Guest guest Posted February 28, 2007 Report Share Posted February 28, 2007 That is great that people see her for herself and not as a child with scoliosis. I am so happy for her...I know it's been such a long road. Noelle (12-2-01) Ian (8-15-04) Olivia I wanted to share something that's been happening over the last year, that I hadnt really figured out, until yesterday. As most of you know, Olivia has been in casts, braces all of her life. Last year, she underwent her 1st surgical procedure(veptr dual rods attached to her pelvic structure) because she had come to the end of the road in casts and braces. A month ago, Olivia told me that she did not like her teacher, because he didnt pay attention to her! Well, this really upset me.....I didnt take action, because I had to think about it for a while. The teacher seems like a really good, caring, guy....There had to be something else going on.....Well, I think I just figured it out. Olivia is used to getting just a little more attention from people, due to her very obvious casts and braces (w/ neck support)....Now, that she no longer wears them, she doesnt stand out as much, and the attention she used to recieve is less. She is just like the other kids...No one even notices her scoliosis. I think I am so excited about this, because to everyone at her school, she is Olivia... Not Olivia with scoliosis. This means a lot to a 9 year old girl, who is growing up and wanting to fit in and be like the rest. Very young children with scoliosis, dont care what others think. They usually take their cues from their parents, and how the parents feel about it. Little ones can be taught to take pride in their casts and braces. I look back on it, and that was the easy time. No questions, no feelings of being left out, no worries about ~not~ looking exactly like the other kids, sad because she cant keep up, etc.....I am 100% convinced that Olivia looks so good, because she did wear casts for so long, and over the years they improved her overall body shape. ( Remember, her curves were over 100). Anyway, sorry about the ramble. I am just relieved that Olivia isnt starved for attention. She is just used to getting a lot. Now, she is just one of the kids. She can choose to work harder to get the attention, or not....Just like any other kid. One more thing that I have to share. Apparently, the teacher had a few minutes of free time after lunch yesterday, and he decided to have a contest to see who could hold their breath the longest. Guess who won?!! (out of 45 kids) Olivia!! Not bad for 76% lung function, heh? She won a pencil. This makes me a true believer of the bi-pap breathing exersizes she has been doing since age 2. I feel like we are very lucky, and I am very grateful for my childs health. I know what Livs life could have been, and we are nowhere near that place! Not today, anyway! Thanks for listening. HRH Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2007 Report Share Posted March 3, 2007 Hi , Thank you for sharing this experience. It is wonderful to hear about Olivia. Someday, if she doesn't already know, she will find out how her life, courage, strength, story, and the tenacity of her mother, have helped so many people. Team Olivia!! Love, Raegan 3, 16 mo. Olivia I wanted to share something that's been happening over the last year, that I hadnt really figured out, until yesterday. As most of you know, Olivia has been in casts, braces all of her life. Last year, she underwent her 1st surgical procedure(veptr dual rods attached to her pelvic structure) because she had come to the end of the road in casts and braces. A month ago, Olivia told me that she did not like her teacher, because he didnt pay attention to her! Well, this really upset me.....I didnt take action, because I had to think about it for a while. The teacher seems like a really good, caring, guy....There had to be something else going on.....Well, I think I just figured it out. Olivia is used to getting just a little more attention from people, due to her very obvious casts and braces (w/ neck support).... Now, that she no longer wears them, she doesnt stand out as much, and the attention she used to recieve is less. She is just like the other kids...No one even notices her scoliosis. I think I am so excited about this, because to everyone at her school, she is Olivia... Not Olivia with scoliosis. This means a lot to a 9 year old girl, who is growing up and wanting to fit in and be like the rest. Very young children with scoliosis, dont care what others think. They usually take their cues from their parents, and how the parents feel about it. Little ones can be taught to take pride in their casts and braces. I look back on it, and that was the easy time. No questions, no feelings of being left out, no worries about ~not~ looking exactly like the other kids, sad because she cant keep up, etc.....I am 100% convinced that Olivia looks so good, because she did wear casts for so long, and over the years they improved her overall body shape. ( Remember, her curves were over 100). Anyway, sorry about the ramble. I am just relieved that Olivia isnt starved for attention. She is just used to getting a lot. Now, she is just one of the kids. She can choose to work harder to get the attention, or not....Just like any other kid. One more thing that I have to share. Apparently, the teacher had a few minutes of free time after lunch yesterday, and he decided to have a contest to see who could hold their breath the longest. Guess who won?!! (out of 45 kids) Olivia!! Not bad for 76% lung function, heh? She won a pencil. This makes me a true believer of the bi-pap breathing exersizes she has been doing since age 2. I feel like we are very lucky, and I am very grateful for my childs health. I know what Livs life could have been, and we are nowhere near that place! Not today, anyway! Thanks for listening. HRH ________________________________________________________________________________\ ____ Sucker-punch spam with award-winning protection. Try the free Beta. http://advision.webevents./mailbeta/features_spam.html Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 5, 2007 Report Share Posted March 5, 2007 How wonderful! You and Olivia are true angels..... Tyler 4 Matson 12 months dx 12/06 Lily 1 month > > Hi , > Thank you for sharing this experience. It is wonderful to hear about Olivia. Someday, if she doesn't already know, she will find out how her life, courage, strength, story, and the tenacity of her mother, have helped so many people. Team Olivia!! > Love, > Raegan 3, 16 mo. > > > Olivia > > I wanted to share something that's been happening over the last year, that I > hadnt really figured out, until yesterday. As most of you know, Olivia has > been in casts, braces all of her life. Last year, she underwent her 1st > surgical procedure(veptr dual rods attached to her pelvic structure) because > she had come to the end of the road in casts and braces. > A month ago, Olivia told me that she did not like her teacher, because he > didnt pay attention to her! Well, this really upset me.....I didnt take > action, because I had to think about it for a while. The teacher seems like > a really good, caring, guy....There had to be something else going > on.....Well, I think I just figured it out. > Olivia is used to getting just a little more attention from people, due to > her very obvious casts and braces (w/ neck support).... Now, that she no > longer wears them, she doesnt stand out as much, and the attention she used > to recieve is less. She is just like the other kids...No one even notices > her scoliosis. I think I am so excited about this, because to everyone at > her school, she is Olivia... Not Olivia with scoliosis. This means a lot > to a 9 year old girl, who is growing up and wanting to fit in and be like > the rest. > Very young children with scoliosis, dont care what others think. They > usually take their cues from their parents, and how the parents feel about > it. Little ones can be taught to take pride in their casts and braces. I > look back on it, and that was the easy time. No questions, no feelings of > being left out, no worries about ~not~ looking exactly like the other kids, > sad because she cant keep up, etc.....I am 100% convinced that Olivia looks > so good, because she did wear casts for so long, and over the years they > improved her overall body shape. ( Remember, her curves were over 100). > Anyway, sorry about the ramble. I am just relieved that Olivia isnt starved > for attention. She is just used to getting a lot. Now, she is just one of > the kids. She can choose to work harder to get the attention, or > not....Just like any other kid. > One more thing that I have to share. Apparently, the teacher had a few > minutes of free time after lunch yesterday, and he decided to have a contest > to see who could hold their breath the longest. Guess who won?!! (out of 45 > kids) Olivia!! Not bad for 76% lung function, heh? She won a pencil. This > makes me a true believer of the bi-pap breathing exersizes she has been > doing since age 2. I feel like we are very lucky, and I am very grateful > for my childs health. I know what Livs life could have been, and we are > nowhere near that place! Not today, anyway! > > Thanks for listening. > > HRH > > > > > > > ______________________________________________________________________ ______________ > Sucker-punch spam with award-winning protection. > Try the free Beta. > http://advision.webevents./mailbeta/features_spam.html > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 5, 2007 Report Share Posted March 5, 2007 How wonderful! You and Olivia are true angels..... Tyler 4 Matson 12 months dx 12/06 Lily 1 month > > Hi , > Thank you for sharing this experience. It is wonderful to hear about Olivia. Someday, if she doesn't already know, she will find out how her life, courage, strength, story, and the tenacity of her mother, have helped so many people. Team Olivia!! > Love, > Raegan 3, 16 mo. > > > Olivia > > I wanted to share something that's been happening over the last year, that I > hadnt really figured out, until yesterday. As most of you know, Olivia has > been in casts, braces all of her life. Last year, she underwent her 1st > surgical procedure(veptr dual rods attached to her pelvic structure) because > she had come to the end of the road in casts and braces. > A month ago, Olivia told me that she did not like her teacher, because he > didnt pay attention to her! Well, this really upset me.....I didnt take > action, because I had to think about it for a while. The teacher seems like > a really good, caring, guy....There had to be something else going > on.....Well, I think I just figured it out. > Olivia is used to getting just a little more attention from people, due to > her very obvious casts and braces (w/ neck support).... Now, that she no > longer wears them, she doesnt stand out as much, and the attention she used > to recieve is less. She is just like the other kids...No one even notices > her scoliosis. I think I am so excited about this, because to everyone at > her school, she is Olivia... Not Olivia with scoliosis. This means a lot > to a 9 year old girl, who is growing up and wanting to fit in and be like > the rest. > Very young children with scoliosis, dont care what others think. They > usually take their cues from their parents, and how the parents feel about > it. Little ones can be taught to take pride in their casts and braces. I > look back on it, and that was the easy time. No questions, no feelings of > being left out, no worries about ~not~ looking exactly like the other kids, > sad because she cant keep up, etc.....I am 100% convinced that Olivia looks > so good, because she did wear casts for so long, and over the years they > improved her overall body shape. ( Remember, her curves were over 100). > Anyway, sorry about the ramble. I am just relieved that Olivia isnt starved > for attention. She is just used to getting a lot. Now, she is just one of > the kids. She can choose to work harder to get the attention, or > not....Just like any other kid. > One more thing that I have to share. Apparently, the teacher had a few > minutes of free time after lunch yesterday, and he decided to have a contest > to see who could hold their breath the longest. Guess who won?!! (out of 45 > kids) Olivia!! Not bad for 76% lung function, heh? She won a pencil. This > makes me a true believer of the bi-pap breathing exersizes she has been > doing since age 2. I feel like we are very lucky, and I am very grateful > for my childs health. I know what Livs life could have been, and we are > nowhere near that place! Not today, anyway! > > Thanks for listening. > > HRH > > > > > > > ______________________________________________________________________ ______________ > Sucker-punch spam with award-winning protection. > Try the free Beta. > http://advision.webevents./mailbeta/features_spam.html > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 19, 2007 Report Share Posted March 19, 2007 -, We are praying and thinking of you and Olivia. We hope everything goes well in SLC on Wednesday. Many prayers, and Matt Tyler 4 Matson 13 months (dx Dec 06) Lily 7 weeks -- In infantile scoliosis treatment , " heather hyatt " wrote: > > I sent this e-mail earlier, but dont see it coming through..... > Again... > Olivias veptr rods are migrating. The rods are protruding significantly, at > the shoulders. I think there may be some rib breakage at the top anchoring > points, but she shows no signs of pain...(?) We are headed to SLC, on Weds. > > Please pray for my girl. > > HRH > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 19, 2007 Report Share Posted March 19, 2007 Good luck and Olivia. As always, prayers and thoughts with you. Olivia is such a brave girl! /Cole heather hyatt wrote: I sent this e-mail earlier, but dont see it coming through..... Again... Olivias veptr rods are migrating. The rods are protruding significantly, at the shoulders. I think there may be some rib breakage at the top anchoring points, but she shows no signs of pain...(?) We are headed to SLC, on Weds. Please pray for my girl. HRH --------------------------------- No need to miss a message. Get email on-the-go with for Mobile. Get started. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 19, 2007 Report Share Posted March 19, 2007 Thanks . Thanks . If my daughters ribs are broken, I will work harder than ever before in trying to make Early Treatment a primary option for infants/children with progressive infantile scoliosis!!! No child/family should have to go through this. 9 years ago early treatment was not an option, but today it should be offered at every hospital. Families should have the Early Treatment option, ~before~ any surgery is recommended. HRH Re: Olivia -, We are praying and thinking of you and Olivia. We hope everything goes well in SLC on Wednesday. Many prayers, and Matt Tyler 4 Matson 13 months (dx Dec 06) Lily 7 weeks -- In infantile scoliosis treatment , " heather hyatt " wrote: > > I sent this e-mail earlier, but dont see it coming through..... > Again... > Olivias veptr rods are migrating. The rods are protruding significantly, at > the shoulders. I think there may be some rib breakage at the top anchoring > points, but she shows no signs of pain...(?) We are headed to SLC, on Weds. > > Please pray for my girl. > > HRH > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 19, 2007 Report Share Posted March 19, 2007 , Of course.............I will be praying for Olivia. Let us know how things go. Tasha heather hyatt wrote: I sent this e-mail earlier, but dont see it coming through..... Again... Olivias veptr rods are migrating. The rods are protruding significantly, at the shoulders. I think there may be some rib breakage at the top anchoring points, but she shows no signs of pain...(?) We are headed to SLC, on Weds. Please pray for my girl. HRH --------------------------------- It's here! Your new message! Get new email alerts with the free Toolbar. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 19, 2007 Report Share Posted March 19, 2007 , Give Olivia a gentle hug from us. Call me when you get to town. I'll be in SLC on Friday. Braydon's VEPTR has migrated too, but in a very different fashion, I'm guessing. In Braydon's case, the migration has been a slow process, not causing any discomfort or problem with the natural ribs. The migration through the ribs sounds much worse than it is. I promise. Take care! Carmell Mom to Kara, idiopathic scoliosis and hypothyroidism, Blake 16, GERD, and Braydon 11, VACTERL-congenital scoliosis (fusion surgery 5/96), VEPTR patient #137 (implant 8/01), Thoracic Insufficiency Syndrome (TIS), rib anomalies, missing coccyx, fatty filum/TC (released 4/99 & 12/06), anal stenosis, chronic constipation, horseshoe (cross-fused) kidney, dbl ureter in left kidney, ureterocele (excized 6/95), kidney reflux (reimplant surgery 1/97), neurogenic bladder, dysplastic right leg w/right clubfoot with 8 toes (repaired 2/96, 3/96, 1/97, 3/04), tibial torsion, 4cm length discrepancy-wears 3cm lift, pes cavus, SUA, GERD, Gastroparesis, etc. http://carmellb-ivil.tripod.com/myfamily/ Congenital scoliosis support group http://health./group/CongenitalScoliosisSupport/ ________________________________________________________________________________\ ____ Looking for earth-friendly autos? Browse Top Cars by " Green Rating " at Autos' Green Center. http://autos./green_center/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 19, 2007 Report Share Posted March 19, 2007 , I hope all is well with Olivia. She's a tough cookie that's for sure. I will keep my fingers crossed that all goes well. Noelle (12-2-01) Ian (8-15-04) Olivia I sent this e-mail earlier, but dont see it coming through..... Again... Olivias veptr rods are migrating. The rods are protruding significantly, at the shoulders. I think there may be some rib breakage at the top anchoring points, but she shows no signs of pain...(?) We are headed to SLC, on Weds. Please pray for my girl. HRH Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 19, 2007 Report Share Posted March 19, 2007 heather, of course, my prayers are with you and olivia. good luck with your appointment. i hope you get some good news. she deserves it! my best, deshea > I sent this e-mail earlier, but dont see it coming through..... > Again... > Olivias veptr rods are migrating. The rods are protruding > significantly, at > the shoulders. I think there may be some rib breakage at the top > anchoring > points, but she shows no signs of pain...(?) We are headed to SLC, > on Weds. > > Please pray for my girl. > > HRH > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 20, 2007 Report Share Posted March 20, 2007 , Olivia is in our thoughts and our prayers. You're right-on a postive note-she's not in pain or discomfort. Hope all goes well on wednesday. Good Luck, Aekta, Dave & Maxwell > > I sent this e-mail earlier, but dont see it coming through..... > Again... > Olivias veptr rods are migrating. The rods are protruding significantly, at > the shoulders. I think there may be some rib breakage at the top anchoring > points, but she shows no signs of pain...(?) We are headed to SLC, on Weds. > > Please pray for my girl. > > HRH > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 20, 2007 Report Share Posted March 20, 2007 Our thoughts and prayers are with you and Olivia. We look forward to hearing from you when you return. Love, and Raegan 3yrs 17 months Olivia I sent this e-mail earlier, but dont see it coming through..... Again... Olivias veptr rods are migrating. The rods are protruding significantly, at the shoulders. I think there may be some rib breakage at the top anchoring points, but she shows no signs of pain...(?) We are headed to SLC, on Weds. Please pray for my girl. HRH ________________________________________________________________________________\ ____ Food fight? Enjoy some healthy debate in the Answers Food & Drink Q & A. http://answers./dir/?link=list & sid=396545367 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 20, 2007 Report Share Posted March 20, 2007 Good luck and Olivia We wish you all the best and hope for good results and better results than you are expecting.. We will be sending prayers Love Bert and Bridget heather hyatt wrote: I sent this e-mail earlier, but dont see it coming through..... Again... Olivias veptr rods are migrating. The rods are protruding significantly, at the shoulders. I think there may be some rib breakage at the top anchoring points, but she shows no signs of pain...(?) We are headed to SLC, on Weds. Please pray for my girl. HRH --------------------------------- Get your own web address. Have a HUGE year through Yahoo! Small Business. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 20, 2007 Report Share Posted March 20, 2007 , You are in our family's prayers as always. I am so sorry you have to go through all of this! You are such a strength for you daughter. I admire your dedication and ambition on her behalf. Good luck and keep us updated!!! Hansen > > I sent this e-mail earlier, but dont see it coming through..... > Again... > Olivias veptr rods are migrating. The rods are protruding significantly, at > the shoulders. I think there may be some rib breakage at the top anchoring > points, but she shows no signs of pain...(?) We are headed to SLC, on Weds. > > Please pray for my girl. > > HRH > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 20, 2007 Report Share Posted March 20, 2007 , She's in our prayers. Take care. Jerry Olivia I sent this e-mail earlier, but dont see it coming through..... Again... Olivias veptr rods are migrating. The rods are protruding significantly, at the shoulders. I think there may be some rib breakage at the top anchoring points, but she shows no signs of pain...(?) We are headed to SLC, on Weds. Please pray for my girl. HRH Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 20, 2007 Report Share Posted March 20, 2007 , You are in our prayers. Hope everything goes well in SLC. tried to call Monday night to let you know I Recieved the article thank you. Devyn's surgery for the Chiari is scheduled for next thursday the 29th at Denver childrens. They have said we will have to wait till june now to cast. Again good luck and hope to talk to you when you return. Rochelle West > > I sent this e-mail earlier, but dont see it coming through..... > Again... > Olivias veptr rods are migrating. The rods are protruding significantly, at > the shoulders. I think there may be some rib breakage at the top anchoring > points, but she shows no signs of pain...(?) We are headed to SLC, on Weds. > > Please pray for my girl. > > HRH > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 21, 2007 Report Share Posted March 21, 2007 , We are praying for you both! Please take Care. Amy & Adelaide heather hyatt wrote: Thanks . Thanks . If my daughters ribs are broken, I will work harder than ever before in trying to make Early Treatment a primary option for infants/children with progressive infantile scoliosis!!! No child/family should have to go through this. 9 years ago early treatment was not an option, but today it should be offered at every hospital. Families should have the Early Treatment option, ~before~ any surgery is recommended. HRH Re: Olivia -, We are praying and thinking of you and Olivia. We hope everything goes well in SLC on Wednesday. Many prayers, and Matt Tyler 4 Matson 13 months (dx Dec 06) Lily 7 weeks -- In infantile scoliosis treatment , " heather hyatt " wrote: > > I sent this e-mail earlier, but dont see it coming through..... > Again... > Olivias veptr rods are migrating. The rods are protruding significantly, at > the shoulders. I think there may be some rib breakage at the top anchoring > points, but she shows no signs of pain...(?) We are headed to SLC, on Weds. > > Please pray for my girl. > > HRH > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 21, 2007 Report Share Posted March 21, 2007 We wish you every luck and success. I can only imagine how worried you are! Glad Oliviia isn't phased! xoxox Abigail and Nadia --------------------------------- No need to miss a message. Get email on-the-go with for Mobile. Get started. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 22, 2007 Report Share Posted March 22, 2007 - Good luck to you guys I have a thought about broken ribs....You said she was not in pain so maybe there aren't any broken ribs ......would'nt she be in same pain so maybe that is a good note? Keep us posted and good luck and Adan -- In infantile scoliosis treatment , Amy Norenberg wrote: > > , > We are praying for you both! Please take Care. > Amy & Adelaide > > heather hyatt wrote: > Thanks . > Thanks . > If my daughters ribs are broken, I will work harder than ever before in trying to make Early Treatment a primary option for infants/children with progressive infantile scoliosis!!! No child/family should have to go through this. 9 years ago early treatment was not an option, but today it should be offered at every hospital. Families should have the Early Treatment option, ~before~ any surgery is recommended. > > HRH > Re: Olivia > > -, > We are praying and thinking of you and Olivia. We hope everything > goes well in SLC on Wednesday. > Many prayers, > and Matt > Tyler 4 > Matson 13 months (dx Dec 06) > Lily 7 weeks > > -- In infantile scoliosis treatment , " heather hyatt " > <heather@> wrote: > > > > I sent this e-mail earlier, but dont see it coming through..... > > Again... > > Olivias veptr rods are migrating. The rods are protruding > significantly, at > > the shoulders. I think there may be some rib breakage at the top > anchoring > > points, but she shows no signs of pain...(?) We are headed to SLC, > on Weds. > > > > Please pray for my girl. > > > > HRH > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2007 Report Share Posted March 27, 2007 Sending again.... Re: called re: Olivia HI Everyone, Shellie here. called me this evening with an update. All those prayers were heard, because Olivia is fine. Her xrays show that the Veptrs are fine and NO ribs are broken. The protrusion is actually an area of fluid between layers of skin. They are going to take care of that tomorrow and do a mini-expansion of the Veptrs. Mini, because they need to keep an eye on the area. Mini also (as opposed to not expanding) because if you wait too long between expansions some spines become rigid. is very relieved and thanks everyone for thinking of her and Olivia. She will call me again tomorrow with another update on how things go. Shellie heather hyatt wrote: Thanks for all of your positive thoughts and prayers. We leave first thing in the a.m., and should be to SLC before evryone gets to work (LOL)!! Olivia is doing great, and doesnt even realize my concern. Dont want to scare her. I'll have Shellie post for us, when we figure out whats going on. Love, HRH --------------------------------- Bored stiff? Loosen up... Download and play hundreds of games for free on Games. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2007 Report Share Posted March 27, 2007 , Glad to hear your are home and getting ready for a FABULOUS trip! You both could use some time away from medical stress and trauma to ENJOY life! Good for you. I wish I would have called you while you were here... I know how worried you were, but glad it wasn't as serious as you thought. Braydon has quite a large bursa over the bottom part of his chestwall device. They've drained it a few times during routine expansion surgeries, but it always comes back. Its just how his body heals. We'll be anxious to hear how your cruise goes, and how the trip to VA goes, and so many adventures in your life. Let me know if I can do anything to help. Carmell Mom to Kara, idiopathic scoliosis and hypothyroidism, Blake 16, GERD, and Braydon 11, VACTERL-congenital scoliosis (fusion surgery 5/96), VEPTR patient #137 (implant 8/01), Thoracic Insufficiency Syndrome (TIS), rib anomalies, missing coccyx, fatty filum/TC (released 4/99 & 12/06), anal stenosis, chronic constipation, horseshoe (cross-fused) kidney, dbl ureter in left kidney, ureterocele (excized 6/95), kidney reflux (reimplant surgery 1/97), neurogenic bladder, dysplastic right leg w/right clubfoot with 8 toes (repaired 2/96, 3/96, 1/97, 3/04), tibial torsion, 4cm length discrepancy-wears 3cm lift, pes cavus, SUA, GERD, Gastroparesis, etc. http://carmellb-ivil.tripod.com/myfamily/ Congenital scoliosis support group http://health./group/CongenitalScoliosisSupport/ ________________________________________________________________________________\ ____ Never miss an email again! Toolbar alerts you the instant new Mail arrives. http://tools.search./toolbar/features/mail/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2007 Report Share Posted March 28, 2007 Great news and love to Olivia too from me and Bridget. Have a wonderful trip and enjoy the ocean and the sand. Catch a wave for us.. Love Bert and Bridget heather hyatt wrote: Sending again.... Re: called re: Olivia HI Everyone, Shellie here. called me this evening with an update. All those prayers were heard, because Olivia is fine. Her xrays show that the Veptrs are fine and NO ribs are broken. The protrusion is actually an area of fluid between layers of skin. They are going to take care of that tomorrow and do a mini-expansion of the Veptrs. Mini, because they need to keep an eye on the area. Mini also (as opposed to not expanding) because if you wait too long between expansions some spines become rigid. is very relieved and thanks everyone for thinking of her and Olivia. She will call me again tomorrow with another update on how things go. Shellie heather hyatt wrote: Thanks for all of your positive thoughts and prayers. We leave first thing in the a.m., and should be to SLC before evryone gets to work (LOL)!! Olivia is doing great, and doesnt even realize my concern. Dont want to scare her. I'll have Shellie post for us, when we figure out whats going on. Love, HRH --------------------------------- Bored stiff? Loosen up... Download and play hundreds of games for free on Games. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2007 Report Share Posted March 28, 2007 I am really sorry that we didnt connect, Carmell. There was so much going on at the hospital, I could barely take a break. We were able to see Kylie, Bethany, & Breann this time, so Olivia really had fun. This was the 1st time that Bethany and Liv were able to meet, and it was great to see all of them " hanging out " together. They are all growing up into amazing young women, who have a lot to do in this lifetime. I think that our doc is going to try to schedule expansions for Breann & Liv together, which makes all of our lives a lot easier....They both did great, and were walking around by evening, right after the expansions.. That darn bursa almost gave me a heart attack! I was sick to my stomach last week, thinking her rods had migrated through! The protrusion was significant, and I would have never thought it to be a bursa. It made both rods protrude. Anyway, we lucked out, again! I am so relieved. All you can do is continue providing your solid experience on this group. You know we all appreciate what you have to say, Carmell. I'll be in touch, when we get home. Olivia is so excited about her wish, she can hardly stand it. She has never seen the beach. She is trying to go to bed early every night, so the next day will be here quicker! Now, thats exitement! Thanks for recommending the M-A-W, and going to bat for us!!! This vacation has been a long time coming, and we are beside ourselves. The limo will be here to pick us up on Sat....Oh, and her best friend since kindergarden is coming with us!! Yeah! HRH Re: Fw: Olivia , Glad to hear your are home and getting ready for a FABULOUS trip! You both could use some time away from medical stress and trauma to ENJOY life! Good for you. I wish I would have called you while you were here... I know how worried you were, but glad it wasn't as serious as you thought. Braydon has quite a large bursa over the bottom part of his chestwall device. They've drained it a few times during routine expansion surgeries, but it always comes back. Its just how his body heals. We'll be anxious to hear how your cruise goes, and how the trip to VA goes, and so many adventures in your life. Let me know if I can do anything to help. Carmell Mom to Kara, idiopathic scoliosis and hypothyroidism, Blake 16, GERD, and Braydon 11, VACTERL-congenital scoliosis (fusion surgery 5/96), VEPTR patient #137 (implant 8/01), Thoracic Insufficiency Syndrome (TIS), rib anomalies, missing coccyx, fatty filum/TC (released 4/99 & 12/06), anal stenosis, chronic constipation, horseshoe (cross-fused) kidney, dbl ureter in left kidney, ureterocele (excized 6/95), kidney reflux (reimplant surgery 1/97), neurogenic bladder, dysplastic right leg w/right clubfoot with 8 toes (repaired 2/96, 3/96, 1/97, 3/04), tibial torsion, 4cm length discrepancy-wears 3cm lift, pes cavus, SUA, GERD, Gastroparesis, etc. http://carmellb-ivil.tripod.com/myfamily/ Congenital scoliosis support group http://health./group/CongenitalScoliosisSupport/ __________________________________________________________ Never miss an email again! Toolbar alerts you the instant new Mail arrives. http://tools.search./toolbar/features/mail/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2007 Report Share Posted March 28, 2007 “She is trying to go to bed early every night, so the next day will be here quicker! Now, thats exitement!” The real question is, is she even sleeping? Lol, If I was her and expecting a trip like that, I would find it very hard to sleep besides doing anything else. Have a blast on this trip, you 2 deserve it. Betty -- No virus found in this outgoing message. Checked by AVG Free Edition. Version: 7.5.446 / Virus Database: 268.18.18/734 - Release Date: 3/26/2007 2:31 PM Quote Link to comment Share on other sites More sharing options...
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