Guest guest Posted January 18, 2006 Report Share Posted January 18, 2006 Hi Peggy Sue, Yeah, dry eyes is one of the symptoms of this autoimmune disease, AND a side effect of some of the meds we take. I figure it's the least of our problems LOL. BUT, among us, no problem is too small to mention, we is all we got and all we got is we! (gentle) hugggggs Alice in Alaska http://maryals.blogspot.com/ On Jan 18, 2006, at 12:36 PM, peggy sue wrote: > Hi to all, > Just wanted to give a quick thanks shout to all of you who have > listened. I am new to the group (Jan. 2006), and joined because I > was in denial for so long. It was great to know that I was not > alone in my feelings. I take 10mg of methotrexate a week, and > Daypro (NSAIDS) for imflammation. The daypro has started really > messing up my stomach. The last few times I have taken it, I spend > the next day in the bathroom. I am trying different ways to take > it. The dr suggested I take it with pepto or prilosec or something > like that. It helps but still upsetting. A new side affect is my > eyes. I can't seem to be able to wear my contacts any more. Anyone > else have that problem? I have been wearing contacts for 30 years > with no problems. Now it seeems like my eyes can't breathe with the > contacts in. Guess I am stuck with glasses for now. > Thanks again for being my support, I hope in the future I too can > be some support. > Peg > > > --------------------------------- > 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 20, 2006 Report Share Posted January 20, 2006 Hi, I don't think I've seen you post here before and I just wanted to say welcome. This is a wonderful group with lots of support!!! I hope you find what yous eek here. If you ever need to talk, feel free to contact me. Yanosz Descouedresz Email: yanosz@... On : yanoszd The Road goes ever on and on Down from the door where it began. Now far ahead the Road has gone, And I must follow, if I can, Pursuing it with eager feet, Until it joins some larger way Where many paths and errands meet. And whither then? I cannot say. [ ] Thanks > Hi to all, > Just wanted to give a quick thanks shout to all of you who have listened. I am new to the group (Jan. 2006), and joined because I was in denial for so long. It was great to know that I was not alone in my feelings. I take 10mg of methotrexate a week, and Daypro (NSAIDS) for imflammation. The daypro has started really messing up my stomach. The last few times I have taken it, I spend the next day in the bathroom. I am trying different ways to take it. The dr suggested I take it with pepto or prilosec or something like that. It helps but still upsetting. A new side affect is my eyes. I can't seem to be able to wear my contacts any more. Anyone else have that problem? I have been wearing contacts for 30 years with no problems. Now it seeems like my eyes can't breathe with the contacts in. Guess I am stuck with glasses for now. > Thanks again for being my support, I hope in the future I too can be some support. > Peg > > > --------------------------------- > 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 26, 2006 Report Share Posted January 26, 2006 You're welcome, . Take care, > > > Just wanted to say thank you for emailing me that article about little > Nolan. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 26, 2006 Report Share Posted January 26, 2006 You're welcome, . Take care, > > > Just wanted to say thank you for emailing me that article about little > Nolan. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 2, 2006 Report Share Posted March 2, 2006 Carolyn, I have been reading all of your posts and I only want to tell you that personally I think your PT needs to be more open minded. It is not HER child! And if, in your heart of hearts, you think banding is best then go for it. We are also at CT in Paramus. My husband and I were also turned off by our consult but decided to go with it. Our therapist there, , has been super wonderful. We graduate a week from tomorrow and I can say it is without one single regret! Good luck! Meagancarolyn fox <cdfox@...> wrote: I was skeptical when our PT showed me how to apply pressure on Malcolm’s skull with my fingertips. Ok, now I know that it’s not me. My husband and I had already agreed before we met Wanda at cranial technologies about getting the band for Malcolm. If cranial technologies thought a band was warranted, we agreed that we would proceed on getting him the band asap. We were impressed with the results other parents have had and didn’t think there was much of a choice in eventually getting our son a helmet. When I told our PT about seeing cranial technologies and getting a helmet, she was upset. She doesn’t believe in helmet therapy and thinks they’re only for severe cases. She believes that Malcolm’s plagio and tort are correctable through PT. While I’m not a PT, it doesn’t make sense to me that you can correct plagio and tort solely through PT in Malcolm’s case, especially since he was breech and born with plagio and tort. Malcolm’s head was pressed against my right rib case almost throughout the pregnancy. He only occasionally veered left of my belly button before week 20. After week 20 of my pregnancy, I don’t recall him ever on the left side of my abdomen. I started to self-doubt myself and get more frustrated and confused today when our PT implied that there was a choice in treating Malcolm’s plagio and tort. I really don’t see a choice. Either we band him asap and achieve some level of symmetry and roundness to his head or we don’t and pray that his head will improve in time, which it hasn’t done for 4 months despite aggressive repositioning and pt. Thanks for restoring my confidence and making me think I’m not nuts. I really wish we didn’t have to make these decisions and go through this ordeal. This is a nightmare to me. I know there are plenty of life-threatening circumstances for infants that are more pressing and deserving of attention for doctors, but there must be easier ways dealing with this. Why do doctors, pts, insurance companies, etc. make it so difficult when it doesn’t have to be? They make you feel incompetent, a complete failure for not doing more and leading you to believe that you have the power to correct this when you may not. Thanks again Carolyn in NYC Mum to Malcolm – 4 months old – born breech with plagio and tort Relax. virus scanning helps detect nasty viruses! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 2, 2006 Report Share Posted March 2, 2006 Carolyn, I have been reading all of your posts and I only want to tell you that personally I think your PT needs to be more open minded. It is not HER child! And if, in your heart of hearts, you think banding is best then go for it. We are also at CT in Paramus. My husband and I were also turned off by our consult but decided to go with it. Our therapist there, , has been super wonderful. We graduate a week from tomorrow and I can say it is without one single regret! Good luck! Meagancarolyn fox <cdfox@...> wrote: I was skeptical when our PT showed me how to apply pressure on Malcolm’s skull with my fingertips. Ok, now I know that it’s not me. My husband and I had already agreed before we met Wanda at cranial technologies about getting the band for Malcolm. If cranial technologies thought a band was warranted, we agreed that we would proceed on getting him the band asap. We were impressed with the results other parents have had and didn’t think there was much of a choice in eventually getting our son a helmet. When I told our PT about seeing cranial technologies and getting a helmet, she was upset. She doesn’t believe in helmet therapy and thinks they’re only for severe cases. She believes that Malcolm’s plagio and tort are correctable through PT. While I’m not a PT, it doesn’t make sense to me that you can correct plagio and tort solely through PT in Malcolm’s case, especially since he was breech and born with plagio and tort. Malcolm’s head was pressed against my right rib case almost throughout the pregnancy. He only occasionally veered left of my belly button before week 20. After week 20 of my pregnancy, I don’t recall him ever on the left side of my abdomen. I started to self-doubt myself and get more frustrated and confused today when our PT implied that there was a choice in treating Malcolm’s plagio and tort. I really don’t see a choice. Either we band him asap and achieve some level of symmetry and roundness to his head or we don’t and pray that his head will improve in time, which it hasn’t done for 4 months despite aggressive repositioning and pt. Thanks for restoring my confidence and making me think I’m not nuts. I really wish we didn’t have to make these decisions and go through this ordeal. This is a nightmare to me. I know there are plenty of life-threatening circumstances for infants that are more pressing and deserving of attention for doctors, but there must be easier ways dealing with this. Why do doctors, pts, insurance companies, etc. make it so difficult when it doesn’t have to be? They make you feel incompetent, a complete failure for not doing more and leading you to believe that you have the power to correct this when you may not. Thanks again Carolyn in NYC Mum to Malcolm – 4 months old – born breech with plagio and tort Relax. virus scanning helps detect nasty viruses! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2006 Report Share Posted March 3, 2006 Carolyn, I have been really busy, but have been reading your posts. So my question is........Are you getting a new PT? CAROLG > > I was skeptical when our PT showed me how to apply pressure on Malcolm's > skull with my fingertips. Ok, now I know that it's not me. > > > > My husband and I had already agreed before we met Wanda at cranial > technologies about getting the band for Malcolm. If cranial technologies > thought a band was warranted, we agreed that we would proceed on getting him > the band asap. We were impressed with the results other parents have had > and didn't think there was much of a choice in eventually getting our son a > helmet. > > > > When I told our PT about seeing cranial technologies and getting a helmet, > she was upset. She doesn't believe in helmet therapy and thinks they're > only for severe cases. She believes that Malcolm's plagio and tort are > correctable through PT. > > > While I'm not a PT, it doesn't make sense to me that you can correct plagio > and tort solely through PT in Malcolm's case, especially since he was breech > and born with plagio and tort. Malcolm's head was pressed against my right > rib case almost throughout the pregnancy. He only occasionally veered left > of my belly button before week 20. After week 20 of my pregnancy, I don't > recall him ever on the left side of my abdomen. > > > > I started to self-doubt myself and get more frustrated and confused today > when our PT implied that there was a choice in treating Malcolm's plagio and > tort. I really don't see a choice. Either we band him asap and achieve > some level of symmetry and roundness to his head or we don't and pray that > his head will improve in time, which it hasn't done for 4 months despite > aggressive repositioning and pt. > > > > Thanks for restoring my confidence and making me think I'm not nuts. I > really wish we didn't have to make these decisions and go through this > ordeal. This is a nightmare to me. I know there are plenty of > life-threatening circumstances for infants that are more pressing and > deserving of attention for doctors, but there must be easier ways dealing > with this. Why do doctors, pts, insurance companies, etc. make it so > difficult when it doesn't have to be? They make you feel incompetent, a > complete failure for not doing more and leading you to believe that you have > the power to correct this when you may not. > > > > Thanks again > > > > Carolyn in NYC > > Mum to Malcolm - 4 months old - born breech with plagio and tort > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2006 Report Share Posted March 3, 2006 Carolyn, I have been really busy, but have been reading your posts. So my question is........Are you getting a new PT? CAROLG > > I was skeptical when our PT showed me how to apply pressure on Malcolm's > skull with my fingertips. Ok, now I know that it's not me. > > > > My husband and I had already agreed before we met Wanda at cranial > technologies about getting the band for Malcolm. If cranial technologies > thought a band was warranted, we agreed that we would proceed on getting him > the band asap. We were impressed with the results other parents have had > and didn't think there was much of a choice in eventually getting our son a > helmet. > > > > When I told our PT about seeing cranial technologies and getting a helmet, > she was upset. She doesn't believe in helmet therapy and thinks they're > only for severe cases. She believes that Malcolm's plagio and tort are > correctable through PT. > > > While I'm not a PT, it doesn't make sense to me that you can correct plagio > and tort solely through PT in Malcolm's case, especially since he was breech > and born with plagio and tort. Malcolm's head was pressed against my right > rib case almost throughout the pregnancy. He only occasionally veered left > of my belly button before week 20. After week 20 of my pregnancy, I don't > recall him ever on the left side of my abdomen. > > > > I started to self-doubt myself and get more frustrated and confused today > when our PT implied that there was a choice in treating Malcolm's plagio and > tort. I really don't see a choice. Either we band him asap and achieve > some level of symmetry and roundness to his head or we don't and pray that > his head will improve in time, which it hasn't done for 4 months despite > aggressive repositioning and pt. > > > > Thanks for restoring my confidence and making me think I'm not nuts. I > really wish we didn't have to make these decisions and go through this > ordeal. This is a nightmare to me. I know there are plenty of > life-threatening circumstances for infants that are more pressing and > deserving of attention for doctors, but there must be easier ways dealing > with this. Why do doctors, pts, insurance companies, etc. make it so > difficult when it doesn't have to be? They make you feel incompetent, a > complete failure for not doing more and leading you to believe that you have > the power to correct this when you may not. > > > > Thanks again > > > > Carolyn in NYC > > Mum to Malcolm - 4 months old - born breech with plagio and tort > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 9, 2006 Report Share Posted March 9, 2006 I just wanted to say thank you for responding. We will definitely try that. Suzanne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 9, 2006 Report Share Posted March 9, 2006 I just wanted to say thank you for responding. We will definitely try that. Suzanne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 17, 2006 Report Share Posted August 17, 2006 Meredith, where are you in Canada? I am in Ontario and covered under Section 8 for Enbrel. I think but can find out for sure if any provinces are not covered. Hugs June [ ] thanks Thanks Rhonda, , and Janet for responding to my questions. I have been doing pretty good during the summer. Last winter was definitely not fun and I am worried now the fall is just around the corner. I get pain in my shoulders and back but the pain in my chest really bothers me. It will just be achy, but can escalate to sharp stabbing pain. My Rheumy decided to do heart tests on me back in February because he said that chest pain is not usual in RA patients. But of course the tests came back fine and the month of worrying I would die of a heart attack was wasted. I am only on Methatrexate and Hydroxcloroquine right now as I am not on any health benefits. I have heard wonderful things about Enbrel but I would not be able to go on that because it is too costly and have no coverage. I see my Rheumy again the beginning of September. My hands and elbows only hurt once in awhile. I have many nodules on them. Meredith from Canada Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 18, 2006 Report Share Posted August 18, 2006 Meredith, Have you tried the drug companies? I get my meds free all of them for only twenty one dollars every three months, and that is for them filling out all the paperwork, so I don't have to worry with it. ( I take Plaquenil, Zoloft, Prevacide, Metformin, Potassium, Doxycycline, Lorazepam). I have a place here called spring creek health cooperative,that is the ones who helped me. Check with your Human Resources Dept., or Health Dept. to found out if they offer these type of services, if not you can go tthrought the internet and get all the infor. Oh yeah ask your doctor about this too, he should be able to help. If you will let me know if this was any help. Rhonda P.S. you can send personal email to bigsis135@...--- maybe this could help others too. [ ] thanks > Thanks Rhonda, , and Janet for responding to my questions. I have > been doing pretty good during the summer. Last winter was definitely not > fun and I am worried now the fall is just around the corner. I get pain > in my shoulders and back but the pain in my chest really bothers me. It > will just be achy, but can escalate to sharp stabbing pain. My Rheumy > decided to do heart tests on me back in February because he said that > chest pain is not usual in RA patients. But of course the tests came back > fine and the month of worrying I would die of a heart attack was wasted. > I am only on Methatrexate and Hydroxcloroquine right now as I am not on > any health benefits. I have heard wonderful things about Enbrel but I > would not be able to go on that because it is too costly and have no > coverage. I see my Rheumy again the beginning of September. My hands and > elbows only hurt once in awhile. I have many nodules on them. > > Meredith from Canada > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 23, 2006 Report Share Posted August 23, 2006 June, I am also in Ontario. I will look in this Section 8. Meredith in Canada. Meredith, where are you in Canada? I am in Ontario and covered under Section 8 for Enbrel. I think but can find out for sure if any provinces are not covered. Hugs June [ ] thanks Thanks Rhonda, , and Janet for responding to my questions. I have been doing pretty good during the summer. Last winter was definitely not fun and I am worried now the fall is just around the corner. I get pain in my shoulders and back but the pain in my chest really bothers me. It will just be achy, but can escalate to sharp stabbing pain. My Rheumy decided to do heart tests on me back in February because he said that chest pain is not usual in RA patients. But of course the tests came back fine and the month of worrying I would die of a heart attack was wasted. I am only on Methatrexate and Hydroxcloroquine right now as I am not on any health benefits. I have heard wonderful things about Enbrel but I would not be able to go on that because it is too costly and have no coverage. I see my Rheumy again the beginning of September. My hands and elbows only hurt once in awhile. I have many nodules on them. Meredith from Canada Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 2, 2006 Report Share Posted September 2, 2006 It just occurred to me that if you are under 65 you would apply to Trillium which is another arm of the government. Your pharmacy or your rheumy should have the forms available. Everyone in Ontario is eligible for coverage for drugs not covered on the ODB plan. Let me know how you make out. You could also get in touch with Enliven Services who will help you with paperwork. Their phone # is 1-877-936-2735 or look up the web site www.enbrelca and enter DIN #02242905. Hugs June [ ] thanks Thanks Rhonda, , and Janet for responding to my questions. I have been doing pretty good during the summer. Last winter was definitely not fun and I am worried now the fall is just around the corner. I get pain in my shoulders and back but the pain in my chest really bothers me. It will just be achy, but can escalate to sharp stabbing pain. My Rheumy decided to do heart tests on me back in February because he said that chest pain is not usual in RA patients. But of course the tests came back fine and the month of worrying I would die of a heart attack was wasted. I am only on Methatrexate and Hydroxcloroquine right now as I am not on any health benefits. I have heard wonderful things about Enbrel but I would not be able to go on that because it is too costly and have no coverage. I see my Rheumy again the beginning of September. My hands and elbows only hurt once in awhile. I have many nodules on them. Meredith from Canada Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 1, 2006 Report Share Posted October 1, 2006 Michele, I'm glad it was helpful. Hang in there! Caroline > From: <isoaa@...> > Reply-< > > Date: Sun, 01 Oct 2006 11:03:26 -0400 (EDT) > < > > Subject: Thanks > > Caroline and Everyone here : > > Thanks for the great article. It was extremely helpful. > And thanks to all of you for support that could not > have come at a better time. > > God Bless Everyone! > > Michele Cerruto > Greenville, SC. > > " Ms. Michele " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 15, 2006 Report Share Posted October 15, 2006 Eileen, Since we go to California I'm not sure about the Neurospect situation in New York. Maybe someone will can jump in here and fill you in. Best of luck... Caroline > From: tebog2 <tebog2@...> > Reply-< > > Date: Mon, 16 Oct 2006 01:22:01 +0000 > < > > Subject: Thanks > > Thank you Caroline & for your quick responses. I am going to > call the New York office first thing in the a.m. Do they do the > Neurospect testing there too? I am really anxious to start this > process, although I am cautiously hopeful. > > I look forward to communicating with you all and really appreciate > your help!! > > Eileen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 16, 2006 Report Share Posted October 16, 2006 Hi Eileen: I am Eileen too and we just had our first appt with Dr. R in NY on Friday..He told me they are not doing NeuroSpects on the east coast but hopefully in DC soon....I dont know much more than that as my son was totally out of control and it was a difficult appt for him....Eileen B. --------------------------------- Get your own web address for just $1.99/1st yr. We'll help. Small Business. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 15, 2006 Report Share Posted November 15, 2006 Hi Nice to meet you too. I'm sure we have a lot in common. Lynne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2006 Report Share Posted December 3, 2006 My state has started getting better about mold and landlords. I believe that they now or soon will have to sign a form saying there is no mold, roaches, in the apartment or home for rent. I am not sure on details but they will condemn a place but then where do you go when they condemn the home. That happened to me in one place we were getting out cuz they were about to condemn the place cuz of a roof leak and a moldy roof. So they made the landlord put on a new roof but I moved out before that all started. > > > When will the government step in and start setting air quality > guidelines? > > The only department that is suppose to do something, looks the other > way. (The > > Department of business and professional regulations) There would be > less > > lawsuits if this department would investigate uninhabitable housing > (TEST) and > > make these apartment owners clean up their mold or demolish and > start over. I > > wonder how these people can sleep at night and I can only hope they > will one > > day have to answer to god. To all the victims, I pray for your > recovery and > > hope that we will all make a difference from our journeys in some > way or > > another. > > > > GOD BLESS > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2006 Report Share Posted December 3, 2006 , may I ask what state you are in that has these laws? Is is CA? Thanks, Jocelyn > > My state has started getting better about mold and landlords. I > believe that they now or soon will have to sign a form saying there > is no mold, roaches, in the apartment or home for rent. I am not sure > on details but they will condemn a place but then where do you go > when they condemn the home. That happened to me in one place we were > getting out cuz they were about to condemn the place cuz of a roof > leak and a moldy roof. So they made the landlord put on a new roof > but I moved out before that all started. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2006 Report Share Posted December 3, 2006 My state is Delaware. I guess it is a start that they are doing something. --- In , " Jocelyn Brown " <brownje@...> wrote: > > , may I ask what state you are in that has these laws? Is is CA? > Thanks, > Jocelyn > > --- In , " ldelp84227 " <ldelp84227@> wrote: > > > > My state has started getting better about mold and landlords. I > > believe that they now or soon will have to sign a form saying there > > is no mold, roaches, in the apartment or home for rent. I am not sure > > on details but they will condemn a place but then where do you go > > when they condemn the home. That happened to me in one place we were > > getting out cuz they were about to condemn the place cuz of a roof > > leak and a moldy roof. So they made the landlord put on a new roof > > but I moved out before that all started. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2006 Report Share Posted December 3, 2006 In many places in CA now tenants have to sign a waiver of all rights before they are even considered for an apartment. Basically, they have to agree in advance that nomatter what the situation really is, its 'not the landlord's fault'.. This doesn't mean that landlords will repair issues, it just means that they don't have the option of suing. On 12/3/06, Jocelyn Brown <brownje@...> wrote: > > , may I ask what state you are in that has these laws? Is is CA? > Thanks, > Jocelyn > > > > > > My state has started getting better about mold and landlords. I > > believe that they now or soon will have to sign a form saying there > > is no mold, roaches, in the apartment or home for rent. I am not sure > > on details but they will condemn a place but then where do you go > > when they condemn the home. That happened to me in one place we were > > getting out cuz they were about to condemn the place cuz of a roof > > leak and a moldy roof. So they made the landlord put on a new roof > > but I moved out before that all started. > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2006 Report Share Posted December 3, 2006 Thanks for the update on CA. Guess we better consider buying instead of renting when we relocate back there in a couple of months. Jocelyn > > > > > > My state has started getting better about mold and landlords. I > > > believe that they now or soon will have to sign a form saying there > > > is no mold, roaches, in the apartment or home for rent. I am not sure > > > on details but they will condemn a place but then where do you go > > > when they condemn the home. That happened to me in one place we were > > > getting out cuz they were about to condemn the place cuz of a roof > > > leak and a moldy roof. So they made the landlord put on a new roof > > > but I moved out before that all started. > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 19, 2007 Report Share Posted February 19, 2007 Gretchen, My daughter was so excited after we recived your email that she went to see her teachers this morning before school. Everyone was so wonderful when she showed them your email and were very open to anything she thought would help. I had already given her a laptop because home work has been so difficult for her and they have agreed to allow her to use it in class. Thank you for the web site, we will love it! I am sure we are going to enjoy very much, already we feel far less lost then yesterday. Lissa Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 4, 2007 Report Share Posted April 4, 2007 Hi , I take the cleanse and flush am, 30 min. (at least) before I eat. Flush 30 min before 2nd meal, and cleanse and flush 30 min before last meal. If you burp, you will taste product, but not unpleasant to me. On 3rd week of gall cleanse. I also take raw. unfiltered, organic, apple cider vinegar 3 times per day ( 1oz. x 3 ). Also eating and blending organic apples/juice daily. Will give report on site after next ultrasound <eaquita@...> wrote: Hi there, Thanks for checking in . I went ahead and ordered the GallCleanse, but haven't started taking it yet. It says to take on an empty stomach. Do you take it in the a.m. when you get up? and before you go to bed? When would my tomach be empty besides when I first wake up? I guess I wonder how empty is empty. I'm looking forward to your next ultrasound. Thanks again for your info. Quote Link to comment Share on other sites More sharing options...
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