Re: Saline implants and link to Multiple Sclerosis?

[Guest guest]

Hi Jill,

Welcome to saline support . . .

We can't be sure that you don't have MS . . . but the

only way you'll know if it's implant related is to

have your implants properly removed. Many, many women

have been diagnosed with a host of serious autoimmune

diseases that mysteriously disappear after being

explanted and detoxing.

Personally, knowing what I do after watching women

come through here for years, I wouldn't accept MS as a

diagnoses right now. After your implants are removed,

and you've made a serious effort to detox, if the

symptoms aren't improving in a year, I'd take another

look at it.

Some of the women (Patty?) have been diagnosed with

brain lesions that have resolved! . . . . Until they

care enough to test those of us who are sick, we won't

know why women get sick after getting implants . . .

Please look through the messages and the archives . .

.. I think you'll see yourself in many of them. . .

The good news is that, regardless of your current

diagnosis, you have an excellent chance of getting

much better! We're here to help. If you have any

questions, let us know.

Hugs and prayers,

Rogene

[Guest guest]

Hi Jill,

I had my implants done in May of 2005, and I started having symptoms

within a week of getting them. Initially I had joint swelling but

it got really bad in September, and when the joints swelled up, I

started having numbness in my fingers and toes, that in time became

pain in my fingertips and toes, kind of under the nails. Also

experienced headaches in my temples and dizziness. I had my

implants removed in November of 2005 and am so relieved to have them

out. My symptoms haven't eased up all that much yet, however I

fully believe the implants caused all of these symptoms, because

what a coincidence that suddenly after getting implants, I start

having all these issues. It takes most women at least a year to get

better after having the implants removed, so I didn't go into the

explant expecting that I'd see a miraculous change right away. My

right arm goes numb, especially when I wake up in the AM. I also

have sleep disturbances. I had an MRI on my neck recently, and I

did see that my head was included, so I don't know if they have to

specifically target the brain in MRI's, but as far as I know I don't

have any lesions - but I have definitely heard of other women with

implants reporting lesions on the brain.

Good luck, we're here for you.

Sis

>

> Hi guys. My name is Jill and this is my first post.

>

> I am 36 YO. I had saline implants in April of 2005. In August of

> 2005 I had some knee issues/pain. I was told I had chondromalacia

of

> the patella and given anti-inflammatory medication as well as a

> cortisone shot that provided great relief. In February of 2006, I

> woke up one day with right arm pain that in a few days time

> developed into complete numbness. Medical attention ensued and I

> have been unofficially diagnosed as having Multiple Sclerosis. I

> have an MRI of my brain and cervical spine that shows lesions.

(two

> on my brain and one on my spinal cord) I am awaiting the results

of

> a spinal tap.

> The neurologist seemed a bit baffled by my MRI of my brain. He

> wouldn't definately say that I did indeed have MS.

>

> Anyway..this all seems so surreal to me. I was perfectly healthy

my

> entire life. I had a CAT scan of my brain in 2002 for some

migraines

> that I was having and it was clean. I then gave birth in 2003 and

> had no MS attack following. (usually MS flares up postpartum) Fast

> forward to having implants in 2005 and then ending up with MS or

MS

> like symptoms in 2006 and something seems array to me???

>

> Has anyone here had a limb go completely numb? What about brain

> lesions or a spinal cord lesion?

>

> Thanks..sorry this is so long.

>

> Jill

>