Guest guest Posted June 10, 2002 Report Share Posted June 10, 2002 Hello ! I'm feeling okay; thanks for asking! I would have never guessed the meaning of your company's name. That is lovely. God Bless You ! Tony Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 24, 2003 Report Share Posted March 24, 2003 I will get a picture of them and send them to you tomorrow! -----Original Message----- From: tazz001@... [mailto:tazz001@...] Sent: Monday, March 24, 2003 6:54 PM Subject: [ ] ! Hi ! DARK PURPLE ! THEY MOST BE SO BEAUTIFUL! Love, Tony Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 7, 2003 Report Share Posted July 7, 2003 Tony with all you have going on I am very touched that you had time to think of me. Of course as big as your heart is it is really no surprise. Have you talked to your mom? Is she coming up? I hope all goes well with your appointment today, will be praying for you. the WV hillbilly Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 17, 2005 Report Share Posted June 17, 2005 In a message dated 6/17/2005 5:54:42 A.M. Eastern Daylight Time, writes: I am considering writing a book (maybe a pipe-dream...), I think NOT ... start typing, girl! Pipe-dream ... scmipe-dream! The best way to start a book or other piece of written work is to write in what is called " stream of consciousness " . That means, just write what you wa nt to say -- don't edit, spellcheck or anything else. Just get it OUT there Editing and all that comes on the second draft. Go, go, go! :-) Love and Prayers, Beth ~*~*~*~*~*~*~*~* Read my blog at www.ThinkBigAboutHealing.blogspot.com ~*~*~*~*~*~*~*~* Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 17, 2005 Report Share Posted June 17, 2005 Thanks Beth! Words of encouragement are always welcome and so needed! If I ever do get that book written (and published) you'll get the first copy - free of charge, of course! Love, > > > In a message dated 6/17/2005 5:54:42 A.M. Eastern Daylight Time, writes: > > I am considering writing a book (maybe a pipe-dream...), > > I think NOT ... start typing, girl! Pipe-dream ... scmipe-dream! > > The best way to start a book or other piece of written work is to write in > what is called " stream of consciousness " . That means, just write what you wa > nt to say -- don't edit, spellcheck or anything else. Just get it OUT there > Editing and all that comes on the second draft. > > Go, go, go! :-) > > > Love and Prayers, > Beth > > ~*~*~*~*~*~*~*~* > Read my blog at www.ThinkBigAboutHealing.blogspot.com > > ~*~*~*~*~*~*~*~* > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 29, 2007 Report Share Posted January 29, 2007 Thanks Nola. I just need a doctor to ptescribe it .Nola <oothappam@...> wrote: Dear , I'm in a situation like yours.Very progressive MS. I started on LDN last February. At that time I was already disabled and using a wheelchair. I am still in my chair now, but I had an appointment with my neurologist last Monday and for the very first time--I've not progressed! I see him every 5 months. It took time but I can really say that the LDN hs slowed my progression. I can't say if it has stopped it but definately it has slowed down. In 2003 I was walking, living a normal life. 2004, I was limping. 2005, Using a walker and 2006, using a chair. I was progressing very fast and probably by now I'd be in bed , I think, if it were not for LDN. So, please give it a try! You've nothing to lose and can gain a lot. It doesnt cost much and the only side effects I have had were a little weight loss, which is welcome because I was on steroids for 1 year and gained 60 lbs, and vivid dreams which I like! So--its only been good for me. Nola in California [sPAM] Re: [low dose naltrexone] Re:LDN Hi all, Do any of you take LDN for MS? I have recently been diagnosed with PPMS and it is really cripppling me. I have become disabled. I can no longer walk, I am wondering if LDN will help me. I am desperate. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 19, 2008 Report Share Posted March 19, 2008 Very cute too! Sounds like he's quite the guy.... Janice [sPAM][ ] ! [] [] Good for ! I've been wondering about his progress. We hear lots about his diet challenges- but not so about his speech progress. It is still very true that once they learn what words can do for them- they never stop talking again. Wait till he's babbling to you in the car- than you know all your work has done wonders! > > was standing there holding his cup and said to me: I want water. > It's empty. > > Getting better every day. I love it! > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 20, 2008 Report Share Posted March 20, 2008 The speech generally has been on the climb for a good while. Still, you know how it is, you get scared to talk about it lest something goes south. The articulation and the sheer number of words are the big win. The gains started really coming once we got self-initiated speech. We still have things to concern ourselves with (his legs) but we are surely in a happy place. The big gains were solidified recently with his sister stuck home from school for 2 weeks with the flu. He had to fight to get a word in edgewise and he did! The Prompt therapy is the thing I credit with initially planting the seed of " if you talk you will be heard and if you don't you will be left out. " That was something neither EI nor I could get across consistently. We were hoping preschool would do that but he has not gotten there due to illnesses with one of us each week for the past month. > > > > was standing there holding his cup and said to me: I want > water. > > It's empty. > > > > Getting better every day. I love it! > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 20, 2008 Report Share Posted March 20, 2008 I believe him to be so...as all of our children are. The thing I love about all kids, not just my own, is their resilience. I'd love to bottle that. > > > > was standing there holding his cup and said to me: I want > water. > > It's empty. > > > > Getting better every day. I love it! > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 20, 2008 Report Share Posted March 20, 2008 Liz, Looks like our boys are definetely zooming thanks to PROMPT! therapy. It is amazing how it moves them right along. Great news on and his " spring forward " mode. Colleen [ ] Re: ! The speech generally has been on the climb for a good while. Still, you know how it is, you get scared to talk about it lest something goes south. The articulation and the sheer number of words are the big win. The gains started really coming once we got self-initiated speech. We still have things to concern ourselves with (his legs) but we are surely in a happy place. The big gains were solidified recently with his sister stuck home from school for 2 weeks with the flu. He had to fight to get a word in edgewise and he did! The Prompt therapy is the thing I credit with initially planting the seed of " if you talk you will be heard and if you don't you will be left out. " That was something neither EI nor I could get across consistently. We were hoping preschool would do that but he has not gotten there due to illnesses with one of us each week for the past month. > > > > was standing there holding his cup and said to me: I want > water. > > It's empty. > > > > Getting better every day. I love it! > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 20, 2008 Report Share Posted March 20, 2008 This therapist is good. He only goes once per week and we don't wind up going every week due to illness but he still improves. The old EI therapist suspects part of it is him wanting to please her since all of his other girlfriends left him after he aged out. I see that at play, the little flirt! > > > > > > was standing there holding his cup and said to me: I want > > water. > > > It's empty. > > > > > > Getting better every day. I love it! > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 11, 2009 Report Share Posted March 11, 2009 i'm really scared at the moment because my heart rate has been crazy high for the past 2 weeks. i was hospitalized and told i have tachycardia. the doctor said nothing else. i'm also have sharp stabbing chest pains and twitching. has this happened to anyone else? i'm soo scared. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 17, 2009 Report Share Posted March 17, 2009 > >Hi- I feel for you. I just went thru my bout with tachycardia myself and I am 3 yrs post explant. I did have a catheter ablation done for 1 problem they found during an EPS study, which needs to be done by a cardiologist trained specifically in that area. And the only way to get to the bottom of your heart issues, is to see a cardiologist. But, I will add this. In my case, I have fibromyalgia/chronic fatigue since implant rupture, and have not been supplementing and supporting my body as I should be for this condition. I just started taking Corvalen M and will start Co-Q10 to help my heart function. I already feel a difference. Dr. Kolb's Silicone Protocol has so much information on there that may be pertinent to your condition. She sees alot of patients with " heart " issues, ranging from infection , toxins, and then again, real heart issues that have to be addressed. Good luck to you and I am doing really well after my procedure, if it comes to that for you. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2009 Report Share Posted March 29, 2009 , I'm so pleased for you and proud of you! Congratulations, big time! Harper ************** Feeling the pinch at the grocery store? Make meals for Under $10. (http://food.aol.com/frugal-feasts?ncid=emlcntusfood00000002) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 10, 2009 Report Share Posted June 10, 2009 > So, After i painted my room with y-shield i started feeling even worse , > the only reason I could think that was the cause is that the paint is > grounded to the electrical ground somwhere, and since the ground caries rf > , that is probably reradiating that back to me from the paint. > > Ok so after one month of delaying I got an electrician to come to my house > to help me troubleshoot this problem. > > We completely disconnected the ground cpnnection to all outlets from my > room and to his and my surprise the paint was still grounded and had just > as strong a ground as before. He told me its possible that the ground > could be coming from the wall because one of my walls is made of plaster > ( I had no idea) because plaster contains minerals an stuff it can be > conductive. Then when we were testing one of the outlets to check if it > was grounded ( btw my house is grounded by flex cable not with a ground > wire to each outlet) and the ground was disconnected from my room so there > was supposed to be no ground from the metal case but the oulet tester > showed that it was grounded! Now we knew that my entire plaster wall was > grounded because the metal case was touching the plaster, we tested the > plaster to see if indeed it was grounded an it was. > > Even though the yshield paint isnt directly touching the plaster because > of 5-6 coats of paint underneath, Im guesiing its still grounded by it > because the previews layers still have a little conductivity and the area > is so large and its also probably touching directly in a few small areas. > > > The only solution he came up with was to take the paint off from that wall > and repaint it with a paint called lastatamedic that is like a plastic so > there would be no conductivity between the y shield and the plaster when i > paint with y-shield over it. > > Any other suggestions on how to Fix this problem will be appreciated.! > > (btw hes the coolest guy I explained to him what Im doing and he was very > interested and open minded about it. He also told me that he used to do > surveys in my area for the electric company and that many people made > complains about the power lines and cell towers making them feel bad here. > > Sorry is some parts may sound confusing or dont make sense Im kinda tired > and sick. > > Cristian Cristian, Before you go through all the trouble or repainting, consider the following: 1- If the plaster was grounded before painting, then the paint is grounded as well, how is grounding related to your symptoms becoming worse with paint? 2- Have you checked with an RF meter? It seems to me that a proper diagnosis before re-painting might be wise. 3- A large conductive object (such as the conductive paint or the plaster) IS a ground. The more massive the conductive material, the better the ground. Think of ground as a reservoir of electrons. Earth is the most massive ground we have access to, but not the only ground. How are you testing for ground? Emil Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 10, 2009 Report Share Posted June 10, 2009 > So, After i painted my room with y-shield i started feeling even worse , > the only reason I could think that was the cause is that the paint is > grounded to the electrical ground somwhere Maybe you're also reacting to offgassing from the paint? Are you chemically sensitive as well? Marc Quote Link to comment Share on other sites More sharing options...
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