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Just wanted to introduce myself. I'm , a 35 yr. old Mom of 2.

I got saline implants w/ a silicone shell in 2004.

In late '04, I started having weird skin issues, rashes, hives etc. I'd always

go to my General Practitioner and get a steroid shot. Everything would be fine

for a few months.

In 2007, I began having migraines and my blood pressure soared. I was put on

meds. I'm not over weight nor do I have a family history of high BP.

In 2008, I was having 20-40 day monthly cycles. My GYNO found polyps and cysts.

The year before, my Pap was beautiful.

In 2009, I started having achy joints. The pain was intermittent, but just in

the same joints. I thought maybe I was working out too hard. I eased off, but

the aches got worse and spread to other areas.

My skin was still breaking out, and I developed a cough and low grade fever

that stuck around for about 4 months. My children both got H1N1 and I thought I

had the flu as well.

Again, I went to the GP. My flu test was negative, so she (Doctor) asked if she

could run some other blood tests.

2 weeks later, I went to the GP to find out I had 4 positive blood tests and

got a referral to a Rheumatologist.

Long story short- I'm on Plaquenil and have a diagnosis of Systemic Lupus. My

levels are so low compared to most Lupus patients.

I strongly suspect my implants to be a big contributor to my illness even

though I have saline implants. Am I going crazy, or is there a connection?

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