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Hi everyone, what a great webpage and group! Thanks for the invite

Rogene. Its great to be a part of the group, and share information.

I look forward to meeting those of you I don't know and sharing with

some of you that I have already crossed paths with over the years.

I am new to the Saline Group, but not to this issue. I've been

suffering since 1982 when I had silicone implants following a mastectomy.

After many problems with them, I switched to what I thought was

the " safe saline " and I had a saline rupture less then a year later.

My story can be found at this link--

http://www.geocities.com/implantinfonet/saline2.html

To date I have the DX of CFS, FMS, MCS, Connective Tissue Disease,

Lupus, MS like Syndrome, Benign Brain Tumor, Pseudo Cerebri Tumor,

Pulmonary Hypertension and Right Sided Heart Failure...and the list goes

on...

I was one of the unfortuate ones that did not the implants removed

properly,(didn't know better) therefore the silicone had more time to

travel around my body causing more damage. I finally found out from Dr.

Feng that the old silicone capsules were still in my system and had them

rmoved in 1996 and I have seen some improvements in my health.

The things I have found most helpful has been following a good sleep

schedule, knowing my limitations and sticking to them and following a

good life style diet (gluten free) and exercise along with Chiro care.

I am not " cured " but my days are much fuller and less painful and the

flares are kept to a minimum. I still remain hopeful because God has

built our body and He knows how to repair it =)

BTW.. Has anyone found anything to help with the " cognitive fog " and

memory problems?

Wishing everyone a wonderful night. Hugs, Rosie =)

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Welcome Rosie,

I just finished reading your webpage . . . It sounds

like the same ole tune we've heard from soooooo many

women. You would think, by now, the doctors would have

wised up!

Regarding your brain fog. . . have you done any

detoxing? i.e. taken antifungals or probiotics? Liver

flushes? We have a lot of suggested detox programs in

the archive section. If it's there, one of us has

tried it!

Sweating is very important too . . . a number of us

are using 'far infrared saunas'. . . If you'll do a

web search for that term, you'll learn a lot more than

I can tell you in a message! The health effect is

considerably different than the standard dry or steam

sauna.

Anyone who has taken antibiotics needs to be treated

for systemic yeast/fungal problems. Especially when

your system has taken a huge whack from breast

implants!

Check the detox section, and if you have any

questions, let us know!

(Rosie's friend Judy Frey recently passed away in

Florida)

Hugs and prayers,

Rogene

--- implantinfonet <implantinfonet@...> wrote:

>

> Hi everyone, what a great webpage and group! Thanks

> for the invite

> Rogene. Its great to be a part of the group, and

> share information.

> I look forward to meeting those of you I don't know

> and sharing with

> some of you that I have already crossed paths with

> over the years.

>

> I am new to the Saline Group, but not to this issue.

> I've been

> suffering since 1982 when I had silicone implants

> following a mastectomy.

> After many problems with them, I switched to what I

> thought was

> the " safe saline " and I had a saline rupture less

> then a year later.

> My story can be found at this link--

> http://www.geocities.com/implantinfonet/saline2.html

>

> To date I have the DX of CFS, FMS, MCS, Connective

> Tissue Disease,

> Lupus, MS like Syndrome, Benign Brain Tumor, Pseudo

> Cerebri Tumor,

> Pulmonary Hypertension and Right Sided Heart

> Failure...and the list goes

> on...

>

> I was one of the unfortuate ones that did not the

> implants removed

> properly,(didn't know better) therefore the silicone

> had more time to

> travel around my body causing more damage. I

> finally found out from Dr.

> Feng that the old silicone capsules were still in my

> system and had them

> rmoved in 1996 and I have seen some improvements in

> my health.

>

> The things I have found most helpful has been

> following a good sleep

> schedule, knowing my limitations and sticking to

> them and following a

> good life style diet (gluten free) and exercise

> along with Chiro care.

>

> I am not " cured " but my days are much fuller and

> less painful and the

> flares are kept to a minimum. I still remain

> hopeful because God has

> built our body and He knows how to repair it =)

>

> BTW.. Has anyone found anything to help with the

> " cognitive fog " and

> memory problems?

>

> Wishing everyone a wonderful night. Hugs, Rosie =)

>

>

>

>

>

>

>

>

>

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