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Dear friends,

I find myself at that time of year again, when I must again renew the Survivors of Salines website. If you are not familiar with it, I would urge you to pay a visit. There are around 100 pages on it, and since 1998 I have endeavored to place factual medical information on it so that women who are seeking information about saline-filled silicone breast implants can know that they may be getting themselves in trouble - and women who are already in trouble can find validation and support.

I answer each letter myself, and though there is not much new on the page, the information is a solid resource. I do not post new info on legal matters, nor do I feel it is my place to post healing protocols. I'm not a lawyer or a doctor. I share what I know about getting well, both from my own experience and from that of others, but only when asked, and I urge women to seek medical counsel.

Last year I closed down the site because of lack of funding, and one woman stepped up to the plate and paid for another year of Homestead web hosting. I will be eternally grateful to her! I am writing this letter because I again need help. I am in even more financial difficulty this year than last. While I want to be there for women who need information, I am a divorced woman living on very low income and unable to work. Worse, my mother wants me to move out so she can sell the house and go live with my youngest brother, and because of my severe chemical sensitivity I have nowhere to go. I am on a list for section 8 housing, but cannot live in an apt building because they use pesticides and all manner of other chemicals. I am on a section 8 voucher list in CA (NJ wouldn't even return my calls), but the wait is several years.

Anyway, I have placed a PayPal button on the site (link below), and I hope some of you will find it in your hearts to make a small donation to give us another year of Survivors of Salines. I can't believe I am asking for this kind of help; I was the self-reliant wife of an Army officer and a business owner to whom other people turned for help. Good grief, how life can turn on a dime... or a breast implant!

With love,

Eileen

Eileen Swanson

www.homestead.com/sosalines/sos.html

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You do a good job with the site.

Lynda

At 09:46 PM 7/21/2004, you wrote:

>Dear friends,

>

>I find myself at that time of year again, when I must again renew the

>Survivors of Salines website. If you are not familiar with it, I would

>urge you to pay a visit. There are around 100 pages on it, and since 1998

>I have endeavored to place factual medical information on it so that women

>who are seeking information about saline-filled silicone breast implants

>can know that they may be getting themselves in trouble - and women who

>are already in trouble can find validation and support.

>

>I answer each letter myself, and though there is not much new on the page,

>the information is a solid resource. I do not post new info on legal

>matters, nor do I feel it is my place to post healing protocols. I'm not

>a lawyer or a doctor. I share what I know about getting well, both from

>my own experience and from that of others, but only when asked, and I urge

>women to seek medical counsel.

>

>Last year I closed down the site because of lack of funding, and one woman

>stepped up to the plate and paid for another year of Homestead web

>hosting. I will be eternally grateful to her! I am writing this letter

>because I again need help. I am in even more financial difficulty this

>year than last. While I want to be there for women who need information,

>I am a divorced woman living on very low income and unable to

>work. Worse, my mother wants me to move out so she can sell the house and

>go live with my youngest brother, and because of my severe chemical

>sensitivity I have nowhere to go. I am on a list for section 8 housing,

>but cannot live in an apt building because they use pesticides and all

>manner of other chemicals. I am on a section 8 voucher list in CA (NJ

>wouldn't even return my calls), but the wait is several years.

>

>Anyway, I have placed a PayPal button on the site (link below), and I hope

>some of you will find it in your hearts to make a small donation to give

>us another year of Survivors of Salines. I can't believe I am asking for

>this kind of help; I was the self-reliant wife of an Army officer and a

>business owner to whom other people turned for help. Good grief, how life

>can turn on a dime... or a breast implant!

>

>With love,

>Eileen

>

>Eileen Swanson

><http://www.homestead.com/sosalines/sos.html>www.homestead.com/sosalines/sos.ht\

ml

>

>

>

>

>

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  • 5 years later...
Guest guest

hi tagreed..answer to question 5....sub mucous fibrosisdunt kno the rest....rgds...jasmineFrom: tagreed ghanem <tagreedgh@...>Subject: urgent need Date: Tuesday, 13 April, 2010, 10:37 PM

Hi Guys can any one help me please for these questions1-

if the patient present to practice cant close or open his mouth for left side (muscle of mustication) what is the answer upper motor neuron of the left side or upper motor neuron of the right side,or lower

motor nueron of left side, or lower motor nueron of right side, is it

the same principle of contralateral side 2.how do u sterelize articulator3.what do u mean wet area & dry area of the practice4.technique

& material for taking imprsion for adult with gag reflrx5.which

one have more likly to malignant tranformationhyperplastic candiasis or submucous fibrosis or erosive lichan planus or keratosis6.

which muscle affect in snoring7. why periapical granuloma there is no pain8.time of closur of anterior fontanell & post fontanelthanks

u very much in advance for ur helpTaghreed

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