Guest guest Posted August 27, 2002 Report Share Posted August 27, 2002 Cory - I am new to the group, and just saw your message. I am a 26 year old female, and have had fms since 11 years old, though my mom thinks I had symptoms since I was much younger. I am interested in talking to someone of my age, with symptoms starting in early childhoood. I think that in some ways, my symptoms are different than someone who didn't have any symptoms until later on. I think that perhaps my body was able to adjust in some ways, since I did a lot of growing and maturing, in the midst of the pain and other stuff. Have you thought about any of that at all? Are there others in this group who have also been dealing with fms since childhood? > Hello Everyone- > > My name is Cory Hart; I am a 27-year-old male. I was diagnosed with > Fibromyalgia in late 1999. I have been suffering with the pain since > I was about 7-8 years old. Lately I have been in a real bad flare. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 27, 2002 Report Share Posted August 27, 2002 Cory - I am new to the group, and just saw your message. I am a 26 year old female, and have had fms since 11 years old, though my mom thinks I had symptoms since I was much younger. I am interested in talking to someone of my age, with symptoms starting in early childhoood. I think that in some ways, my symptoms are different than someone who didn't have any symptoms until later on. I think that perhaps my body was able to adjust in some ways, since I did a lot of growing and maturing, in the midst of the pain and other stuff. Have you thought about any of that at all? Are there others in this group who have also been dealing with fms since childhood? > Hello Everyone- > > My name is Cory Hart; I am a 27-year-old male. I was diagnosed with > Fibromyalgia in late 1999. I have been suffering with the pain since > I was about 7-8 years old. Lately I have been in a real bad flare. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 27, 2002 Report Share Posted August 27, 2002 Cory - I am new to the group, and just saw your message. I am a 26 year old female, and have had fms since 11 years old, though my mom thinks I had symptoms since I was much younger. I am interested in talking to someone of my age, with symptoms starting in early childhoood. I think that in some ways, my symptoms are different than someone who didn't have any symptoms until later on. I think that perhaps my body was able to adjust in some ways, since I did a lot of growing and maturing, in the midst of the pain and other stuff. Have you thought about any of that at all? Are there others in this group who have also been dealing with fms since childhood? > Hello Everyone- > > My name is Cory Hart; I am a 27-year-old male. I was diagnosed with > Fibromyalgia in late 1999. I have been suffering with the pain since > I was about 7-8 years old. Lately I have been in a real bad flare. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 27, 2002 Report Share Posted August 27, 2002 Hello- No, I never thought about it like that! You may be on to something. Would you like to write a story or article about it? If so E-mail me. Sincerely, Cory www.nomf.com > > Hello Everyone- > > > > My name is Cory Hart; I am a 27-year-old male. I was diagnosed with > > Fibromyalgia in late 1999. I have been suffering with the pain > since > > I was about 7-8 years old. Lately I have been in a real bad flare. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 27, 2002 Report Share Posted August 27, 2002 Hello- No, I never thought about it like that! You may be on to something. Would you like to write a story or article about it? If so E-mail me. Sincerely, Cory www.nomf.com > > Hello Everyone- > > > > My name is Cory Hart; I am a 27-year-old male. I was diagnosed with > > Fibromyalgia in late 1999. I have been suffering with the pain > since > > I was about 7-8 years old. Lately I have been in a real bad flare. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 27, 2002 Report Share Posted August 27, 2002 Hello- No, I never thought about it like that! You may be on to something. Would you like to write a story or article about it? If so E-mail me. Sincerely, Cory www.nomf.com > > Hello Everyone- > > > > My name is Cory Hart; I am a 27-year-old male. I was diagnosed with > > Fibromyalgia in late 1999. I have been suffering with the pain > since > > I was about 7-8 years old. Lately I have been in a real bad flare. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 4, 2002 Report Share Posted October 4, 2002 ?? How is Rebel? I was so worried about you dealing with the stress from that and from Mom, how is she doing?? Better I hope! > Take care Everyone, and if you need me, drop me a line... > Hallock@a... > > Love and {{{HUGZ}}} to Everyone!!! > : Thanks for asking. Rebel is not doing well. I spent the afternoon at the vet with him . Finally did a chest x-ray and labs ( at my insistance). CXR was not good. Either small pulmonary emboli,pulmonary edema (my vote),or lung cancer. Needless to say I am almost a basket case. He started him on Ascriptin ( asprin with maloxx)and lasix. I am to call him ASAP if I have any questions or problems over the weekend. he said he checks the answering machine at the office several times a day, just in case. I am scheduled for surgery in Oct 16th and he HAS to be better. Either that or my sister will have to come a dog sit. no way am I leaving him in the house with my father in law only checking on him a couple of times a day, Besides with the lasix he has to be walked more often. Thanks for thinking of me. Take care . -SC Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 4, 2002 Report Share Posted October 4, 2002 ?? How is Rebel? I was so worried about you dealing with the stress from that and from Mom, how is she doing?? Better I hope! > Take care Everyone, and if you need me, drop me a line... > Hallock@a... > > Love and {{{HUGZ}}} to Everyone!!! > : Thanks for asking. Rebel is not doing well. I spent the afternoon at the vet with him . Finally did a chest x-ray and labs ( at my insistance). CXR was not good. Either small pulmonary emboli,pulmonary edema (my vote),or lung cancer. Needless to say I am almost a basket case. He started him on Ascriptin ( asprin with maloxx)and lasix. I am to call him ASAP if I have any questions or problems over the weekend. he said he checks the answering machine at the office several times a day, just in case. I am scheduled for surgery in Oct 16th and he HAS to be better. Either that or my sister will have to come a dog sit. no way am I leaving him in the house with my father in law only checking on him a couple of times a day, Besides with the lasix he has to be walked more often. Thanks for thinking of me. Take care . -SC Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 4, 2002 Report Share Posted October 4, 2002 ?? How is Rebel? I was so worried about you dealing with the stress from that and from Mom, how is she doing?? Better I hope! > Take care Everyone, and if you need me, drop me a line... > Hallock@a... > > Love and {{{HUGZ}}} to Everyone!!! > : Thanks for asking. Rebel is not doing well. I spent the afternoon at the vet with him . Finally did a chest x-ray and labs ( at my insistance). CXR was not good. Either small pulmonary emboli,pulmonary edema (my vote),or lung cancer. Needless to say I am almost a basket case. He started him on Ascriptin ( asprin with maloxx)and lasix. I am to call him ASAP if I have any questions or problems over the weekend. he said he checks the answering machine at the office several times a day, just in case. I am scheduled for surgery in Oct 16th and he HAS to be better. Either that or my sister will have to come a dog sit. no way am I leaving him in the house with my father in law only checking on him a couple of times a day, Besides with the lasix he has to be walked more often. Thanks for thinking of me. Take care . -SC Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2002 Report Share Posted October 30, 2002 In a message dated 10/30/2002 9:23:16 AM Central Standard Time, wendi_manley@... writes: > ~Wendi > Welcome Wendi! I have two girls with CF and 1 without. We found out about my girls CF when my oldest was 6. At one time I thought we would try for a fourth but after there diagnoses I decided there was know way I could handle 3 kids with CF. I just didn't want to take the chance. I wish you the very best. Deb A Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2002 Report Share Posted October 30, 2002 In a message dated 10/30/2002 9:23:16 AM Central Standard Time, wendi_manley@... writes: > ~Wendi > Welcome Wendi! I have two girls with CF and 1 without. We found out about my girls CF when my oldest was 6. At one time I thought we would try for a fourth but after there diagnoses I decided there was know way I could handle 3 kids with CF. I just didn't want to take the chance. I wish you the very best. Deb A Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2002 Report Share Posted October 30, 2002 In a message dated 10/30/2002 9:23:16 AM Central Standard Time, wendi_manley@... writes: > ~Wendi > Welcome Wendi! I have two girls with CF and 1 without. We found out about my girls CF when my oldest was 6. At one time I thought we would try for a fourth but after there diagnoses I decided there was know way I could handle 3 kids with CF. I just didn't want to take the chance. I wish you the very best. Deb A Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2002 Report Share Posted October 30, 2002 Hi Wendi, welcome to the list. We are in the same situation. We are " working " on our second child for more than a year now after thinking about it for four years. Since preimplantation diagnosis (PID) isn't allowed here in Germany and we don't wanna have another child wcf (a very difficult decision) we have to play russian roulette. Recently I spoke with a geneticst about CVS vs. amnio. While generally amnio is the standard way of prenatal testing she prefers a CVS for the CF testing. She said that she needs the blood of both parents first (to make sure that one can distinguish between cells from the mother and cells from the fetus) and then a CVS is performed at 12 or 13 weeks. You'll get the results within 10 days then. The only downside is that there is a higher risk of a miscarriage with CVS (1% vs. 0.3% with amnios). Hope this helps. The whole question of prenatal testing is highly sensibel and in the end a personal decision of the parents. But fortunately we have been able on this list to discuss it mature and calmly. Peace Torsten, dad of Fiona 5wcf > Hello- > I am brand new to this group. I am really looking forward to having people > to talk to who understand what I am going through. I am the mother of a > wonderful 2 and a 1/2 year old. Her name is Peyton . She was > diagnosed with CF at 13 months. Thus far we have been very fortunate, she > had been very healthy and her specialist is happy with her progress since > the diagnosis. (She was diagnosed because of failure to thrive.) My > husband and I have always wanted 2+ children and looked forward to raising > a family. Peyton is our first child. After her diagnosis I was hesitant > to have more children, however I feel that had a lot to do with the > initial shock and fear of the unknown. Now that we have settled into a > routine and my nerves have calmed down, we are trying to have another > child. Although we have not conceived yet, (been trying for 6 months) I > am weighing the pros and cons and options of prenatal testing, CVS versus > amnio. Can anyone who has been in this situation offer suggestions? I > look forward to hearing from you! > > Thanks! > ~Wendi > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2002 Report Share Posted October 30, 2002 Hi Wendi, welcome to the list. We are in the same situation. We are " working " on our second child for more than a year now after thinking about it for four years. Since preimplantation diagnosis (PID) isn't allowed here in Germany and we don't wanna have another child wcf (a very difficult decision) we have to play russian roulette. Recently I spoke with a geneticst about CVS vs. amnio. While generally amnio is the standard way of prenatal testing she prefers a CVS for the CF testing. She said that she needs the blood of both parents first (to make sure that one can distinguish between cells from the mother and cells from the fetus) and then a CVS is performed at 12 or 13 weeks. You'll get the results within 10 days then. The only downside is that there is a higher risk of a miscarriage with CVS (1% vs. 0.3% with amnios). Hope this helps. The whole question of prenatal testing is highly sensibel and in the end a personal decision of the parents. But fortunately we have been able on this list to discuss it mature and calmly. Peace Torsten, dad of Fiona 5wcf > Hello- > I am brand new to this group. I am really looking forward to having people > to talk to who understand what I am going through. I am the mother of a > wonderful 2 and a 1/2 year old. Her name is Peyton . She was > diagnosed with CF at 13 months. Thus far we have been very fortunate, she > had been very healthy and her specialist is happy with her progress since > the diagnosis. (She was diagnosed because of failure to thrive.) My > husband and I have always wanted 2+ children and looked forward to raising > a family. Peyton is our first child. After her diagnosis I was hesitant > to have more children, however I feel that had a lot to do with the > initial shock and fear of the unknown. Now that we have settled into a > routine and my nerves have calmed down, we are trying to have another > child. Although we have not conceived yet, (been trying for 6 months) I > am weighing the pros and cons and options of prenatal testing, CVS versus > amnio. Can anyone who has been in this situation offer suggestions? I > look forward to hearing from you! > > Thanks! > ~Wendi > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2002 Report Share Posted October 30, 2002 WELCOME to the list. You will find many varied answers to all questions, BUT , that is what is so very great about it here & on the other CF lists as well.. My daughter has her first child who had CF (18 years ago) & that was followed by 2 more. Non CF . They are all very happy. ERIN is currently in hospital , hopefully to get out soon. This is her first time too. It wasn't a good one, but has ending well .they love having siblings, so it really is such a personal decision to make. The testing prior to delivery would let you be more prepared if the wee one does have CF & also confirm , if it doesn't have. Your choice-not one anyone else can do . Bless you in whatever way you go. ENJOY those precious babies:):) LOVE & HUGS, grandmomBEV Hello Everyone Hello- I am brand new to this group. I am really looking forward to having people to talk to who understand what I am going through. I am the mother of a wonderful 2 and a 1/2 year old. Her name is Peyton . She was diagnosed with CF at 13 months. Thus far we have been very fortunate, she had been very healthy and her specialist is happy with her progress since the diagnosis. (She was diagnosed because of failure to thrive.) My husband and I have always wanted 2+ children and looked forward to raising a family. Peyton is our first child. After her diagnosis I was hesitant to have more children, however I feel that had a lot to do with the initial shock and fear of the unknown. Now that we have settled into a routine and my nerves have calmed down, we are trying to have another child. Although we have not conceived yet, (been trying for 6 months) I am weighing the pros and cons and options of prenatal testing, CVS versus amnio. Can anyone who has been in this situation offer suggestions? I look forward to hearing from you! Thanks! ~Wendi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2002 Report Share Posted October 30, 2002 Torsten this is very interesting - we were looking down the amnio way. Could you explain CVS and why they think it is better for CF testing. Looking at the miscarrige statistics there amnio seems more sensible. Please could you tell us more. thank you in advance. Best wishes Lucinda Fleming-, with son Dylan 19 months wcf, from Durham in the UK Reply-To: cfparents To: cfparents Subject: Re: Hello Everyone Date: Wed, 30 Oct 2002 15:35:07 -0000 Hi Wendi, welcome to the list. We are in the same situation. We are " working " on our second child for more than a year now after thinking about it for four years. Since preimplantation diagnosis (PID) isn't allowed here in Germany and we don't wanna have another child wcf (a very difficult decision) we have to play russian roulette. Recently I spoke with a geneticst about CVS vs. amnio. While generally amnio is the standard way of prenatal testing she prefers a CVS for the CF testing. She said that she needs the blood of both parents first (to make sure that one can distinguish between cells from the mother and cells from the fetus) and then a CVS is performed at 12 or 13 weeks. You'll get the results within 10 days then. The only downside is that there is a higher risk of a miscarriage with CVS (1% vs. 0.3% with amnios). Hope this helps. The whole question of prenatal testing is highly sensibel and in the end a personal decision of the parents. But fortunately we have been able on this list to discuss it mature and calmly. Peace Torsten, dad of Fiona 5wcf > Hello- > I am brand new to this group. I am really looking forward to having people > to talk to who understand what I am going through. I am the mother of a > wonderful 2 and a 1/2 year old. Her name is Peyton . She was > diagnosed with CF at 13 months. Thus far we have been very fortunate, she > had been very healthy and her specialist is happy with her progress since > the diagnosis. (She was diagnosed because of failure to thrive.) My > husband and I have always wanted 2+ children and looked forward to raising > a family. Peyton is our first child. After her diagnosis I was hesitant > to have more children, however I feel that had a lot to do with the > initial shock and fear of the unknown. Now that we have settled into a > routine and my nerves have calmed down, we are trying to have another > child. Although we have not conceived yet, (been trying for 6 months) I > am weighing the pros and cons and options of prenatal testing, CVS versus > amnio. Can anyone who has been in this situation offer suggestions? I > look forward to hearing from you! > > Thanks! > ~Wendi > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2002 Report Share Posted October 30, 2002 Torsten this is very interesting - we were looking down the amnio way. Could you explain CVS and why they think it is better for CF testing. Looking at the miscarrige statistics there amnio seems more sensible. Please could you tell us more. thank you in advance. Best wishes Lucinda Fleming-, with son Dylan 19 months wcf, from Durham in the UK Reply-To: cfparents To: cfparents Subject: Re: Hello Everyone Date: Wed, 30 Oct 2002 15:35:07 -0000 Hi Wendi, welcome to the list. We are in the same situation. We are " working " on our second child for more than a year now after thinking about it for four years. Since preimplantation diagnosis (PID) isn't allowed here in Germany and we don't wanna have another child wcf (a very difficult decision) we have to play russian roulette. Recently I spoke with a geneticst about CVS vs. amnio. While generally amnio is the standard way of prenatal testing she prefers a CVS for the CF testing. She said that she needs the blood of both parents first (to make sure that one can distinguish between cells from the mother and cells from the fetus) and then a CVS is performed at 12 or 13 weeks. You'll get the results within 10 days then. The only downside is that there is a higher risk of a miscarriage with CVS (1% vs. 0.3% with amnios). Hope this helps. The whole question of prenatal testing is highly sensibel and in the end a personal decision of the parents. But fortunately we have been able on this list to discuss it mature and calmly. Peace Torsten, dad of Fiona 5wcf > Hello- > I am brand new to this group. I am really looking forward to having people > to talk to who understand what I am going through. I am the mother of a > wonderful 2 and a 1/2 year old. Her name is Peyton . She was > diagnosed with CF at 13 months. Thus far we have been very fortunate, she > had been very healthy and her specialist is happy with her progress since > the diagnosis. (She was diagnosed because of failure to thrive.) My > husband and I have always wanted 2+ children and looked forward to raising > a family. Peyton is our first child. After her diagnosis I was hesitant > to have more children, however I feel that had a lot to do with the > initial shock and fear of the unknown. Now that we have settled into a > routine and my nerves have calmed down, we are trying to have another > child. Although we have not conceived yet, (been trying for 6 months) I > am weighing the pros and cons and options of prenatal testing, CVS versus > amnio. Can anyone who has been in this situation offer suggestions? I > look forward to hearing from you! > > Thanks! > ~Wendi > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2002 Report Share Posted October 30, 2002 Torsten this is very interesting - we were looking down the amnio way. Could you explain CVS and why they think it is better for CF testing. Looking at the miscarrige statistics there amnio seems more sensible. Please could you tell us more. thank you in advance. Best wishes Lucinda Fleming-, with son Dylan 19 months wcf, from Durham in the UK Reply-To: cfparents To: cfparents Subject: Re: Hello Everyone Date: Wed, 30 Oct 2002 15:35:07 -0000 Hi Wendi, welcome to the list. We are in the same situation. We are " working " on our second child for more than a year now after thinking about it for four years. Since preimplantation diagnosis (PID) isn't allowed here in Germany and we don't wanna have another child wcf (a very difficult decision) we have to play russian roulette. Recently I spoke with a geneticst about CVS vs. amnio. While generally amnio is the standard way of prenatal testing she prefers a CVS for the CF testing. She said that she needs the blood of both parents first (to make sure that one can distinguish between cells from the mother and cells from the fetus) and then a CVS is performed at 12 or 13 weeks. You'll get the results within 10 days then. The only downside is that there is a higher risk of a miscarriage with CVS (1% vs. 0.3% with amnios). Hope this helps. The whole question of prenatal testing is highly sensibel and in the end a personal decision of the parents. But fortunately we have been able on this list to discuss it mature and calmly. Peace Torsten, dad of Fiona 5wcf > Hello- > I am brand new to this group. I am really looking forward to having people > to talk to who understand what I am going through. I am the mother of a > wonderful 2 and a 1/2 year old. Her name is Peyton . She was > diagnosed with CF at 13 months. Thus far we have been very fortunate, she > had been very healthy and her specialist is happy with her progress since > the diagnosis. (She was diagnosed because of failure to thrive.) My > husband and I have always wanted 2+ children and looked forward to raising > a family. Peyton is our first child. After her diagnosis I was hesitant > to have more children, however I feel that had a lot to do with the > initial shock and fear of the unknown. Now that we have settled into a > routine and my nerves have calmed down, we are trying to have another > child. Although we have not conceived yet, (been trying for 6 months) I > am weighing the pros and cons and options of prenatal testing, CVS versus > amnio. Can anyone who has been in this situation offer suggestions? I > look forward to hearing from you! > > Thanks! > ~Wendi > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 5, 2002 Report Share Posted November 5, 2002 Walt, so sorry you had such a bad attack. I hope it clears up soon. You've got my prayers that the pain reduces soon. Kimber -- Kimber Vallejo, CA hominid2@... Southwest and California Representative Pancreatitis Association, International Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 5, 2002 Report Share Posted November 5, 2002 Walt, so sorry you had such a bad attack. I hope it clears up soon. You've got my prayers that the pain reduces soon. Kimber -- Kimber Vallejo, CA hominid2@... Southwest and California Representative Pancreatitis Association, International Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 5, 2002 Report Share Posted November 5, 2002 Walt, so sorry you had such a bad attack. I hope it clears up soon. You've got my prayers that the pain reduces soon. Kimber -- Kimber Vallejo, CA hominid2@... Southwest and California Representative Pancreatitis Association, International Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 14, 2002 Report Share Posted December 14, 2002 Hi Walt Nice to meet another from the NW. I was starting to feel lonely. :-) I am from Portland. Drop me a line if you want. K Hello everyone Hi there it has been a couple of weeks now on my new diet and meds. It seems to have stablized everything very well so far My new diet is rather sparse, but works. Oatmeal w/Resource Plus (ensure) morning and night and a PBJ in the afternoons. My meds are MSContin 45mgx3, Morformin, doxepin, reglan, Creon 10/20's with meals. Colace and Milk of Magnisia(sp.) This is really simple and my weight has stabilized. I have have had days with no pain all day. Yet, I have started muscle pain aroud my joints( shoulder, ankle) for about a couple of months now. My PCP is having me see a rhymotolgyst (sp.) for a posible muscle biopsy? Walt Tacoma, WA PANCREATITIS Association, Intl. Online e-mail group To reply to this message hit & quot;reply & quot; or send an e-mail to: Pancreatitis (AT) Yahoo Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 14, 2002 Report Share Posted December 14, 2002 Hi Walt Nice to meet another from the NW. I was starting to feel lonely. :-) I am from Portland. Drop me a line if you want. K Hello everyone Hi there it has been a couple of weeks now on my new diet and meds. It seems to have stablized everything very well so far My new diet is rather sparse, but works. Oatmeal w/Resource Plus (ensure) morning and night and a PBJ in the afternoons. My meds are MSContin 45mgx3, Morformin, doxepin, reglan, Creon 10/20's with meals. Colace and Milk of Magnisia(sp.) This is really simple and my weight has stabilized. I have have had days with no pain all day. Yet, I have started muscle pain aroud my joints( shoulder, ankle) for about a couple of months now. My PCP is having me see a rhymotolgyst (sp.) for a posible muscle biopsy? Walt Tacoma, WA PANCREATITIS Association, Intl. Online e-mail group To reply to this message hit & quot;reply & quot; or send an e-mail to: Pancreatitis (AT) Yahoo Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2009 Report Share Posted March 4, 2009 Actually,, I feel like Darth Vader with it on: And I get the uncontrollable urge to say: " , I am your mother " !! lol, Later NSIP 08 NC > > Subject: Re: Hello Everyone > To: Breathe-Support > Date: Wednesday, March 4, 2009, 4:04 PM > C....I know, don't we look funny in the mask?? I > call mine my snorkel. > Sure hope you sleep better after the adjustment. > Are you using the full mask or the blue gel nose mask? > Good luck w/ new pulmodude. > MamaSher; 70, IPF 3-06, OR. > Nasturtiums > Don't fret about tomorrow, God is already there! > > Hello Everyone > > > Hi my Name is Card > today I was fitted for my CPAP Mask I call it my going > diving gear > I had to Laugh my husband was with me and laughing at me > while I was trying the mask on ..will see how it goes. I > can'twait to see my kid's reaction and my dog's > when I wear the mask . Snorkel snorkel.. > I am trying to look at getting a new Pulmornary Doc.I see > my Primary Doc tommorow.to see what she can help me with new > refereal. > > Thanks Card > Springfield Mass > IPF SEPT 08 > SLEEP APENA 08 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 9, 2009 Report Share Posted March 9, 2009 Lucky you....my tech missed the artery 8 times in my wrist before switching to elbow. Then she blamed it on me being too tense. I explained later to her that if you'd just been poked eight times you'd be tense too. > > Hi Everyone > Just wanted to check in and let everyone know I had my Blood Gas Test done today it went ok harldy felt the needle just a little pinch.. > in the Wrist. just wanted to say I enjoyed talking to Peggy and Joyce Ken Baker and Lou hope she is doing well.I am trying to get used of CPAP mask. at night very uncomfortable, plus very bad sinus infection. > trouble breathing is hard enough .very tired. > > Thank you Card 9-08 iPF > wish you all the best > Quote Link to comment Share on other sites More sharing options...
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