Guest guest Posted March 7, 2001 Report Share Posted March 7, 2001 Ask the one I just posted about scar tissue. R At 02:57 PM 3/7/01 -0500, Moulton wrote: Please, if you have any questions you'd like this physiatrist to answer, now is the time to submit them to Sue. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 9, 2001 Report Share Posted March 9, 2001 Hi everyone, Here is the list of questions so far. Ihave not taken out ant duplictes yet, or arranged them in any kind of order either. I hope to do that tonight or tomorrow. With all the discussion going on about Core Questions I thought that you might want to see what we have so far, and I' hoping that these questions might spark questions that you have not thought of yet. Please email me directly at: JRF25@... if you havequstions to add to this list. Thanks, Sue Mc Questions for Specialists 1. What effect might chronic pain have on cognitive functioning, even if the chronic pain is relatively well controlled? 2. Could chronic pain cause memory loss, loss of language fluency, etc? 3. Might the drugs associated with chronic pain control also cause a loss of cognitive functioning? 4. I am three years post-op from cord release surgery. I continue to have symptoms with mild new ones accumulating - most recently started taking detrol to help with bladder spasms and major leakage. My neurosurgeon says he dismisses his patients when they are 19 or so (I'm middle aged) and does not wish to see me any more. There are no other neurosurgeons in my area who deal with tethered spinal cord. Should I insist on seeing mine again, or look elsewhere for follow-up, if I can convince my insurance company? 5. Why are muscle spasms so common as a lasting problem after surgery? 6. What is the advantage of seeing a pain management doctor, as opposed to seeing a primary care physician for pain relief meds? 7. What would you consider adequate monitoring and pain control for a patient with TCS? 8. Are you ever concerned that a patient will become addicted to pain relief meds? 9. What is the difference between addiction and dependence? 10. What do you do with a chronic pain patient if you are unsure that she/he is abusing meds? 11. Could it be that the patient is not abusing meds but is under medicated, and uneducated on alternatives? 12. How do you treat a patient that has chronic pain but is also a recovering addict? 13. What is break through pain? 14. What is the difference between referred pain and radiating pain? 15. Do you treat pain in children differently than in adults? 16. Do patients with chronic severe pain get a high from narcotics? 17. What is an epidural injection? 18. How many epidurals (cortisone) can a person have in a year? 19. What about alternative medicine for pain (herbs, Reike, acupuncture)? 20. What is a pain psychologist or neuropsychologist? 21. Are they different than regular psychologists or psychiatrists? 22. What does a pain, or neuro, psychologist do? 23. How does stress effect chronic pain? 24. How does chronic pain effect one's ability to deal with stress? 25. How does pain, external, affect blood pressure and the heart rate? 26. Are support groups helpful? 27. Do men and women experience or deal with pain differently? 28. How much will a MRI show in relation to a tethered cord? i.e.: Will it show nerves " stuck " in a lipoma? Will it show which nerves are tangled or out of place? 29. Which part of the spinal cord controls or is responsible for spasticity/spasms in the legs/buttocks? Would nerve blocks stop this? 30. Which exercises would you recommend for people that have a tethered spinal cord? 31. There are many people we have in our groups that have declined within a short period after surgery. If there is nothing wrong anatomically after surgery, what in your opinion would be the cause of this in so many? 32. Would you recommend someone with a tethered spinal cord be a candidate for a spinal cord stim for pain control? If so, what type of pain do you foresee this controlling? 33. Some of us have been referred for intrathecal pumps. What are the long term implications of these? Do you recommend testing for allergic reactions to any of the pump's components before implanting or the test dose? 34. With such a small amount of medicine needed to have control over pain with the pump, does your body still have a physical dependence on the medicine given? 35. Would please explain the difference between addiction and physical dependence in regard to narcotics given to those with chronic pain? 36. For your patients with chronic spasticity that deforms the feet and toes (i.e.: hammer toes, tight heel cords, raised arches, etc) do you recommend surgery for them? There has been discussion on this issue because of the fact that the spasticity is not under control and continues, the surgery may only be a temporary fix at best. 37. What is your opinion on eastern medicine such as acupuncture, etc? 38. Do you ever use or recommend nerve blocks for pain control in someone that has a tethered spinal cord or pain from the spinal cord? 39. Many of us had had to have laminectomies during our surgeries. What, in your opinion, are the long term implications of having 2-7 disks that have had laminectomies? Does this make our backs inherently weaker? If so, what can we do to minimize the effects? 40. Are botox injections that are done to help ease the effects of spasticity dangerous if done for a long time over the life of a person? 41. On the subject of intermittent self catheterization: 42. a) What are the long term effects of this? 43. Do you foresee any new research into this field that may make it possible for some to be able to empty on their own without the use of a catheter? 44. Given the implications of a tethered cord, could this cause someone's blood pressure to be lower than their normal? 45. How important do you see the role of the physiatrist with someone that has damage due to a tethered spinal cord? 46. If you are familiar with Chiari 1 malformations, what are the symptoms and is there anyway to separate which symptoms would be from the tether and which are from the Chiari? There has been much talk about Chiari's relation to Fibromyalgia. What is your take on this relationship? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 10, 2001 Report Share Posted March 10, 2001 Here is another Question, if you want to ask it. If the Trauma from Surgery(Spinal Shock?) caused Leg Spasms, immediately following Surgery, in your opinion, normally how long should they last? When would these Leg Spasms be considered Abnormal after Surgery, and may indicate another problem arising, in your opinion? If you can reword it to make it sound better that would be fine, as long as Subject is kept in tact. Take Care, Brande, RHIT mymocha@... > 5. Why are muscle spasms so common as a lasting problem after surgery? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 23, 2008 Report Share Posted November 23, 2008 Hi , I'm so sorry you are feeling bad. It's good to hear from you again. I know the issue with your son is weighing heavy on you. It seems like you've had a good relationship with his adoptive parents since the adoption. If I were you, I believe I would just have a talk with his adoptive parents and tell them that your cirrhosis is caused by Hep C and that there is a small chance that your son could be infected as well. Explain however that you are not sure that you even had the virus when you were carrying him. Tell them he should be tested just to be sure. They don't even have to tell him until the results are in. They can just carry him if for a checkup and ask the doctor to order the test as a part of the regular lab workup. It can be handled discreetly and there's no need to make a big deal of it unless absolutely necessary. I will be praying for you and for your son. Let us know how things turn out. Hugs.......... Diane ________________________________ To: livercirrhosissupport Sent: Sunday, November 23, 2008 12:36:21 PM Subject: questions hello family,I haven't posted for a couple weeks,I have been going through the " I hate the world syndrome " My platlets are 81,now shouldn't I get some new ones(I'm trying to be humorous)I had wrist surgery in the beginning of July and my bruising is still VERY here...and this FREEZING all the time Crap is for the birds,isn't there any vitamin to help?I also have a serious dilema..I gave my son up for adoption 16 yrs ago thruogh a private adoption,I know the parents,and they have always sent me pictures and keep me had kept in touch,well i hadn't heard a word in a couple years and she sent me some recent pictures (usually for the last 7 yrs. the have always gone on some sort of Carribean cruise and he gets to put up a tree for the first time in a long time,so happy that made me,but i need to know if he deffinatly has the HepC if i had it when he was born? I don't want to alarm them if I don't have to but I don't think that is possible,I feel so horrible inside if I have harmed him.They don't know about the Hepc (YET)They know I have cirrohsis but think it is from me drinking.What do I do? Thank you.God Bless, oh! this backwards sleeping thing is really confusing to me also and I try to get the nights to be nights but for some reason the daylight makes me want to sleep....Go figure. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 23, 2008 Report Share Posted November 23, 2008 Diane,thanks for the uplift,but the sad part is I had a blood transfusion in the mid 80's , and didn't find out I had hepC till 2001,he was born in 93.What I meant to ask is it a deffinate that he would be born positive? I know I have to tell them but that means he has had it all his life and could be very bad off,there is a new girl on here that is 21 can't remember her name,but the timing was weird because she was born with it and is very sad over all this and that is what made me think Oh shit! what about my son,I guess it was the selfish part of me that honestly never even thought about that issue. It had been so long and it is still painfull even though I know he has had a lovely life. Subject: Re: questions To: livercirrhosissupport Date: Sunday, November 23, 2008, 2:16 PM Hi , I'm so sorry you are feeling bad. It's good to hear from you again. I know the issue with your son is weighing heavy on you. It seems like you've had a good relationship with his adoptive parents since the adoption. If I were you, I believe I would just have a talk with his adoptive parents and tell them that your cirrhosis is caused by Hep C and that there is a small chance that your son could be infected as well. Explain however that you are not sure that you even had the virus when you were carrying him. Tell them he should be tested just to be sure. They don't even have to tell him until the results are in. They can just carry him if for a checkup and ask the doctor to order the test as a part of the regular lab workup. It can be handled discreetly and there's no need to make a big deal of it unless absolutely necessary. I will be praying for you and for your son. Let us know how things turn out. Hugs........ .. Diane ____________ _________ _________ __ From: italybell69 <italybell69@ yahoo.com> To: livercirrhosissuppo rtyahoogroups (DOT) com Sent: Sunday, November 23, 2008 12:36:21 PM Subject: questions hello family,I haven't posted for a couple weeks,I have been going through the " I hate the world syndrome " My platlets are 81,now shouldn't I get some new ones(I'm trying to be humorous)I had wrist surgery in the beginning of July and my bruising is still VERY here...and this FREEZING all the time Crap is for the birds,isn't there any vitamin to help?I also have a serious dilema..I gave my son up for adoption 16 yrs ago thruogh a private adoption,I know the parents,and they have always sent me pictures and keep me had kept in touch,well i hadn't heard a word in a couple years and she sent me some recent pictures (usually for the last 7 yrs. the have always gone on some sort of Carribean cruise and he gets to put up a tree for the first time in a long time,so happy that made me,but i need to know if he deffinatly has the HepC if i had it when he was born? I don't want to alarm them if I don't have to but I don't think that is possible,I feel so horrible inside if I have harmed him.They don't know about the Hepc (YET)They know I have cirrohsis but think it is from me drinking.What do I do? Thank you.God Bless, oh! this backwards sleeping thing is really confusing to me also and I try to get the nights to be nights but for some reason the daylight makes me want to sleep....Go figure. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 23, 2008 Report Share Posted November 23, 2008 I'm sorry , I misunderstood. That's not unusal for me though! LOL! As for whether it is definite, I don't know. I know there are people here better qualified to answer that question than I. I will be praying for you and for your son. I know this is painful for you. I want you to know that I admire you for the decisions you have made. It's can't be easy to give up a child, yet you made the decision you felt best for your child. You are to be commended for that. Hugs........... Diane ________________________________ To: livercirrhosissupport Sent: Sunday, November 23, 2008 2:52:52 PM Subject: Re: questions Diane,thanks for the uplift,but the sad part is I had a blood transfusion in the mid 80's , and didn't find out I had hepC till 2001,he was born in 93.What I meant to ask is it a deffinate that he would be born positive? I know I have to tell them but that means he has had it all his life and could be very bad off,there is a new girl on here that is 21 can't remember her name,but the timing was weird because she was born with it and is very sad over all this and that is what made me think Oh shit! what about my son,I guess it was the selfish part of me that honestly never even thought about that issue. It had been so long and it is still painfull even though I know he has had a lovely life. From: diane chandler <dianechandler@ att.net> Subject: Re: questions To: livercirrhosissuppo rtyahoogroups (DOT) com Date: Sunday, November 23, 2008, 2:16 PM Hi , I'm so sorry you are feeling bad. It's good to hear from you again. I know the issue with your son is weighing heavy on you. It seems like you've had a good relationship with his adoptive parents since the adoption. If I were you, I believe I would just have a talk with his adoptive parents and tell them that your cirrhosis is caused by Hep C and that there is a small chance that your son could be infected as well. Explain however that you are not sure that you even had the virus when you were carrying him. Tell them he should be tested just to be sure. They don't even have to tell him until the results are in. They can just carry him if for a checkup and ask the doctor to order the test as a part of the regular lab workup. It can be handled discreetly and there's no need to make a big deal of it unless absolutely necessary. I will be praying for you and for your son. Let us know how things turn out. Hugs........ .. Diane ____________ _________ _________ __ From: italybell69 <italybell69@ yahoo.com> To: livercirrhosissuppo rtyahoogroups (DOT) com Sent: Sunday, November 23, 2008 12:36:21 PM Subject: questions hello family,I haven't posted for a couple weeks,I have been going through the " I hate the world syndrome " My platlets are 81,now shouldn't I get some new ones(I'm trying to be humorous)I had wrist surgery in the beginning of July and my bruising is still VERY here...and this FREEZING all the time Crap is for the birds,isn't there any vitamin to help?I also have a serious dilema..I gave my son up for adoption 16 yrs ago thruogh a private adoption,I know the parents,and they have always sent me pictures and keep me had kept in touch,well i hadn't heard a word in a couple years and she sent me some recent pictures (usually for the last 7 yrs. the have always gone on some sort of Carribean cruise and he gets to put up a tree for the first time in a long time,so happy that made me,but i need to know if he deffinatly has the HepC if i had it when he was born? I don't want to alarm them if I don't have to but I don't think that is possible,I feel so horrible inside if I have harmed him.They don't know about the Hepc (YET)They know I have cirrohsis but think it is from me drinking.What do I do? Thank you.God Bless, oh! this backwards sleeping thing is really confusing to me also and I try to get the nights to be nights but for some reason the daylight makes me want to sleep....Go figure. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 23, 2008 Report Share Posted November 23, 2008 Hi , I got hepatitis in 78 and had my son in 96. I did not find out that I had hep c until 2003. My husband and son were both tested and both came back negative. I was so thankful that I didn't pass it on to either of them. Sue ________________________________ To: livercirrhosissupport Sent: Sunday, November 23, 2008 2:52:52 PM Subject: Re: questions Diane,thanks for the uplift,but the sad part is I had a blood transfusion in the mid 80's , and didn't find out I had hepC till 2001,he was born in 93.What I meant to ask is it a deffinate that he would be born positive? I know I have to tell them but that means he has had it all his life and could be very bad off,there is a new girl on here that is 21 can't remember her name,but the timing was weird because she was born with it and is very sad over all this and that is what made me think Oh shit! what about my son,I guess it was the selfish part of me that honestly never even thought about that issue. It had been so long and it is still painfull even though I know he has had a lovely life. From: diane chandler <dianechandler@ att.net> Subject: Re: questions To: livercirrhosissuppo rtyahoogroups (DOT) com Date: Sunday, November 23, 2008, 2:16 PM Hi , I'm so sorry you are feeling bad. It's good to hear from you again. I know the issue with your son is weighing heavy on you. It seems like you've had a good relationship with his adoptive parents since the adoption. If I were you, I believe I would just have a talk with his adoptive parents and tell them that your cirrhosis is caused by Hep C and that there is a small chance that your son could be infected as well. Explain however that you are not sure that you even had the virus when you were carrying him. Tell them he should be tested just to be sure. They don't even have to tell him until the results are in. They can just carry him if for a checkup and ask the doctor to order the test as a part of the regular lab workup. It can be handled discreetly and there's no need to make a big deal of it unless absolutely necessary. I will be praying for you and for your son. Let us know how things turn out. Hugs........ .. Diane ____________ _________ _________ __ From: italybell69 <italybell69@ yahoo.com> To: livercirrhosissuppo rtyahoogroups (DOT) com Sent: Sunday, November 23, 2008 12:36:21 PM Subject: questions hello family,I haven't posted for a couple weeks,I have been going through the " I hate the world syndrome " My platlets are 81,now shouldn't I get some new ones(I'm trying to be humorous)I had wrist surgery in the beginning of July and my bruising is still VERY here...and this FREEZING all the time Crap is for the birds,isn't there any vitamin to help?I also have a serious dilema..I gave my son up for adoption 16 yrs ago thruogh a private adoption,I know the parents,and they have always sent me pictures and keep me had kept in touch,well i hadn't heard a word in a couple years and she sent me some recent pictures (usually for the last 7 yrs. the have always gone on some sort of Carribean cruise and he gets to put up a tree for the first time in a long time,so happy that made me,but i need to know if he deffinatly has the HepC if i had it when he was born? I don't want to alarm them if I don't have to but I don't think that is possible,I feel so horrible inside if I have harmed him.They don't know about the Hepc (YET)They know I have cirrohsis but think it is from me drinking.What do I do? Thank you.God Bless, oh! this backwards sleeping thing is really confusing to me also and I try to get the nights to be nights but for some reason the daylight makes me want to sleep....Go figure. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 23, 2008 Report Share Posted November 23, 2008 Sue,thank you for the uplift,I know it is a possibility but that is better than he has it " for sure " case.I am still not possitive how I got HepC I had the transfusion in the 80's,never was an I.V. user,do you know the stats. on getting it from having sex? From: diane chandler <dianechandler@ att.net> Subject: Re: questions To: livercirrhosissuppo rtyahoogroups (DOT) com Date: Sunday, November 23, 2008, 2:16 PM Hi , I'm so sorry you are feeling bad. It's good to hear from you again. I know the issue with your son is weighing heavy on you. It seems like you've had a good relationship with his adoptive parents since the adoption. If I were you, I believe I would just have a talk with his adoptive parents and tell them that your cirrhosis is caused by Hep C and that there is a small chance that your son could be infected as well. Explain however that you are not sure that you even had the virus when you were carrying him. Tell them he should be tested just to be sure. They don't even have to tell him until the results are in. They can just carry him if for a checkup and ask the doctor to order the test as a part of the regular lab workup. It can be handled discreetly and there's no need to make a big deal of it unless absolutely necessary. I will be praying for you and for your son. Let us know how things turn out. Hugs........ .. Diane ____________ _________ _________ __ From: italybell69 <italybell69@ yahoo.com> To: livercirrhosissuppo rtyahoogroups (DOT) com Sent: Sunday, November 23, 2008 12:36:21 PM Subject: questions hello family,I haven't posted for a couple weeks,I have been going through the " I hate the world syndrome " My platlets are 81,now shouldn't I get some new ones(I'm trying to be humorous)I had wrist surgery in the beginning of July and my bruising is still VERY here...and this FREEZING all the time Crap is for the birds,isn't there any vitamin to help?I also have a serious dilema..I gave my son up for adoption 16 yrs ago thruogh a private adoption,I know the parents,and they have always sent me pictures and keep me had kept in touch,well i hadn't heard a word in a couple years and she sent me some recent pictures (usually for the last 7 yrs. the have always gone on some sort of Carribean cruise and he gets to put up a tree for the first time in a long time,so happy that made me,but i need to know if he deffinatly has the HepC if i had it when he was born? I don't want to alarm them if I don't have to but I don't think that is possible,I feel so horrible inside if I have harmed him.They don't know about the Hepc (YET)They know I have cirrohsis but think it is from me drinking.What do I do? Thank you.God Bless, oh! this backwards sleeping thing is really confusing to me also and I try to get the nights to be nights but for some reason the daylight makes me want to sleep....Go figure. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 26, 2008 Report Share Posted November 26, 2008 Some conditions are more obviously related from parent to child, such as Hep C. But there are lots of other things a child can get or be at risk of getting because of the genetic pool of the child's parents. I am also a birth mother. When I found my son, I had to tell him that heart and artery problems, thyroid problems, and allergies and asthma ran in my family. He had already checked on the blood pressure record because he is an airline pilot and every time they sent him in for a physical his bp was high. Turned out he just reacted to white coats at that time. But he is still at risk for high bp, high cholesterol, heart attacks, arthritis. And then a couple of years after I found him, I was diagnosed with non alcoholic cirrhosis with a possibility of a genetic factor. And I have peripheral neuropathy, and my daughter has it and my brother was just diagnosed with that too, so maybe that is genetic too. I really gave this guy a lousy medical background. But, he is better off for knowing it. Now he can watch for signs. I am not telling you this to tell you you should contact his adoptive parents, just to let you know that there are others out there who feel a responsibility for the risks their children run because of their biological parents medical problems. Because a doctor told me and my brothers to be checked for heart problems frequently after my father died of a heart attack and my mother had a heart attack about one month later, I still haven't had a heart attack even though I have 7 stents in my body, have had triple bypass surgery and carotid artery surgery. Jan H > hello family,I haven't posted for a couple weeks,I have been going > through the " I hate the world syndrome " My platlets are 81,now shouldn't > I get some new ones(I'm trying to be humorous)I had wrist surgery in > the beginning of July and my bruising is still VERY here...and this > FREEZING all the time Crap is for the birds,isn't there any vitamin to > help?I also have a serious dilema..I gave my son up for adoption 16 yrs > ago thruogh a private adoption,I know the parents,and they have always > sent me pictures and keep me had kept in touch,well i hadn't heard a > word in a couple years and she sent me some recent pictures (usually > for the last 7 yrs. the have always gone on some sort of Carribean > cruise and he gets to put up a tree for the first time in a long > time,so happy that made me,but i need to know if he deffinatly has the > HepC if i had it when he was born? I don't want to alarm them if I > don't have to but I don't think that is possible,I feel so horrible > inside if I have harmed him.They don't know about the Hepc (YET)They > know I have cirrohsis but think it is from me drinking.What do I do? > Thank you.God Bless, oh! this backwards sleeping thing is really > confusing to me also and I try to get the nights to be nights but for > some reason the daylight makes me want to sleep....Go figure. > > > -- Jan H Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 30, 2008 Report Share Posted November 30, 2008 Thanks Jan for the advice. Hugs, > hello family,I haven't posted for a couple weeks,I have been going > through the " I hate the world syndrome " My platlets are 81,now shouldn't > I get some new ones(I'm trying to be humorous)I had wrist surgery in > the beginning of July and my bruising is still VERY here...and this > FREEZING all the time Crap is for the birds,isn't there any vitamin to > help?I also have a serious dilema..I gave my son up for adoption 16 yrs > ago thruogh a private adoption,I know the parents,and they have always > sent me pictures and keep me had kept in touch,well i hadn't heard a > word in a couple years and she sent me some recent pictures (usually > for the last 7 yrs. the have always gone on some sort of Carribean > cruise and he gets to put up a tree for the first time in a long > time,so happy that made me,but i need to know if he deffinatly has the > HepC if i had it when he was born? I don't want to alarm them if I > don't have to but I don't think that is possible,I feel so horrible > inside if I have harmed him.They don't know about the Hepc (YET)They > know I have cirrohsis but think it is from me drinking.What do I do? > Thank you.God Bless, oh! this backwards sleeping thing is really > confusing to me also and I try to get the nights to be nights but for > some reason the daylight makes me want to sleep....Go figure. > > > -- Jan H Quote Link to comment Share on other sites More sharing options...
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