Guest guest Posted October 30, 2001 Report Share Posted October 30, 2001 Vee, Hi, Welcome to the group. Yes, Dr. Levin is a wonderful doctor. I had my surgery with him in Dec, 2000. He gave me a 75% chance to concieve and I concieved in July but unfortantely I miscarried. So I know his surgery for me was successful. If you have any questions please ask! 26 Misty 30 Ricky 9 Shelby 8 TL 8-27-93 done by a surgeon dumb enough to listen to me *lol* TR 12-18-00 - Dr. Levin Baby Fenton (Angel in Heaven) >From: shazeon01@... >Reply-To: TubalLigationReversal >To: TubalLigationReversal >Subject: new to the group >Date: Mon, 29 Oct 2001 23:34:21 -0000 > >Hi everyone, I am new to the support group. I don't do any online >communicating, except e-mail, so I've been trying to figure out for >about a week how to get on-line so I can learn how to join in on >being supportive. I am looking for help from Dr. Levin. I guess >this is his support group. I have read his info over the net and >just received some literature from him in the mail. I want to have a >baby, carry a baby, be able to lie down with my fiance and know that >thier is a chance that we will be able to become pregnant. And I >have been searching for answers for over ten years now. I'd like to >hear some of the experiences some of you may have had with Dr. >Levin. Is he as good as it all reads? Has he really helped all of >these women become " whole " again? I don't know much about statistics >and all of that, I just want to know is it worth getting my hopes >up. This would be the ultimate dream come true to be able to have >children again. I am tired of being depressed and feeling jealous >when I see a pregnant woman or a newborn child. I want my own, and I >know that God does not condone these negative feelings. I had >inquired about a the operative procedure performed by my surgeon, he >states in his return letter that the procedure he used is >lapaposcopic bipolar tubal fulgeration. That sounds scary and >irreversable, I do not even see where Dr. Levin describes this in his >literature. Is anyone out there familiar with this type of surgery? >If so please respond to me, I am very afraid and becoming discouraged >again. Thanks to you all for letting me join in and God Bless you >all and good luck! >Vee > _________________________________________________________________ Get your FREE download of MSN Explorer at http://explorer.msn.com/intl.asp Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2001 Report Share Posted October 30, 2001 Hi Vee, welcome to the group. Love, Becky Mullen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2001 Report Share Posted October 30, 2001 Welcome to the group. I'm new too. I just joined over the weekend, so everything is still new to me, as well. I can say that these ladies have really been caring and concerned about each of us. It is a loving group and I think you'll like it here. I do! Amethyst Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2001 Report Share Posted October 31, 2001 Welcome to the group qtepy. What's your name? Congrats on your phone consult! You'll feel much better after talking to Dr Levin. It makes it all seem more real. If I can help ya out just hollar,Donna --- qtepy4ever@... wrote: > Just wanted to say that I am new to the group. I am > trying to raise > funds for my TR. My phone consult is 11/9. Does > anyone have any > ideas. Just a note, this group thing is very new to > me and I will > have to train myself on it so please be patient with > me. > > Oh, and just an overview...I am 32 with one child. > I had a TL at the > age of 22 after the birth of my daughter. I have > raised her alone > since day one and have met my soul mate of two years > now and we are > planning our wedding. He has no children. My > prayers are that God > blesses me in the ability to have a TR and that my > husband (to be) > and I can have a family together. > > GOD BLESS ALL OF YOU!!! > > ===== Donna Fannin 34 DH Kenny 33 DD's Angie & 15 & 16 DS (bubby)14 TL 3-15-93 TR 8-20-01 __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 1, 2001 Report Share Posted November 1, 2001 Vee, I didn't have the same procedure done. I had my reversal By Dr L in May 01. I am now 5 1/2 months pg. I do know and believe. If it can be reversed Dr L will do it or attempt to . He his a very wonderful doctor. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 26, 2005 Report Share Posted November 26, 2005 Dear I now eat the whole egg raw. I just put the raw eggs in a drinking glass and break them up with a spoon. Like drinking scrambled eggs. I was just eating the egg yoke when I noticed the pain going away. Here is an article I found on raw eggs. http://www.regenerativenutrition.com/content.asp?id=268 " Kindscher (Charter) " wrote: Hi , Boy Aajonus sure had a very interesting life so far. I know my grandmother ate raw meat all the time, she lived to be 99 years old with no illness, other then some diemtia the last year. How do you stomach the raw eggs that just seems gross. This is something I will have to spend some more time reading about. I already use raw milk and raw cheese, just not raw meat and eggs. Thanks for sharing. http://www.rawpaleodiet.org/ I don't stick with the diet 100% but I try and get as close as I can. When I started drinking raw cow milk my headaches quit. I also experienced fast pain relief after eating raw chicken egg yokes. My health is improving. Its a slow process! I wish it was quick. Here is another website I highly recomend reading everything on it. http://www.drbass.com/index.html This interview with Aajonus Vonderplanitz will blow your mind away http://www.drbass.com/aajonus.html The interview is a bit long but well worth reading. Neither of these two web sites are mine. Just out spreading the word. I live in Louisiana and work for the US postal service. Costanza --------------------------------- Yahoo! Music Unlimited - Access over 1 million songs. Try it free. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2008 Report Share Posted January 2, 2008 Thank you for your response Norma, I wish there were some friends or family willing to help out, but that avenue has been exhausted. It's just him. I can't do it because I haven't earned the trust of his loved one yet. I can help with a lot of things, but I'm not allowed to help with meds, restroom trips, showers or baths, or helping to get dressed. I just clean and try to hold a conversation with his loved one as often as possible. Re: New to the group Hi Holly, How wonderful of you to write. You have every reason to be concerned because caregiving can certainly take its toll. Since I don't know the specifics of the situation, I can't comment directly but the most important thing--IF AT ALL POSSIBLE--is for your man to get help so he can have a life. Is there any way he can get someone to relieve him a few days a week (for two or three hours a day)? How about two hours two times a week? Can he go out for two hours while you clean? And then can someone else relieve both of you for an evening each week so that you can go out? I would also suggest that he exercise whenever he can to relieve the stress. Hope this helps a little, Norma " wonderingwhattod o " <wonderingwhattod To o@...> LBDcaregivers@ yahoogroups. com Sent by: cc LBDcaregivers@ yah oogroups.com Subject New to the group 01/02/2008 01:04 PM Please respond to LBDcaregivers@ yah oogroups.com Hi to everyone, my name is Holly and I'm new to the group. I've heard such great things about this group and I am seeking some advice. My situation is a bit different thou, I am not a direct caregiver. I have fallen in love with someone who is a caregiver. Someone that spends all day, every day in the same four walls. He receives no help from friends or family, just me and most of the time I don't know what I can do. I always feel so helpless. We talk about LBD from time to time, but he mostly talks with all of you, and I am ok with that. In fact, I am thankful for this group and giving him other people that can relate to him better than I. But what really concerns me is him and his condition. While he says he isn't stressed out, the stress is taking its toll physically on him. All sorts of things are started to go wrong or pop up. I think he feels no one understands him (excluding the group). That he is going stir crazy being inside all day, every day. He gets no relief, so he can't get out at all. I even feel that he doesn't think I understand. I feel I do understand, I just don't go thru the same exact experiences he does. I have the freedom to come and go. And I don't know how I can help him. When I can, I help with his loved one, or I will help with house work. But my main concern is for him. He is the love of my life and I want to spend the rest of my life with him. I'm just afraid that there may be nothing left of him by the time this is over. In a couple of years, I may have to be his caregiver. What can I do to help him? Thank you Holly Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2008 Report Share Posted January 2, 2008 Holly - Welcome to the group. I can think of a few things you can do to help out the person who is caring for their loved one. * Just 'being there' for him is a great help. You are his outlet, when someone is a 24/7 caregiver having someone who visits and talk about what the rest of the world is doing is great. * You can continue to 'be there' for his loved one - a different face, someone different to talk with is wonderful for the loved one. Even your visiting with his loved one allows him to break free and do some things around the house that needs to get done. * You can do research. Caregiving takes a lot of time - if you can do the research for him I'm sure he'll be appreciative. Find in-home caregivers in his area, that are free (volunteers) or inexpensive could help. With your help he could find a caregiver who would allow him to get out and do something out of the house with you. Do the research of adult day centers - the costs and etc. which would also allow you & him to get a break. There's tons of stuff in our Links section that he may not have had the chance to look into - but you can do the research for him. http://health.groups.yahoo.com/group/LBDcaregivers/links/ * Housekeeping is always welcome. Running errands is a huge help too. If you work it out so that he can come to this board and pose questions and/or vent, and you utilize the board as a research area - I bet that would be very helpful for him. And again... just your being there for him may be all that he needs. Thank you for caring for the caregiver! > > Hi to everyone, my name is Holly and I'm new to the group. I've heard > such great things about this group and I am seeking some advice. My > situation is a bit different thou, I am not a direct caregiver. I > have fallen in love with someone who is a caregiver. Someone that > spends all day, every day in the same four walls. He receives no help > from friends or family, just me and most of the time I don't know what > I can do. I always feel so helpless. We talk about LBD from time to > time, but he mostly talks with all of you, and I am ok with that. In > fact, I am thankful for this group and giving him other people that > can relate to him better than I. But what really concerns me is him > and his condition. While he says he isn't stressed out, the stress is > taking its toll physically on him. All sorts of things are started to > go wrong or pop up. I think he feels no one understands him (excluding > the group). That he is going stir crazy being inside all day, every > day. He gets no relief, so he can't get out at all. I even feel that > he doesn't think I understand. I feel I do understand, I just don't > go thru the same exact experiences he does. I have the freedom to > come and go. And I don't know how I can help him. When I can, I help > with his loved one, or I will help with house work. But my main > concern is for him. He is the love of my life and I want to spend the > rest of my life with him. I'm just afraid that there may be nothing > left of him by the time this is over. In a couple of years, I may > have to be his caregiver. What can I do to help him? Thank you Holly > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2008 Report Share Posted January 8, 2008 Hello and Good Evening; My name is Charla and I am 45 years old. My father has LBD and PSP. He was diagnosed a little over a year and a half ago. My husband and I sold our house which was 2 1/2 hours away from my home town and moved in with my dad to take care of him because I was not going to put him in a NH. His disease has progressed and the last few days he has been sleeping a lot. I have told him it is okay to let go and I asked him if he was holding on for me and he shook his head yes. I told him not to. I love my dad very much and this has been a up and down roller coaster ride from the beginning. I'm really not ready to say goodbye, but he has no quality of life anymore as he is totally incontinent and has been for months and can no longer walk or stand on his own. I just wish he still had his mind. He has worked so hard all of his life and next week he will be 78 years old. He is a strong man and a fighter which shows as last October the Neurologist said he had 3 months to live if he was lucky, he has surpassed that by far and although he has had bad days before; this seems different. He has aspirated more and he has to have all food pureed and liquids thickened to honey consistency. Hope to gain some peace through all of this. Blessings, Charla Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2008 Report Share Posted January 9, 2008 Hi, Charla, Welcome to the list. I'm sending prayers and hugs your way. Gladys -- New to the Group Hello and Good Evening; My name is Charla and I am 45 years old. My father has LBD and PSP. He was diagnosed a little over a year and a half ago. My husband and I sold our house which was 2 1/2 hours away from my home town and moved in with my dad to take care of him because I was not going to put him in a NH. His disease has progressed and the last few days he has been sleeping a lot. I have told him it is okay to let go and I asked him if he was holding on for me and he shook his head yes. I told him not to. I love my dad very much and this has been a up and down roller coaster ride from the beginning. I'm really not ready to say goodbye, but he has no quality of life anymore as he is totally incontinent and has been for months and can no longer walk or stand on his own. I just wish he still had his mind. He has worked so hard all of his life and next week he will be 78 years old. He is a strong man and a fighter which shows as last October the Neurologist said he had 3 months to live if he was lucky, he has surpassed that by far and although he has had bad days before; this seems different. He has aspirated more and he has to have all food pureed and liquids thickened to honey consistency. Hope to gain some peace through all of this. Blessings, Charla Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2008 Report Share Posted January 9, 2008 HI Charla and welcome to the group. Your post tugged at my heart. It is so hard to watch our LO's quality of life decline. We just never know how far this darned disease will take our LO's. My mom has been bed-bound for a few years now and I wrestle with the issue of wanting her here yet acknowledging that her quality of life is nil. Sending you, your father and husband strength for the road ahead. Courage Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2008 Report Share Posted January 9, 2008 --- Dear Charla, Welcome to the group.Youll find many wonderful caring caregivers here.Im Ron and I take care of my mother with lbd in her home.I know the sacrifices youve had to make moving home first hand..My heart goes out to you, your husband and your dear father.My heartfelt best to you Ron In LBDcaregivers , " Gladys Stefany " wrote: > > Hi, Charla, > > Welcome to the list. I'm sending prayers and hugs your way. > > Gladys > > -- New to the Group > > Hello and Good Evening; > > My name is Charla and I am 45 years old. My father has LBD and PSP. He was > diagnosed a little over a year and a half ago. My husband and I sold our > house which was 2 1/2 hours away from my home town and moved in with my dad > to take care of him because I was not going to put him in a NH. His disease > has progressed and the last few days he has been sleeping a lot. I have > told him it is okay to let go and I asked him if he was holding on for me > and he shook his head yes. I told him not to. I love my dad very much and > this has been a up and down roller coaster ride from the beginning. I'm > really not ready to say goodbye, but he has no quality of life anymore as he > is totally incontinent and has been for months and can no longer walk or > stand on his own. I just wish he still had his mind. He has worked so hard > all of his life and next week he will be 78 years old. He is a strong man > and a fighter which shows as last October the Neurologist said he had 3 > months to live if he was lucky, he has surpassed that by far and although he > has had bad days before; this seems different. He has aspirated more and he > has to have all food pureed and liquids thickened to honey consistency. > > Hope to gain some peace through all of this. > > Blessings, > > Charla > > Quote Link to comment Share on other sites More sharing options...
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