Re: Re: Skin Rash and other symptoms

[Guest guest]

Hi Terri,

For some doctors, CFS and fibro are the same diagnosis and both are

considered autoimmune problems. How does your doc want to treat your

problems?

Kenda

> ,

> Thank you so much for sharing with us how you are doing, I am so

> happy for you!!!!. It is so important for others to share their

> healing so we that are still fighting can keep going. Knowing there

> is light at the end of the tunnel. Thank you again for inspiring me,

> I just saw a new Dr,Saturday, he read over my whole history and said

> you have CFS as well as autoimmune no Dr, up until this point has

> confirmed what I already knew, It was nice having thei confirmation

> after 10 years of tests and searching, They all want to say it is

> the Fibro, but I knew there is more going on,

> Terri P

>

>

>

>

>

>>

>> Hi everyone. I wanted to let everyone know how well I am doing

> since

>> I was explanted in July. It took a while for my body to settle

> down

>> from the surgery and for my immune system to calm down......but I

> do

>> not have my symptons any more. The Skin Rash I suffered with for

> over

>> 2 years (pictures are on shutterfly), the fatigue, the bloating,

> the

>> GI stuff....is all gone. My energy levels are steadily getting

>> better. I have been working out 3 or 4 times a week and am

> starting

>> to also loose " the weight " that I now associate with " allergic

> toxic

>> weight gain " from implants.

>>

>> Now I feel I can " get on with my life " . I haven't been to a

> doctor

>> for over 3 plus months now!!! For two years, I was going almost

> every

>> other week. No infections.....etc.

>>

>> Without a doubt, my symptons were related to my " saline "

> implants. I

>> am just sorry and sad that the FDA has lifted the ban on

> silicone.

>> Hugs to everyone

>>

>>

>

>