Guest guest Posted March 29, 2002 Report Share Posted March 29, 2002 Thanks Marci, I hope you are doing well too! Anne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2002 Report Share Posted March 29, 2002 I'm here , just busy as ever! No time for the computer these days. Spring cleaning, over active psycho toddler, more spring cleaning more crazy toddler are keeping me busy busy busy. There are days when I do not even get a chance to shower!! Curse Swear!!! Anne Mom of Livia DOC Grad 12/01 CANADA > Nice to hear from you again Anne!! I was wondering where you went > > ' Mom Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2002 Report Share Posted March 29, 2002 Kendra, How are you feeling these days? I hope all is well with you and your little peanut! Oh and hubby too huh lol. Has he found work yet? Hows the teeny tiny wee one? everything going ok? lol soo many questions! Anne > Good to hear from you Anne! ) > Kendra > Sorry > > > Hi guys, I am so sorry to have not been very active lately. I keep > meaning to pop by on Tuesdays for chat but by the time I remember, > it is too late and I am ready for bed. Livia has been keeping me > very busy these days, and I am finding little time for myself other > than when she sleeps at night and by that time i am exhausted and > trying to do the million things I have forgotten to do earlier. lol > > I will try my darndest to become active again in this community, but > I might not get to all the posts.lol There are so many!! > > I just thought I would let you all know " whats up " in Anne world, > and let you know I have not forgotten about all you wonderful moms > and dads, and certainly not all the beautiful babys! > > > Anne > Mom of Livia > DOC Grad 12/01 > Canada > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2002 Report Share Posted March 29, 2002 Darci, I am in Edmonton and Liv recieved treatment at the University Hosp. Occupational therapy clinic. Anne > Hi Anne, where in Canada are you from? Where did you go to get the DOC > band? (i guess you must be in Calgary?) > > Darcy (father to Madeleine) > Toronto > > Sorry > > > Hi guys, I am so sorry to have not been very active lately. I keep > meaning to pop by on Tuesdays for chat but by the time I remember, > it is too late and I am ready for bed. Livia has been keeping me > very busy these days, and I am finding little time for myself other > than when she sleeps at night and by that time i am exhausted and > trying to do the million things I have forgotten to do earlier. lol > > I will try my darndest to become active again in this community, but > I might not get to all the posts.lol There are so many!! > > I just thought I would let you all know " whats up " in Anne world, > and let you know I have not forgotten about all you wonderful moms > and dads, and certainly not all the beautiful babys! > > > Anne > Mom of Livia > DOC Grad 12/01 > Canada > > > > For more plagio info Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2002 Report Share Posted March 29, 2002 Everything's good here Anne! Thanx for asking! Hanna is great - but sooooooo 2!!! She's really stubborn and EVERYTHING is a challenge these days. She's not going shopping for a while, that's for sure! Bed time is the worst. It takes a good hour to get her to bed. *sigh* As for the "wee one", he's doing good. Very squirmy and growing quickly! I feel so huge already, and we're only 1/2 way there! still hasn't found work. It's been 4 months now. He hasn't been looking very hard tho. I think he enjoys his home life a little too much!!! Time to get his butt in gear tho! The severance will run out soon! How are things with you? How's your leg? I hear Livia is keeping you very busy! ;o) How is Preston liking his job? Keep in touch! Kendra Sorry> > > Hi guys, I am so sorry to have not been very active lately. I keep > meaning to pop by on Tuesdays for chat but by the time I remember, > it is too late and I am ready for bed. Livia has been keeping me > very busy these days, and I am finding little time for myself other > than when she sleeps at night and by that time i am exhausted and > trying to do the million things I have forgotten to do earlier. lol> > I will try my darndest to become active again in this community, but > I might not get to all the posts.lol There are so many!!> > I just thought I would let you all know "whats up" in Anne world, > and let you know I have not forgotten about all you wonderful moms > and dads, and certainly not all the beautiful babys!> > > Anne> Mom of Livia> DOC Grad 12/01> Canada> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 30, 2002 Report Share Posted March 30, 2002 Kendra, It is so good to hear that everything is going great with the pregnancy. Hard to believe when just a few short months ago I said I was probably not going to have any more when just today I was throwing the idea around in my head lol. (babies are like tattoo's, you can't only have one!) So Hanna's horns have sprouted huh? Don't worry it will only get worse!(just kidding) I hope she does not sprout the tail when her baby brother arrives. I am keeping my eyes and ears open, hoping to have " the perfect job " pop out, so that you can get out from underfoot. I know what a pain that can be. Preston is in the groove of his job. I have not heard any complaints YET. My knee is still screwed, but I can expect that for the rest of my life. It pops in and out at will, and will continue to do so until I go have surgery. It is not an option at the moment. We need my meager 2days a week paycheck to get by, and chasing a toddler on crutches would not be very easy. Well, I have to run to work now (ICK!) Anne > > Good to hear from you Anne! ) > > Kendra > > Sorry > > > > > > Hi guys, I am so sorry to have not been very active lately. I > keep > > meaning to pop by on Tuesdays for chat but by the time I > remember, > > it is too late and I am ready for bed. Livia has been keeping me > > very busy these days, and I am finding little time for myself > other > > than when she sleeps at night and by that time i am exhausted > and > > trying to do the million things I have forgotten to do earlier. > lol > > > > I will try my darndest to become active again in this community, > but > > I might not get to all the posts.lol There are so many!! > > > > I just thought I would let you all know " whats up " in Anne > world, > > and let you know I have not forgotten about all you wonderful > moms > > and dads, and certainly not all the beautiful babys! > > > > > > Anne > > Mom of Livia > > DOC Grad 12/01 > > Canada > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2002 Report Share Posted August 4, 2002 I am sleep deprived and when I get this way I clean ...figure I will burn myself out and the body will crash...when I clean I think....so excuse the length of this but I have to get it out...I found this group trying to help my sister-in-law...who had called me hysterically after being diagnosed with RA...she figured having scleroderma-lupus I could help. I told her i didnt know much about RA and suggested a group so she could read and learn and she asked me to find one as she was a compuetr newbie. I reluctantly agreed as I had just decided to not do the support group thing anymore...here is why ...I signed up for a scleroderma group...the is 5 women who basically -++++are the group..members were welcomed when they first signed up...but if you asked a question it was ignored...there was constant drivvel amongst the five about men-in-tool belts but never any concrete info..one of the newbies said something and was told to get a life....if she was looking for information hit the scleroderma sights....and if she wanted to cry and whine find a local support group...and the drivvle went on...one asked what was the matter that they didnt want to talk to her and she got lamb basted...then me being redheaded and the person they lambbasted a cyber friend I shot off my mouth...ok fingers ....and was told I was a grouchy pants....so I left and decided that was it....when I found this group...I was amazed the moderators did not snippety-do-da the messages...not every message had to go through them...there was a wealth of information as well as real people that cared and communicated with each other..I looked at the message activity and was amazed at all the different people that were posting...I felt welcomed ...I understand in any group there is people for whatever reason you will seem to bond with and others not...but this group seems to accept all...I have never felt unwelcome even with the fact I didnt have RA...the combo of articles...humor...crying...caring cyber hugs and the rest...all make this group a real group....I have found another scleroderma group that is kind...and have digest sent to me to keep current with all new info in the scleroderma field and with others symptoms..I barely ever post there as for me it is more for info...this group as others has said is like family....I realize opinions are like a$$$holes and evryone has one...but in this group I have always felt it was OK to give mine....and the saying you can please some of the people some of the time but not all the people all the time does come to mind...people in this group are sick and in pain and sometimes things are said that may be taken wrong by others that are sick and in pain...but on the whole it is a great group...I am sorry this is so long ...and once again I am expressing an opinion but I had to get this out...Kathi in OK Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2002 Report Share Posted August 4, 2002 Kathi in OK, Your message is extremely eloquent and straight from the heart. I couldn't agree with you more about this group. Personally, I feel grateful every day to have found you. My love to all. Al in IL > I am sleep deprived and when I get this way I clean ...figure I will > burn myself out and the body will crash...when I clean I think....so > excuse the length of this but I have to get it out...I found this > group trying to help my sister-in-law...who had called me hysterically > after being diagnosed with RA...she figured having scleroderma- lupus I > could help. I told her i didnt know much about RA and suggested a > group so she could read and learn and she asked me to find one as she > was a compuetr newbie. I reluctantly agreed as I had just decided to > not do the support group thing anymore...here is why ...I signed up > for a scleroderma group...the is 5 women who basically -++++are the > group..members were welcomed when they first signed up...but if you > asked a question it was ignored...there was constant drivvel amongst > the five about men-in-tool belts but never any concrete info..one of > the newbies said something and was told to get a life....if she was > looking for information hit the scleroderma sights....and if she > wanted to cry and whine find a local support group...and the drivvle > went on...one asked what was the matter that they didnt want to talk > to her and she got lamb basted...then me being redheaded and the > person they lambbasted a cyber friend I shot off my mouth...ok fingers > ...and was told I was a grouchy pants....so I left and decided that > was it....when I found this group...I was amazed the moderators did > not snippety-do-da the messages...not every message had to go through > them...there was a wealth of information as well as real people that > cared and communicated with each other..I looked at the message > activity and was amazed at all the different people that were > posting...I felt welcomed ...I understand in any group there is people > for whatever reason you will seem to bond with and others not...but > this group seems to accept all...I have never felt unwelcome even with > the fact I didnt have RA...the combo of > articles...humor...crying...caring cyber hugs and the rest...all make > this group a real group....I have found another scleroderma group that > is kind...and have digest sent to me to keep current with all new info > in the scleroderma field and with others symptoms..I barely ever post > there as for me it is more for info...this group as others has said is > like family....I realize opinions are like a$$$holes and evryone has > one...but in this group I have always felt it was OK to give > mine....and the saying you can please some of the people some of the > time but not all the people all the time does come to mind...people in > this group are sick and in pain and sometimes things are said that may > be taken wrong by others that are sick and in pain...but on the whole > it is a great group...I am sorry this is so long ...and once again I > am expressing an opinion but I had to get this out...Kathi in OK Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2002 Report Share Posted August 4, 2002 Hi Al, I just had to say that you are the nicest guy. A lot of men are less communicative, but you are such fun to have in the group. Hugs, Carol [ ] Re: Sorry Kathi in OK, Your message is extremely eloquent and straight from the heart. I couldn't agree with you more about this group. Personally, I feel grateful every day to have found you. My love to all. Al in IL > I am sleep deprived and when I get this way I clean ...figure I will > burn myself out and the body will crash...when I clean I think....so > excuse the length of this but I have to get it out...I found this > group trying to help my sister-in-law...who had called me hysterically > after being diagnosed with RA...she figured having scleroderma- lupus I > could help. I told her i didnt know much about RA and suggested a > group so she could read and learn and she asked me to find one as she > was a compuetr newbie. I reluctantly agreed as I had just decided to > not do the support group thing anymore...here is why ...I signed up > for a scleroderma group...the is 5 women who basically -++++are the > group..members were welcomed when they first signed up...but if you > asked a question it was ignored...there was constant drivvel amongst > the five about men-in-tool belts but never any concrete info..one of > the newbies said something and was told to get a life....if she was > looking for information hit the scleroderma sights....and if she > wanted to cry and whine find a local support group...and the drivvle > went on...one asked what was the matter that they didnt want to talk > to her and she got lamb basted...then me being redheaded and the > person they lambbasted a cyber friend I shot off my mouth...ok fingers > ...and was told I was a grouchy pants....so I left and decided that > was it....when I found this group...I was amazed the moderators did > not snippety-do-da the messages...not every message had to go through > them...there was a wealth of information as well as real people that > cared and communicated with each other..I looked at the message > activity and was amazed at all the different people that were > posting...I felt welcomed ...I understand in any group there is people > for whatever reason you will seem to bond with and others not...but > this group seems to accept all...I have never felt unwelcome even with > the fact I didnt have RA...the combo of > articles...humor...crying...caring cyber hugs and the rest...all make > this group a real group....I have found another scleroderma group that > is kind...and have digest sent to me to keep current with all new info > in the scleroderma field and with others symptoms..I barely ever post > there as for me it is more for info...this group as others has said is > like family....I realize opinions are like a$$$holes and evryone has > one...but in this group I have always felt it was OK to give > mine....and the saying you can please some of the people some of the > time but not all the people all the time does come to mind...people in > this group are sick and in pain and sometimes things are said that may > be taken wrong by others that are sick and in pain...but on the whole > it is a great group...I am sorry this is so long ...and once again I > am expressing an opinion but I had to get this out...Kathi in OK Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2002 Report Share Posted August 4, 2002 Hi Carol, What a sweet and nice thing to say. Thank you very much. Hugs, Al > > I am sleep deprived and when I get this way I clean ...figure I > will > > burn myself out and the body will crash...when I clean I > think....so > > excuse the length of this but I have to get it out...I found this > > group trying to help my sister-in-law...who had called me > hysterically > > after being diagnosed with RA...she figured having scleroderma- > lupus I > > could help. I told her i didnt know much about RA and suggested a > > group so she could read and learn and she asked me to find one as > she > > was a compuetr newbie. I reluctantly agreed as I had just decided > to > > not do the support group thing anymore...here is why ...I signed up > > for a scleroderma group...the is 5 women who basically -++++are the > > group..members were welcomed when they first signed up...but if you > > asked a question it was ignored...there was constant drivvel > amongst > > the five about men-in-tool belts but never any concrete info..one > of > > the newbies said something and was told to get a life....if she was > > looking for information hit the scleroderma sights....and if she > > wanted to cry and whine find a local support group...and the > drivvle > > went on...one asked what was the matter that they didnt want to > talk > > to her and she got lamb basted...then me being redheaded and the > > person they lambbasted a cyber friend I shot off my mouth...ok > fingers > > ...and was told I was a grouchy pants....so I left and decided that > > was it....when I found this group...I was amazed the moderators did > > not snippety-do-da the messages...not every message had to go > through > > them...there was a wealth of information as well as real people > that > > cared and communicated with each other..I looked at the message > > activity and was amazed at all the different people that were > > posting...I felt welcomed ...I understand in any group there is > people > > for whatever reason you will seem to bond with and others not...but > > this group seems to accept all...I have never felt unwelcome even > with > > the fact I didnt have RA...the combo of > > articles...humor...crying...caring cyber hugs and the rest...all > make > > this group a real group....I have found another scleroderma group > that > > is kind...and have digest sent to me to keep current with all new > info > > in the scleroderma field and with others symptoms..I barely ever > post > > there as for me it is more for info...this group as others has said > is > > like family....I realize opinions are like a$$$holes and evryone > has > > one...but in this group I have always felt it was OK to give > > mine....and the saying you can please some of the people some of > the > > time but not all the people all the time does come to mind...people > in > > this group are sick and in pain and sometimes things are said that > may > > be taken wrong by others that are sick and in pain...but on the > whole > > it is a great group...I am sorry this is so long ...and once again > I > > am expressing an opinion but I had to get this out...Kathi in OK > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2002 Report Share Posted August 4, 2002 Kathi, no need to apologize for anything you've said. I feel as you do about our group. And, of course, you were and are always welcome here! And so are OT posts. Says so right in the description of our group at the site. We do need fun and interesting stories and jokes and consolation and to get to know one another. Everyone is entitled to her or his opinion here and is free to express it as long as no unkindness toward others is involved. We've been very lucky that there has been very little nastiness or controversy in the history of the group. More than that, we are blessed to have each other and in that we are able to interact on a variety of levels in a strongly positive way. As you point out, many people are sick and tired. They have limited energy. Sometimes the mail is overwhelming. Last month was a record - 2094 posts! When people join, they don't know what to expect. Or sometimes the group changes character a bit. Or the mail load changes. Or the person's own situation changes. If an individual chooses to leave, he or she has an opportunity to send a reason to the moderators. The most common reason for leaving is too much mail. That's OK though. See that as just a fact, not necessarily a negative criticism. Don't let it cramp your style. You either, Debs! As you and others have pointed out, there are ways to minimize how much mail one has to go through. All work and no play makes RA-Support a dull group. Besides, the boring stuff is my department. PS. How many extra emails have we generated on this topic, LOL???? [ ] RE: Sorry > I am sleep deprived and when I get this way I clean ...figure I will > burn myself out and the body will crash...when I clean I think....so > excuse the length of this but I have to get it out...I found this > group trying to help my sister-in-law...who had called me hysterically > after being diagnosed with RA...she figured having scleroderma-lupus I > could help. I told her i didnt know much about RA and suggested a > group so she could read and learn and she asked me to find one as she > was a compuetr newbie. I reluctantly agreed as I had just decided to > not do the support group thing anymore...here is why ...I signed up > for a scleroderma group...the is 5 women who basically -++++are the > group..members were welcomed when they first signed up...but if you > asked a question it was ignored...there was constant drivvel amongst > the five about men-in-tool belts but never any concrete info..one of > the newbies said something and was told to get a life....if she was > looking for information hit the scleroderma sights....and if she > wanted to cry and whine find a local support group...and the drivvle > went on...one asked what was the matter that they didnt want to talk > to her and she got lamb basted...then me being redheaded and the > person they lambbasted a cyber friend I shot off my mouth...ok fingers > ...and was told I was a grouchy pants....so I left and decided that > was it....when I found this group...I was amazed the moderators did > not snippety-do-da the messages...not every message had to go through > them...there was a wealth of information as well as real people that > cared and communicated with each other..I looked at the message > activity and was amazed at all the different people that were > posting...I felt welcomed ...I understand in any group there is people > for whatever reason you will seem to bond with and others not...but > this group seems to accept all...I have never felt unwelcome even with > the fact I didnt have RA...the combo of > articles...humor...crying...caring cyber hugs and the rest...all make > this group a real group....I have found another scleroderma group that > is kind...and have digest sent to me to keep current with all new info > in the scleroderma field and with others symptoms..I barely ever post > there as for me it is more for info...this group as others has said is > like family....I realize opinions are like a$$$holes and evryone has > one...but in this group I have always felt it was OK to give > mine....and the saying you can please some of the people some of the > time but not all the people all the time does come to mind...people in > this group are sick and in pain and sometimes things are said that may > be taken wrong by others that are sick and in pain...but on the whole > it is a great group...I am sorry this is so long ...and once again I > am expressing an opinion but I had to get this out...Kathi in OK Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 5, 2002 Report Share Posted August 5, 2002 Oops, we¹re generating another one I just have to add my two cents. We¹ve always shared our lives other than our illnesses. It¹s nice to hear about things going on in everyone¹ life. This group is an extension of my family. Yes, It¹s a large one with many different personalities that makes it so interesting. When we have a lot of people leaving due to the large amount of mail, I try to think about what I can do to accommodate everyone, but I just can¹t. Other than marking the subject OT, there is nothing else we can do. There are several options to help deal with the large quantity, either getting the digest or reading it from the website. Occasionally you will see me mention that these other options exist, and this if for the benefit of those that are having a difficult time managing the mail. It is not said to curtail conversations in any way. I just want the new members to know that there are alternatives to mail delivery. To restrict the quantity of mail is to strip away the personality of the list. We just can¹t talk about being ill 24/7. I¹ve always wondered if only nice people get RA since our group is full of wonderful, caring, and considerate people who do what they can to comfort and support a fellow sufferer. It is a pleasure to see how we all get along so well. a Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 5, 2002 Report Share Posted August 5, 2002 Kathi, I¹m sorry the scleraderma group was like that, but sure glad you found us. Although this group was originally started for RA, it has grown to include any of the autoimmune diseases. They are all related, but just affects a different part of our body. Many of these diseases are treated the same. I hope our group can always remain a free spirit, with no censorship. Hugs, a > I am sleep deprived and when I get this way I clean ...figure I will > burn myself out and the body will crash...when I clean I think....so > excuse the length of this but I have to get it out...I found this > group trying to help my sister-in-law...who had called me hysterically > after being diagnosed with RA...she figured having scleroderma-lupus I > could help. I told her i didnt know much about RA and suggested a > group so she could read and learn and she asked me to find one as she > was a compuetr newbie. I reluctantly agreed as I had just decided to > not do the support group thing anymore...here is why ...I signed up > for a scleroderma group...the is 5 women who basically -++++are the > group..members were welcomed when they first signed up...but if you > asked a question it was ignored...there was constant drivvel amongst > the five about men-in-tool belts but never any concrete info..one of > the newbies said something and was told to get a life....if she was > looking for information hit the scleroderma sights....and if she > wanted to cry and whine find a local support group...and the drivvle > went on...one asked what was the matter that they didnt want to talk > to her and she got lamb basted...then me being redheaded and the > person they lambbasted a cyber friend I shot off my mouth...ok fingers > ...and was told I was a grouchy pants....so I left and decided that > was it....when I found this group...I was amazed the moderators did > not snippety-do-da the messages...not every message had to go through > them...there was a wealth of information as well as real people that > cared and communicated with each other..I looked at the message > activity and was amazed at all the different people that were > posting...I felt welcomed ...I understand in any group there is people > for whatever reason you will seem to bond with and others not...but > this group seems to accept all...I have never felt unwelcome even with > the fact I didnt have RA...the combo of > articles...humor...crying...caring cyber hugs and the rest...all make > this group a real group....I have found another scleroderma group that > is kind...and have digest sent to me to keep current with all new info > in the scleroderma field and with others symptoms..I barely ever post > there as for me it is more for info...this group as others has said is > like family....I realize opinions are like a$$$holes and evryone has > one...but in this group I have always felt it was OK to give > mine....and the saying you can please some of the people some of the > time but not all the people all the time does come to mind...people in > this group are sick and in pain and sometimes things are said that may > be taken wrong by others that are sick and in pain...but on the whole > it is a great group...I am sorry this is so long ...and once again I > am expressing an opinion but I had to get this out...Kathi in OK > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 5, 2002 Report Share Posted August 5, 2002 << I¹ve always wondered if only nice people get RA since our group is full of wonderful, caring, and considerate people who do what they can to comfort and support a fellow sufferer. It is a pleasure to see how we all get along so well. >> It really is something the way we all get along so well, with no real personality conflicts. Maybe coping with chronic pain makes us more tolerant of the little things. Or the adversary inflicts RA on the Lord’s choicest spirits, in an attempt to try their faith. I was musing about that the other day, thinking that in spite of my feeling alone, the Lord has been there with me the whole time. Just like the poem “Footprints”. Hope nobody is offended by the spiritual thoughts. And I hope everyone has a pain free day! Love and hugs, Carol Re: [ ] RE: Sorry Oops, we¹re generating another one I just have to add my two cents. We¹ve always shared our lives other than our illnesses. It¹s nice to hear about things going on in everyone¹ life. This group is an extension of my family. Yes, It¹s a large one with many different personalities that makes it so interesting. When we have a lot of people leaving due to the large amount of mail, I try to think about what I can do to accommodate everyone, but I just can¹t. Other than marking the subject OT, there is nothing else we can do. There are several options to help deal with the large quantity, either getting the digest or reading it from the website. Occasionally you will see me mention that these other options exist, and this if for the benefit of those that are having a difficult time managing the mail. It is not said to curtail conversations in any way. I just want the new members to know that there are alternatives to mail delivery. To restrict the quantity of mail is to strip away the personality of the list. We just can¹t talk about being ill 24/7. I¹ve always wondered if only nice people get RA since our group is full of wonderful, caring, and considerate people who do what they can to comfort and support a fellow sufferer. It is a pleasure to see how we all get along so well. a Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 5, 2002 Report Share Posted August 5, 2002 I think that only strong people get RA and nice too. We are a tough bunch for sure or did I just happen upon a great group. But let me add there are onmly nice people on most of my lists or they get kicked off! Temple 3 Fox Haven Way Chelmsford, MA 01824 dat2352@... www.homestead.com/kuddlekrittersfarm/index.html www.homestead.com/kuddlekrittersdairygoats/index.html www.homestead.com/kuddlekraft/index.html Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 6, 2002 Report Share Posted August 6, 2002 Carol, He¹s been trying my faith for an awfully long time now. I wish He¹d take my word for it and give me a break LOL! Footprints has always been special to me too. I have to say that my faith is what has kept me sane and carried me through many surgical procedures. I don¹t know where I¹d be without my faith. Hugs, a > << I¹ve always wondered if only nice people get RA since our group is full > of > wonderful, caring, and considerate people who do what they can to comfort > and support a fellow sufferer. It is a pleasure to see how we all get > along so well. >> > > It really is something the way we all get along so well, with no real > personality conflicts. Maybe coping with chronic pain makes us more > tolerant of the little things. Or the adversary inflicts RA on the Lord’s > choicest spirits, in an attempt to try their faith. I was musing about that > the other day, thinking that in spite of my feeling alone, the Lord has been > there with me the whole time. Just like the poem “Footprints”. > > Hope nobody is offended by the spiritual thoughts. And I hope everyone has > a pain free day! > > Love and hugs, > Carol > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 9, 2002 Report Share Posted August 9, 2002 Kathi in OK, I'm sorry that you went through all that with that other group and I am extremely happy that you found this one. I'm sending you one, big, humongous (but gentle) hug. Love ya Stacey in PA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 9, 2002 Report Share Posted August 9, 2002 Hi Al, I agree with Carol wholeheartedly. I'm glad you're here with us. Stacey in PA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 10, 2002 Report Share Posted August 10, 2002 Thank you Stacey....and I will always remember you were the first one to welcome me.....hugs back to you..Kathi in OK --- staceycrwfrd@... wrote: > Kathi in OK, > I'm sorry that you went through all that with that > other group and I am > extremely happy that you found this one. I'm > sending you one, big, humongous > (but gentle) hug. > Love ya > Stacey in PA > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 10, 2002 Report Share Posted August 10, 2002 Hi Stacey, So am I. Thank you for making me feel so welcome. Hugs, Al > Hi Al, > I agree with Carol wholeheartedly. I'm glad you're here with us. > Stacey in PA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 9, 2002 Report Share Posted December 9, 2002 Please forgive my double post but my computer is sending emails before i am ready or have corrected my spelling Joanne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 27, 2003 Report Share Posted February 27, 2003 LOL!! You don't have to hide! It's not your fault the link is too long to post. How about telling us the name of the product you are talking about? Then we can to to onestepahead.com and check it out? > I tried to put a website for a plagio-preventer type thing. It > obviously did not work....I am sorry...I am going to hide > somewhere.... > > Sponagle Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 27, 2003 Report Share Posted February 27, 2003 > > I tried to put a website for a plagio-preventer type thing. It > > obviously did not work....I am sorry...I am going to hide > > somewhere.... > > > > Sponagle Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 27, 2003 Report Share Posted February 27, 2003 Thanks! A few ppl posted that the head N' back to sleep didn't really do what they wanted it too. I checked it out in BabiesRUs and the pillow part really did look too small. Someone on here posted about the Head and Body support from DEX. I went to Target and liked it so much I bought 2 of them! Dex has since changed the name to Secure Sleeper Head and Body Support System. You can check it out here: http://www.dexproducts.com/Pages/HeadandBodySupport.html I just hope it does what I want it too! > > > I tried to put a website for a plagio-preventer type thing. It > > > obviously did not work....I am sorry...I am going to hide > > > somewhere.... > > > > > > Sponagle Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 27, 2003 Report Share Posted February 27, 2003 Jeff- We've never heard anything too positive about the Head N back to Sleep thing. Don't feel too bad about not knowing about it last year! Quote Link to comment Share on other sites More sharing options...
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