Guest guest Posted April 26, 2005 Report Share Posted April 26, 2005 Welcome Judy. You have found a great group of supportive mito patients. We are here to help and support you. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 26, 2005 Report Share Posted April 26, 2005 Judy Welcome to the group. You have come to the right place to meet others with mito. The group is good at sharing experiences and support. Jump right in when you are ready. We often have various subjects/conversations going on at once, so ask if you get lost in what we are posting. laurie > > > > hi there my name is judy. i have been diagnosed with mito. about 3 > years ago. no one here where i live even my dr. knows about this > disease. i just want to talk to people with it so i know that i am not > alone. thank you for listening to me. > take care > judy > > > > > > > > > > Medical advice, information, opinions, data and statements contained herein > are not necessarily those of the list moderators. The author of this e mail > is entirely responsible for its content. List members are reminded of their > responsibility to evaluate the content of the postings and consult with > their physicians regarding changes in their own treatment. > > Personal attacks are not permitted on the list and anyone who sends one is > automatically moderated or removed depending on the severity of the attack. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 26, 2005 Report Share Posted April 26, 2005 Welcome Judy, You have come to the right place to get support and information I just wanted to say hi and welcome. Donna K ---- thewoodbandits thewoodbandits@...> wrote: > > > > hi there my name is judy. i have been diagnosed with mito. about 3 > years ago. no one here where i live even my dr. knows about this > disease. i just want to talk to people with it so i know that i am not > alone. thank you for listening to me. > take care > judy > > > > > > > > > > Medical advice, information, opinions, data and statements contained herein are not necessarily those of the list moderators. The author of this e mail is entirely responsible for its content. List members are reminded of their responsibility to evaluate the content of the postings and consult with their physicians regarding changes in their own treatment. > > Personal attacks are not permitted on the list and anyone who sends one is automatically moderated or removed depending on the severity of the attack. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 26, 2005 Report Share Posted April 26, 2005 ---Welcome Judy. It is nice to have you on board. Dawn A In , " thewoodbandits " wrote: > > > hi there my name is judy. i have been diagnosed with mito. about 3 > years ago. no one here where i live even my dr. knows about this > disease. i just want to talk to people with it so i know that i am not > alone. thank you for listening to me. > take care > judy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 26, 2005 Report Share Posted April 26, 2005 Judy, Welcome! I am recently diagnosed and struggling with trying to understand all of this and the maze of doctors, tests etc. Just wanted to say hi and hope you stick around! LILQT4U1984@... wrote: Welcome Judy. You have found a great group of supportive mito patients. We are here to help and support you. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 26, 2005 Report Share Posted April 26, 2005 HI Judy, welcome to the group. If you have any questions that you need answered just ask..... and we will do our best to answer them for you. We have alot of people here on the list who are very knowledgable. Have you checked out any of the following sites?: www.umdf.org www.mdausa.org Hugs, Ann-Marie hi there i'm new hi there my name is judy. i have been diagnosed with mito. about 3 years ago. no one here where i live even my dr. knows about this disease. i just want to talk to people with it so i know that i am not alone. thank you for listening to me. take care judy Medical advice, information, opinions, data and statements contained herein are not necessarily those of the list moderators. The author of this e mail is entirely responsible for its content. List members are reminded of their responsibility to evaluate the content of the postings and consult with their physicians regarding changes in their own treatment. Personal attacks are not permitted on the list and anyone who sends one is automatically moderated or removed depending on the severity of the attack. ------------------------------------------------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 26, 2005 Report Share Posted April 26, 2005 Judy, Welcome to the group. I have found this group to be filled with caring and supportive people. I'm sorry for the reason you are here, but glad that you found the group. Smiles, a On Tue, 26 Apr 2005 05:46:26 -0000 " thewoodbandits " thewoodbandits@...> writes: hi there my name is judy. i have been diagnosed with mito. about 3 years ago. no one here where i live even my dr. knows about this disease. i just want to talk to people with it so i know that i am not alone. thank you for listening to me. take care judy Quote Link to comment Share on other sites More sharing options...
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