Guest guest Posted September 9, 2003 Report Share Posted September 9, 2003 Hi, I'm not sure what your name is? But I'm glad that your here. This is a wonderful group of ladies. :-) Hugs~ Donna Lay EDD 10/25/03 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 9, 2003 Report Share Posted September 9, 2003 Welcome Tammy New to the group > Good morning, > > I have just joined the group and wanted to say hello to everyone. I > had a tubal ligation over 10 years ago because my husband at the time > didn't want any more children (I have a son)and now that I am re- > married to a wonderful man I am anxious to have the reversal so we > can try to expand our family. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 9, 2003 Report Share Posted September 9, 2003 Welcome Tammy New to the group > Good morning, > > I have just joined the group and wanted to say hello to everyone. I > had a tubal ligation over 10 years ago because my husband at the time > didn't want any more children (I have a son)and now that I am re- > married to a wonderful man I am anxious to have the reversal so we > can try to expand our family. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 9, 2003 Report Share Posted September 9, 2003 Welcome Tammy New to the group > Good morning, > > I have just joined the group and wanted to say hello to everyone. I > had a tubal ligation over 10 years ago because my husband at the time > didn't want any more children (I have a son)and now that I am re- > married to a wonderful man I am anxious to have the reversal so we > can try to expand our family. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 9, 2003 Report Share Posted September 9, 2003 Welcome Tammy and best wishes on your TR journey! Hugs, > Good morning, > > I have just joined the group and wanted to say hello to everyone. I > had a tubal ligation over 10 years ago because my husband at the time > didn't want any more children (I have a son)and now that I am re- > married to a wonderful man I am anxious to have the reversal so we > can try to expand our family. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 9, 2003 Report Share Posted September 9, 2003 Welcome, Tammy! New to the group Good morning, I have just joined the group and wanted to say hello to everyone. I had a tubal ligation over 10 years ago because my husband at the time didn't want any more children (I have a son)and now that I am re- married to a wonderful man I am anxious to have the reversal so we can try to expand our family. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 9, 2003 Report Share Posted September 9, 2003 Welcome Tammy! I had my TL 10 years ago this December and we are saving for my TR. These ladies are great for answering questions!! I am pretty new too. Lesley New to the group Good morning, I have just joined the group and wanted to say hello to everyone. I had a tubal ligation over 10 years ago because my husband at the time didn't want any more children (I have a son)and now that I am re- married to a wonderful man I am anxious to have the reversal so we can try to expand our family. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 15, 2003 Report Share Posted September 15, 2003 What aprt of ky im from russell co . New to the group HELLO EVERYONE. FIRST LET ME SAY THANKS FOR ALLOWING ME TO JOIN THE GROUP. MY NAME IS MELISA SLONE. I AM FROM KENTUCKY, ABOUT FOUR HOURS FROM DR LEVIN. MY JOURNEY HAS JUST BEGUN. I WOULD LIKE TO GET A TR ASAP SO I CAN USE ALL YOUR ADVICE. ALL YOUR HELP WILL BE GREATLY APPRECIATED. THANKS A BUNCH MELISA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 15, 2003 Report Share Posted September 15, 2003 --- Welcome Melisa! Jump in ask questions, and learn alot here. hugs~~kelly In TubalLigationReversal , " melisa310 " wrote: > HELLO EVERYONE. FIRST LET ME SAY THANKS FOR ALLOWING ME TO JOIN THE > GROUP. MY NAME IS MELISA SLONE. I AM FROM KENTUCKY, ABOUT FOUR HOURS > FROM DR LEVIN. MY JOURNEY HAS JUST BEGUN. I WOULD LIKE TO GET A TR > ASAP SO I CAN USE ALL YOUR ADVICE. ALL YOUR HELP WILL BE GREATLY > APPRECIATED. > THANKS A BUNCH > MELISA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 15, 2003 Report Share Posted September 15, 2003 wecome melissa.you will get lots of advice from here.Dr.Levin did my surgery and he is the greatest.you will love him and venica. Amy > HELLO EVERYONE. FIRST LET ME SAY THANKS FOR ALLOWING ME TO JOIN THE > GROUP. MY NAME IS MELISA SLONE. I AM FROM KENTUCKY, ABOUT FOUR HOURS > FROM DR LEVIN. MY JOURNEY HAS JUST BEGUN. I WOULD LIKE TO GET A TR > ASAP SO I CAN USE ALL YOUR ADVICE. ALL YOUR HELP WILL BE GREATLY > APPRECIATED. > THANKS A BUNCH > MELISA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 5, 2005 Report Share Posted January 5, 2005 Leroy, Have been going through a really rough time myself, or would have said hello sooner! Welcome to this group and hope that you get as much out of it as I do! The people here are awesome and are my new best friends and family, even though I really do love my other family! You will find great answers to questions and find that many of us even speak to one another on the phone! I really hope that you find the support and help that you need here and also some new friends! I am also 40 and have RSD in my right knee and have had it for 2 and 1/2 years, so already feel like we have something in common. I also fell at work! Well I hope that you write soon and keep in touch with us all! LOL and Best Wishes Always!!! Dawnjomal1@... wrote: Hi all, Please help me to Welcome Leroy, who sent this to me directly... Leroy, welcome to the group. I'm sure you will find lots and lots of caring and compassion here.. Hugs, Jo Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 9, 2005 Report Share Posted May 9, 2005 Hi , I just wanted to welcome you to the group. This is truly a wonderful group to be a part of. I have found much support from many wonderful ladies. Jump right in and don't be afraid to ask questions. We all try to help when we can and offer words of encouragement. Best of luck to you! Lyn 26, UD pregnant w/ #1 6weeks!!! -- New to the Group Hello all- My name is and I am new to this group. I have known for about 2 years that I have a septate uterus. I have been married for almost 2 years and we are starting to talk about trying to conceive. I am really nervous about what will happen because of the septate. I just wanted to say hi and I am glad I found some support. Share bookmarks: http://groups.yahoo.com/group/MullerianAnomalies/links/ Share files: http://groups.yahoo.com/group/MullerianAnomalies/files/ The Congenital Uterine Anomalies Home Page: http://www.wegrokit.com/uterineanomalies/ es/ The Congenital Uterine Anomalies Home Page: http://www.wegrokit.com/uterineanomalies/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 9, 2005 Report Share Posted May 9, 2005 Hi and welcome! This board is great...there are lots of SU mommys here, so I'm sure there will be many ladies who can answer any of your questions. Wishing you all the best... UU, 30 DS 8-31-03 2 m/cs Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 10, 2005 Report Share Posted May 10, 2005 , Welcome! You'll find lots of support and help on this site. Many women have SU's and don't ever discover it and never have a problem with any pregnancy. Many of us have had the 50/50 chance of where the baby implants either on the septum or on a " good " spot. Ask lots of questions and be satisfied with the answers your doctor gives you. I've had one successful pregnancy with a septum. I have had the septum removed now per my doctors recommendation and will see how things work with a new pregnancy. Good luck! Kari SU removed 8/04 ds 6/02 mc x2 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2005 Report Share Posted May 14, 2005 Hi I have a question I hope you don't mind ... Are you sure you have a SU? A few women in this board, myself included, have been misdiagnosed. For instance I was told for +10 years I was BU and I was infact SU. Apparently (if you read the FILES section here) the best way to diagnose SU or BU (or sometimes a combination of both) is to have a lap/hyst = laparoscopy (look at the uterus from the outside) and hysteroscopy (look at the uterus from the inside) ... This is usually done under general anesthesia because it's surgery (outpatient procedure but surgery anyway) - If you happen to be SU then the dr usually can perform the resection at that very moment (that was my case last march). Please keep us posted and good luck with your August appt. Gabi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 16, 2005 Report Share Posted May 16, 2005 Gabi- You know I don't know if I am infact SU. As I am sure you have read my other post about me getting pregnant when I was 17 and terminating the pregancy because of my parents. It wasn't until about 3 or 4 years later that I got my medical records and saw that they had put on my sheet that I was SU. I have never talked to my doctor about it so I am going to ask in August. I appreciate your questions and I will keep you updated about what the doctor says. Gabi gabi151@...> wrote: Hi I have a question I hope you don't mind ... Are you sure you have a SU? A few women in this board, myself included, have been misdiagnosed. For instance I was told for +10 years I was BU and I was infact SU. Apparently (if you read the FILES section here) the best way to diagnose SU or BU (or sometimes a combination of both) is to have a lap/hyst = laparoscopy (look at the uterus from the outside) and hysteroscopy (look at the uterus from the inside) ... This is usually done under general anesthesia because it's surgery (outpatient procedure but surgery anyway) - If you happen to be SU then the dr usually can perform the resection at that very moment (that was my case last march). Please keep us posted and good luck with your August appt. Gabi Share bookmarks: http://groups.yahoo.com/group/MullerianAnomalies/links/ Share files: http://groups.yahoo.com/group/MullerianAnomalies/files/ The Congenital Uterine Anomalies Home Page: http://www.wegrokit.com/uterineanomalies/ es/ The Congenital Uterine Anomalies Home Page: http://www.wegrokit.com/uterineanomalies/ --------------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 7, 2006 Report Share Posted January 7, 2006 Welcome , We've all been where you are now ... new to group stuff, afraid for our child, and at our wits end. That's the starting point. For many of us, just finding this group was/is the beginning of our forward progress & our education. The Eggshells book is crucial to understanding bpd, and a couple of other helpful books are Co-Dependent No More, and Boundaries. I highly recommend both. For me, the concept of boundaries to *protect* myself was an eye-opener and a huge part of my ongoing recovery from fear. The Co-Dependent book showed me how, in love, I wasn't allowing my son to gain strength by working through his battles on his own. There's a fine line between supporting & taking on our child's issues ourselves, and it was a line I had trouble initially identifying. I know you'll receive excellent advice from everyone here, as we've all walked in your shoes. Don't give up hope. I'll post an update on my own situation this weekend, as we've seen a real improvement in our 24yr. old son. Maybe even more importantly, I'VE improved!!! I'm learning to claim my own life back, and I'm finding lots of little daily things to give me joy. Hang on, and don't hesitate to share. A burden shared is often a burden lightened. Joan ----Original Message Follows---- Reply-To: WTOParentsOfBPs To: WTOParentsOfBPs Subject: New to the group Date: Sat, 07 Jan 2006 14:39:34 -0000 Hello, I am new to this group stuff and really have no clue at all about using these groups. I found my way here by reading the book " Stop Walking on Eggshells " This group was recommended in the book. My daughter had a most difficult year(2005). Hospitalized twice and has been in ongoing therapy for almost 2 years/ She is 15. She has just begun DBT. A good part of my battle is just getting her there, let alone for her to participate. She is very resistent. I am afraid. I will be the one using the skills learned and really question if she will ever be capable. I am afraid for my daughter, for not only what today will bring, but tomorrow will bring as well. I am at wits end and can use any helpful info. Thanks, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 13, 2006 Report Share Posted January 13, 2006 Hi : I don't normally post - but read the postings continuously. Wanted to welcome you personally. I, as well, have a 16 year old daughter with BPD. She is currently in a residential treatment center, which utilizes DBT. In a nut-shell - baby steps forward, a few steps backward. Progress is slow, but I feel that there is not a quick fix to this life-long illness (which I reitterate to my daughter (and family) constantly). It is a long road we are traveling. Wishing you and your family the best, and don't hesitate to contact me. geargirl68 geargirl68@...> wrote: Hello, I am new to this group stuff and really have no clue at all about using these groups. I found my way here by reading the book " Stop Walking on Eggshells " This group was recommended in the book. My daughter had a most difficult year(2005). Hospitalized twice and has been in ongoing therapy for almost 2 years/ She is 15. She has just begun DBT. A good part of my battle is just getting her there, let alone for her to participate. She is very resistent. I am afraid. I will be the one using the skills learned and really question if she will ever be capable. I am afraid for my daughter, for not only what today will bring, but tomorrow will bring as well. I am at wits end and can use any helpful info. Thanks, Problems? Ask our friendly List Manager for help, @.... SEND HER ANY POSTS THAT CONCERN YOU; DO NOT RESPOND ONLINE. Essential reading to help you feel better and understand the BP in your life are: • SWOE ( " Stop Walking on Eggshells”) and the SWOE Workbook (for everyone) • HOPE FOR PARENTS Call 888-35-SHELL () to order your copies. From Randi Kreger, Owner of BPDCentral and the WTO Online Community Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 14, 2006 Report Share Posted January 14, 2006 Hi e, How long has your daughter been in a residential placement? How did that come about? I can only imagine it must have been a most difficult decision. My sister keeps telling me that that is what I should be looking into. You are seeing progress and that must feel good. Thank you for the support and best wishes for you and your family as well. e rachelebohnet@...> wrote: Hi : I don't normally post - but read the postings continuously. Wanted to welcome you personally. I, as well, have a 16 year old daughter with BPD. She is currently in a residential treatment center, which utilizes DBT. In a nut-shell - baby steps forward, a few steps backward. Progress is slow, but I feel that there is not a quick fix to this life-long illness (which I reitterate to my daughter (and family) constantly). It is a long road we are traveling. Wishing you and your family the best, and don't hesitate to contact me. Problems? Ask our friendly List Manager for help, @.... SEND HER ANY POSTS THAT CONCERN YOU; DO NOT RESPOND ONLINE. Essential reading to help you feel better and understand the BP in your life are: • SWOE ( " Stop Walking on Eggshells”) and the SWOE Workbook (for everyone) • HOPE FOR PARENTS Call 888-35-SHELL () to order your copies. From Randi Kreger, Owner of BPDCentral and the WTO Online Community Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 15, 2008 Report Share Posted March 15, 2008 Go to www.canaryclub.org and order an adrenal saliva test. Dont; wonder abotu it. -- Artistic Grooming- Hurricane WV http://www.stopthethyroidmadness.com/ http://health.groups.yahoo.com/group/NaturalThyroidHormonesADRENALS/ http://health.groups.yahoo.com/group/RT3_T3/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 20, 2008 Report Share Posted April 20, 2008 ***Note from Co-Owner: The ending " algia " means pain such as in Fibroyalgia. *** Hello Marci, I know I had heard of FM but always thought it was some sort of cancer. After all most things that end with an " algia " are, right? Imagine when the Doc came in and told me I had this. I started getting light headed. I had to sit down. It's kind of funny now but at that very moment it was a big YIKES! By the way. Mine progressed really fast. I went from annoying pain in my chest to crippling pain in a matter of a few weeks. It took nearly 3 months before I was given the right diagnosis. So far as I can tell we are in the right place. If someone doesn't already know something they know where to look for the answers. The part I like is that we may all have the same thing, but we are still all so different. It gives us a chance to find the ways that might work for us. A little of this and a little of that. We just need the right recipe. ;0) The fog has cleared a little so I'm off to bed while I can still find it. Ha! Take care, Jan > > Hello. My name is Marci and I just found this group. I would love > to talk to other people who have this disease. I am 36 years old and > have been diagnosed for about 3 years. I know they say it doesn't Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 28, 2008 Report Share Posted April 28, 2008 Hi, My name is Doreen and I have just contacted the SSI people and learned I have degenerative RA something, a touchy skin thing, Severe Fibro. degineritive musclar something, We're having fun now! I am from Dover,Delaware and Have been diagnosed since 2004? I am not used to not being active. I have depression from it and anxiety. Memory troubles and I went from a college vocab to maybe a 4th grade vocab if I'm lucky. I try to keep a sense of humor. I am on several medicines. which make my all doped up and they help a little bit. I am very happy to have found all of you and I hope we can learn new ways to beat all of this. Sincerely, The Pagan Pixie Dover,Delaware --------------------------------- Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 28, 2008 Report Share Posted April 28, 2008 Hi Doreen and welcome to the group :-) Hugs, Annie Doreen Pierce thepaganpixie@...> wrote: Hi, My name is Doreen and I have just contacted the SSI people and learned I have degenerative RA something, a touchy skin thing, Severe Fibro. degineritive musclar something, We're having fun now! I am from Dover,Delaware and Have been diagnosed since 2004? I am not used to not being active. I have depression from it and anxiety. Memory troubles and I went from a college vocab to maybe a 4th grade vocab if I'm lucky. I try to keep a sense of humor. I am on several medicines. which make my all doped up and they help a little bit. I am very happy to have found all of you and I hope we can learn new ways to beat all of this. Sincerely, The Pagan Pixie Dover,Delaware --------------------------------- Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now. Quote Link to comment Share on other sites More sharing options...
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