Guest guest Posted January 9, 2006 Report Share Posted January 9, 2006 Welcome to our group. Welcoming you to our support and information " family " is like a double edged sword. I'm glad that you found us, but I am sorry that it is under these conditions. Hopefully you were able to locate us soon enough to where we can educate and guide you before this type of exposure gets out of control. As you can see, you will find excellant information and guidance by many of what we call the " Olde Moldies " and some of the excellant professionals we have on the board. It effects many individuals differently and the levels of severity, effecting many different systems. Including mentally, physically, emotionally and definately financially. There are some situations that are unavoidable when you have many ill and desperate individuals looking for a quick cure/answers and a silver bullet. There isn't any. In order to overcome the affects of mold exposure it is a long, drawnout, strict process that will include many protocols in order to recover to a somewhat normal life. Since we have had many new members join it is difficult at times for me to address each and everyone, that's why we have many people on this board that will offer help and you will get to know them. If you would like more one on one assistance you can contact me personally by email and at that time to make it easier I can send you my number. Or to save on long distance costs I can call you. I hope you will find the answers and the guidance you are looking for. KC, Moderator Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2006 Report Share Posted January 9, 2006 Hi, I just joined the group. I am a mother to an 8 year old with PDD/developmental delay. My son and my husband tested positive for lyme disease though I didn't. I have CFS like symptoms with lots of aches and pains and flu like symptoms on and off. We all got good relief from our symptoms when we moved from OR to AZ and I started looking into mold issues. Recently when I tested my son and myself for HLA (to rule out lyme autoimmunity), I found out (from 'Mold Warriors') that my son has the dreaded HLA combination for mold, so is my husband and I am 'multisusceptible'. We have an appointment with Dr. SHoemaker for the end of this month. I can't wait for it. The more I read his book, the more I am able to connect the pieces in my son. Did anyone get tested and treated for CoagNegStaph ? What are the experiences ? Thanks Jay tigerpaw2c <tigerpaw2c@...> wrote: Welcome to our group. Welcoming you to our support and information " family " is like a double edged sword. I'm glad that you found us, but I am sorry that it is under these conditions. Hopefully you were able to locate us soon enough to where we can educate and guide you before this type of exposure gets out of control. As you can see, you will find excellant information and guidance by many of what we call the " Olde Moldies " and some of the excellant professionals we have on the board. It effects many individuals differently and the levels of severity, effecting many different systems. Including mentally, physically, emotionally and definately financially. There are some situations that are unavoidable when you have many ill and desperate individuals looking for a quick cure/answers and a silver bullet. There isn't any. In order to overcome the affects of mold exposure it is a long, drawnout, strict process that will include many protocols in order to recover to a somewhat normal life. Since we have had many new members join it is difficult at times for me to address each and everyone, that's why we have many people on this board that will offer help and you will get to know them. If you would like more one on one assistance you can contact me personally by email and at that time to make it easier I can send you my number. Or to save on long distance costs I can call you. I hope you will find the answers and the guidance you are looking for. KC, Moderator FAIR USE NOTICE: Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2006 Report Share Posted January 9, 2006 I did. I know others have. I had a bad reaction to one of the antibiotics used, but was told that's not usually the case. I did feel better for a bit after that, and was happy to be breathing better than I had in years. I think it's come back already, though. So I'll be looking into that very shortly. Good luck on your visit! I hope you and your family feel better soon. jay krishnaa <jkrishnaa@...> wrote: Did anyone get tested and treated for CoagNegStaph ? What are the experiences ? Serena There is no such thing as an anomaly. Recheck your original premise. ...Ayn Rand, paraphrased --------------------------------- Photos Ring in the New Year with Photo Calendars. Add photos, events, holidays, whatever. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2006 Report Share Posted January 9, 2006 Hi Serena, Thank you for sharing your response. Why do you think the CoagnegStaph is back ? Is it possible that your bad reaction to one of the antibiotics was a herx due to addressing some bacteria ? My son and my husband also have tested high positive for bartonella, so I am waiting to combine treatment (if CNS is also present) as Rifampin is used to treat bart also. Thanks Jay > Did anyone get tested and treated for CoagNegStaph ? What are the experiences ? > > > > Serena > > There is no such thing as an anomaly. Recheck your original premise. > ... Ayn Rand, paraphrased > > > > > --------------------------------- > Photos > Ring in the New Year with Photo Calendars. Add photos, events, holidays, whatever. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2006 Report Share Posted January 9, 2006 Jay, We had visited Dr.Shoemaker within the last few months so it's too early to give you any type of results for except my wife has two staph infections. She will be starting on the antibodics this month, possibly. We'll let you know in the future the outcome. KC > Did anyone get tested and treated for CoagNegStaph ? What are the experiences ? > > > > Serena > > There is no such thing as an anomaly. Recheck your original premise. > ... Ayn Rand, paraphrased > > > > > --------------------------------- > Photos > Ring in the New Year with Photo Calendars. Add photos, events, holidays, whatever. > > Quote Link to comment Share on other sites More sharing options...
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