Guest guest Report post Posted May 13, 2002 Bridgett, HI, I am a Mom of two daughter with CF on is 9 and one is 5. I also have an 8 year old that doesn't have CF. You will meet lots of friends on here because this group is great. Deb A Quote Share this post Link to post Share on other sites
Guest guest Report post Posted May 13, 2002 Hello Bridgette, You have come to the right place. Just like our CF kids, us CF parents are a pretty special bunch. My daughter Sian (pronounced Sharn) will be six in August. She is double D508, and has mostly GI symptoms, plus exercise induced asthma. My elder daughter has no CF, but has asthma and is currently off school sick after falling in the playground but not breaking her neck! Useful things X-rays, but I'm contemplating banning monkey bars..... Love & hugs to all Mum to Cate 9yrs wocf and Sian 5yrs wcf Canberra Australia Quote Share this post Link to post Share on other sites
Guest guest Report post Posted May 14, 2002 Bridgette, Welcome to the list. I'm sure you'll find many new friends and lots of support. What is your daughter's name? I hope she is well. hugs, C Mommy to Mick and Alli, 2 yo twins wcf --- phat_grits phat_grits@...> wrote: > Hello my name is Bridgette Sumrall and I have a 9 > month old daughter > with CF. I hope to make many new friends here.. hope > to hear from > some soon... > Bridgette > > > __________________________________________________ Quote Share this post Link to post Share on other sites
Guest guest Report post Posted May 14, 2002 hello bridgette, i am patty, mom of 2 daughters with cf..Age 20 and 16 years old..patty Quote Share this post Link to post Share on other sites
Guest guest Report post Posted May 14, 2002 Welcome Bridgette. This is a good place to learn. Cindy mom of 3 - 2 w/cf 1 n/cf hello > Hello my name is Bridgette Sumrall and I have a 9 month old daughter > with CF. I hope to make many new friends here.. hope to hear from > some soon... > Bridgette > > > > > 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 Share this post Link to post Share on other sites
Guest guest Report post Posted May 14, 2002 Hi Bridgette, Welcome to the group. I hope you find the support you need here and any information that will help you with your daughter. Mom to Elliot 15mths wcf Quote Share this post Link to post Share on other sites
Guest guest Report post Posted May 14, 2002 Welcome Bridgette, My name is Deana and I have a 5 1/2 year old son wcf and an 11 year old daughter with no cf nor is she a carrier. You have come to the right place, we are here to answer ??, to lend a shoulder to cry on, and to listen if you need to vent........... How is your daughter doing now? Take care, Deana mom to 5 1/2 wcf and 11 no cf > > >Hello my name is Bridgette Sumrall and I have a 9 month old daughter >with CF. I hope to make many new friends here.. hope to hear from >some soon... >Bridgette > > _________________________________________________________________ Send and receive Hotmail on your mobile device: http://mobile.msn.com Quote Share this post Link to post Share on other sites
Guest guest Report post Posted July 2, 2002 Hi Cherity, welcome to the list! Hope your girls are doing well. I am from Germany, so can't help you with your question. But if you take a look into our archive and search for SSI you'll find a lot of messages from people, who are in the same situation. Peace Torsten, dad of Fiona 5wcf > Hello, I am new here. I am searching for some info and support on > obtaining SSI Disability for my girls w/CF. Anyone with an idea's or > if you receive it please email me! Thanks! > > Cherity > SAHMof2CFGirls@a... Quote Share this post Link to post Share on other sites
Guest guest Report post Posted July 3, 2002 I don't have any information about the SSI disability. I did want to welcome you to the list though. You might want to search previous messages on the cfparents group page at yahoo. A lot of us seem to be very busy with summer at the moment and it could take a while for your question to be answered. :-) Dawn mom of 4, 6 and under, the youngest wcf __________________________________________________ Quote Share this post Link to post Share on other sites
Guest guest Report post Posted July 3, 2002 I don't have any information about the SSI disability. I did want to welcome you to the list though. You might want to search previous messages on the cfparents group page at yahoo. A lot of us seem to be very busy with summer at the moment and it could take a while for your question to be answered. :-) Dawn mom of 4, 6 and under, the youngest wcf __________________________________________________ Quote Share this post Link to post Share on other sites
Guest guest Report post Posted July 3, 2002 I don't have any information about the SSI disability. I did want to welcome you to the list though. You might want to search previous messages on the cfparents group page at yahoo. A lot of us seem to be very busy with summer at the moment and it could take a while for your question to be answered. :-) Dawn mom of 4, 6 and under, the youngest wcf __________________________________________________ Quote Share this post Link to post Share on other sites
Guest guest Report post Posted July 3, 2002 We applied for our daughter in April and have heard from them a week ago. Because she is in the bottom of the fith percent for age in weight they are pushing it hard and it is going befor the final board. I guess it just depends on the extent of their problems. -- Bonnie Merkerison mom of three Miranda 8 wocf Trenton 5 wocf and Brooklyn 7months wcf -- Quote Share this post Link to post Share on other sites
Guest guest Report post Posted August 20, 2002 What a perfect name for the steps you have taken. Hope, let me be one of the first of many to welcome you. Unfortunatley do to my crazy travel schedule, I pop in and out a bit, but no matter where I am at in the world, I can still get to the folks online. You are among friends, for sure. Please let us know if you need anything. Craig Big-T and the Bada-Bings www.BigT-Music.com ---- " hopie612001 " hopie612001@...> wrote: > My name is Hope, and I am a new member, I had my surgery June 21 > 2001, I was 395lbs when I had the surgery, and I am now at 245lbs > however I still have more to go, wish me luck.I hope to meet new > friends here, and maybe share my story. > Again Hello and take care > Hope > > > > Homepage: http://groups.yahoo.com/group/Graduate-OSSG > > Unsubscribe: mailto:Graduate-OSSG-unsubscribe > > > > > Quote Share this post Link to post Share on other sites
Guest guest Report post Posted August 20, 2002 Hope, Welcome. I too come and go on this list, posting only occasionally but read faithfully and look forward to getting to know you. Debbie in Gig Harbor ladybostons@... Open RNY Jan 1999 320 ~ 200 Quote Share this post Link to post Share on other sites
Guest guest Report post Posted August 29, 2002 One little tip on getting in all those vitamins....I use a pill container that I got at Shop Rite. It has7 little cases that snap into the base. Each little case is marked with a day of the week and has 4 sections per day. You can snap out the little case for the day and take it with you. I fill this up weekly. Then I know if I have missed something that day. It definitely helps a lot. I think I paid around $8 for it. One other tip....since that iron needs to be taken by itself, and since I get up in the middle of the night to use the bathroom anyway...I take the iron in the middle of the night and with water only. Suggestions for the rest....read over the " pouch rules for dummies " . Not everyone follows this exactly, but reading it helps to get your head back on track and thinking about what you need to do. Do you need the suggested vitamins list? If so, let me know and I will post it or send it to you. I think both the pouch rules and the vitamin list are in the files section of the website, but I have them too if you need them. And try to avoid those carbs. They are what keep calling us back constantly, don't they? This journey becomes a LOT harder as you get farther post-op, doesn't it? I know it is really difficult to lose weight now that I am 2 yrs post-op. I exercise like crazy, take all my protein and vitamins, etc, etc...and the weight is coming off very VERY slowly now. Don't beat yourself up. Just look over all those things we were told from the beginning to give yourself a refresher course. You've done a great job!!!! Remember that. And you can keep on going too. It just isn't easy anymore. Chrissie shihtzumom@... http://users.snip.net/~shihtzumom My WLS Journey: http://millennium.fortunecity.com/doddington/691/WLS/this_is_me.htm ----- Original Message ----- From: mikki69712000 Hi my name is . I live in NJ, and had my surgery June of 2000 and abdominaplasty in June of 2001 (BTW Hi Chrissie a/k/a shitzumom). I have lost approx 130 lbs. My surgeon was Dr. Greenbaum in Willingboro. I need some help with the maintenance of my tool. It's getting a bit rusty and I don't want that to happen. I am having a problem with Protein and my vitamins as well. I can't seem to continuously get them in. I had the open rny short limb. When there are so many other issues in life, how does everyone keep their tool running like a well oiled machine. I seem to have lost touch with that. Thanks for any help that anyone may give, and thanks for listening. W. Homepage: http://groups.yahoo.com/group/Graduate-OSSG Unsubscribe: mailto:Graduate-OSSG-unsubscribe Quote Share this post Link to post Share on other sites
Guest guest Report post Posted August 29, 2002 Chrissie, I was told that we need vitamin C to help the iron get absorbed. You might want to think about taking a vitamin C pill when you take the iron..... Helene shihtzumom wrote: > One little tip on getting in all those vitamins....I use a pill container that I got at Shop Rite. It has7 little cases that snap into the base. Each little case is marked with a day of the week and has 4 sections per day. You can snap out the little case for the day and take it with you. I fill this up weekly. Then I know if I have missed something that day. It definitely helps a lot. I think I paid around $8 for it. > > One other tip....since that iron needs to be taken by itself, and since I get up in the middle of the night to use the bathroom anyway...I take the iron in the middle of the night and with water only. > > Suggestions for the rest....read over the " pouch rules for dummies " . Not everyone follows this exactly, but reading it helps to get your head back on track and thinking about what you need to do. > > Do you need the suggested vitamins list? If so, let me know and I will post it or send it to you. > > I think both the pouch rules and the vitamin list are in the files section of the website, but I have them too if you need them. > > And try to avoid those carbs. They are what keep calling us back constantly, don't they? > This journey becomes a LOT harder as you get farther post-op, doesn't it? I know it is really difficult to lose weight now that I am 2 yrs post-op. I exercise like crazy, take all my protein and vitamins, etc, etc...and the weight is coming off very VERY slowly now. Don't beat yourself up. Just look over all those things we were told from the beginning to give yourself a refresher course. You've done a great job!!!! Remember that. And you can keep on going too. It just isn't easy anymore. > > Chrissie > shihtzumom@... > http://users.snip.net/~shihtzumom > My WLS Journey: http://millennium.fortunecity.com/doddington/691/WLS/this_is_me.htm > ----- Original Message ----- From: mikki69712000 > Hi my name is . I live in NJ, and had my surgery June of > 2000 and abdominaplasty in June of 2001 (BTW Hi Chrissie a/k/a > shitzumom). I have lost approx 130 lbs. My surgeon was Dr. > Greenbaum in Willingboro. I need some help with the maintenance of > my tool. It's getting a bit rusty and I don't want that to happen. > I am having a problem with Protein and my vitamins as well. I can't > seem to continuously get them in. I had the open rny short limb. > When there are so many other issues in life, how does everyone keep > their tool running like a well oiled machine. I seem to have lost > touch with that. Thanks for any help that anyone may give, and > thanks for listening. > > W. > > Homepage: http://groups.yahoo.com/group/Graduate-OSSG > > Unsubscribe: mailto:Graduate-OSSG-unsubscribe > > > > Quote Share this post Link to post Share on other sites
Guest guest Report post Posted August 30, 2002 WELCOME, We are so very glad to have you. I am just a grandmom to an 18 yr old but have also been very close to her. I look forward to hearing about your delightful family. LOVE & HUGS, grandmomBEV Hello Hi to all on the list. This is the first time I have been on this list so I would like to introduce myself. My name is Sandie s and I am the mum of an 8 yo cf daughter and a 10 yo son without cf. We are from Australia. I am very interested to here the different experiences of other parents and hope to learn new information regarding treatments etc. Hopefully I will get to know most of you over time. Sandie s Quote Share this post Link to post Share on other sites
Guest guest Report post Posted August 30, 2002 Hi Sandie, My name is and I have 2 children, 1 with cf and 1without. I also live in Australia. What state are you in? You'll find great people on this list. Mum to Liam 8wocf & Eilish 5wcf Hello Hi to all on the list. This is the first time I have been on this list so I would like to introduce myself. My name is Sandie s and I am the mum of an 8 yo cf daughter and a 10 yo son without cf. We are from Australia. I am very interested to here the different experiences of other parents and hope to learn new information regarding treatments etc. Hopefully I will get to know most of you over time. Sandie s Quote Share this post Link to post Share on other sites
Guest guest Report post Posted August 30, 2002 Sandy and Trev, Welcome to the group, I have only been here a short time and have already learned a few things I had no clue about, I sure you will to. (Iowa) mother of 2 Mandy (13 wcf) and Cyle (11 wocf) Trev & Sandie's Mail wrote:Hi to all on the list. This is the first time I have been on this list so I would like to introduce myself. My name is Sandie s and I am the mum of an 8 yo cf daughter and a 10 yo son without cf. We are from Australia. I am very interested to here the different experiences of other parents and hope to learn new information regarding treatments etc. Hopefully I will get to know most of you over time. Sandie s Quote Share this post Link to post Share on other sites
Guest guest Report post Posted August 30, 2002 I do take vitamin C with my iron. I just didn't mention that as we were just talking about when to take the iron. Thanks, Chrissie ----- Original Message ----- From: hwd112 Chrissie, I was told that we need vitamin C to help the iron get absorbed. You might want to think about taking a vitamin C pill when you take the iron..... Quote Share this post Link to post Share on other sites
Guest guest Report post Posted August 30, 2002 Hi , Thank you for your welcome to the group. You wanted to know what part of Australia I live in. We live in Queensland, about 45mins from Brisbane. Tammy (8yo wcf) is treated at the RCH in Brisbane. I would like to know what part of Australia you come from. Cheers, Sandie s Quote Share this post Link to post Share on other sites
Guest guest Report post Posted September 1, 2002 Hi Sandie, Guess what - there's a few of us Ozzies on the various CF lists! Glad that you found us (which is a very different thing from glad that you're here - I wouldn't wish CF on anybody!) And while I'm here, I'll just let everyone know that Sian turned 6!! Love & hugs, - Mum to Cate 9yrs wocf and Sian 6yrs wcf Canberra Australia- Quote Share this post Link to post Share on other sites
Guest guest Report post Posted September 1, 2002 YEAH...........And a great big HAPPY BIRTHDAY SIAN !! LOVE & HUGS, gRANDMOMbev Re: Hello Hi Sandie, Guess what - there's a few of us Ozzies on the various CF lists! Glad that you found us (which is a very different thing from glad that you're here - I wouldn't wish CF on anybody!) And while I'm here, I'll just let everyone know that Sian turned 6!! Love & hugs, - Mum to Cate 9yrs wocf and Sian 6yrs wcf Canberra Australia- 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 Share this post Link to post Share on other sites
Guest guest Report post Posted September 1, 2002 Happy Birthday Sian!!! Deb A Quote Share this post Link to post Share on other sites
Guest guest Report post Posted October 11, 2002 WOW, what a great weight loss. I snack (if I have to) on teriyaki beef jerky (small ones - I buys the small bag). I also buy sugarless toffee candies. I am not a great on avoiding all carbs, but I do enjoy these. I allow myself some carbs, but I try to stay focused on protein. How about a boiled egg? My guess would be anything low fat, high protein (yogurt). Exercise and drink water. Whatever you're doing, it must be right...look how far you've come. Enjoy yourself, you're unique. I am sure your friend has a whole other set of circumstances. Janene West Haven,CT 8/20/01 297/191 Hello I try to find snacks that I can eat that will not put weight on me. Do anyone have any ideals? I would be thankful for any ideals anyone that have had the surgery around the length of time as me or longer. I could use some help with this. I have a friend that had the surgery but she has gain some of her weight back.This scares me. My starting weight was 304 and now I weight 126. Looking forward from hearing for someone. Quote Share this post Link to post Share on other sites