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Suzi,

I am 43 and was just diagnosed one year ago after a lifetime of problems!

As soon as I was diagnosed, my general practitioner ran a series of tests,

including a bone

density scan.

I also was diagnosed with osteopenia.

They were very encouraging that it can improve. I joined a gym and have been

going

regularly, which is supposed to help.

My doctor said it would be a waste of time to try medication for it until my

intestines

healed. And, actually, from what I've read about those meds, I'm not sure I'd

even want to!

I do take calcium supplements (in capsules, so it is easier to absorb!).

I've been gluten free fo 11 months and I was just thinking I need to check with

my doctor

to see when she wants to check if anything has improved since I've healed.

Best of luck,

Ellen in land

>

> Anyone else diagnosised with this? I guess I am on my way to

> osteoporosis, I am 41. :(

> Suzi

>

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Suzi,

I am 43 and was just diagnosed one year ago after a lifetime of problems!

As soon as I was diagnosed, my general practitioner ran a series of tests,

including a bone

density scan.

I also was diagnosed with osteopenia.

They were very encouraging that it can improve. I joined a gym and have been

going

regularly, which is supposed to help.

My doctor said it would be a waste of time to try medication for it until my

intestines

healed. And, actually, from what I've read about those meds, I'm not sure I'd

even want to!

I do take calcium supplements (in capsules, so it is easier to absorb!).

I've been gluten free fo 11 months and I was just thinking I need to check with

my doctor

to see when she wants to check if anything has improved since I've healed.

Best of luck,

Ellen in land

>

> Anyone else diagnosised with this? I guess I am on my way to

> osteoporosis, I am 41. :(

> Suzi

>

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Suzi,

I am 43 and was just diagnosed one year ago after a lifetime of problems!

As soon as I was diagnosed, my general practitioner ran a series of tests,

including a bone

density scan.

I also was diagnosed with osteopenia.

They were very encouraging that it can improve. I joined a gym and have been

going

regularly, which is supposed to help.

My doctor said it would be a waste of time to try medication for it until my

intestines

healed. And, actually, from what I've read about those meds, I'm not sure I'd

even want to!

I do take calcium supplements (in capsules, so it is easier to absorb!).

I've been gluten free fo 11 months and I was just thinking I need to check with

my doctor

to see when she wants to check if anything has improved since I've healed.

Best of luck,

Ellen in land

>

> Anyone else diagnosised with this? I guess I am on my way to

> osteoporosis, I am 41. :(

> Suzi

>

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What does a bone density scan involve? The GI doc thinks I should do

that one, now that I'm finally healing after going GF. I'm 43 too. My

sister, 53, has osteoporosis. And so does my mom (in her 80s),

something wicked. (She even broke her wrist while SLEEPING! How scary

is THAT??!!)

> >

> > Anyone else diagnosised with this? I guess I am on my way to

> > osteoporosis, I am 41. :(

> > Suzi

> >

>

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What does a bone density scan involve? The GI doc thinks I should do

that one, now that I'm finally healing after going GF. I'm 43 too. My

sister, 53, has osteoporosis. And so does my mom (in her 80s),

something wicked. (She even broke her wrist while SLEEPING! How scary

is THAT??!!)

> >

> > Anyone else diagnosised with this? I guess I am on my way to

> > osteoporosis, I am 41. :(

> > Suzi

> >

>

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What does a bone density scan involve? The GI doc thinks I should do

that one, now that I'm finally healing after going GF. I'm 43 too. My

sister, 53, has osteoporosis. And so does my mom (in her 80s),

something wicked. (She even broke her wrist while SLEEPING! How scary

is THAT??!!)

> >

> > Anyone else diagnosised with this? I guess I am on my way to

> > osteoporosis, I am 41. :(

> > Suzi

> >

>

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> Anyone else diagnosised with this? I guess I am on my way to

> osteoporosis, I am 41. :(

==========

43 in a week with osteoporosis. docs are blaming a combination of

undiagnosed CD for 42 years and 10 years on steroids for what we now

know where symptoms of gluten intolerance.

Be very careful about letting the doctors talk you into taking

Bisphosphanates. they have not been proven to treat osteoporosis.

If you do a good literature search you will see that the underlying

premise is dodgy. They are also implicated in a dreadful disease

called avascular necrosis (your bones die). Believe me when I say

that you don't want AVN. I have it and it is painful beyond your

worst imaginings. Then of course there is the increased risk of

esophageal cancer that this class of drug brings with it.

Docs put their patients of Fosomax and its brethren very easily and

don't tell you that controlled studies show that women on these

bisphosphonates break their bones just as often as non treated women.

If you are able to, start doing weight bearing exercise and be extra

careful about being 100% GF. You have to ensure that your gut is

completely healed so that it can absorb the nutrients it needs. I am

still battling with the small intestinal damaged caused by the

undiagnosed CD. my doc has put me on this calcium supplement http://

www.nutramed.com/anonline/scripts/prodView.asp?idproduct=32 as he

says that the absorption is good.

Shez

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You're not necessarily doomed. Many people report significant

improvements to bone density after going GF. You do need to be very

careful you are compliant with the diet. Also take supplements and do

weight bearing exercise as much as you are able.

Sue in Denver

>

> Anyone else diagnosised with this? I guess I am on my way to

> osteoporosis, I am 41. :(

> Suzi

>

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Dx with it at 36...I don't think we are doomed....we

just found it earlier than most people do, we caught

it and maybe now we won't have osteoporosis ( sp)

--- zoemom2001 wrote:

> You're not necessarily doomed. Many people report

> significant

> improvements to bone density after going GF. You do

> need to be very

> careful you are compliant with the diet. Also take

> supplements and do

> weight bearing exercise as much as you are able.

>

> Sue in Denver

>

>

> >

> > Anyone else diagnosised with this? I guess I am on

> my way to

> > osteoporosis, I am 41. :(

> > Suzi

> >

>

>

>

>

>

__________________________________________________

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A bone density scan (I think it may be called a Dexa scan, or something like

that) is a

special type of x-ray.

You lay on your back on a special table and it x-rays certain parts of your

body. The

radiologist measures this for bone density.

If I remember correctly, I may take about a half-hour or so. It was very easy

and

comfortable.

Ellen in land

> > >

> > > Anyone else diagnosised with this? I guess I am on my way to

> > > osteoporosis, I am 41. :(

> > > Suzi

> > >

> >

>

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I was just diagnosed about 3 weeks ago with it. I have been GF now for 3 1/2 years. I should have been on a GF diet over 20 years ago but all the Drs. said it was IBS.

I am 52 and I also have Fibromyligia, Chronic Fatigue Syndrome, Restless Leg Syndrome, I go in every month for medial nerve blocks in my lower spine.I can not do very much any more I have to use a cane all the time and when we go out to do our shopping I have to use a motorized cart or it would take me 3 hours in the store and I could fall very easy. You name it and I more then likely have it. I have suffered from depression since I was in my teens. I am a recovering alcoholic, drug addict I have not used anything in over 14 years now.

All the different medications that I am on the Drs. think have caused my bones to thin as fast as they have.

Hugs!!!!

Anyone else diagnosised with this? I guess I am on my way to osteoporosis, I am 41. :( Suzi

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I was just diagnosed about 3 weeks ago with it. I have been GF now for 3 1/2 years. I should have been on a GF diet over 20 years ago but all the Drs. said it was IBS.

I am 52 and I also have Fibromyligia, Chronic Fatigue Syndrome, Restless Leg Syndrome, I go in every month for medial nerve blocks in my lower spine.I can not do very much any more I have to use a cane all the time and when we go out to do our shopping I have to use a motorized cart or it would take me 3 hours in the store and I could fall very easy. You name it and I more then likely have it. I have suffered from depression since I was in my teens. I am a recovering alcoholic, drug addict I have not used anything in over 14 years now.

All the different medications that I am on the Drs. think have caused my bones to thin as fast as they have.

Hugs!!!!

Anyone else diagnosised with this? I guess I am on my way to osteoporosis, I am 41. :( Suzi

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I was diagnosed with osteopenia at 35.

I am now 38, and have been gf for 4 years, and taken plenty of calcium, etc.

I have recently found that it has not been enough, and I have had more bone

loss. I believe I will choose Miacalcin, only because it does not seem to

have the same negative gut effects as the others. Anyone else having any

luck?

Suzie

From: SillyYaks [mailto:SillyYaks ] On Behalf Of

Sent: Saturday, January 21, 2006

7:19 PM

To: SillyYaks

Subject: Re:

Osteopenia

I was just

diagnosed about 3 weeks ago with it. I have been GF now for 3 1/2 years.

I should have been on a GF diet over 20 years ago but all the Drs.

said it was IBS.

I am 52 and I

also have Fibromyligia, Chronic Fatigue Syndrome, Restless Leg Syndrome,

I go in every month for medial nerve blocks in my lower spine.I can not

do very much any more I have to use a cane all the time and when we go out to

do our shopping I have to use a motorized cart or it would take me 3 hours in

the store and I could fall very easy. You name it and I more then likely

have it. I have suffered from depression since I was in my teens. I am a

recovering alcoholic, drug addict I have not used anything in over 14 years

now.

All the different

medications that I am on the Drs. think have caused my bones to thin as fast

as they have.

Hugs!!!!

Anyone else diagnosised with this? I guess I am on

my way to

osteoporosis, I am 41. :(

Suzi

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I was diagnosed with osteopenia at 35.

I am now 38, and have been gf for 4 years, and taken plenty of calcium, etc.

I have recently found that it has not been enough, and I have had more bone

loss. I believe I will choose Miacalcin, only because it does not seem to

have the same negative gut effects as the others. Anyone else having any

luck?

Suzie

From: SillyYaks [mailto:SillyYaks ] On Behalf Of

Sent: Saturday, January 21, 2006

7:19 PM

To: SillyYaks

Subject: Re:

Osteopenia

I was just

diagnosed about 3 weeks ago with it. I have been GF now for 3 1/2 years.

I should have been on a GF diet over 20 years ago but all the Drs.

said it was IBS.

I am 52 and I

also have Fibromyligia, Chronic Fatigue Syndrome, Restless Leg Syndrome,

I go in every month for medial nerve blocks in my lower spine.I can not

do very much any more I have to use a cane all the time and when we go out to

do our shopping I have to use a motorized cart or it would take me 3 hours in

the store and I could fall very easy. You name it and I more then likely

have it. I have suffered from depression since I was in my teens. I am a

recovering alcoholic, drug addict I have not used anything in over 14 years

now.

All the different

medications that I am on the Drs. think have caused my bones to thin as fast

as they have.

Hugs!!!!

Anyone else diagnosised with this? I guess I am on

my way to

osteoporosis, I am 41. :(

Suzi

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Hi

I'm a lurker here.

I was diagnosed almost a year ago(on my 40th birthday) with

osteopenia in my neck and lower back and mild osteoporosis in my

hips. I've been gf since Sept 2003.

I do have a family history(my mom can sneeze and crack a rib)plus I

had a total hysterectomy in 2002, not on hormone replacement, had an

eating disorder in college, over-exercised and I'm lactose

intolerant, so lots of other factors besides Celiacs.

Anyways my Gynocologist is big in to " here's a pill " He put me on

Actonel. I tried it for 3 months and felt horrible. I'm almost sure

its what caused my hypothyroid. My thyroid levels were perfect right

before going on Actonel. I had horrible joint pain while on it too.

Yet my mom takes it with no problems.

My internist took me off the Actonel, she said to take 1500mg of

calcium, exercise every day-need to start weight training though, she

said that would make a huge difference and as soon as the pool opens

at our new Ymca, she said I need to take water aerobics.

Dana

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Hi

I'm a lurker here.

I was diagnosed almost a year ago(on my 40th birthday) with

osteopenia in my neck and lower back and mild osteoporosis in my

hips. I've been gf since Sept 2003.

I do have a family history(my mom can sneeze and crack a rib)plus I

had a total hysterectomy in 2002, not on hormone replacement, had an

eating disorder in college, over-exercised and I'm lactose

intolerant, so lots of other factors besides Celiacs.

Anyways my Gynocologist is big in to " here's a pill " He put me on

Actonel. I tried it for 3 months and felt horrible. I'm almost sure

its what caused my hypothyroid. My thyroid levels were perfect right

before going on Actonel. I had horrible joint pain while on it too.

Yet my mom takes it with no problems.

My internist took me off the Actonel, she said to take 1500mg of

calcium, exercise every day-need to start weight training though, she

said that would make a huge difference and as soon as the pool opens

at our new Ymca, she said I need to take water aerobics.

Dana

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Hi

I'm a lurker here.

I was diagnosed almost a year ago(on my 40th birthday) with

osteopenia in my neck and lower back and mild osteoporosis in my

hips. I've been gf since Sept 2003.

I do have a family history(my mom can sneeze and crack a rib)plus I

had a total hysterectomy in 2002, not on hormone replacement, had an

eating disorder in college, over-exercised and I'm lactose

intolerant, so lots of other factors besides Celiacs.

Anyways my Gynocologist is big in to " here's a pill " He put me on

Actonel. I tried it for 3 months and felt horrible. I'm almost sure

its what caused my hypothyroid. My thyroid levels were perfect right

before going on Actonel. I had horrible joint pain while on it too.

Yet my mom takes it with no problems.

My internist took me off the Actonel, she said to take 1500mg of

calcium, exercise every day-need to start weight training though, she

said that would make a huge difference and as soon as the pool opens

at our new Ymca, she said I need to take water aerobics.

Dana

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AH , My heart goes out to you. Your story is so sad! I wish you

the very best and will pray for your health! Is it true, then that Irish

are more prone to Celiacs? My side of the family is Irish--just wondering.

TIA,

& Mike

Osteopenia

Hi everyone,

I've been reading the posts today on osteopenia and I had to write in.

I too have osteopenia and have been on the GF diet since my diagnosis last

August. I was misdiagnosed for almost 20 years with multiple stomach

problems. I'm 38 and the only way these so called GI experts found out that

I had Celiac disease was because I broke 4 bones in just over a year. I had

the bone density test done and it showed that I had bones of an 80 year old.

I am a very tall and very thin Irish redhead, and was a ballet dancer for

many years of my life. I found out that these factors were against me once

I learned more about Celiac disease. Since then, I take 1800 mg. of calcium

a day that's not including all the peanut butter and chocolate ice cream I

can eat in a week. Anyway, my recent bone scan showed no sign of

improvement being on a strict GF diet. My doctor said drugs like Fosamax

would not work for me so I started the drug Forteo on Jan 12th.

Unfortunately, this drug is not an easy pill to take. For it is an injection

I have to give myself every 24 hours for the next 2 years. Primary site, in

your abdomen. It's not pretty, my stomach is covered in bruises. So how

this drug works differently from Fosamax that it actually creates new bone.

It does have it side effects like any other drug though; I get horrible

nausea and dizziness. To a point where you don't even want to get in a car.

Just curious to see if any of you with bone troubles are on Forteo. I just

dread the hours of 6 to 9 p.m.

when it's supposed to given. I usually wait until 8:59 when my husband is

hanging over me to make sure I do it. I'm just so tired of living in a cast.

Thanks for listening to me vent.

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AH , My heart goes out to you. Your story is so sad! I wish you

the very best and will pray for your health! Is it true, then that Irish

are more prone to Celiacs? My side of the family is Irish--just wondering.

TIA,

& Mike

Osteopenia

Hi everyone,

I've been reading the posts today on osteopenia and I had to write in.

I too have osteopenia and have been on the GF diet since my diagnosis last

August. I was misdiagnosed for almost 20 years with multiple stomach

problems. I'm 38 and the only way these so called GI experts found out that

I had Celiac disease was because I broke 4 bones in just over a year. I had

the bone density test done and it showed that I had bones of an 80 year old.

I am a very tall and very thin Irish redhead, and was a ballet dancer for

many years of my life. I found out that these factors were against me once

I learned more about Celiac disease. Since then, I take 1800 mg. of calcium

a day that's not including all the peanut butter and chocolate ice cream I

can eat in a week. Anyway, my recent bone scan showed no sign of

improvement being on a strict GF diet. My doctor said drugs like Fosamax

would not work for me so I started the drug Forteo on Jan 12th.

Unfortunately, this drug is not an easy pill to take. For it is an injection

I have to give myself every 24 hours for the next 2 years. Primary site, in

your abdomen. It's not pretty, my stomach is covered in bruises. So how

this drug works differently from Fosamax that it actually creates new bone.

It does have it side effects like any other drug though; I get horrible

nausea and dizziness. To a point where you don't even want to get in a car.

Just curious to see if any of you with bone troubles are on Forteo. I just

dread the hours of 6 to 9 p.m.

when it's supposed to given. I usually wait until 8:59 when my husband is

hanging over me to make sure I do it. I'm just so tired of living in a cast.

Thanks for listening to me vent.

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Thanks for your thoughts karen. Yes, studies show that 1 in 50

persons in Ireland have Celiac disease. Pretty amazing.

- In SillyYaks , " & Mike "

<Mikea@a...> wrote:

>

> AH , My heart goes out to you. Your story is so sad! I

wish you

> the very best and will pray for your health! Is it true, then

that Irish

> are more prone to Celiacs? My side of the family is Irish--just

wondering.

>

>

>

>

> TIA,

>

> & Mike

>

>

> Osteopenia

>

> Hi everyone,

>

> I've been reading the posts today on osteopenia and I had to write

in.

> I too have osteopenia and have been on the GF diet since my

diagnosis last

> August. I was misdiagnosed for almost 20 years with multiple

stomach

> problems. I'm 38 and the only way these so called GI experts

found out that

> I had Celiac disease was because I broke 4 bones in just over a

year. I had

> the bone density test done and it showed that I had bones of an 80

year old.

> I am a very tall and very thin Irish redhead, and was a ballet

dancer for

> many years of my life. I found out that these factors were

against me once

> I learned more about Celiac disease. Since then, I take 1800 mg.

of calcium

> a day that's not including all the peanut butter and chocolate ice

cream I

> can eat in a week. Anyway, my recent bone scan showed no sign of

> improvement being on a strict GF diet. My doctor said drugs like

Fosamax

> would not work for me so I started the drug Forteo on Jan 12th.

> Unfortunately, this drug is not an easy pill to take. For it is an

injection

> I have to give myself every 24 hours for the next 2 years.

Primary site, in

> your abdomen. It's not pretty, my stomach is covered in bruises.

So how

> this drug works differently from Fosamax that it actually creates

new bone.

> It does have it side effects like any other drug though; I get

horrible

> nausea and dizziness. To a point where you don't even want to get

in a car.

> Just curious to see if any of you with bone troubles are on

Forteo. I just

> dread the hours of 6 to 9 p.m.

> when it's supposed to given. I usually wait until 8:59 when my

husband is

> hanging over me to make sure I do it. I'm just so tired of living

in a cast.

> Thanks for listening to me vent.

>

>

>

>

>

>

>

>

>

>

>

>

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Thanks for your thoughts karen. Yes, studies show that 1 in 50

persons in Ireland have Celiac disease. Pretty amazing.

- In SillyYaks , " & Mike "

<Mikea@a...> wrote:

>

> AH , My heart goes out to you. Your story is so sad! I

wish you

> the very best and will pray for your health! Is it true, then

that Irish

> are more prone to Celiacs? My side of the family is Irish--just

wondering.

>

>

>

>

> TIA,

>

> & Mike

>

>

> Osteopenia

>

> Hi everyone,

>

> I've been reading the posts today on osteopenia and I had to write

in.

> I too have osteopenia and have been on the GF diet since my

diagnosis last

> August. I was misdiagnosed for almost 20 years with multiple

stomach

> problems. I'm 38 and the only way these so called GI experts

found out that

> I had Celiac disease was because I broke 4 bones in just over a

year. I had

> the bone density test done and it showed that I had bones of an 80

year old.

> I am a very tall and very thin Irish redhead, and was a ballet

dancer for

> many years of my life. I found out that these factors were

against me once

> I learned more about Celiac disease. Since then, I take 1800 mg.

of calcium

> a day that's not including all the peanut butter and chocolate ice

cream I

> can eat in a week. Anyway, my recent bone scan showed no sign of

> improvement being on a strict GF diet. My doctor said drugs like

Fosamax

> would not work for me so I started the drug Forteo on Jan 12th.

> Unfortunately, this drug is not an easy pill to take. For it is an

injection

> I have to give myself every 24 hours for the next 2 years.

Primary site, in

> your abdomen. It's not pretty, my stomach is covered in bruises.

So how

> this drug works differently from Fosamax that it actually creates

new bone.

> It does have it side effects like any other drug though; I get

horrible

> nausea and dizziness. To a point where you don't even want to get

in a car.

> Just curious to see if any of you with bone troubles are on

Forteo. I just

> dread the hours of 6 to 9 p.m.

> when it's supposed to given. I usually wait until 8:59 when my

husband is

> hanging over me to make sure I do it. I'm just so tired of living

in a cast.

> Thanks for listening to me vent.

>

>

>

>

>

>

>

>

>

>

>

>

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Thanks for your thoughts karen. Yes, studies show that 1 in 50

persons in Ireland have Celiac disease. Pretty amazing.

- In SillyYaks , " & Mike "

<Mikea@a...> wrote:

>

> AH , My heart goes out to you. Your story is so sad! I

wish you

> the very best and will pray for your health! Is it true, then

that Irish

> are more prone to Celiacs? My side of the family is Irish--just

wondering.

>

>

>

>

> TIA,

>

> & Mike

>

>

> Osteopenia

>

> Hi everyone,

>

> I've been reading the posts today on osteopenia and I had to write

in.

> I too have osteopenia and have been on the GF diet since my

diagnosis last

> August. I was misdiagnosed for almost 20 years with multiple

stomach

> problems. I'm 38 and the only way these so called GI experts

found out that

> I had Celiac disease was because I broke 4 bones in just over a

year. I had

> the bone density test done and it showed that I had bones of an 80

year old.

> I am a very tall and very thin Irish redhead, and was a ballet

dancer for

> many years of my life. I found out that these factors were

against me once

> I learned more about Celiac disease. Since then, I take 1800 mg.

of calcium

> a day that's not including all the peanut butter and chocolate ice

cream I

> can eat in a week. Anyway, my recent bone scan showed no sign of

> improvement being on a strict GF diet. My doctor said drugs like

Fosamax

> would not work for me so I started the drug Forteo on Jan 12th.

> Unfortunately, this drug is not an easy pill to take. For it is an

injection

> I have to give myself every 24 hours for the next 2 years.

Primary site, in

> your abdomen. It's not pretty, my stomach is covered in bruises.

So how

> this drug works differently from Fosamax that it actually creates

new bone.

> It does have it side effects like any other drug though; I get

horrible

> nausea and dizziness. To a point where you don't even want to get

in a car.

> Just curious to see if any of you with bone troubles are on

Forteo. I just

> dread the hours of 6 to 9 p.m.

> when it's supposed to given. I usually wait until 8:59 when my

husband is

> hanging over me to make sure I do it. I'm just so tired of living

in a cast.

> Thanks for listening to me vent.

>

>

>

>

>

>

>

>

>

>

>

>

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Hold on! Don't get depressed. I might have something you and your

doctor can discuss about trying. It's called Calcitriol. It's a

pill.

I was diagnosed with Celiac Disease about 2 1/2 years ago. I had my

first bone scan about 1 month after I was diagnosed. I had and

still have osteopenia. But I have improved a great deal! I have

had a total of 3 bone scans and my bone density has improved 4%

since the last bone scan in 2004. Woo Hoo! The scan technician

(doctor) was amazed that it had improved that much in 1 year and

asked what I was taking so that he could recommend it to his other

patients. I still take it to this day and will continue until my

endocrinologist says that it's time to quit.

I hope this might help you too! Good luck!

Becky

>

> Hi everyone,

>

> I've been reading the posts today on osteopenia and I had to write

> in.

> I too have osteopenia and have been on the GF diet since my

> diagnosis last August. I was misdiagnosed for almost 20 years

with

> multiple stomach problems. I'm 38 and the only way these so

called

> GI experts found out that I had Celiac disease was because I broke

4

> bones in just over a year. I had the bone density test done and it

> showed that I had bones of an 80 year old. I am a very tall and

> very thin Irish redhead, and was a ballet dancer for many years of

> my life. I found out that these factors were against me once I

> learned more about Celiac disease. Since then, I take 1800 mg. of

> calcium a day that's not including all the peanut butter and

> chocolate ice cream I can eat in a week. Anyway, my recent bone

> scan showed no sign of improvement being on a strict GF diet. My

> doctor said drugs like Fosamax would not work for me so I started

> the drug Forteo on Jan 12th. Unfortunately, this drug is not an

> easy pill to take. For it is an injection I have to give myself

> every 24 hours for the next 2 years. Primary site, in your

> abdomen. It's not pretty, my stomach is covered in bruises. So

how

> this drug works differently from Fosamax that it actually creates

> new bone. It does have it side effects like any other drug

though;

> I get horrible nausea and dizziness. To a point where you don't

> even want to get in a car. Just curious to see if any of you with

> bone troubles are on Forteo. I just dread the hours of 6 to 9

p.m.

> when it's supposed to given. I usually wait until 8:59 when my

> husband is hanging over me to make sure I do it. I'm just so tired

> of living in a cast. Thanks for listening to me vent.

>

>

>

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Hold on! Don't get depressed. I might have something you and your

doctor can discuss about trying. It's called Calcitriol. It's a

pill.

I was diagnosed with Celiac Disease about 2 1/2 years ago. I had my

first bone scan about 1 month after I was diagnosed. I had and

still have osteopenia. But I have improved a great deal! I have

had a total of 3 bone scans and my bone density has improved 4%

since the last bone scan in 2004. Woo Hoo! The scan technician

(doctor) was amazed that it had improved that much in 1 year and

asked what I was taking so that he could recommend it to his other

patients. I still take it to this day and will continue until my

endocrinologist says that it's time to quit.

I hope this might help you too! Good luck!

Becky

>

> Hi everyone,

>

> I've been reading the posts today on osteopenia and I had to write

> in.

> I too have osteopenia and have been on the GF diet since my

> diagnosis last August. I was misdiagnosed for almost 20 years

with

> multiple stomach problems. I'm 38 and the only way these so

called

> GI experts found out that I had Celiac disease was because I broke

4

> bones in just over a year. I had the bone density test done and it

> showed that I had bones of an 80 year old. I am a very tall and

> very thin Irish redhead, and was a ballet dancer for many years of

> my life. I found out that these factors were against me once I

> learned more about Celiac disease. Since then, I take 1800 mg. of

> calcium a day that's not including all the peanut butter and

> chocolate ice cream I can eat in a week. Anyway, my recent bone

> scan showed no sign of improvement being on a strict GF diet. My

> doctor said drugs like Fosamax would not work for me so I started

> the drug Forteo on Jan 12th. Unfortunately, this drug is not an

> easy pill to take. For it is an injection I have to give myself

> every 24 hours for the next 2 years. Primary site, in your

> abdomen. It's not pretty, my stomach is covered in bruises. So

how

> this drug works differently from Fosamax that it actually creates

> new bone. It does have it side effects like any other drug

though;

> I get horrible nausea and dizziness. To a point where you don't

> even want to get in a car. Just curious to see if any of you with

> bone troubles are on Forteo. I just dread the hours of 6 to 9

p.m.

> when it's supposed to given. I usually wait until 8:59 when my

> husband is hanging over me to make sure I do it. I'm just so tired

> of living in a cast. Thanks for listening to me vent.

>

>

>

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Just another short word. I was diagnosed at 29. I hope all of you

will discuss this with your doctor. I still take 1750mg of calcium

citrate (it's easier to digest) a day. I also take 2 prenatal

vitamins a day as a multivitamin. Hope this helps!

Becky

> >

> > Hi everyone,

> >

> > I've been reading the posts today on osteopenia and I had to

write

> > in.

> > I too have osteopenia and have been on the GF diet since my

> > diagnosis last August. I was misdiagnosed for almost 20 years

> with

> > multiple stomach problems. I'm 38 and the only way these so

> called

> > GI experts found out that I had Celiac disease was because I

broke

> 4

> > bones in just over a year. I had the bone density test done and

it

> > showed that I had bones of an 80 year old. I am a very tall and

> > very thin Irish redhead, and was a ballet dancer for many years

of

> > my life. I found out that these factors were against me once I

> > learned more about Celiac disease. Since then, I take 1800 mg.

of

> > calcium a day that's not including all the peanut butter and

> > chocolate ice cream I can eat in a week. Anyway, my recent bone

> > scan showed no sign of improvement being on a strict GF diet. My

> > doctor said drugs like Fosamax would not work for me so I

started

> > the drug Forteo on Jan 12th. Unfortunately, this drug is not an

> > easy pill to take. For it is an injection I have to give myself

> > every 24 hours for the next 2 years. Primary site, in your

> > abdomen. It's not pretty, my stomach is covered in bruises. So

> how

> > this drug works differently from Fosamax that it actually

creates

> > new bone. It does have it side effects like any other drug

> though;

> > I get horrible nausea and dizziness. To a point where you don't

> > even want to get in a car. Just curious to see if any of you

with

> > bone troubles are on Forteo. I just dread the hours of 6 to 9

> p.m.

> > when it's supposed to given. I usually wait until 8:59 when my

> > husband is hanging over me to make sure I do it. I'm just so

tired

> > of living in a cast. Thanks for listening to me vent.

> >

> >

> >

>

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