fears, but

> > they are nothing compared to any of you guys. I want to stay

> > healthy. In case you are wondering, I get annual mammograms (my

> > living sister had skipped two), and do self exams (although how I

> will

> > know when I find something is beyond me). I keep myself healthy

> with

> > good food, and exercise. So, I guess I am here to " listen " and

> learn.

> >

> Colleen, eating health is sure the best place to start plus getting

> those mammograms. But with the history of your family you need to

> be vigliant in keeping your seld checked. I didn't have any history

> in my family but got it any way. I will be finishing my chemo this

> comeing Tuesday. THe last one I had has been the worse so

> far,,,they all have been bad but this one I haven;t been without

> pain.I ususaly have at lest 3 to 4 good days but not this last

> treatment, So I am dreading my next one even though it is my final

> one!!!Amen MY body is just warn out from the treatments,,,I have no

> muscles left my skin sags from losing so much weight and of course

> bald as a cue ball....lol I can't wait to finally start feeling

> better when ever that might be!!!! I start my rads the 16th and will

> be finished with them the end of NOV. THen they put me on

> arimidex,for 5 yrs. But if I get muscule and joint pains with it I

> will stop taking it. I am so tired of being in pain.!!!!

>

> Steph

>

Hello, Steph. Thanks for the welcome and the information. I hope

everything gets easier for you. I do the self exams, but wish I was

more sure that I would feel what it is I need to feel (or not need!).

Everyone's family history starts somewhere; with my family, it was

my late sister. No one had had breast cancer before in the family, as

far as I know. But, after my other sister got it, and had missed a

couple of her mammograms, I know that, even if we had to drop health

insurance when the premiums get too high, we will continue to afford

annual mammograms. Colleen

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Of course you are welcome Colleen :-) Its great you want to learn and that you

do check yourself etc. Feel free to ask any questions you may have.

Hugs

nne

Breast Cancer Patients Soul Mates for Life

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

BreastCancerStories.com

http://www.breastcancerstories.com/content/view/433/161/

Angel Feather Loomer

www.angelfeatherloomer.blogspot.com

Check out my other ornaments at

www.geocities.com/chucky5741/bcornament.html

Lots of info and gifts at:

www.cancerclub.com

new member

Hello. My name is Colleen and I don't know, after reading a lot of

the posted messages, if it is appropriate that I be a member of this

group, but I got accepted, so here goes. I am 51 years old,

peri-menopausal, with a high risk of breast cancer. My eldest sister

got it at 33, and fought it, and eventually died at 43 (1987). My

mother got it in her 70's, and had a mastectomy, but had had

Alzheimer's, which is what she died from at age 75 in 1997. I thought

my elder sister and I would go through our lives unscathed, but no go.

She, at 58, was diagnosed last year, and just finished up all the

chemo and radiation. So, here I am, the only female in my immediate

family to not yet have breast cancer. I have high deductible health

insurance, with a company that requests and usually gets, nearly

annual rate hikes. I joined this group just after hearing about their

latest request on the news. I guess I was upset. I have fears, but

they are nothing compared to any of you guys. I want to stay

healthy. In case you are wondering, I get annual mammograms (my

living sister had skipped two), and do self exams (although how I will

know when I find something is beyond me). I keep myself healthy with

good food, and exercise. So, I guess I am here to " listen " and learn.

------------------------------------------------------------------------------

No virus found in this incoming message.

Checked by AVG Free Edition.

Version: 7.1.407 / Virus Database: 268.12.9/458 - Release Date: 9/27/2006

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nne: Thanks for the second welcome. I already have bunches of

questions, and already, before I even posted my message, had one of my

fears sort of eased. I am going to try to read the messages and get

my answers. If, after a while, my question is still there, I will

indeed post it. Better health to you all! Colleen

>

> Of course you are welcome Colleen :-) Its great you want to learn

and that you do check yourself etc. Feel free to ask any questions you

may have.

> Hugs

> nne

> Breast Cancer Patients Soul Mates for Life

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

> BreastCancerStories.com

> http://www.breastcancerstories.com/content/view/433/161/

> Angel Feather Loomer

> www.angelfeatherloomer.blogspot.com

> Check out my other ornaments at

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

> Lots of info and gifts at:

> www.cancerclub.com

> new member

>

>

> Hello. My name is Colleen and I don't know, after reading a lot of

> the posted messages, if it is appropriate that I be a member of this

> group, but I got accepted, so here goes. I am 51 years old,

> peri-menopausal, with a high risk of breast cancer. My eldest sister

> got it at 33, and fought it, and eventually died at 43 (1987). My

> mother got it in her 70's, and had a mastectomy, but had had

> Alzheimer's, which is what she died from at age 75 in 1997. I thought

> my elder sister and I would go through our lives unscathed, but no go.

> She, at 58, was diagnosed last year, and just finished up all the

> chemo and radiation. So, here I am, the only female in my immediate

> family to not yet have breast cancer. I have high deductible health

> insurance, with a company that requests and usually gets, nearly

> annual rate hikes. I joined this group just after hearing about their

> latest request on the news. I guess I was upset. I have fears, but

> they are nothing compared to any of you guys. I want to stay

> healthy. In case you are wondering, I get annual mammograms (my

> living sister had skipped two), and do self exams (although how I will

> know when I find something is beyond me). I keep myself healthy with

> good food, and exercise. So, I guess I am here to " listen " and learn.

>

>

>

>

>

>

>

------------------------------------------------------------------------------

>

>

> No virus found in this incoming message.

> Checked by AVG Free Edition.

> Version: 7.1.407 / Virus Database: 268.12.9/458 - Release Date:

9/27/2006

>

>

>

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Hi Colleen and welcome. With your family history, I believe I'd be

as proactive as you are about B/C. So first, good for you!

Secondly, along with your yearly Mammo's I think I'd ask about

getting your primary to request an ultrasound or digital mammo. All

B/C's are not seen on mammo's and an ultrasound or digital may make

you feel more secure. Don't know if your insurance company will go

for it, but it's worth a try. Again, welcome.

Ellen

>

> Hello. My name is Colleen and I don't know, after reading a lot of

> the posted messages, if it is appropriate that I be a member of

this

> group, but I got accepted, so here goes. I am 51 years old,

> peri-menopausal, with a high risk of breast cancer. My eldest

sister

> got it at 33, and fought it, and eventually died at 43 (1987). My

> mother got it in her 70's, and had a mastectomy, but had had

> Alzheimer's, which is what she died from at age 75 in 1997. I

thought

> my elder sister and I would go through our lives unscathed, but no

go.

> She, at 58, was diagnosed last year, and just finished up all the

> chemo and radiation. So, here I am, the only female in my

immediate

> family to not yet have breast cancer. I have high deductible

health

> insurance, with a company that requests and usually gets, nearly

> annual rate hikes. I joined this group just after hearing about

their

> latest request on the news. I guess I was upset. I have fears, but

> they are nothing compared to any of you guys. I want to stay

> healthy. In case you are wondering, I get annual mammograms (my

> living sister had skipped two), and do self exams (although how I

will

> know when I find something is beyond me). I keep myself healthy

with

> good food, and exercise. So, I guess I am here to " listen " and

learn.

>

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Hi Colleen, I'm new here too. Have you explored genetic screening?

It might help to know if you are BRCA1 or 2 as you would know how

aggressive to be in getting regular exams. Your OB/GYN should be

able to help you with this. If not, a local hospital with cancer

treatment facilities should have counselors who know how to help

with this.

Maya

> Hello. My name is Colleen and I don't know, after reading a lot of

> the posted messages, if it is appropriate that I be a member of

this

> group, but I got accepted, so here goes. I am 51 years old,

> peri-menopausal, with a high risk of breast cancer. My eldest

sister

> got it at 33, and fought it, and eventually died at 43 (1987). My

> mother got it in her 70's, and had a mastectomy, but had had

> Alzheimer's, which is what she died from at age 75 in 1997. I

thought

> my elder sister and I would go through our lives unscathed, but no

go.

> She, at 58, was diagnosed last year, and just finished up all the

> chemo and radiation. So, here I am, the only female in my

immediate

> family to not yet have breast cancer. I have high deductible

health

> insurance, with a company that requests and usually gets, nearly

> annual rate hikes. I joined this group just after hearing about

their

> latest request on the news. I guess I was upset. I have fears, but

> they are nothing compared to any of you guys. I want to stay

> healthy. In case you are wondering, I get annual mammograms (my

> living sister had skipped two), and do self exams (although how I

will

> know when I find something is beyond me). I keep myself healthy

with

> good food, and exercise. So, I guess I am here to " listen " and

learn.

>

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  • 3 months later...

Hi

I am now 18. I was also diagnosed at 14. And I had to do my final year of school last year with the extra burden of PSC. It was a very hard year for me, as I couldnt control the way i was feeling, and some days when I needed to do 6 hours work I was only able to do 2 due to my health. It was a challenging year but also a rewarding one. The only advice I can give your son is too just WORK when he is feeling up to it, just to do extra hours when he is feeling fine, just incase he goes through a bad spell there won't be so much pressure on him.

I wish him all the luck for this next year. And if he wants I am defenietly avaliable to email him.

Love Terri(18)

Diagnosed PSC 2002

Send instant messages to your online friends http://uk.messenger.yahoo.com

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  • 7 months later...

thatks a lot dawn i appreciate your help!Dawn wrote: , First off, this is NOT your fault. Many of us are still trying to figure out why we ended up with something like this. I would suggest that you stop trying to have intercourse all together for now. You are young, there will be plenty of time.There are many other ways to be sexual and intimate with your husband that does not require intercourse. By continuing to try, you are just going to aggravate the nerves that are already

wound-for-sound. You were lucky to have found a doc that even recognizes this condition in such a short amount of time. Yes it's depressing, but you can get through it. Don't try to live up to 'what you should be'. Just try to take one day at a time. Find joy in the simple things.Dawn Zimbro wrote:>> Hi, My name is ,> I'm 23 years old and have been married since May. I have just recently been diagnosed with a possible vulvar vestibulitis. I have my apt with a specialist in late October. I was wondering if anyone has any suggestions to reduce pain during sex that i can try until i see the gynourologist. My husband and I almost never have it at all because it is so painfull for me, and it is really starting to take a toll on my marriage. I get really depressed that its all my fault and that I'm not living up to what i should be. Thank You> >

> Suprise AZ

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  • 2 years later...
Guest guest

Thanks for your responses Kitty and Alan.

I have test results but no RT3 test done. My ferritin was checked but was only

told it was normal. I did request the result but it wasn't sent.

TSH 0.66, FT4 15 (9 -21), FT3 1.5 (0.9 -2.5)

I did a saliva adrenal stress profile at the end of January this year. My last

sample was taken at 9.30pm as I had a really bad reaction to not having any

coffee during the test - really bad head and felt sick for most of the day so

couldn't last any longer.

Cortisol levels:

Sample 1: 15.7 (12-22), S2: 3.6 ((5.0-9.0), S3: 5.0 (3.0-7.0), S4: 22.4

(1.0-3.0)

DHEA levels: am: 1.32, pm: 1.07 (0.30-1.00)

Adrenal stress stage - Alarm stage

Comment on last sample level - suggestive of malfunctioning of the hypothalmic

adrenal axis feedback system. Associated with REM sleep disturbance and

depression.

DHEA levels - elevated, reflecting elevated ACTH with an imbalanced response

from the adrenals, could be due to an inappropriate DHEA response. ???

I had a quick look at the FAQ's but will have a better look. I still have my

thyroid, was told I had primary hypothyroidism. At the moment I'm on 175mcgrms

thyroxine and taking a multi vit and mineral, selenium, vit D3( was below range

in this) and vitaminC.

I will have a read at Dr Rind method and start this.

Alan, I have done a gluten free diet/detox. this was about 4 years ago and I

kept on it for 6 weeks. I did the diet because my energy, stamina and fatigue

were so poor. the difference wasn't huge. I keep my gluten intake under control

although,especially during the day as it does make me feel even more tired. Most

days I have none. Also, I don't really have joint pain. I get muscle aches when

very fatigued.

About RT3 test, is it done by the NHS? Would I have to wait for my endo

appointment or would my GP be able to do the FT3 and RT3?

Once again I would be grateful for your response.

Vivienne

>

> > sorry to see you here but hope we can help! Do you have any blood results

from you last visit? Have you ever had your adrenals tested via saliva cortisol

testing? How about ferritin or RT3? Just the fact that

>

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