Guest guest Posted March 18, 2005 Report Share Posted March 18, 2005 --Oh boy, I'm in tears from reading that. What a beautiful soul. I wish I could've experienced her like you all did when she was alive, but just reading that has touched me to the core of my being. thanks Lea.. I'm going to save this one, print it and bring it with me the night before explant. Now I know why there is so much love here. You all are amazing. Love... Dawn - In , " Lea " <devans@c...> wrote: > I found this a minute ago, we all loved Kathi. We will miss her so > much....bless her precious heart...love....Lea > ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~````````````````` > > > Subject: Fw: To help clarify my situation............ > > > > > > To help clarify my situation............ > > > > > > > Thank you to all who have written! Your encouragement and advice > mean > > > more than you will ever know! > > > > > > I was implanted in '78 with Surgitek polyerathanes. In '80 I began > > > losing my ability to get a spoon, cup or fork to my mouth and > actually > > > hit it without spilling and my legs would just give out for no > reason. > > > There would be weeks go by when I could barely stand let alone walk > or > > > straighten up. After a ton of tests and many types of doctors, they > > > concurred that it was a form of collagen vascular but could not > identify > > > as it seemed to be a mix of almost all and some unknown but that it > was > > > progressive and non fatal. They said they really could not do much > to > > > help except to treat symptoms. I had many periods of remissions and > did > > > fairly well until '93 when one implant was ruptured during a > mammogram. > > > I went to ER about four hours after the imaging in my first full > blown > > > asthma attack only to be laughed at and stared at and sent home > saying > > > noting need be done except to keep it packed in ice to keep it from > > > moving while it settled. I called my cousin who worked for a PS and > she > > > told me that he told her when she got her implants that if they ever > > > ruptured to get to a hospital and have them and the residuals > removed > > > ASAP because it could kill her. I called my doctor at the time and > he > > > said he would get me into a PS but just keep it packed and wait, (he > was > > > angry with the call but did have the tech who did the mammo fired) > > > > > > It took 6 months to get the insurance to ok removal. I was able to > find > > > a loop hole but had to really fight. It was a four hour surgery > because > > > I had the implants attached to the chest wall and there was alot of > > > scrapping and sanding done he said. Most of the silicone had > (230cc) > > > had migrated away and he could not do anything about that even > though we > > > could see it clearly through ultra sound and mri. At that time the > > > recommended removal was to break down the capsule to enable it to > > > deteriorate and be thrown off by the body or harmlessly absorbed > into > > > the body. HA!! > > > > > > We can now see it through out the diaphragm, stomach, liver, ribs, > > > chest, heart, throat, stomach, and colon not to mention all the > abscess > > > like and tumor like growths through out my body. > > > I have since been from 80-90% disabled, bouncing back and forth and > an > > > occasional 60-70%. I am unable to breathe, My internal body is in > a > > > constant stand of chronic inflammation (organs included) as I am > > > allergic to silicone. What a turn about........ caused by break > down > > > in the immune system. A suffer almost a 85% state of anaphylaxis at > > > some level. My current testing show that I have a hypersensitive > rate > > > of 96% over the average. My blood does not transport oxygen as it > > > should, starvingmy tissues, muscles and organs of this necessary > > > element. This is caused by the hypersensitivity and chemical > poisoning. > > > My IgM runs 150 - 180 and over and my compliment CH is usually > around 5 > > > or 8. Blood gases are good and lungs are clear and moving air at > times > > > but the blood just cannot carry it being hindered from the chemical > > damage. > > > > > > The seizures and tremors have stopped for the most part, just > tremors > > > occasionally now. I still pass out if I raise my arms or try to hold > or > > > carry anything. > > > > > > I have regularly detoxed and maintain an organic lifestyle for > years, > > > have had my blood filter a few times and cannot take antibiotics > unless > > > absolutely have to because I have a terrible yeast/fungus problem. > > > Antibiotics always cause a sever bout of thrush swelling my throat > even > > > more. I also have become sensitive or allergic to many antibiotics. > As I > > > suffer many bouts of pneumonia, it is best to leave what there is > for > > > emergencies since our bodies have a tendency to become immune to > them > > > after much use. I have even had bouts of fungus growing in large > > > patches up and down my legs and feet that would not respond to > > > treatment. After a week of heavy dosing with Diflucan it will clear > for > > > 6 months to a year but always comes back. > > > > > > As with many of you, I have no support and little if any help. I > have a > > > 10 year old granddaughter who does help me bathe on weekends and > tries > > > to pick up alittle but you know how they are at that age.......my > > > husband is here but will only help in menial ways if at that and is > of > > > no support at all. (that is a whole other story) One daughter lives > far > > > away and it would be a tremendous hardship for her to even visit and > the > > > other is here but I can truly say she has barely a minute for > herself. I > > > raised three of my granddaughters for 10 years and they do what they > can > > > in the little time they are ever here but live away now and cannot > get > > > back. My mother was vibrant until she had silicone implant post > > > mastectomy in '93 against my advice and now she has great difficulty > > > breathing enough to barely help herself. Up top that time, she > cleaned > > > offices and homes and moved furniture on a regular basis, strong, > > > vibrant and able, health as could be and years younger than her age > but > > > now ....well you know how that goes. She is in denial that it might > even > > > be the implant. My sister had Surgitk in '82. She is in remission > > > right now and doing very well but went through 5 years where she > could > > > not leave her home very often, she was unable to walk, scooted up > and > > > down stairs on her knees or butt and her ankles would swell so that > they > > > fell over the tops of her shoes. She does now have severe cardio > and > > > cardio vascular damage. She to is in denial of the implant > connection. > > > > > > For the most part I treat symptoms organically and with as much > exercise > > > (ha!) as I can give my body in ANYWAY I can. I have a continuing > > > ability to become sensitive to almost every drug I take, which could > be > > > God's way of telling me enough! Depend on Me > alone.................We > > > need doctors, they are his gift to us, his hands inthe earth but > they > > > are human and they have been lied to and the truths hidden from > them, > > > research has been so limited and the only thing we have left after > God > > > is each other, coming together and sharing what works for us, what > does > > > not work, and any information we can gather and taking this and > > > educating whoever we can. > > > > > > I do believe in the body's ability to heal itself and that 95% of it > is > > > a matter of a healthy spirit and mind, being positive, refusing > > > negativity and I do believe in my heart that I will see victory over > > > this, getting through it is not easy but........... > > > as long as you let nothing rob you of gratitude for what you have, > joy > > > of just being alive and faith, then it cannot devour you. > > > > > > I love you! > > > Kathi > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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