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I am so sorry to hear of your pain and swelling. At least you can take some

comfort in knowing that there are a lot of other people out there who have gone

through similar pain. We know how you feel.

My Dr. told me that eating meat can increase inflamation. I've heard that

it's good to avoid nightshade vegatables (tomatoes, peppers, etc. ). I've heard

that fish oil pills help with inflamation.

I personally love to take baths when I am all swollen. If you are able to get

in and out of the tub you might try that. I've heard peroxide baths mentioned

on here several times. I think you put a bunch of epsom salt in the tub, soak

in it and then fill the tub with a dilution of hydrogen peroxide.

My thoughts and prayers are with you. I hope the situation with the IV's gets

resolved soon.

Clara

madelyfs <madelyfs@...> wrote:

Hello everyone. Thank you again for all the responses I received

when I last posted about the painful nodules and the leg swelling. I

had one thank you message returned (Korea) so again thank you so

much. My SD seems to be getting worse because I continue to have

problems with the swelling and the pain in my feet and lower legs

even when I first get up in the mornings. I've been working on

trying to get the IV treatments. Dr. Franco in CA send me the RX

for the IV's but now I'm trying to get

a home health service to administer the IV's. The

only co. that my insurance might possibly cover

doesn't come to my hometown. So I asked Dr. Franco

about the injections so that I could possibly

administer them myself. Anyway to make a long story

short I seem to be playing a waiting came. I ask Dr.

Franco questions and it takes about a week for an

answer. Things are moving very slowly and during this

waiting game I am suffering quite a bit. I'm really

becoming scared now because of the pain and swelling

in my feet and lower legs. I still have the erethyma

nodosum and I'm just miserable. I feel that while I'm

waiting my body is being further damaged and I feel

helpless. Is there something I should be doing while

I wait. I often wonder if I'm not seeing something

that I could be doing. Any advice would be helpful.

Could I be possibly eating something that is

triggering the swelling? I'm starting to be concerned about

something possibly going on with my kidneys. Thanks, Debra

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

Sports Fantasy Football ’06 - Go with the leader. Start your league

today!

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Clara, thanks so much for your response. I think I'll

try the peroxide baths tonight. I'm also trying to

watch what I eat. Thanks again, Debra

--- Clara Hurtado Lee <divaclarita@...> wrote:

> I am so sorry to hear of your pain and swelling. At

> least you can take some comfort in knowing that

> there are a lot of other people out there who have

> gone through similar pain. We know how you feel.

>

> My Dr. told me that eating meat can increase

> inflamation. I've heard that it's good to avoid

> nightshade vegatables (tomatoes, peppers, etc. ).

> I've heard that fish oil pills help with

> inflamation.

>

> I personally love to take baths when I am all

> swollen. If you are able to get in and out of the

> tub you might try that. I've heard peroxide baths

> mentioned on here several times. I think you put a

> bunch of epsom salt in the tub, soak in it and then

> fill the tub with a dilution of hydrogen peroxide.

>

> My thoughts and prayers are with you. I hope the

> situation with the IV's gets resolved soon.

>

> Clara

>

> madelyfs <madelyfs@...> wrote:

> Hello everyone. Thank you again for all

> the responses I received

> when I last posted about the painful nodules and the

> leg swelling. I

> had one thank you message returned (Korea) so again

> thank you so

> much. My SD seems to be getting worse because I

> continue to have

> problems with the swelling and the pain in my feet

> and lower legs

> even when I first get up in the mornings. I've been

> working on

> trying to get the IV treatments. Dr. Franco in CA

> send me the RX

> for the IV's but now I'm trying to get

> a home health service to administer the IV's. The

> only co. that my insurance might possibly cover

> doesn't come to my hometown. So I asked Dr. Franco

> about the injections so that I could possibly

> administer them myself. Anyway to make a long story

> short I seem to be playing a waiting came. I ask Dr.

> Franco questions and it takes about a week for an

> answer. Things are moving very slowly and during

> this

> waiting game I am suffering quite a bit. I'm really

> becoming scared now because of the pain and swelling

> in my feet and lower legs. I still have the erethyma

> nodosum and I'm just miserable. I feel that while

> I'm

> waiting my body is being further damaged and I feel

> helpless. Is there something I should be doing while

> I wait. I often wonder if I'm not seeing something

> that I could be doing. Any advice would be helpful.

> Could I be possibly eating something that is

> triggering the swelling? I'm starting to be

> concerned about

> something possibly going on with my kidneys. Thanks,

> Debra

>

>

>

>

>

>

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

> Sports Fantasy Football ’06 - Go with the

> leader. Start your league today!

>

> [Non-text portions of this message have been

> removed]

>

>

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Guest guest

I'm curious about this stuff in the bath thing. I have an infectious

diseases doc that tells me I need to take my bath once a month with a

cup of bleach in it. (Yes I take a bath more than once a month. I just

put bleach in it once a month for a week.) The Doc says It's supposed

to kill certain naturally occuring bacteria on the outside of the skin.

Anybody have any idea about this??? Related to the peroxide or epsom

salts?

michael

>

> I am so sorry to hear of your pain and swelling. At least you can

take some comfort in knowing that there are a lot of other people out

there who have gone through similar pain. We know how you feel.

>

> My Dr. told me that eating meat can increase inflamation. I've

heard that it's good to avoid nightshade vegatables (tomatoes, peppers,

etc. ). I've heard that fish oil pills help with inflamation.

>

> I personally love to take baths when I am all swollen. If you are

able to get in and out of the tub you might try that. I've heard

peroxide baths mentioned on here several times. I think you put a

bunch of epsom salt in the tub, soak in it and then fill the tub with a

dilution of hydrogen peroxide.

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Hi ,

I read about using bleach in some old health books (written in the 70s) but

doing this did not resonate with me. I have filters on my showers to take

out chlorine (and other chemicals) so it did not make sense to add

essentially chlorine back into the bath water and soak in it. I feel much

safer soaking in peroxide and certainly recommend it for whenever you feel

'icky.' Peroxide will certainly kill bacteria and it's never been linked to

cancer whereas the dioxins in bleach certainly have been. Hope this helps.

El

rheumatic Re: Help needed!!

I'm curious about this stuff in the bath thing. I have an infectious

diseases doc that tells me I need to take my bath once a month with a

cup of bleach in it. (Yes I take a bath more than once a month. I just

put bleach in it once a month for a week.) The Doc says It's supposed

to kill certain naturally occuring bacteria on the outside of the skin.

Anybody have any idea about this??? Related to the peroxide or epsom

salts?

michael

>

> I am so sorry to hear of your pain and swelling. At least you can

take some comfort in knowing that there are a lot of other people out

there who have gone through similar pain. We know how you feel.

>

> My Dr. told me that eating meat can increase inflamation. I've

heard that it's good to avoid nightshade vegatables (tomatoes, peppers,

etc. ). I've heard that fish oil pills help with inflamation.

>

> I personally love to take baths when I am all swollen. If you are

able to get in and out of the tub you might try that. I've heard

peroxide baths mentioned on here several times. I think you put a

bunch of epsom salt in the tub, soak in it and then fill the tub with a

dilution of hydrogen peroxide.

To unsubscribe, email: rheumatic-unsubscribeegroups

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Guest guest

...That's the first I have heard of putting a cup of bleach into the

bath water. I know Hydrogen Peroxide is an antibacterial and use that. It

does not have the smell of bleach and I do hate the bleach smell. Wouldn't

going swimming be good then too?? That is chlorine that is used to keep the

water clean. Just a thought!! Martha

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Guest guest

Thanks Martha... I appreciate the thought. The problem I have is I am a

double leg amputee... Swimming is a bit difficult for me. The other

problem I have is after I drain the bath water, I have to run myself

under the faucet because I need to wash the layer of bleach water off

me... It's kinda hard when you don't have one of those detachable

shower heads... The job gets done, but it's really a pain in the

patoot...

Thanks to everyone for all the ideas and help... The websites have been

helpful too... Thank ya'll

michael

keep the

> water clean. Just a thought!! Martha

>

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hi debra,

if you are concerned about your kidneys do a urine culture and a urine analysis.

have your doc order the tests on a two months basis. do you test ASO positive? I

had ankle swelling until I had a course of 6 weeks of ampicilline.

good luck

anna

a general question: does anybody here know of real people with RA that moved to

Arizona or NM -read dry, hot weather-and got much better?

rheumatic Help needed!!

Hello everyone. Thank you again for all the responses I received

when I last posted about the painful nodules and the leg swelling. I

had one thank you message returned (Korea) so again thank you so

much. My SD seems to be getting worse because I continue to have

problems with the swelling and the pain in my feet and lower legs

even when I first get up in the mornings. I've been working on

trying to get the IV treatments. Dr. Franco in CA send me the RX

for the IV's but now I'm trying to get

a home health service to administer the IV's. The

only co. that my insurance might possibly cover

doesn't come to my hometown. So I asked Dr. Franco

about the injections so that I could possibly

administer them myself. Anyway to make a long story

short I seem to be playing a waiting came. I ask Dr.

Franco questions and it takes about a week for an

answer. Things are moving very slowly and during this

waiting game I am suffering quite a bit. I'm really

becoming scared now because of the pain and swelling

in my feet and lower legs. I still have the erethyma

nodosum and I'm just miserable. I feel that while I'm

waiting my body is being further damaged and I feel

helpless. Is there something I should be doing while

I wait. I often wonder if I'm not seeing something

that I could be doing. Any advice would be helpful.

Could I be possibly eating something that is

triggering the swelling? I'm starting to be concerned about

something possibly going on with my kidneys. Thanks, Debra

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Guest guest

Erethyma nodosum and lower leg edema eventually respond very well to

conventional treatment and medication. If they did not respond completely

with the initial treatment, then simply revisit for more treatment. I know

I had to go in at least three times to completely resolve the erethyma

nodosum and the ensuing infection.

rheumatic Help needed!!

Hello everyone. Thank you again for all the responses I received

when I last posted about the painful nodules and the leg swelling. I

had one thank you message returned (Korea) so again thank you so

much. My SD seems to be getting worse because I continue to have

problems with the swelling and the pain in my feet and lower legs

even when I first get up in the mornings. I've been working on

trying to get the IV treatments. Dr. Franco in CA send me the RX

for the IV's but now I'm trying to get

a home health service to administer the IV's. The

only co. that my insurance might possibly cover

doesn't come to my hometown. So I asked Dr. Franco

about the injections so that I could possibly

administer them myself. Anyway to make a long story

short I seem to be playing a waiting came. I ask Dr.

Franco questions and it takes about a week for an

answer. Things are moving very slowly and during this

waiting game I am suffering quite a bit. I'm really

becoming scared now because of the pain and swelling

in my feet and lower legs. I still have the erethyma

nodosum and I'm just miserable. I feel that while I'm

waiting my body is being further damaged and I feel

helpless. Is there something I should be doing while

I wait. I often wonder if I'm not seeing something

that I could be doing. Any advice would be helpful.

Could I be possibly eating something that is

triggering the swelling? I'm starting to be concerned about

something possibly going on with my kidneys. Thanks, Debra

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Guest guest

>I ask Dr.

> Franco questions and it takes about a week for an

> answer. Things are moving very slowly and during this

> waiting game

Hi Debra, I know it sometimes seems like a long time to wait for a

response from Dr. Franco and/or his staff. I've been there. He and his

staff routinely work until 7:00 p.m. in the evenings (he sees patients

on Mondays - Wednesdays, and processes insurance paperwork on Thursdays)

-- in fact, I received a return call from , Dr. Franco's nurse

this week. I had left a message earlier in the day and to my surprise

she called me that evening, asked if I could talk to Dr. Franco right

then, as he will be out of town in July. (Few doctors will even talk to

their patients on the phone, and many insist they make an office

appointment.) Keep trying -- Dr. Franco is one of the few doctors who

really understands rheumatic diseases. He's worth the wait. Take care,

~Connie

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Guest guest

Also, try calling DR Sinnott, he is still in Iowa right? I have called

a few times and he has been great about taking my calls. Just another

idea...hope this helps....

rheumatic Re: Help needed!!

>

>

> >I ask Dr.

> > Franco questions and it takes about a week for an

> > answer. Things are moving very slowly and during this

> > waiting game

>

> Hi Debra, I know it sometimes seems like a long time to wait for a

> response from Dr. Franco and/or his staff. I've been there. He and his

> staff routinely work until 7:00 p.m. in the evenings (he sees patients

> on Mondays - Wednesdays, and processes insurance paperwork on Thursdays)

> -- in fact, I received a return call from , Dr. Franco's nurse

> this week. I had left a message earlier in the day and to my surprise

> she called me that evening, asked if I could talk to Dr. Franco right

> then, as he will be out of town in July. (Few doctors will even talk to

> their patients on the phone, and many insist they make an office

> appointment.) Keep trying -- Dr. Franco is one of the few doctors who

> really understands rheumatic diseases. He's worth the wait. Take care,

>

> ~Connie

>

>

>

>

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When my doctor returns from vacation I will ask for

the kidney tests. I feel really ignorant but which

test shows if you are ASO positive? Thanks, Debra

--- ionstanciu <ionstanciu@...> wrote:

> hi debra,

> if you are concerned about your kidneys do a urine

> culture and a urine analysis. have your doc order

> the tests on a two months basis. do you test ASO

> positive? I had ankle swelling until I had a course

> of 6 weeks of ampicilline.

> good luck

> anna

>

> a general question: does anybody here know of real

> people with RA that moved to Arizona or NM -read

> dry, hot weather-and got much better?

> rheumatic Help needed!!

>

>

> Hello everyone. Thank you again for all the

> responses I received

> when I last posted about the painful nodules and

> the leg swelling. I

> had one thank you message returned (Korea) so

> again thank you so

> much. My SD seems to be getting worse because I

> continue to have

> problems with the swelling and the pain in my feet

> and lower legs

> even when I first get up in the mornings. I've

> been working on

> trying to get the IV treatments. Dr. Franco in CA

> send me the RX

> for the IV's but now I'm trying to get

> a home health service to administer the IV's. The

> only co. that my insurance might possibly cover

> doesn't come to my hometown. So I asked Dr. Franco

> about the injections so that I could possibly

> administer them myself. Anyway to make a long

> story

> short I seem to be playing a waiting came. I ask

> Dr.

> Franco questions and it takes about a week for an

> answer. Things are moving very slowly and during

> this

> waiting game I am suffering quite a bit. I'm

> really

> becoming scared now because of the pain and

> swelling

> in my feet and lower legs. I still have the

> erethyma

> nodosum and I'm just miserable. I feel that while

> I'm

> waiting my body is being further damaged and I

> feel

> helpless. Is there something I should be doing

> while

> I wait. I often wonder if I'm not seeing something

> that I could be doing. Any advice would be

> helpful.

> Could I be possibly eating something that is

> triggering the swelling? I'm starting to be

> concerned about

> something possibly going on with my kidneys.

> Thanks, Debra

>

>

>

>

>

> [Non-text portions of this message have been

> removed]

>

>

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Yes, I realize how busy they are. I have spoken to

several times and have also spoken to Dr.

Franco in the past. Its just very frustrating right

now because of the pain I'm in and because my hometown

doctor doesn't really know how to help me and if I go

back to the traditional rheumy he'll just put me on

all that awful medicine. I'm just really concerned

about the inflammmation and shooting pain I've been

experiencing lately. This condition just seems to be

getting worse. Do you know if Dr. Franco is going to

be gone all of July? Thanks, Debra

--- conniehache <hache37@...> wrote:

>

>

> >I ask Dr.

> > Franco questions and it takes about a week for an

> > answer. Things are moving very slowly and during

> this

> > waiting game

>

> Hi Debra, I know it sometimes seems like a long time

> to wait for a

> response from Dr. Franco and/or his staff. I've

> been there. He and his

> staff routinely work until 7:00 p.m. in the evenings

> (he sees patients

> on Mondays - Wednesdays, and processes insurance

> paperwork on Thursdays)

> -- in fact, I received a return call from ,

> Dr. Franco's nurse

> this week. I had left a message earlier in the day

> and to my surprise

> she called me that evening, asked if I could talk to

> Dr. Franco right

> then, as he will be out of town in July. (Few

> doctors will even talk to

> their patients on the phone, and many insist they

> make an office

> appointment.) Keep trying -- Dr. Franco is one of

> the few doctors who

> really understands rheumatic diseases. He's worth

> the wait. Take care,

>

> ~Connie

>

>

>

> [Non-text portions of this message have been

> removed]

>

>

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Guest guest

Jeffery what is the conventional treatment and

medication for the erethyma nodosum? I still have it

and it seems to be getting worse. I have shooting

pains in my legs. I also have a small sore on my

right ankle that has not completely healed in almost

two months. Thanks, Debra

--- Jeffery scott <jefferysa@...> wrote:

> Erethyma nodosum and lower leg edema eventually

> respond very well to

> conventional treatment and medication. If they did

> not respond completely

> with the initial treatment, then simply revisit for

> more treatment. I know

> I had to go in at least three times to completely

> resolve the erethyma

> nodosum and the ensuing infection.

>

> rheumatic Help needed!!

>

> Hello everyone. Thank you again for all the

> responses I received

> when I last posted about the painful nodules and

> the leg swelling. I

> had one thank you message returned (Korea) so

> again thank you so

> much. My SD seems to be getting worse because I

> continue to have

> problems with the swelling and the pain in my

> feet and lower legs

> even when I first get up in the mornings. I've

> been working on

> trying to get the IV treatments. Dr. Franco in CA

> send me the RX

> for the IV's but now I'm trying to get

> a home health service to administer the IV's. The

> only co. that my insurance might possibly cover

> doesn't come to my hometown. So I asked Dr.

> Franco

> about the injections so that I could possibly

> administer them myself. Anyway to make a long

> story

> short I seem to be playing a waiting came. I ask

> Dr.

> Franco questions and it takes about a week for an

> answer. Things are moving very slowly and during

> this

> waiting game I am suffering quite a bit. I'm

> really

> becoming scared now because of the pain and

> swelling

> in my feet and lower legs. I still have the

> erethyma

> nodosum and I'm just miserable. I feel that while

> I'm

> waiting my body is being further damaged and I

> feel

> helpless. Is there something I should be doing

> while

> I wait. I often wonder if I'm not seeing

> something

> that I could be doing. Any advice would be

> helpful.

> Could I be possibly eating something that is

> triggering the swelling? I'm starting to be

> concerned about

> something possibly going on with my kidneys.

> Thanks, Debra

>

>

>

>

>

> [Non-text portions of this message have been

> removed]

>

>

>

>

> To unsubscribe, email:

> rheumatic-unsubscribeegroups

>

>

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Guest guest

Debbie, does he talk to people who are not his regular

patients?

--- DEBBIE GIBSON <Debbullwinkle@...> wrote:

> Also, try calling DR Sinnott, he is still in

> Iowa right? I have called

> a few times and he has been great about taking my

> calls. Just another

> idea...hope this helps....

> rheumatic Re: Help needed!!

>

>

> >

> >

> > >I ask Dr.

> > > Franco questions and it takes about a week for

> an

> > > answer. Things are moving very slowly and during

> this

> > > waiting game

> >

> > Hi Debra, I know it sometimes seems like a long

> time to wait for a

> > response from Dr. Franco and/or his staff. I've

> been there. He and his

> > staff routinely work until 7:00 p.m. in the

> evenings (he sees patients

> > on Mondays - Wednesdays, and processes insurance

> paperwork on Thursdays)

> > -- in fact, I received a return call from

> , Dr. Franco's nurse

> > this week. I had left a message earlier in the

> day and to my surprise

> > she called me that evening, asked if I could talk

> to Dr. Franco right

> > then, as he will be out of town in July. (Few

> doctors will even talk to

> > their patients on the phone, and many insist they

> make an office

> > appointment.) Keep trying -- Dr. Franco is one of

> the few doctors who

> > really understands rheumatic diseases. He's worth

> the wait. Take care,

> >

> > ~Connie

> >

> >

> >

> > [Non-text portions of this message have been

> removed]

> >

> >

> >

> >

> > To unsubscribe, email:

> rheumatic-unsubscribeegroups

> >

> >

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Guest guest

Yes, I have never been to see him...but had some general questions about the

AP and he was very helpful.

rheumatic Re: Help needed!!

> >

> >

> > >

> > >

> > > >I ask Dr.

> > > > Franco questions and it takes about a week for

> > an

> > > > answer. Things are moving very slowly and during

> > this

> > > > waiting game

> > >

> > > Hi Debra, I know it sometimes seems like a long

> > time to wait for a

> > > response from Dr. Franco and/or his staff. I've

> > been there. He and his

> > > staff routinely work until 7:00 p.m. in the

> > evenings (he sees patients

> > > on Mondays - Wednesdays, and processes insurance

> > paperwork on Thursdays)

> > > -- in fact, I received a return call from

> > , Dr. Franco's nurse

> > > this week. I had left a message earlier in the

> > day and to my surprise

> > > she called me that evening, asked if I could talk

> > to Dr. Franco right

> > > then, as he will be out of town in July. (Few

> > doctors will even talk to

> > > their patients on the phone, and many insist they

> > make an office

> > > appointment.) Keep trying -- Dr. Franco is one of

> > the few doctors who

> > > really understands rheumatic diseases. He's worth

> > the wait. Take care,

> > >

> > > ~Connie

> > >

> > >

> > >

> > > [Non-text portions of this message have been

> > removed]

> > >

> > >

> > >

> > >

> > > To unsubscribe, email:

> > rheumatic-unsubscribeegroups

> > >

> > >

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Guest guest

ASO test is a blood test that shows if there is strep infection in your system.

If you're positive you must be treated with pennicillin, ampicillin or

amoxicillin tilll you get the ASO negative.

rheumatic Help needed!!

>

>

> Hello everyone. Thank you again for all the

> responses I received

> when I last posted about the painful nodules and

> the leg swelling. I

> had one thank you message returned (Korea) so

> again thank you so

> much. My SD seems to be getting worse because I

> continue to have

> problems with the swelling and the pain in my feet

> and lower legs

> even when I first get up in the mornings. I've

> been working on

> trying to get the IV treatments. Dr. Franco in CA

> send me the RX

> for the IV's but now I'm trying to get

> a home health service to administer the IV's. The

> only co. that my insurance might possibly cover

> doesn't come to my hometown. So I asked Dr. Franco

> about the injections so that I could possibly

> administer them myself. Anyway to make a long

> story

> short I seem to be playing a waiting came. I ask

> Dr.

> Franco questions and it takes about a week for an

> answer. Things are moving very slowly and during

> this

> waiting game I am suffering quite a bit. I'm

> really

> becoming scared now because of the pain and

> swelling

> in my feet and lower legs. I still have the

> erethyma

> nodosum and I'm just miserable. I feel that while

> I'm

> waiting my body is being further damaged and I

> feel

> helpless. Is there something I should be doing

> while

> I wait. I often wonder if I'm not seeing something

> that I could be doing. Any advice would be

> helpful.

> Could I be possibly eating something that is

> triggering the swelling? I'm starting to be

> concerned about

> something possibly going on with my kidneys.

> Thanks, Debra

>

>

>

>

>

> [Non-text portions of this message have been

> removed]

>

>

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Guest guest

Hi El;

I have Scleroderma and my doctor told me to stay away from

chlorine.She says it is one of the causes of this disease.As much so as

benzene.The only patient she ever lost had worked in a manufacturing

company that bottled household bleach. Lynne

ehgooding wrote:

> Hi ,

>

> I read about using bleach in some old health books (written in the

> 70s) but

> doing this did not resonate with me. I have filters on my showers to take

> out chlorine (and other chemicals) so it did not make sense to add

> essentially chlorine back into the bath water and soak in it. I feel much

> safer soaking in peroxide and certainly recommend it for whenever you feel

> 'icky.' Peroxide will certainly kill bacteria and it's never been

> linked to

> cancer whereas the dioxins in bleach certainly have been. Hope this helps.

> El

>

> rheumatic Re: Help needed!!

>

> I'm curious about this stuff in the bath thing. I have an infectious

> diseases doc that tells me I need to take my bath once a month with a

> cup of bleach in it. (Yes I take a bath more than once a month. I just

> put bleach in it once a month for a week.) The Doc says It's supposed

> to kill certain naturally occuring bacteria on the outside of the skin.

> Anybody have any idea about this??? Related to the peroxide or epsom

> salts?

>

> michael

>

>

> >

> > I am so sorry to hear of your pain and swelling. At least you can

> take some comfort in knowing that there are a lot of other people out

> there who have gone through similar pain. We know how you feel.

> >

> > My Dr. told me that eating meat can increase inflamation. I've

> heard that it's good to avoid nightshade vegatables (tomatoes, peppers,

> etc. ). I've heard that fish oil pills help with inflamation.

> >

> > I personally love to take baths when I am all swollen. If you are

> able to get in and out of the tub you might try that. I've heard

> peroxide baths mentioned on here several times. I think you put a

> bunch of epsom salt in the tub, soak in it and then fill the tub with a

> dilution of hydrogen peroxide.

>

> To unsubscribe, email: rheumatic-unsubscribeegroups

> <mailto:rheumatic-unsubscribe%40>

>

>

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Are you interested in cleansing out your body? Have a Happy and Healthy Day, Kopera M.H.© Copyright 2007 www.sCorner.com . All rights reserved | Privacy Policy WARNING: None of the above statements have been evaluated or approved by the Food and Drug Administration or the American Medical Association. The information provided on this site is intended for your general knowledge only and is

not a substitute for professional medical advice or treatment for specific medical conditions. Always seek the advice of your physician or other qualified health care provider before using any herbal products. From: gracedawn0175 <gracedawn0175@...> Sent: Saturday, July 25, 2009

7:59:12 AMSubject: Help needed!!

Hello. I have been in serious need of help for a decision on how and what to do for my breast explantation. I got them about three years ago (saline under) and I was so paranoid they were going to be too big for my size 2 frame. And they were. I asked for a full C but instead received a full D. I have tried to deal with it and bought and entire new wardrobe since I wore xs size before. Now I am happy if a medium fits. I never wanted to draw that much attention to my chest. But with that being said, here is the real reason I am here.

Between Vanderbilt Hospital *I live in Nashville* and the Mayo Clinic, they cannot find what is wrong with me. Did I mention about 30k in testing? I am now waiting to see an endocrinologist about this orthostatic tachycardia that I have to see if it could be related to an adrenal issue. I am so tired of doctors and not feeling well.

Did I also mention I am 34 years old and on 80mg of Nadalol just to control my heart rate? However, my norepinepherine is high as well as my aldosterone levels are through the roof.

These symptoms have been progressively getting worse since the implants three years ago. I really think I need them out. I am worried about the cost since I just paid Vanderbilt 2k for all of their tests that told me nothing. Mayos bills are arriving as I type.

My question. Anyone heard of correlation of saline implants and orthostatic tachycardia or other endocrine disorders? Also, who in Nashville does the explant?? There has to be someone here in this big wealthy city.

I would appreciate ANY help! THANK YOU in advance!

Dawn stressin in Nashville... .

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