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Re: DHEA

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Hi ,

I was on DHEA last year thru my rhuemy. Didn't seem to do squat for

me. You can buy it over the counter currently and started at small

dosages - worked my way up to the highest you can safely take under a

doctors orders and still didn't do nothing for me - but hopefully it

can help others that suffer from lupus.

Good luck with it.

Deanna

> Hi!! Has anyone ever been on DHEA??? I am enrolled in a new study-

> it is on reducing vascular damage in female SLE patients using

DHEA.

> I haven't started yet, but am supposed to soon. I will let you all

> know what they find out. DHEA is supposed to be approved for use

in

> lupus in the next year or so. Supposed to help reduce flares, but

I

> don't know what dose or anything. It's a double blind study, so I

> won't know when I get it or the placebo. I will let you know when

I

> get results (takes about 5 months total). Hope you are all doing

> well, take care friends!!!!

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Guest guest

Hi ,

I was on DHEA last year thru my rhuemy. Didn't seem to do squat for

me. You can buy it over the counter currently and started at small

dosages - worked my way up to the highest you can safely take under a

doctors orders and still didn't do nothing for me - but hopefully it

can help others that suffer from lupus.

Good luck with it.

Deanna

> Hi!! Has anyone ever been on DHEA??? I am enrolled in a new study-

> it is on reducing vascular damage in female SLE patients using

DHEA.

> I haven't started yet, but am supposed to soon. I will let you all

> know what they find out. DHEA is supposed to be approved for use

in

> lupus in the next year or so. Supposed to help reduce flares, but

I

> don't know what dose or anything. It's a double blind study, so I

> won't know when I get it or the placebo. I will let you know when

I

> get results (takes about 5 months total). Hope you are all doing

> well, take care friends!!!!

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Guest guest

Hi ,

I was on DHEA last year thru my rhuemy. Didn't seem to do squat for

me. You can buy it over the counter currently and started at small

dosages - worked my way up to the highest you can safely take under a

doctors orders and still didn't do nothing for me - but hopefully it

can help others that suffer from lupus.

Good luck with it.

Deanna

> Hi!! Has anyone ever been on DHEA??? I am enrolled in a new study-

> it is on reducing vascular damage in female SLE patients using

DHEA.

> I haven't started yet, but am supposed to soon. I will let you all

> know what they find out. DHEA is supposed to be approved for use

in

> lupus in the next year or so. Supposed to help reduce flares, but

I

> don't know what dose or anything. It's a double blind study, so I

> won't know when I get it or the placebo. I will let you know when

I

> get results (takes about 5 months total). Hope you are all doing

> well, take care friends!!!!

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Guest guest

-Thanks Deanna, I don't really hold out hope for myself, but I hope

that my participating might help them gain more knowledge about what

it does and does not do. I guess they will be doing ultrasounds of

my arms, has to do with vascular damage repair and heart disease

related to lupus in women. I'll post when I know more. Thanks for

your response...take care

- In LUPIES , " Deanna H. " wrote:

> Hi ,

> I was on DHEA last year thru my rhuemy. Didn't seem to do squat for

> me. You can buy it over the counter currently and started at small

> dosages - worked my way up to the highest you can safely take under

a

> doctors orders and still didn't do nothing for me - but hopefully

it

> can help others that suffer from lupus.

> Good luck with it.

> Deanna

>

>

>

> > Hi!! Has anyone ever been on DHEA??? I am enrolled in a new

study-

>

> > it is on reducing vascular damage in female SLE patients using

> DHEA.

> > I haven't started yet, but am supposed to soon. I will let you

all

> > know what they find out. DHEA is supposed to be approved for use

> in

> > lupus in the next year or so. Supposed to help reduce flares,

but

> I

> > don't know what dose or anything. It's a double blind study, so

I

> > won't know when I get it or the placebo. I will let you know

when

> I

> > get results (takes about 5 months total). Hope you are all doing

> > well, take care friends!!!!

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Guest guest

-Thanks Deanna, I don't really hold out hope for myself, but I hope

that my participating might help them gain more knowledge about what

it does and does not do. I guess they will be doing ultrasounds of

my arms, has to do with vascular damage repair and heart disease

related to lupus in women. I'll post when I know more. Thanks for

your response...take care

- In LUPIES , " Deanna H. " wrote:

> Hi ,

> I was on DHEA last year thru my rhuemy. Didn't seem to do squat for

> me. You can buy it over the counter currently and started at small

> dosages - worked my way up to the highest you can safely take under

a

> doctors orders and still didn't do nothing for me - but hopefully

it

> can help others that suffer from lupus.

> Good luck with it.

> Deanna

>

>

>

> > Hi!! Has anyone ever been on DHEA??? I am enrolled in a new

study-

>

> > it is on reducing vascular damage in female SLE patients using

> DHEA.

> > I haven't started yet, but am supposed to soon. I will let you

all

> > know what they find out. DHEA is supposed to be approved for use

> in

> > lupus in the next year or so. Supposed to help reduce flares,

but

> I

> > don't know what dose or anything. It's a double blind study, so

I

> > won't know when I get it or the placebo. I will let you know

when

> I

> > get results (takes about 5 months total). Hope you are all doing

> > well, take care friends!!!!

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Guest guest

-Thanks Deanna, I don't really hold out hope for myself, but I hope

that my participating might help them gain more knowledge about what

it does and does not do. I guess they will be doing ultrasounds of

my arms, has to do with vascular damage repair and heart disease

related to lupus in women. I'll post when I know more. Thanks for

your response...take care

- In LUPIES , " Deanna H. " wrote:

> Hi ,

> I was on DHEA last year thru my rhuemy. Didn't seem to do squat for

> me. You can buy it over the counter currently and started at small

> dosages - worked my way up to the highest you can safely take under

a

> doctors orders and still didn't do nothing for me - but hopefully

it

> can help others that suffer from lupus.

> Good luck with it.

> Deanna

>

>

>

> > Hi!! Has anyone ever been on DHEA??? I am enrolled in a new

study-

>

> > it is on reducing vascular damage in female SLE patients using

> DHEA.

> > I haven't started yet, but am supposed to soon. I will let you

all

> > know what they find out. DHEA is supposed to be approved for use

> in

> > lupus in the next year or so. Supposed to help reduce flares,

but

> I

> > don't know what dose or anything. It's a double blind study, so

I

> > won't know when I get it or the placebo. I will let you know

when

> I

> > get results (takes about 5 months total). Hope you are all doing

> > well, take care friends!!!!

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Guest guest

Okay I tried Dhea for at least six months and it did nothing for me.

On the other hand my vet was telling me to try my dog on coq10. and

ester c for her arthritis( she is young 1.5 yrs old.). well we kept

talking and he told me that it works for people also with auto-immune

diseases. He told me to take 50 mg. per 50 lbs of body weight for the

coq10. He said it has to do with something called adt or adp in the

cells? anyways it helps that thing carry oxygen to cells. Well a few

weeks later I read a report that a lot of lupus patients have a lower

level of the adp or adt( whatever it is ). He also told me that a lot

of the medicines we take lower the levels of these chemicals in our

blood stream. Well it has been about 6 weeks now and I feel much

better. I mean we have nothing to loose we already feel like crap so

anything above that is better. You all have a great day I went back to

work today after 2 weeks off for my laproscopy and I am tired.... bye

for now. marion

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Guest guest

Okay I tried Dhea for at least six months and it did nothing for me.

On the other hand my vet was telling me to try my dog on coq10. and

ester c for her arthritis( she is young 1.5 yrs old.). well we kept

talking and he told me that it works for people also with auto-immune

diseases. He told me to take 50 mg. per 50 lbs of body weight for the

coq10. He said it has to do with something called adt or adp in the

cells? anyways it helps that thing carry oxygen to cells. Well a few

weeks later I read a report that a lot of lupus patients have a lower

level of the adp or adt( whatever it is ). He also told me that a lot

of the medicines we take lower the levels of these chemicals in our

blood stream. Well it has been about 6 weeks now and I feel much

better. I mean we have nothing to loose we already feel like crap so

anything above that is better. You all have a great day I went back to

work today after 2 weeks off for my laproscopy and I am tired.... bye

for now. marion

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Share on other sites

Guest guest

Okay I tried Dhea for at least six months and it did nothing for me.

On the other hand my vet was telling me to try my dog on coq10. and

ester c for her arthritis( she is young 1.5 yrs old.). well we kept

talking and he told me that it works for people also with auto-immune

diseases. He told me to take 50 mg. per 50 lbs of body weight for the

coq10. He said it has to do with something called adt or adp in the

cells? anyways it helps that thing carry oxygen to cells. Well a few

weeks later I read a report that a lot of lupus patients have a lower

level of the adp or adt( whatever it is ). He also told me that a lot

of the medicines we take lower the levels of these chemicals in our

blood stream. Well it has been about 6 weeks now and I feel much

better. I mean we have nothing to loose we already feel like crap so

anything above that is better. You all have a great day I went back to

work today after 2 weeks off for my laproscopy and I am tired.... bye

for now. marion

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Guest guest

I have been taking the dhea for 3 months now, and I feel great! I

was so tired before, so thought it was worht the shot. My memory has

improved, I can focus, no more brain fog, and no more headaches. I

take 50 mg daily.

> Hi . I was reading your post on DHEA and I have been on and

off of it for about a year and a half. So far it seems to be helping

with my fatigue, I think. I'm still tired alot but when I come off

of it for awhile I notice that I'm more tired. I have noticed more

facial hair and acne, but nair hair and retnia A seems to take care

of most of it. What type research are you doing? I would love to

hear more. If you want to email me direct you can at nursealso@c...

Oh, I started taking 25mg daily and have worked up to 75mg. Just

F.Y.I. Take care, Helen

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I'm very interested the usage of DHEA for Lupus patients. I've read

about 2 studies, where it helped relieve Lupus symptoms. I asked

my rheumy about it and he didn't want to even discuss it. He won't

talk about anything that isn't FDA approved. I'm going to try it.

Robyn

In LUPIES , " bandit5125 " wrote:

> I have been taking the dhea for 3 months now, and I feel great! I

> was so tired before, so thought it was worht the shot. My memory

has

> improved, I can focus, no more brain fog, and no more headaches. I

> take 50 mg daily.

>

>

>

> > Hi . I was reading your post on DHEA and I have been on

and

> off of it for about a year and a half. So far it seems to be

helping

> with my fatigue, I think. I'm still tired alot but when I come off

> of it for awhile I notice that I'm more tired. I have noticed more

> facial hair and acne, but nair hair and retnia A seems to take

care

> of most of it. What type research are you doing? I would love to

> hear more. If you want to email me direct you can at

nursealso@c...

> Oh, I started taking 25mg daily and have worked up to 75mg. Just

> F.Y.I. Take care, Helen

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Guest guest

I buy the dhea at walmart, its about 9.00 a bottle for 50 pills at

50 mg. It has worked wonders for me, my only concern was one of the

side effects was hair loss, but it never happened to me. I strarted

taking one every other day, then went to one every day and have done

well on it. Good luck!!!!-

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