Guest guest Posted April 26, 2002 Report Share Posted April 26, 2002 Angie, Thank you so much for letting us know about your father. I will definitely keep him and all of you in my prayers. Please keep us up to date on him as much as possible. God bless, Belinda > Hello to everyone. My Dad wanted me to e-mail everyone to update you on his > latest status. He is currently at Shore Memorial Hospital fighting pneumonia. > He is listed in critical condition due to his need for assistance with > breathing. My Mom, Kris, Beth and myself are all here in NJ. The doctors, > nurses, and specialists are all providing the best care possible for him. > Please keep him in your thoughts and prayers. > Angie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 10, 2002 Report Share Posted May 10, 2002 Thank you for the blank e-mail. Was it a reflective piece? LOL Rosemary in New York with three children with CF - they are 11, 9, 5....... I coined the phrase " BREATHE DAMMIT " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2002 Report Share Posted May 14, 2002 I sure know allot of research must have been done on THAT one :):) Hi < Love YA, GrandmomBEV Re: (no subject) Thank you for the blank e-mail. Was it a reflective piece? LOL Rosemary in New York with three children with CF - they are 11, 9, 5....... I coined the phrase " BREATHE DAMMIT " PLEASE do not post religious emails to the list. ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. -------------------------------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2002 Report Share Posted May 26, 2002 hi, so glad to hear that your dad is getting home finally. i'm sure he'll be happy to be there. please give him a big hug from me and tell him we're all praying for his recovery. smiles and hugs, di (no subject) Hello again,I just wanted to give everyone an update on my dad. He is scheduled to be released from ICU this Wednesday. The doctor is sending him home. Everyone, especially my mom, is learning how to take care of him with all of his new equiptment. He will remain on a vent. and use a feeding tube even while at home. He is weak and prone to infection, but is anxiously waiting to get back home! Thank you for keeping him in your thoughts and prayers. We all appreciate it.Angie If you do not wish to belong to shydrager, you may unsubscribe by sending a blank email to shydrager-unsubscribe Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 11, 2002 Report Share Posted September 11, 2002 this is the one I sent , It had been sent to me thanks GRANDMOMBEV (no subject) Torsten, This was posted on cystic-l, the words and images say it all. I had this forwarded to me and I thought I'd pass it on. It has sound, so make sure your speakers are on and it's about 7-8 mins long but truly captures the feelings and emotions of 9/11/01. http://www.politicsandprotest.com/ Carol - a native new yorker (mom to 2/cf) PLEASE do not post religious emails to the list. ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. -------------------------------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 11, 2002 Report Share Posted September 11, 2002 Bev and Carol, I just viewed this download and it stirred all the raw feelings that I felt that day. It is a powerful piece and well represents what New York, as a city, and we, as a nation, have endured. Torsten, we may have, in your opinion, the " dumbest US president ever " , but I am proud that he is MY President! Randy ______________________________________________________________ Information contained in this e-mail message may be legally privileged and confidential information intended only for the use of the individual(s) named above. If the reader of this message is not the intended recipient, you are hereby notified that any use, dissemination, distribution, or copying of this e-mail is strictly prohibited. If e-mailed messages include MEDICAL RECORDS, these records ARE PRIVILEGED AND CONFIDENTIAL and may be released only upon written permission of the patient. If you have received this e-mail in error, please immediately notify the sender by telephone at 1- and delete this e-mail. Thank you! ______________________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2002 Report Share Posted September 25, 2002 Hi Christy, you have to add the new addy to your Yahoo Profile and then go to " My Groups " and change the addy under " Mail preferences " . Alternatively you send a mail from your new account to cfparents-subscribe but if you subscribe via mail your new addy isn't registered with Yahoo and you can't use the list features. So the first method is more difficult to do but gives you access to the list archives, files, chat and so on. Hope you figure it out. Peace Torsten, dad of Fiona 5wcf e-mail: torstenkrafft@... (no subject) > Im changing internet connection how to i go about changing to a new email > address? > > thanks christy(shianne 22 months w/cf) > > > PLEASE do not post religious emails to the list. > > > ------------------------------------------- > > > The opinions and information exchanged on this list should > IN NO WAY > be construed as medical advice. > > PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. > > -------------------------------------------------- > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2002 Report Share Posted September 25, 2002 Hi Christy, you have to add the new addy to your Yahoo Profile and then go to " My Groups " and change the addy under " Mail preferences " . Alternatively you send a mail from your new account to cfparents-subscribe but if you subscribe via mail your new addy isn't registered with Yahoo and you can't use the list features. So the first method is more difficult to do but gives you access to the list archives, files, chat and so on. Hope you figure it out. Peace Torsten, dad of Fiona 5wcf e-mail: torstenkrafft@... (no subject) > Im changing internet connection how to i go about changing to a new email > address? > > thanks christy(shianne 22 months w/cf) > > > PLEASE do not post religious emails to the list. > > > ------------------------------------------- > > > The opinions and information exchanged on this list should > IN NO WAY > be construed as medical advice. > > PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. > > -------------------------------------------------- > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2002 Report Share Posted September 25, 2002 Hi Christy, you have to add the new addy to your Yahoo Profile and then go to " My Groups " and change the addy under " Mail preferences " . Alternatively you send a mail from your new account to cfparents-subscribe but if you subscribe via mail your new addy isn't registered with Yahoo and you can't use the list features. So the first method is more difficult to do but gives you access to the list archives, files, chat and so on. Hope you figure it out. Peace Torsten, dad of Fiona 5wcf e-mail: torstenkrafft@... (no subject) > Im changing internet connection how to i go about changing to a new email > address? > > thanks christy(shianne 22 months w/cf) > > > PLEASE do not post religious emails to the list. > > > ------------------------------------------- > > > The opinions and information exchanged on this list should > IN NO WAY > be construed as medical advice. > > PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. > > -------------------------------------------------- > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 I was given enzymes when this all started for me and they seemed to help, but since April I have been on TPN and have had no need for them. Jenise Mansfield, OH Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 I was given enzymes when this all started for me and they seemed to help, but since April I have been on TPN and have had no need for them. Jenise Mansfield, OH Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 I was given enzymes when this all started for me and they seemed to help, but since April I have been on TPN and have had no need for them. Jenise Mansfield, OH Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 In a message dated 11/11/02 11:47:28 PM Eastern Standard Time, KimNY777@... writes: > Just curious .. Does everyone here with pancreatitis take " Enzymes " ? I was > given a script in the hospital to take with meals here at home ... just > never > bothered. ( Those that do take them .. Do you really feel that it makes a > difference ?? . Would appreciate any feed back on this subject. > Yes I do and yes it makes a big difference for me. But remember we are all different. Ya gotta try to seek and implement the best procedure for you, but leave no rock unturned, it's a long journey. Best wishes, Poncho - GA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 In a message dated 11/11/02 11:47:28 PM Eastern Standard Time, KimNY777@... writes: > Just curious .. Does everyone here with pancreatitis take " Enzymes " ? I was > given a script in the hospital to take with meals here at home ... just > never > bothered. ( Those that do take them .. Do you really feel that it makes a > difference ?? . Would appreciate any feed back on this subject. > Yes I do and yes it makes a big difference for me. But remember we are all different. Ya gotta try to seek and implement the best procedure for you, but leave no rock unturned, it's a long journey. Best wishes, Poncho - GA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 In a message dated 11/11/02 11:47:28 PM Eastern Standard Time, KimNY777@... writes: > Just curious .. Does everyone here with pancreatitis take " Enzymes " ? I was > given a script in the hospital to take with meals here at home ... just > never > bothered. ( Those that do take them .. Do you really feel that it makes a > difference ?? . Would appreciate any feed back on this subject. > Yes I do and yes it makes a big difference for me. But remember we are all different. Ya gotta try to seek and implement the best procedure for you, but leave no rock unturned, it's a long journey. Best wishes, Poncho - GA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 In a message dated 11/11/2002 11:51:00 PM Eastern Standard Time, Jenise4790@... writes: > I was given enzymes when this all started for me and they seemed to help, > but > since April I have been on TPN and have had no need for them. > > Jenise > Mansfield, OH Jenise ... What is TPN ?? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 In a message dated 11/11/2002 11:51:00 PM Eastern Standard Time, Jenise4790@... writes: > I was given enzymes when this all started for me and they seemed to help, > but > since April I have been on TPN and have had no need for them. > > Jenise > Mansfield, OH Jenise ... What is TPN ?? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 In a message dated 11/11/2002 11:55:17 PM Eastern Standard Time, poncho9191@... writes: > Yes I do and yes it makes a big difference for me. But remember we are all > different. > Ya gotta try to seek and implement the best procedure for you, but leave no > > rock unturned, it's a long journey. > Best wishes, Poncho - GA > Thank you Poncho. .. I will certainly give them a try now. (((HUGSSSS))) Kim/NY Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 In a message dated 11/11/2002 11:55:17 PM Eastern Standard Time, poncho9191@... writes: > Yes I do and yes it makes a big difference for me. But remember we are all > different. > Ya gotta try to seek and implement the best procedure for you, but leave no > > rock unturned, it's a long journey. > Best wishes, Poncho - GA > Thank you Poncho. .. I will certainly give them a try now. (((HUGSSSS))) Kim/NY Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 In a message dated 11/11/2002 11:55:17 PM Eastern Standard Time, poncho9191@... writes: > Yes I do and yes it makes a big difference for me. But remember we are all > different. > Ya gotta try to seek and implement the best procedure for you, but leave no > > rock unturned, it's a long journey. > Best wishes, Poncho - GA > Thank you Poncho. .. I will certainly give them a try now. (((HUGSSSS))) Kim/NY Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 TPN is Total Parental Nutrition. Basically I feed myself thru an IV port. It is a bag of liquid that has all your nutritional needs when you are unable to eat normal. Jenise Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 TPN is Total Parental Nutrition. Basically I feed myself thru an IV port. It is a bag of liquid that has all your nutritional needs when you are unable to eat normal. Jenise Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 TPN is Total Parental Nutrition. Basically I feed myself thru an IV port. It is a bag of liquid that has all your nutritional needs when you are unable to eat normal. Jenise Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 In a message dated 11/12/2002 1:17:45 AM Eastern Standard Time, casca@... writes: > > I take them all the time with meals and snacks...they make a wonderful > difference for me > > Mark E. Armstrong Thank you Mark ) As I told Poncho I'm definitely going to give them a try after hearing they work for both of you. Again TY (((HUGS))) Kim/NY Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 11, 2002 Report Share Posted November 11, 2002 In a message dated 11/12/2002 1:17:45 AM Eastern Standard Time, casca@... writes: > > I take them all the time with meals and snacks...they make a wonderful > difference for me > > Mark E. Armstrong Thank you Mark ) As I told Poncho I'm definitely going to give them a try after hearing they work for both of you. Again TY (((HUGS))) Kim/NY Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.