Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 Dianne, We are at the point now where we really only go to doctors every couple of months. I find that I feel much better in between appointment cycles than I do when we're in the middle of one. I hate hearing anything other than, " Ma'am this is totally great! " And of course both of my boys are a little different, so I can be very sensitive in discussions about " normal " kids. I think worrying about their cognitive ability is the hardest for me too. And sometimes I wonder why they tell you anything about life expectancy at all. I mean does it help anything? They are so often wrong, and then you spend so much time waiting for the end of your child's life. No parent should have to do that. I mean, we aren't set up that way. I can't imagine what a blackness that would bring around. No wonder you panic. I'm sure that some of the amazing people on here who've suffered a loss can help you maybe find some peace. I agree with about the trauma. I still freak out in hospitals, to the point of physical symptoms. 's heart surgery was a terrible experience. Even though it was 9 months ago, I still have a hard time letting doctors near him unless I am right there. Which, by the way, we have a sedated BAER today that I am dreading. I am actually looking for a counselor now, and may go back on meds myself. (Let me know how you work all of this through Tricare!) From most of what I have read, post partum depression can extend well into the first year or beyond, and therapy AND medication are the most effective treatment. And I think that for me, I may need some time just to experience the greif that is lingering. It's kind of a triple whammy, I'm still sad for the life/child we thought we would have and didn't, and then I'm sad for everything my son has to go through, and on top of it all, worried if he'll even make it. Luckily, is at a shore site now, so he's not been deployed for any of this. But he's still usually not there when I get any news, good or bad. He's still trying to bond with , and tends to distance himself from all the medical stuff. I feel pretty alone sometimes too, very similar to when you try and keep up a cheery deployment front. Does your EFMP have a support group? They have one here that I think I would go to if wasn't home. There is something I saw on Oprah the other day. Don't laugh, I'm serious! This beautiful girl had been terribly burned and disfigured in a car accident. And she said that she gives herself five minutes a day to be angry and sorry for herself, but the rest of the time she has to make her life enjoyable or she may as well have died. That really hit home with me. So, for a few minutes a day, I hate CHARGE, and I feel like crap. Then I try and enjoy my kids. I'm not real good at it yet! I'm thinking about you guys! I hope your ship comes in soon! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 Dianne, We are at the point now where we really only go to doctors every couple of months. I find that I feel much better in between appointment cycles than I do when we're in the middle of one. I hate hearing anything other than, " Ma'am this is totally great! " And of course both of my boys are a little different, so I can be very sensitive in discussions about " normal " kids. I think worrying about their cognitive ability is the hardest for me too. And sometimes I wonder why they tell you anything about life expectancy at all. I mean does it help anything? They are so often wrong, and then you spend so much time waiting for the end of your child's life. No parent should have to do that. I mean, we aren't set up that way. I can't imagine what a blackness that would bring around. No wonder you panic. I'm sure that some of the amazing people on here who've suffered a loss can help you maybe find some peace. I agree with about the trauma. I still freak out in hospitals, to the point of physical symptoms. 's heart surgery was a terrible experience. Even though it was 9 months ago, I still have a hard time letting doctors near him unless I am right there. Which, by the way, we have a sedated BAER today that I am dreading. I am actually looking for a counselor now, and may go back on meds myself. (Let me know how you work all of this through Tricare!) From most of what I have read, post partum depression can extend well into the first year or beyond, and therapy AND medication are the most effective treatment. And I think that for me, I may need some time just to experience the greif that is lingering. It's kind of a triple whammy, I'm still sad for the life/child we thought we would have and didn't, and then I'm sad for everything my son has to go through, and on top of it all, worried if he'll even make it. Luckily, is at a shore site now, so he's not been deployed for any of this. But he's still usually not there when I get any news, good or bad. He's still trying to bond with , and tends to distance himself from all the medical stuff. I feel pretty alone sometimes too, very similar to when you try and keep up a cheery deployment front. Does your EFMP have a support group? They have one here that I think I would go to if wasn't home. There is something I saw on Oprah the other day. Don't laugh, I'm serious! This beautiful girl had been terribly burned and disfigured in a car accident. And she said that she gives herself five minutes a day to be angry and sorry for herself, but the rest of the time she has to make her life enjoyable or she may as well have died. That really hit home with me. So, for a few minutes a day, I hate CHARGE, and I feel like crap. Then I try and enjoy my kids. I'm not real good at it yet! I'm thinking about you guys! I hope your ship comes in soon! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 Dianne, We are at the point now where we really only go to doctors every couple of months. I find that I feel much better in between appointment cycles than I do when we're in the middle of one. I hate hearing anything other than, " Ma'am this is totally great! " And of course both of my boys are a little different, so I can be very sensitive in discussions about " normal " kids. I think worrying about their cognitive ability is the hardest for me too. And sometimes I wonder why they tell you anything about life expectancy at all. I mean does it help anything? They are so often wrong, and then you spend so much time waiting for the end of your child's life. No parent should have to do that. I mean, we aren't set up that way. I can't imagine what a blackness that would bring around. No wonder you panic. I'm sure that some of the amazing people on here who've suffered a loss can help you maybe find some peace. I agree with about the trauma. I still freak out in hospitals, to the point of physical symptoms. 's heart surgery was a terrible experience. Even though it was 9 months ago, I still have a hard time letting doctors near him unless I am right there. Which, by the way, we have a sedated BAER today that I am dreading. I am actually looking for a counselor now, and may go back on meds myself. (Let me know how you work all of this through Tricare!) From most of what I have read, post partum depression can extend well into the first year or beyond, and therapy AND medication are the most effective treatment. And I think that for me, I may need some time just to experience the greif that is lingering. It's kind of a triple whammy, I'm still sad for the life/child we thought we would have and didn't, and then I'm sad for everything my son has to go through, and on top of it all, worried if he'll even make it. Luckily, is at a shore site now, so he's not been deployed for any of this. But he's still usually not there when I get any news, good or bad. He's still trying to bond with , and tends to distance himself from all the medical stuff. I feel pretty alone sometimes too, very similar to when you try and keep up a cheery deployment front. Does your EFMP have a support group? They have one here that I think I would go to if wasn't home. There is something I saw on Oprah the other day. Don't laugh, I'm serious! This beautiful girl had been terribly burned and disfigured in a car accident. And she said that she gives herself five minutes a day to be angry and sorry for herself, but the rest of the time she has to make her life enjoyable or she may as well have died. That really hit home with me. So, for a few minutes a day, I hate CHARGE, and I feel like crap. Then I try and enjoy my kids. I'm not real good at it yet! I'm thinking about you guys! I hope your ship comes in soon! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 In a message dated 7/19/2004 6:24:53 AM Pacific Standard Time, ShKendra@... writes: But he's still usually not there when I get any news, good or bad. He's still trying to bond with , and tends to distance himself from all the medical stuff. I feel pretty alone sometimes too, very similar to when you try and keep up a cheery deployment front. I understand how you feel. goes to as many appointments as he can, but wants me to deal with all the medical and explain what he needs to know to him. Even at his own cardiology appointments (I have been to all but one). Concerning the postpartum, I agree with you. Dianne, you haven't had a chance to just sit. Since Em was born, you have been going, going, going, and must think you are almost gone. Your not though. In addition to Em, you have to worry about military moves and deployment, as well as her sissy's. You are hoping so much for Em and it must seem that each appointment dashes those hopes. Yet, is still here and she knows how much you love her. And so does everyone else. Be angry, cry, even yell if you must. We are here to listen. You are doing a great job as mother and military wife. Hang in there! Take a BIG deep breathe! Talk to someone!!! Praying for you, Em, her sissy's and her deployed daddy, Carolyn Mother of Tanis 2 CHARGE and Denny 3 months Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 In a message dated 7/19/2004 6:24:53 AM Pacific Standard Time, ShKendra@... writes: But he's still usually not there when I get any news, good or bad. He's still trying to bond with , and tends to distance himself from all the medical stuff. I feel pretty alone sometimes too, very similar to when you try and keep up a cheery deployment front. I understand how you feel. goes to as many appointments as he can, but wants me to deal with all the medical and explain what he needs to know to him. Even at his own cardiology appointments (I have been to all but one). Concerning the postpartum, I agree with you. Dianne, you haven't had a chance to just sit. Since Em was born, you have been going, going, going, and must think you are almost gone. Your not though. In addition to Em, you have to worry about military moves and deployment, as well as her sissy's. You are hoping so much for Em and it must seem that each appointment dashes those hopes. Yet, is still here and she knows how much you love her. And so does everyone else. Be angry, cry, even yell if you must. We are here to listen. You are doing a great job as mother and military wife. Hang in there! Take a BIG deep breathe! Talk to someone!!! Praying for you, Em, her sissy's and her deployed daddy, Carolyn Mother of Tanis 2 CHARGE and Denny 3 months Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 In a message dated 7/19/2004 6:24:53 AM Pacific Standard Time, ShKendra@... writes: But he's still usually not there when I get any news, good or bad. He's still trying to bond with , and tends to distance himself from all the medical stuff. I feel pretty alone sometimes too, very similar to when you try and keep up a cheery deployment front. I understand how you feel. goes to as many appointments as he can, but wants me to deal with all the medical and explain what he needs to know to him. Even at his own cardiology appointments (I have been to all but one). Concerning the postpartum, I agree with you. Dianne, you haven't had a chance to just sit. Since Em was born, you have been going, going, going, and must think you are almost gone. Your not though. In addition to Em, you have to worry about military moves and deployment, as well as her sissy's. You are hoping so much for Em and it must seem that each appointment dashes those hopes. Yet, is still here and she knows how much you love her. And so does everyone else. Be angry, cry, even yell if you must. We are here to listen. You are doing a great job as mother and military wife. Hang in there! Take a BIG deep breathe! Talk to someone!!! Praying for you, Em, her sissy's and her deployed daddy, Carolyn Mother of Tanis 2 CHARGE and Denny 3 months Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 , Where are you stationed? We are at 32nd Street Naval Station, San Diego. is on shore duty at Admin due to his own undiagnosed heart condition (being seen at Balboa). We PCS'd in May and have just started the rounds of doctors for our 2 year old Tanis (CHARGE, Tetralogy of Fallot, developmental delays, hearing loss (found out Friday--reevaluation in 3 months for conclusive testing), as well as seems to be a zillion referrals for speech/language and doctors). Carolyn mother of Tanis 2 CHARGE and Denny 3 months Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 , Where are you stationed? We are at 32nd Street Naval Station, San Diego. is on shore duty at Admin due to his own undiagnosed heart condition (being seen at Balboa). We PCS'd in May and have just started the rounds of doctors for our 2 year old Tanis (CHARGE, Tetralogy of Fallot, developmental delays, hearing loss (found out Friday--reevaluation in 3 months for conclusive testing), as well as seems to be a zillion referrals for speech/language and doctors). Carolyn mother of Tanis 2 CHARGE and Denny 3 months Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 , Where are you stationed? We are at 32nd Street Naval Station, San Diego. is on shore duty at Admin due to his own undiagnosed heart condition (being seen at Balboa). We PCS'd in May and have just started the rounds of doctors for our 2 year old Tanis (CHARGE, Tetralogy of Fallot, developmental delays, hearing loss (found out Friday--reevaluation in 3 months for conclusive testing), as well as seems to be a zillion referrals for speech/language and doctors). Carolyn mother of Tanis 2 CHARGE and Denny 3 months Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 Dianne- Going to a therapist is a great idea. You are justified in your feelings. While they may be " normal " for what you're going through, you need to do get some help for them. I am taking anti-depressants and I think there are several others on the list too. I took them before Aubrie because we have a family history of depression. But I was off them when I was pregnant and then didn't think I needed them after her birth. Sure, I cried alot and was sad, but I had reason too. It wasn't like the depression I had before with no basis. Well, finally I got back on meds and it's made a big difference. I've also been to counseling within the past couple years. This gal was a good match. We didn't talk so much about Aubrie's stuff because I had other issues on my mind. But she really helped me get past them and think clearly. A counselor and perhaps medication will help you to better be able to cope with a very difficult situation. It is never easy to get bad news about your child -- even if it's not totally " news " . Being the cheerful strong one 24/7 for your girls with no spouse to give relief -- well, that's just about as hard as it gets. So know that you are not crazy or weak. You are dealing with more than the average person can manage. Take care of yourself. Vent here as much as you need to. Sometimes I find great relief after simply expressing something. And let us know how your counseling session goes. Hugs- Michele W Aubrie's mom Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 Dianne- Going to a therapist is a great idea. You are justified in your feelings. While they may be " normal " for what you're going through, you need to do get some help for them. I am taking anti-depressants and I think there are several others on the list too. I took them before Aubrie because we have a family history of depression. But I was off them when I was pregnant and then didn't think I needed them after her birth. Sure, I cried alot and was sad, but I had reason too. It wasn't like the depression I had before with no basis. Well, finally I got back on meds and it's made a big difference. I've also been to counseling within the past couple years. This gal was a good match. We didn't talk so much about Aubrie's stuff because I had other issues on my mind. But she really helped me get past them and think clearly. A counselor and perhaps medication will help you to better be able to cope with a very difficult situation. It is never easy to get bad news about your child -- even if it's not totally " news " . Being the cheerful strong one 24/7 for your girls with no spouse to give relief -- well, that's just about as hard as it gets. So know that you are not crazy or weak. You are dealing with more than the average person can manage. Take care of yourself. Vent here as much as you need to. Sometimes I find great relief after simply expressing something. And let us know how your counseling session goes. Hugs- Michele W Aubrie's mom Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 - You said that all so beautifully! I love the Oprah story. I will remember that. It makes wonderful sense. Attitude is everthing. I'm convinced that the difference between those who succeed in spite of adversity and those that fail in spite of golden circumstances is attitude. But it's hard to keep a great attitude 24/7. Scheduling 5 min of negativity is a good way to deal with it. I love it! Michele W Aubrie's mom 6 yrs Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 - You said that all so beautifully! I love the Oprah story. I will remember that. It makes wonderful sense. Attitude is everthing. I'm convinced that the difference between those who succeed in spite of adversity and those that fail in spite of golden circumstances is attitude. But it's hard to keep a great attitude 24/7. Scheduling 5 min of negativity is a good way to deal with it. I love it! Michele W Aubrie's mom 6 yrs Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 - You said that all so beautifully! I love the Oprah story. I will remember that. It makes wonderful sense. Attitude is everthing. I'm convinced that the difference between those who succeed in spite of adversity and those that fail in spite of golden circumstances is attitude. But it's hard to keep a great attitude 24/7. Scheduling 5 min of negativity is a good way to deal with it. I love it! Michele W Aubrie's mom 6 yrs Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 Dianne- I think the feeling of being overwhelmed, panicked and paralyzed with grief is normal - at least for me ) However, my reaction came much later. The night of 's birth, I was in the non-maternity section of the OB floor when the pediatric surgeon and hospital pediatrician came in to tell me about the placement of the gastrostomy tube and the tracheo-esophageal fistula, esophageal atresia, the ramifications of this condition and all the possible outcomes of surgery. Immediately after they left, I remember my husband standing beside my bed, giving me a hug, and I experienced a strong feeling of falling backward into a pit as a yelp of grief started to escape my lips - and suddenly it was all swallowed back - and seemed gone. That is what I needed to do to deal with 's situation - our situation. In the years that followed my husband and I were tireless in our optimism and appreciation of every one of 's accomplishments, recoveries from setbacks or lack of setbacks. People marveled at " how we did it " and I was very uncomfortable being perceived as super-human or worse yet - a martyr. I only felt the joy and gratitude of the miracle and beauty of every day of life with , and I couldn't imagine any other possible feeling. Everyday was a great day. " Isn't it great he can breath easier today? " - and I would be so genuinely happy - not experiencing at all the vulnerability of such joy. When our second son was born, for the whole first year every simple thing Elliot acquired easily - breathing, eating, motor achievements was greeted with joy and a bittersweetness - " oh, this is what is could have looked like for . " It was our first time to acknowledge the things did not experience - the ease and fluency of life and breath - but this did not overwhelm or incapacitate. It just made us more joyful and appreciative. When was nine, he decided to run for vice president of his elementary school, and he won. He also went to Space Camp in Huntsville Alabama and was awarded the " Right Stuff Award. " I cried in gulps and heaves. I could feel that some part of me had held my breath all these years and those fears being released. I could feel that I always accepted him as he was, yet I was also tremendously grateful that he was coming so far. It was my first experience of relief so deeply felt that it looked like sadness - because I was releasing a fear that I had already accepted - sort of the counterpart to that sinking feeling of receiving medical or official confirmation of something I already suspected or knew in my heart. I then became acquainted with the idea that this was Post Traumatic Stress, and I was grateful to be done with it. When graduated (culminated) from sixth grade three years ago for two hours I was sobbing as though someone had died. It was easy enough for me to understand that this was my grief unprocessed from when he was born. Now that he had come so far I could safely release the rest of my fears that I swallowed whole that day. And I realized that what I felt two years prior was only a small release. And I was grateful to be done with it. I really thought I was done. Wow, was I wrong. Last year when he graduated (promoted) from middle school I though nothing of it. Middle school was only two years. Then I went into a period of deep depression which in hindsight lasted ten weeks. I was anxious, cold, sweaty, my heart palpitating, feeling like I had just been called to the principal's office, fearful of the phone, of getting mail of stepping outside. Everything I looked at felt like it could be taken away. Trying to count my blessings or find simple joys only had me feel like I was gripping tightly onto sand and it was only slipping through my fingers. My husband and my father's companies were both having tremendous difficulties at the time, and I thought perhaps my anxiety was about that. But throughout it, I had recurrent images of that moment in the non-maternity section of the ob floor that first night - that moment as the grief started to escape my lips and then was swallowed. The moment I felt myself falling back and then was suddenly back in the bed. I thought that I was ridiculous. No financial situation could possibly be as serious as having the life of one's child uncertain. But the image kept replaying. Then I got it. The image was replaying because that is what I was experiencing. It was yet more unprocessed grief. And this grief was tremendous. The first stage was the terrifying pure anxiety - as though my very life were in danger - and the single recurring memory - increasing in its scope over a few weeks. The second stage was my identifying that this was unprocessed grief specific to the conditions of 's birth and my experience of it. The third stage was me exploring that avenue, not having any more detail of why the grief was there or from which events it was built, but to simply be awestruck by the massive scope of it, and talking about it in sobs to my closest friends who were pretty dumbstruck and loving. The fourth stage was as sense of losing down the one fear while acknowledging the possibility of a more intense fear. As could make out the shape of this grief giving me the idea that I would rise above it, I had a more terribly frightening notion that I had no idea if this was the end of it, what more would look like and if I would be able to survive another possibly more intense release or re-discovery of this unprocessed grief at some unknown future time in my life. I thought I was done two years ago, clearly I wasn't. The intensity of this experience was starting to ebb, and yet I was intensely vulnerable and fearful - what if there is more? The fifth stage has occurred gradually over the last year. The intensity faded, and then suddenly daily life just came into focus full of daily joys of gratitude and blessing, and the grief no longer called attention to itself. I was able to experience the gratitude of having, giving and receiving. I was no longer terrified of another experience nor having the memory haunt me. I know I am past it now because when I talk about it I am calm and at peace - not feeling restimulated at all. I talk about it as a simple fact - not with a fearful grip in my heart. I am still close enough to feel a small amount of trepidation that I got through the summer last year at all. It's not as abstract as the physical experience of childbirth seems now. And I now know that if I ever have feelings like that again I might consider seeking help - I would have definitely benefited from that kind of support -. The support of my friends and family was incredible - but truly only two of my friends who have face their own intense challenges in their lives were able to offer me support that was not covered in fear. They had the certainty that I was still myself and that I would come through. They were not afraid of the grief and fear I was showing them, and were able to embrace it and love me with a compassion that let me know I was still whole and would continue to be whole. For others of my friends, they could barely look at me, for I was showing them a possibility that was too frightening for them - just like the way seemed to some of our friends when he was little and so vulnerable - and still they let me know how much they cares and worried for me. But being afraid, sad and terrified, and then seeing fear in the eyes of your friend as they look at you is loving but not exactly comforting. I would love to take that burden and fear off my friends - because if I have to go through this again - seeing how the last three times have increased in intensity logarithmically - I think someone should hang an A-frame sign on me saying " Warning: Only Professionals Should Approach. " I hope this helped. I know it helps me to share it ) take good care, yuka Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 Dianne- I think the feeling of being overwhelmed, panicked and paralyzed with grief is normal - at least for me ) However, my reaction came much later. The night of 's birth, I was in the non-maternity section of the OB floor when the pediatric surgeon and hospital pediatrician came in to tell me about the placement of the gastrostomy tube and the tracheo-esophageal fistula, esophageal atresia, the ramifications of this condition and all the possible outcomes of surgery. Immediately after they left, I remember my husband standing beside my bed, giving me a hug, and I experienced a strong feeling of falling backward into a pit as a yelp of grief started to escape my lips - and suddenly it was all swallowed back - and seemed gone. That is what I needed to do to deal with 's situation - our situation. In the years that followed my husband and I were tireless in our optimism and appreciation of every one of 's accomplishments, recoveries from setbacks or lack of setbacks. People marveled at " how we did it " and I was very uncomfortable being perceived as super-human or worse yet - a martyr. I only felt the joy and gratitude of the miracle and beauty of every day of life with , and I couldn't imagine any other possible feeling. Everyday was a great day. " Isn't it great he can breath easier today? " - and I would be so genuinely happy - not experiencing at all the vulnerability of such joy. When our second son was born, for the whole first year every simple thing Elliot acquired easily - breathing, eating, motor achievements was greeted with joy and a bittersweetness - " oh, this is what is could have looked like for . " It was our first time to acknowledge the things did not experience - the ease and fluency of life and breath - but this did not overwhelm or incapacitate. It just made us more joyful and appreciative. When was nine, he decided to run for vice president of his elementary school, and he won. He also went to Space Camp in Huntsville Alabama and was awarded the " Right Stuff Award. " I cried in gulps and heaves. I could feel that some part of me had held my breath all these years and those fears being released. I could feel that I always accepted him as he was, yet I was also tremendously grateful that he was coming so far. It was my first experience of relief so deeply felt that it looked like sadness - because I was releasing a fear that I had already accepted - sort of the counterpart to that sinking feeling of receiving medical or official confirmation of something I already suspected or knew in my heart. I then became acquainted with the idea that this was Post Traumatic Stress, and I was grateful to be done with it. When graduated (culminated) from sixth grade three years ago for two hours I was sobbing as though someone had died. It was easy enough for me to understand that this was my grief unprocessed from when he was born. Now that he had come so far I could safely release the rest of my fears that I swallowed whole that day. And I realized that what I felt two years prior was only a small release. And I was grateful to be done with it. I really thought I was done. Wow, was I wrong. Last year when he graduated (promoted) from middle school I though nothing of it. Middle school was only two years. Then I went into a period of deep depression which in hindsight lasted ten weeks. I was anxious, cold, sweaty, my heart palpitating, feeling like I had just been called to the principal's office, fearful of the phone, of getting mail of stepping outside. Everything I looked at felt like it could be taken away. Trying to count my blessings or find simple joys only had me feel like I was gripping tightly onto sand and it was only slipping through my fingers. My husband and my father's companies were both having tremendous difficulties at the time, and I thought perhaps my anxiety was about that. But throughout it, I had recurrent images of that moment in the non-maternity section of the ob floor that first night - that moment as the grief started to escape my lips and then was swallowed. The moment I felt myself falling back and then was suddenly back in the bed. I thought that I was ridiculous. No financial situation could possibly be as serious as having the life of one's child uncertain. But the image kept replaying. Then I got it. The image was replaying because that is what I was experiencing. It was yet more unprocessed grief. And this grief was tremendous. The first stage was the terrifying pure anxiety - as though my very life were in danger - and the single recurring memory - increasing in its scope over a few weeks. The second stage was my identifying that this was unprocessed grief specific to the conditions of 's birth and my experience of it. The third stage was me exploring that avenue, not having any more detail of why the grief was there or from which events it was built, but to simply be awestruck by the massive scope of it, and talking about it in sobs to my closest friends who were pretty dumbstruck and loving. The fourth stage was as sense of losing down the one fear while acknowledging the possibility of a more intense fear. As could make out the shape of this grief giving me the idea that I would rise above it, I had a more terribly frightening notion that I had no idea if this was the end of it, what more would look like and if I would be able to survive another possibly more intense release or re-discovery of this unprocessed grief at some unknown future time in my life. I thought I was done two years ago, clearly I wasn't. The intensity of this experience was starting to ebb, and yet I was intensely vulnerable and fearful - what if there is more? The fifth stage has occurred gradually over the last year. The intensity faded, and then suddenly daily life just came into focus full of daily joys of gratitude and blessing, and the grief no longer called attention to itself. I was able to experience the gratitude of having, giving and receiving. I was no longer terrified of another experience nor having the memory haunt me. I know I am past it now because when I talk about it I am calm and at peace - not feeling restimulated at all. I talk about it as a simple fact - not with a fearful grip in my heart. I am still close enough to feel a small amount of trepidation that I got through the summer last year at all. It's not as abstract as the physical experience of childbirth seems now. And I now know that if I ever have feelings like that again I might consider seeking help - I would have definitely benefited from that kind of support -. The support of my friends and family was incredible - but truly only two of my friends who have face their own intense challenges in their lives were able to offer me support that was not covered in fear. They had the certainty that I was still myself and that I would come through. They were not afraid of the grief and fear I was showing them, and were able to embrace it and love me with a compassion that let me know I was still whole and would continue to be whole. For others of my friends, they could barely look at me, for I was showing them a possibility that was too frightening for them - just like the way seemed to some of our friends when he was little and so vulnerable - and still they let me know how much they cares and worried for me. But being afraid, sad and terrified, and then seeing fear in the eyes of your friend as they look at you is loving but not exactly comforting. I would love to take that burden and fear off my friends - because if I have to go through this again - seeing how the last three times have increased in intensity logarithmically - I think someone should hang an A-frame sign on me saying " Warning: Only Professionals Should Approach. " I hope this helped. I know it helps me to share it ) take good care, yuka Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 Dianne- I think the feeling of being overwhelmed, panicked and paralyzed with grief is normal - at least for me ) However, my reaction came much later. The night of 's birth, I was in the non-maternity section of the OB floor when the pediatric surgeon and hospital pediatrician came in to tell me about the placement of the gastrostomy tube and the tracheo-esophageal fistula, esophageal atresia, the ramifications of this condition and all the possible outcomes of surgery. Immediately after they left, I remember my husband standing beside my bed, giving me a hug, and I experienced a strong feeling of falling backward into a pit as a yelp of grief started to escape my lips - and suddenly it was all swallowed back - and seemed gone. That is what I needed to do to deal with 's situation - our situation. In the years that followed my husband and I were tireless in our optimism and appreciation of every one of 's accomplishments, recoveries from setbacks or lack of setbacks. People marveled at " how we did it " and I was very uncomfortable being perceived as super-human or worse yet - a martyr. I only felt the joy and gratitude of the miracle and beauty of every day of life with , and I couldn't imagine any other possible feeling. Everyday was a great day. " Isn't it great he can breath easier today? " - and I would be so genuinely happy - not experiencing at all the vulnerability of such joy. When our second son was born, for the whole first year every simple thing Elliot acquired easily - breathing, eating, motor achievements was greeted with joy and a bittersweetness - " oh, this is what is could have looked like for . " It was our first time to acknowledge the things did not experience - the ease and fluency of life and breath - but this did not overwhelm or incapacitate. It just made us more joyful and appreciative. When was nine, he decided to run for vice president of his elementary school, and he won. He also went to Space Camp in Huntsville Alabama and was awarded the " Right Stuff Award. " I cried in gulps and heaves. I could feel that some part of me had held my breath all these years and those fears being released. I could feel that I always accepted him as he was, yet I was also tremendously grateful that he was coming so far. It was my first experience of relief so deeply felt that it looked like sadness - because I was releasing a fear that I had already accepted - sort of the counterpart to that sinking feeling of receiving medical or official confirmation of something I already suspected or knew in my heart. I then became acquainted with the idea that this was Post Traumatic Stress, and I was grateful to be done with it. When graduated (culminated) from sixth grade three years ago for two hours I was sobbing as though someone had died. It was easy enough for me to understand that this was my grief unprocessed from when he was born. Now that he had come so far I could safely release the rest of my fears that I swallowed whole that day. And I realized that what I felt two years prior was only a small release. And I was grateful to be done with it. I really thought I was done. Wow, was I wrong. Last year when he graduated (promoted) from middle school I though nothing of it. Middle school was only two years. Then I went into a period of deep depression which in hindsight lasted ten weeks. I was anxious, cold, sweaty, my heart palpitating, feeling like I had just been called to the principal's office, fearful of the phone, of getting mail of stepping outside. Everything I looked at felt like it could be taken away. Trying to count my blessings or find simple joys only had me feel like I was gripping tightly onto sand and it was only slipping through my fingers. My husband and my father's companies were both having tremendous difficulties at the time, and I thought perhaps my anxiety was about that. But throughout it, I had recurrent images of that moment in the non-maternity section of the ob floor that first night - that moment as the grief started to escape my lips and then was swallowed. The moment I felt myself falling back and then was suddenly back in the bed. I thought that I was ridiculous. No financial situation could possibly be as serious as having the life of one's child uncertain. But the image kept replaying. Then I got it. The image was replaying because that is what I was experiencing. It was yet more unprocessed grief. And this grief was tremendous. The first stage was the terrifying pure anxiety - as though my very life were in danger - and the single recurring memory - increasing in its scope over a few weeks. The second stage was my identifying that this was unprocessed grief specific to the conditions of 's birth and my experience of it. The third stage was me exploring that avenue, not having any more detail of why the grief was there or from which events it was built, but to simply be awestruck by the massive scope of it, and talking about it in sobs to my closest friends who were pretty dumbstruck and loving. The fourth stage was as sense of losing down the one fear while acknowledging the possibility of a more intense fear. As could make out the shape of this grief giving me the idea that I would rise above it, I had a more terribly frightening notion that I had no idea if this was the end of it, what more would look like and if I would be able to survive another possibly more intense release or re-discovery of this unprocessed grief at some unknown future time in my life. I thought I was done two years ago, clearly I wasn't. The intensity of this experience was starting to ebb, and yet I was intensely vulnerable and fearful - what if there is more? The fifth stage has occurred gradually over the last year. The intensity faded, and then suddenly daily life just came into focus full of daily joys of gratitude and blessing, and the grief no longer called attention to itself. I was able to experience the gratitude of having, giving and receiving. I was no longer terrified of another experience nor having the memory haunt me. I know I am past it now because when I talk about it I am calm and at peace - not feeling restimulated at all. I talk about it as a simple fact - not with a fearful grip in my heart. I am still close enough to feel a small amount of trepidation that I got through the summer last year at all. It's not as abstract as the physical experience of childbirth seems now. And I now know that if I ever have feelings like that again I might consider seeking help - I would have definitely benefited from that kind of support -. The support of my friends and family was incredible - but truly only two of my friends who have face their own intense challenges in their lives were able to offer me support that was not covered in fear. They had the certainty that I was still myself and that I would come through. They were not afraid of the grief and fear I was showing them, and were able to embrace it and love me with a compassion that let me know I was still whole and would continue to be whole. For others of my friends, they could barely look at me, for I was showing them a possibility that was too frightening for them - just like the way seemed to some of our friends when he was little and so vulnerable - and still they let me know how much they cares and worried for me. But being afraid, sad and terrified, and then seeing fear in the eyes of your friend as they look at you is loving but not exactly comforting. I would love to take that burden and fear off my friends - because if I have to go through this again - seeing how the last three times have increased in intensity logarithmically - I think someone should hang an A-frame sign on me saying " Warning: Only Professionals Should Approach. " I hope this helped. I know it helps me to share it ) take good care, yuka Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 Yuka, Thank you so much for what you wrote. My youngest is 3 months old and is already in 6-9 months clothes and the size Tanis was at one year plus. Every day I thank God he is so healthy and fine and growing and progressing. Every day I think, Tanis was leaving the hospital, having surgery, relapse...at this age, this weight, this height, this development. I am so scared of what is to come with Tanis (2, CHARGE, delays, evaluations and testing over the next 3 months) and how Denny won't have to go through any of this but I will be holding my breathe lest anything happens. You have given the " perfect prescription " and " warning label " of what is yet to come. The doctor's didn't know until Tanis was born (36 weeks) that he had Tetralogy of Fallot and other bone deficiencies or anything else. They whisked him out of the room and soon after Children's Hospital came for him. I can remember crying then, and as I stood by his bed in PICU weeks later knowing that if they didn't do surgery real soon, he would die. Sometimes, especially now that we have Denny, I start crying because Tanis still is so far behind in language and development delays/processing. Denny won't be, he's already doing all he should and trying more. My husband doesn't understand the breakdowns, because " I've been so strong and helped get all of us through this. " Fortunately, he usually lends a shoulder for tears and humor to make me smile. That day was the last I saw him cry. He refuses to cry now. Maybe I should give a copy of your letter to my husband's cardiologist and have him evaluate for Post Traumatic Stress Syndrome. Thank you again. I know there are days I want to break down so much, but keep going because there is nothing else I can do. Thank you for the examples of your sons. It will help, especially in the next few months, as Denny " meets his goals " and we set new goals for Tanis. Carolyn Mother of Tanis 2 CHARGE and Denny 3 months (already 13 1/2 pounds and 27 " + long Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 Yuka, Thank you so much for what you wrote. My youngest is 3 months old and is already in 6-9 months clothes and the size Tanis was at one year plus. Every day I thank God he is so healthy and fine and growing and progressing. Every day I think, Tanis was leaving the hospital, having surgery, relapse...at this age, this weight, this height, this development. I am so scared of what is to come with Tanis (2, CHARGE, delays, evaluations and testing over the next 3 months) and how Denny won't have to go through any of this but I will be holding my breathe lest anything happens. You have given the " perfect prescription " and " warning label " of what is yet to come. The doctor's didn't know until Tanis was born (36 weeks) that he had Tetralogy of Fallot and other bone deficiencies or anything else. They whisked him out of the room and soon after Children's Hospital came for him. I can remember crying then, and as I stood by his bed in PICU weeks later knowing that if they didn't do surgery real soon, he would die. Sometimes, especially now that we have Denny, I start crying because Tanis still is so far behind in language and development delays/processing. Denny won't be, he's already doing all he should and trying more. My husband doesn't understand the breakdowns, because " I've been so strong and helped get all of us through this. " Fortunately, he usually lends a shoulder for tears and humor to make me smile. That day was the last I saw him cry. He refuses to cry now. Maybe I should give a copy of your letter to my husband's cardiologist and have him evaluate for Post Traumatic Stress Syndrome. Thank you again. I know there are days I want to break down so much, but keep going because there is nothing else I can do. Thank you for the examples of your sons. It will help, especially in the next few months, as Denny " meets his goals " and we set new goals for Tanis. Carolyn Mother of Tanis 2 CHARGE and Denny 3 months (already 13 1/2 pounds and 27 " + long Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 Yuka, Thank you so much for what you wrote. My youngest is 3 months old and is already in 6-9 months clothes and the size Tanis was at one year plus. Every day I thank God he is so healthy and fine and growing and progressing. Every day I think, Tanis was leaving the hospital, having surgery, relapse...at this age, this weight, this height, this development. I am so scared of what is to come with Tanis (2, CHARGE, delays, evaluations and testing over the next 3 months) and how Denny won't have to go through any of this but I will be holding my breathe lest anything happens. You have given the " perfect prescription " and " warning label " of what is yet to come. The doctor's didn't know until Tanis was born (36 weeks) that he had Tetralogy of Fallot and other bone deficiencies or anything else. They whisked him out of the room and soon after Children's Hospital came for him. I can remember crying then, and as I stood by his bed in PICU weeks later knowing that if they didn't do surgery real soon, he would die. Sometimes, especially now that we have Denny, I start crying because Tanis still is so far behind in language and development delays/processing. Denny won't be, he's already doing all he should and trying more. My husband doesn't understand the breakdowns, because " I've been so strong and helped get all of us through this. " Fortunately, he usually lends a shoulder for tears and humor to make me smile. That day was the last I saw him cry. He refuses to cry now. Maybe I should give a copy of your letter to my husband's cardiologist and have him evaluate for Post Traumatic Stress Syndrome. Thank you again. I know there are days I want to break down so much, but keep going because there is nothing else I can do. Thank you for the examples of your sons. It will help, especially in the next few months, as Denny " meets his goals " and we set new goals for Tanis. Carolyn Mother of Tanis 2 CHARGE and Denny 3 months (already 13 1/2 pounds and 27 " + long Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 Diane, PLEASE don't feel off the wall or abnormal in any way. Almost ALL of us (ok maybe all) have had these feelings of anxiety, depression, etc facing the challenges we go through. It's called STRESS. Nobody other than a robot wouldn't react with strong physical, emotional and scary mind stuff. Don't feel guilty getting whatever help you need. I wish I had, I see now I was kinda a zombie earlier on, and just tried to tough it out, with an occasional valium + go to bed at 7 p.m. escape to stay sane/alive. It gets better as they mature and accomplish new things. They advance and grow just like all children, just on a slower time table. Good luck and treat yourself to a massage as often as you can possibly afford!! love barbra mousouris Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 Diane, PLEASE don't feel off the wall or abnormal in any way. Almost ALL of us (ok maybe all) have had these feelings of anxiety, depression, etc facing the challenges we go through. It's called STRESS. Nobody other than a robot wouldn't react with strong physical, emotional and scary mind stuff. Don't feel guilty getting whatever help you need. I wish I had, I see now I was kinda a zombie earlier on, and just tried to tough it out, with an occasional valium + go to bed at 7 p.m. escape to stay sane/alive. It gets better as they mature and accomplish new things. They advance and grow just like all children, just on a slower time table. Good luck and treat yourself to a massage as often as you can possibly afford!! love barbra mousouris Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 Diane, PLEASE don't feel off the wall or abnormal in any way. Almost ALL of us (ok maybe all) have had these feelings of anxiety, depression, etc facing the challenges we go through. It's called STRESS. Nobody other than a robot wouldn't react with strong physical, emotional and scary mind stuff. Don't feel guilty getting whatever help you need. I wish I had, I see now I was kinda a zombie earlier on, and just tried to tough it out, with an occasional valium + go to bed at 7 p.m. escape to stay sane/alive. It gets better as they mature and accomplish new things. They advance and grow just like all children, just on a slower time table. Good luck and treat yourself to a massage as often as you can possibly afford!! love barbra mousouris Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2004 Report Share Posted July 19, 2004 Carolyn, We're in Fort Meade, at the NSA, in land right now. We just moved here from Norfolk, VA in March. has ToF too! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 20, 2004 Report Share Posted July 20, 2004 Yuka- You are so insightful! I could have cried reading your post. You took me right through the process with you. It's amazing how each of us handles these traumas differently. I had not thought of what we go through as leading to Post Traumatic Stress Syndrome, but now I can see how that might be. I sure did my share of grieving in the first years. It still comes back to haunt me ocassionally, but I think I got the worst of it out right from the start. Let's hope :-) I still get twangs of fear and sadness, but it's not overwhelming anymore. The overwhelming feelings now are just that -- overwhelmed -- with all the appts, the time it takes to stay on top of everything -- fear that I won't be able to keep up or that I won't do a good job, etc. Oh well-- I'm not in a time or place this afternoon to delve into it deeply... Michele w Aubrie's mom 6 yrs Quote Link to comment Share on other sites More sharing options...
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