Guest guest Posted June 9, 2005 Report Share Posted June 9, 2005 Hi, I'm sure you've heard numerous times that the way you are feeling is completely normal. It really is. Things really will get better. Plus, you'll realize that you learn so much from having a child that has a small issue (that is correctable...important to remember). My son has a lot of medical issues, and I know because of it I have become a better person because of him. I no longer take things for granted and have learned what is truly important. Dr. Dobbs is WONDERFUL...we see him also. This is a great group and will be very helpful. Take care, Proud Mom to undiagnosed syndrome: microcephaly, bilateral ptosis, bilateral clubfeet, undescended testes, GERD, low muscle tone, left kidney- hydronephrosis due to Grade IV reflux, right kidney-cysts on upper 20% and low functioning, heart murmur, global developmental delays and a big snuggle-bug that is determined to do things. > > Every day Sydney is getting more relaxed with the casts. They said > she > > wouldnt move them very much but she raises them up about an inch to > > two inches upwards. She is such a strong baby. She doesnt act like > > they bother her until it is late at night when she gets upset and > > tries to curl up. > > > > I am doing a whole lot better. I still have the baby blue and find > > myself crying for no reason BUT because of the postive feedback > about > > Dr. Dobbs and the fact that i can learn so much on this group I am > > coping alot better with her club feet. There is still guilt and we > are > > in the process of trying to find which side of the family had a > > connection to this. > > > > Is there any parents who didnt know about club foot in their family > > intially and had more children? I am very nervous about the fact of > > having another child and having to go through treatment again. I > KNOW > > IT COULD BE WORSE! and that I am very lucky to be getting the > > treatment for Sydney that she is receiving but even though they say > it > > is a 10% chance it still makes me nervous! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 9, 2005 Report Share Posted June 9, 2005 Bless your heart, Mom to . I will pray for you and I admire your outlook! Wow! This group is awesome, you are right about that. You are an inspiration. Jayme Independent Sales Director for the Pampered Chef fullnelson@... www.pamperedchef.biz/jayme " All our dreams can come true, if we have the courage to pursue them. " --Walt Disney Re: doing better Hi, I'm sure you've heard numerous times that the way you are feeling is completely normal. It really is. Things really will get better. Plus, you'll realize that you learn so much from having a child that has a small issue (that is correctable...important to remember). My son has a lot of medical issues, and I know because of it I have become a better person because of him. I no longer take things for granted and have learned what is truly important. Dr. Dobbs is WONDERFUL...we see him also. This is a great group and will be very helpful. Take care, Proud Mom to undiagnosed syndrome: microcephaly, bilateral ptosis, bilateral clubfeet, undescended testes, GERD, low muscle tone, left kidney- hydronephrosis due to Grade IV reflux, right kidney-cysts on upper 20% and low functioning, heart murmur, global developmental delays and a big snuggle-bug that is determined to do things. > > Every day Sydney is getting more relaxed with the casts. They said > she > > wouldnt move them very much but she raises them up about an inch to > > two inches upwards. She is such a strong baby. She doesnt act like > > they bother her until it is late at night when she gets upset and > > tries to curl up. > > > > I am doing a whole lot better. I still have the baby blue and find > > myself crying for no reason BUT because of the postive feedback > about > > Dr. Dobbs and the fact that i can learn so much on this group I am > > coping alot better with her club feet. There is still guilt and we > are > > in the process of trying to find which side of the family had a > > connection to this. > > > > Is there any parents who didnt know about club foot in their family > > intially and had more children? I am very nervous about the fact of > > having another child and having to go through treatment again. I > KNOW > > IT COULD BE WORSE! and that I am very lucky to be getting the > > treatment for Sydney that she is receiving but even though they say > it > > is a 10% chance it still makes me nervous! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 9, 2005 Report Share Posted June 9, 2005 Bless your heart, Mom to . I will pray for you and I admire your outlook! Wow! This group is awesome, you are right about that. You are an inspiration. Jayme Independent Sales Director for the Pampered Chef fullnelson@... www.pamperedchef.biz/jayme " All our dreams can come true, if we have the courage to pursue them. " --Walt Disney Re: doing better Hi, I'm sure you've heard numerous times that the way you are feeling is completely normal. It really is. Things really will get better. Plus, you'll realize that you learn so much from having a child that has a small issue (that is correctable...important to remember). My son has a lot of medical issues, and I know because of it I have become a better person because of him. I no longer take things for granted and have learned what is truly important. Dr. Dobbs is WONDERFUL...we see him also. This is a great group and will be very helpful. Take care, Proud Mom to undiagnosed syndrome: microcephaly, bilateral ptosis, bilateral clubfeet, undescended testes, GERD, low muscle tone, left kidney- hydronephrosis due to Grade IV reflux, right kidney-cysts on upper 20% and low functioning, heart murmur, global developmental delays and a big snuggle-bug that is determined to do things. > > Every day Sydney is getting more relaxed with the casts. They said > she > > wouldnt move them very much but she raises them up about an inch to > > two inches upwards. She is such a strong baby. She doesnt act like > > they bother her until it is late at night when she gets upset and > > tries to curl up. > > > > I am doing a whole lot better. I still have the baby blue and find > > myself crying for no reason BUT because of the postive feedback > about > > Dr. Dobbs and the fact that i can learn so much on this group I am > > coping alot better with her club feet. There is still guilt and we > are > > in the process of trying to find which side of the family had a > > connection to this. > > > > Is there any parents who didnt know about club foot in their family > > intially and had more children? I am very nervous about the fact of > > having another child and having to go through treatment again. I > KNOW > > IT COULD BE WORSE! and that I am very lucky to be getting the > > treatment for Sydney that she is receiving but even though they say > it > > is a 10% chance it still makes me nervous! Quote Link to comment Share on other sites More sharing options...
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