Guest guest Posted October 13, 2007 Report Share Posted October 13, 2007 I second this question. I have never thought to ask what to look for that should prompt a visit to the hospital. For Jim, his wife and myself, I know any answers would be greatly appreciated! TammyJim wrote: Hi all,First of all, thanks for the welcomes a few weeks ago. My wife and I appreciate knowing there is someone out there.And now a quick question:My wife is fairly newly diagnosed with MS and she really hasn't had a chance to sit down and have her questions answered as far as dealing with symptoms goes.. Her PCP and neurologist are out of town, and that has her wondering about at what times you need to seek more immediate medical attention. With the (of course) caveat that you guys aren't doctors, what kind of symptoms onsetting leads you to head directly for the hospital? What kind do you generally let go and just deal with? Thanks,Jim Do you know someone with Multiple Sclerosis? Help find a cure! http://www.nationalmssociety.org/site/PageServer?pagename=HOM_GEN_homepage & amp;s_Affiliate=HOM_GEN_ Join Killeen Barter Trade For Sale at http://finance.groups.yahoo.com/group/KilleenBarterTradeForSale/ Building a website is a piece of cake. Yahoo! Small Business gives you all the tools to get online. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 13, 2007 Report Share Posted October 13, 2007 I second this question. I have never thought to ask what to look for that should prompt a visit to the hospital. For Jim, his wife and myself, I know any answers would be greatly appreciated! TammyJim wrote: Hi all,First of all, thanks for the welcomes a few weeks ago. My wife and I appreciate knowing there is someone out there.And now a quick question:My wife is fairly newly diagnosed with MS and she really hasn't had a chance to sit down and have her questions answered as far as dealing with symptoms goes.. Her PCP and neurologist are out of town, and that has her wondering about at what times you need to seek more immediate medical attention. With the (of course) caveat that you guys aren't doctors, what kind of symptoms onsetting leads you to head directly for the hospital? What kind do you generally let go and just deal with? Thanks,Jim Do you know someone with Multiple Sclerosis? Help find a cure! http://www.nationalmssociety.org/site/PageServer?pagename=HOM_GEN_homepage & amp;s_Affiliate=HOM_GEN_ Join Killeen Barter Trade For Sale at http://finance.groups.yahoo.com/group/KilleenBarterTradeForSale/ Building a website is a piece of cake. Yahoo! Small Business gives you all the tools to get online. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 13, 2007 Report Share Posted October 13, 2007 I second this question. I have never thought to ask what to look for that should prompt a visit to the hospital. For Jim, his wife and myself, I know any answers would be greatly appreciated! TammyJim wrote: Hi all,First of all, thanks for the welcomes a few weeks ago. My wife and I appreciate knowing there is someone out there.And now a quick question:My wife is fairly newly diagnosed with MS and she really hasn't had a chance to sit down and have her questions answered as far as dealing with symptoms goes.. Her PCP and neurologist are out of town, and that has her wondering about at what times you need to seek more immediate medical attention. With the (of course) caveat that you guys aren't doctors, what kind of symptoms onsetting leads you to head directly for the hospital? What kind do you generally let go and just deal with? Thanks,Jim Do you know someone with Multiple Sclerosis? Help find a cure! http://www.nationalmssociety.org/site/PageServer?pagename=HOM_GEN_homepage & amp;s_Affiliate=HOM_GEN_ Join Killeen Barter Trade For Sale at http://finance.groups.yahoo.com/group/KilleenBarterTradeForSale/ Building a website is a piece of cake. Yahoo! Small Business gives you all the tools to get online. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 13, 2007 Report Share Posted October 13, 2007 A tough question to answer. First and foremost, listen to your body. No one knows your body better than yourself. I hesitate to answer because I would not want to plant any seeds of difficulty that may never occur. So the simple answer is when you think that you may need help or a doctor. Seek it. Regards, Tom Re: dealing with symptoms I second this question. I have never thought to ask what to look for that should prompt a visit to the hospital. For Jim, his wife and myself, I know any answers would be greatly appreciated! TammyJim <jrsmithviigmail> wrote: Hi all,First of all, thanks for the welcomes a few weeks ago. My wife and I appreciate knowing there is someone out there.And now a quick question:My wife is fairly newly diagnosed with MS and she really hasn't had a chance to sit down and have her questions answered as far as dealing with symptoms goes.. Her PCP and neurologist are out of town, and that has her wondering about at what times you need to seek more immediate medical attention. With the (of course) caveat that you guys aren't doctors, what kind of symptoms onsetting leads you to head directly for the hospital? What kind do you generally let go and just deal with? Thanks,Jim Do you know someone with Multiple Sclerosis? Help find a cure! http://www.nationalmssociety.org/site/PageServer?pagename=HOM_GEN_homepage & amp;s_Affiliate=HOM_GEN_ Join Killeen Barter Trade For Sale at http://finance.groups.yahoo.com/group/KilleenBarterTradeForSale/ Building a website is a piece of cake. Yahoo! Small Business gives you all the tools to get online. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 13, 2007 Report Share Posted October 13, 2007 There are some things that I would call my nerologist about within 24 hours if they happen to me. He said I should call him and he would directly admit me for IV steroids. Double vision or altered vision, worsening of my walk or if my arms/hands noticibly got weaker. I would not go to my GP because frankly she don't know about this stuff in my estimation, but my neurologist knows all about it. This is just me and my doctors though. Pegi %%%%%%%%%%%%%% Hi all, First of all, thanks for the welcomes a few weeks ago. My wife and I appreciate knowing there is someone out there. And now a quick question: My wife is fairly newly diagnosed with MS and she really hasn't had a chance to sit down and have her questions answered as far as dealing with symptoms goes.. Her PCP and neurologist are out of town, and that has her wondering about at what times you need to seek more immediate medical attention. With the (of course) caveat that you guys aren't doctors, what kind of symptoms onsetting leads you to head directly for the hospital? What kind do you generally let go and just deal with? Thanks, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 13, 2007 Report Share Posted October 13, 2007 Ok, I hold my neuro in high regards. I called him and he called right back within hours. He feels I am having another attack. 3rd one this year. I have poor balance, migraines are back, comprehension problems listening to speech and reading, a new vibration feeling in my left leg. All this coupled with worsening previous symptoms. I agree with my neuro, but is this something I should have considered going to the hospital instead of making a phone call? Would you? Am I looking for symptoms far worse than these to warrant a trip to the hospital? I just need the knowledge to know when bad is bad and a phone call is ok vs. bad is worse and I should go to the ER. I would like to know about anyone else's experience in this if you have had the experience. I don't want to wait until I wake up one morning and have to call 911 for an ambulance because I can't move my legs. Curious about warning signs as I'm sure Jim and his wife also would like to know what some things are that may be expected. I have only been Dx'd for 18 months and I feel as though I've had more than my fair share of exacerbations in that time. Anyone care to share feelings or opinions. I won't take them to heart, but sometimes is helps to hear and know I don't wonder about the same things. Tammytbayuk wrote: A tough question to answer. First and foremost, listen to your body. No one knows your body better than yourself. I hesitate to answer because I would not want to plant any seeds of difficulty that may never occur. So the simple answer is when you think that you may need help or a doctor. Seek it. Regards, Tom Re: dealing with symptoms I second this question. I have never thought to ask what to look for that should prompt a visit to the hospital. For Jim, his wife and myself, I know any answers would be greatly appreciated! TammyJim <jrsmithviigmail> wrote: Hi all,First of all, thanks for the welcomes a few weeks ago. My wife and I appreciate knowing there is someone out there.And now a quick question:My wife is fairly newly diagnosed with MS and she really hasn't had a chance to sit down and have her questions answered as far as dealing with symptoms goes.. Her PCP and neurologist are out of town, and that has her wondering about at what times you need to seek more immediate medical attention. With the (of course) caveat that you guys aren't doctors, what kind of symptoms onsetting leads you to head directly for the hospital? What kind do you generally let go and just deal with? Thanks,Jim Do you know someone with Multiple Sclerosis? Help find a cure! http://www.nationalmssociety.org/site/PageServer?pagename=HOM_GEN_homepage & amp;s_Affiliate=HOM_GEN_ Join Killeen Barter Trade For Sale at http://finance.groups.yahoo.com/group/KilleenBarterTradeForSale/ Building a website is a piece of cake. Yahoo! Small Business gives you all the tools to get online. Do you know someone with Multiple Sclerosis? Help find a cure! http://www.nationalmssociety.org/site/PageServer?pagename=HOM_GEN_homepage & amp;s_Affiliate=HOM_GEN_ Join Killeen Barter Trade For Sale at http://finance.groups.yahoo.com/group/KilleenBarterTradeForSale/ Don't let your dream ride pass you by. Make it a reality with Yahoo! Autos. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 13, 2007 Report Share Posted October 13, 2007 Ok, I hold my neuro in high regards. I called him and he called right back within hours. He feels I am having another attack. 3rd one this year. I have poor balance, migraines are back, comprehension problems listening to speech and reading, a new vibration feeling in my left leg. All this coupled with worsening previous symptoms. I agree with my neuro, but is this something I should have considered going to the hospital instead of making a phone call? Would you? Am I looking for symptoms far worse than these to warrant a trip to the hospital? I just need the knowledge to know when bad is bad and a phone call is ok vs. bad is worse and I should go to the ER. I would like to know about anyone else's experience in this if you have had the experience. I don't want to wait until I wake up one morning and have to call 911 for an ambulance because I can't move my legs. Curious about warning signs as I'm sure Jim and his wife also would like to know what some things are that may be expected. I have only been Dx'd for 18 months and I feel as though I've had more than my fair share of exacerbations in that time. Anyone care to share feelings or opinions. I won't take them to heart, but sometimes is helps to hear and know I don't wonder about the same things. Tammytbayuk wrote: A tough question to answer. First and foremost, listen to your body. No one knows your body better than yourself. I hesitate to answer because I would not want to plant any seeds of difficulty that may never occur. So the simple answer is when you think that you may need help or a doctor. Seek it. Regards, Tom Re: dealing with symptoms I second this question. I have never thought to ask what to look for that should prompt a visit to the hospital. For Jim, his wife and myself, I know any answers would be greatly appreciated! TammyJim <jrsmithviigmail> wrote: Hi all,First of all, thanks for the welcomes a few weeks ago. My wife and I appreciate knowing there is someone out there.And now a quick question:My wife is fairly newly diagnosed with MS and she really hasn't had a chance to sit down and have her questions answered as far as dealing with symptoms goes.. Her PCP and neurologist are out of town, and that has her wondering about at what times you need to seek more immediate medical attention. With the (of course) caveat that you guys aren't doctors, what kind of symptoms onsetting leads you to head directly for the hospital? What kind do you generally let go and just deal with? Thanks,Jim Do you know someone with Multiple Sclerosis? Help find a cure! http://www.nationalmssociety.org/site/PageServer?pagename=HOM_GEN_homepage & amp;s_Affiliate=HOM_GEN_ Join Killeen Barter Trade For Sale at http://finance.groups.yahoo.com/group/KilleenBarterTradeForSale/ Building a website is a piece of cake. Yahoo! Small Business gives you all the tools to get online. Do you know someone with Multiple Sclerosis? Help find a cure! http://www.nationalmssociety.org/site/PageServer?pagename=HOM_GEN_homepage & amp;s_Affiliate=HOM_GEN_ Join Killeen Barter Trade For Sale at http://finance.groups.yahoo.com/group/KilleenBarterTradeForSale/ Don't let your dream ride pass you by. Make it a reality with Yahoo! Autos. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 16, 2007 Report Share Posted October 16, 2007 Hi, I agree with Pegi, I did IV steroids when first diagnosed with my optic neuritis and falling stuff. I basically uese my neurologist as my GP, since like Clarence brings up, they don't know all of our MS problems and it takes them longer to eventually have you go see your neurologist. Does your wife have a nerologist she feels comfortable with. This is very important that she has a good talking comunication time with him/her including you at time. Do you go with her to her appointments? I used to be able to go myself but can't now. Crazy stuff, I always call my feet as "solid ice" as I feel at time they are very heavy and they are not a normal sensation so I can't drive alot, depends. Take care Darlne Kickin Cane Covers. www.canecovers.org -- Re: dealing with symptoms There are some things that I would call my nerologist about within 24 hours if they happen to me. He said I should call him and he would directly admit me for IV steroids. Double vision or altered vision, worsening of my walk or if my arms/hands noticibly got weaker. I would not go to my GP because frankly she don't know about this stuff in my estimation, but my neurologist knows all about it. This is just me and my doctors though.Pegi%%%%%%%%%%%%%%Hi all,First of all, thanks for the welcomes a few weeks ago. My wife and I appreciate knowing there is someone out there.And now a quick question:My wife is fairly newly diagnosed with MS and she really hasn't had a chance to sit down and have her questions answered as far as dealing with symptoms goes.. Her PCP and neurologist are out of town, and that has her wondering about at what times you need to seek more immediate medical attention. With the (of course) caveat that you guys aren't doctors, what kind of symptoms onsetting leads you to head directly for the hospital? What kind do you generally let go and just deal with?Thanks, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 16, 2007 Report Share Posted October 16, 2007 Hi, I agree with Pegi, I did IV steroids when first diagnosed with my optic neuritis and falling stuff. I basically uese my neurologist as my GP, since like Clarence brings up, they don't know all of our MS problems and it takes them longer to eventually have you go see your neurologist. Does your wife have a nerologist she feels comfortable with. This is very important that she has a good talking comunication time with him/her including you at time. Do you go with her to her appointments? I used to be able to go myself but can't now. Crazy stuff, I always call my feet as "solid ice" as I feel at time they are very heavy and they are not a normal sensation so I can't drive alot, depends. Take care Darlne Kickin Cane Covers. www.canecovers.org -- Re: dealing with symptoms There are some things that I would call my nerologist about within 24 hours if they happen to me. He said I should call him and he would directly admit me for IV steroids. Double vision or altered vision, worsening of my walk or if my arms/hands noticibly got weaker. I would not go to my GP because frankly she don't know about this stuff in my estimation, but my neurologist knows all about it. This is just me and my doctors though.Pegi%%%%%%%%%%%%%%Hi all,First of all, thanks for the welcomes a few weeks ago. My wife and I appreciate knowing there is someone out there.And now a quick question:My wife is fairly newly diagnosed with MS and she really hasn't had a chance to sit down and have her questions answered as far as dealing with symptoms goes.. Her PCP and neurologist are out of town, and that has her wondering about at what times you need to seek more immediate medical attention. With the (of course) caveat that you guys aren't doctors, what kind of symptoms onsetting leads you to head directly for the hospital? What kind do you generally let go and just deal with?Thanks, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 16, 2007 Report Share Posted October 16, 2007 Hi, I agree with Pegi, I did IV steroids when first diagnosed with my optic neuritis and falling stuff. I basically uese my neurologist as my GP, since like Clarence brings up, they don't know all of our MS problems and it takes them longer to eventually have you go see your neurologist. Does your wife have a nerologist she feels comfortable with. This is very important that she has a good talking comunication time with him/her including you at time. Do you go with her to her appointments? I used to be able to go myself but can't now. Crazy stuff, I always call my feet as "solid ice" as I feel at time they are very heavy and they are not a normal sensation so I can't drive alot, depends. Take care Darlne Kickin Cane Covers. www.canecovers.org -- Re: dealing with symptoms There are some things that I would call my nerologist about within 24 hours if they happen to me. He said I should call him and he would directly admit me for IV steroids. Double vision or altered vision, worsening of my walk or if my arms/hands noticibly got weaker. I would not go to my GP because frankly she don't know about this stuff in my estimation, but my neurologist knows all about it. This is just me and my doctors though.Pegi%%%%%%%%%%%%%%Hi all,First of all, thanks for the welcomes a few weeks ago. My wife and I appreciate knowing there is someone out there.And now a quick question:My wife is fairly newly diagnosed with MS and she really hasn't had a chance to sit down and have her questions answered as far as dealing with symptoms goes.. Her PCP and neurologist are out of town, and that has her wondering about at what times you need to seek more immediate medical attention. With the (of course) caveat that you guys aren't doctors, what kind of symptoms onsetting leads you to head directly for the hospital? What kind do you generally let go and just deal with?Thanks, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 17, 2007 Report Share Posted October 17, 2007 Thanks for the replies, all...My wife is finally getting going in the right direction with a neurologist, I think. Her previous neuro wouldnt answer any of her questions and basically just repeated 'lose weight' to her over and over again. But as of a few days ago, she's found a neuro that actually wants to spend time explaining everything. BIG IMPROVEMENT! As for me joining her at her appointments, not yet, but I'll start going with her soon. Jim Hi, I agree with Pegi, I did IV steroids when first diagnosed with my optic neuritis and falling stuff. I basically uese my neurologist as my GP, since like Clarence brings up, they don't know all of our MS problems and it takes them longer to eventually have you go see your neurologist. Does your wife have a nerologist she feels comfortable with. This is very important that she has a good talking comunication time with him/her including you at time. Do you go with her to her appointments? I used to be able to go myself but can't now. Crazy stuff, I always call my feet as " solid ice " as I feel at time they are very heavy and they are not a normal sensation so I can't drive alot, depends. Take care Darlne Kickin Cane Covers. www.canecovers.org -- Re: dealing with symptoms There are some things that I would call my nerologist about within 24 hours if they happen to me. He said I should call him and he would directly admit me for IV steroids. Double vision or altered vision, worsening of my walk or if my arms/hands noticibly got weaker. I would not go to my GP because frankly she don't know about this stuff in my estimation, but my neurologist knows all about it. This is just me and my doctors though. Pegi%%%%%%%%%%%%%%Hi all,First of all, thanks for the welcomes a few weeks ago. My wife and I appreciate knowing there is someone out there.And now a quick question:My wife is fairly newly diagnosed with MS and she really hasn't had a chance to sit down and have her questions answered as far as dealing with symptoms goes.. Her PCP and neurologist are out of town, and that has her wondering about at what times you need to seek more immediate medical attention. With the (of course) caveat that you guys aren't doctors, what kind of symptoms onsetting leads you to head directly for the hospital? What kind do you generally let go and just deal with?Thanks, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 17, 2007 Report Share Posted October 17, 2007 Thanks for the replies, all...My wife is finally getting going in the right direction with a neurologist, I think. Her previous neuro wouldnt answer any of her questions and basically just repeated 'lose weight' to her over and over again. But as of a few days ago, she's found a neuro that actually wants to spend time explaining everything. BIG IMPROVEMENT! As for me joining her at her appointments, not yet, but I'll start going with her soon. Jim Hi, I agree with Pegi, I did IV steroids when first diagnosed with my optic neuritis and falling stuff. I basically uese my neurologist as my GP, since like Clarence brings up, they don't know all of our MS problems and it takes them longer to eventually have you go see your neurologist. Does your wife have a nerologist she feels comfortable with. This is very important that she has a good talking comunication time with him/her including you at time. Do you go with her to her appointments? I used to be able to go myself but can't now. Crazy stuff, I always call my feet as " solid ice " as I feel at time they are very heavy and they are not a normal sensation so I can't drive alot, depends. Take care Darlne Kickin Cane Covers. www.canecovers.org -- Re: dealing with symptoms There are some things that I would call my nerologist about within 24 hours if they happen to me. He said I should call him and he would directly admit me for IV steroids. Double vision or altered vision, worsening of my walk or if my arms/hands noticibly got weaker. I would not go to my GP because frankly she don't know about this stuff in my estimation, but my neurologist knows all about it. This is just me and my doctors though. Pegi%%%%%%%%%%%%%%Hi all,First of all, thanks for the welcomes a few weeks ago. My wife and I appreciate knowing there is someone out there.And now a quick question:My wife is fairly newly diagnosed with MS and she really hasn't had a chance to sit down and have her questions answered as far as dealing with symptoms goes.. Her PCP and neurologist are out of town, and that has her wondering about at what times you need to seek more immediate medical attention. With the (of course) caveat that you guys aren't doctors, what kind of symptoms onsetting leads you to head directly for the hospital? What kind do you generally let go and just deal with?Thanks, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 17, 2007 Report Share Posted October 17, 2007 Thanks for the replies, all...My wife is finally getting going in the right direction with a neurologist, I think. Her previous neuro wouldnt answer any of her questions and basically just repeated 'lose weight' to her over and over again. But as of a few days ago, she's found a neuro that actually wants to spend time explaining everything. BIG IMPROVEMENT! As for me joining her at her appointments, not yet, but I'll start going with her soon. Jim Hi, I agree with Pegi, I did IV steroids when first diagnosed with my optic neuritis and falling stuff. I basically uese my neurologist as my GP, since like Clarence brings up, they don't know all of our MS problems and it takes them longer to eventually have you go see your neurologist. Does your wife have a nerologist she feels comfortable with. This is very important that she has a good talking comunication time with him/her including you at time. Do you go with her to her appointments? I used to be able to go myself but can't now. Crazy stuff, I always call my feet as " solid ice " as I feel at time they are very heavy and they are not a normal sensation so I can't drive alot, depends. Take care Darlne Kickin Cane Covers. www.canecovers.org -- Re: dealing with symptoms There are some things that I would call my nerologist about within 24 hours if they happen to me. He said I should call him and he would directly admit me for IV steroids. Double vision or altered vision, worsening of my walk or if my arms/hands noticibly got weaker. I would not go to my GP because frankly she don't know about this stuff in my estimation, but my neurologist knows all about it. This is just me and my doctors though. Pegi%%%%%%%%%%%%%%Hi all,First of all, thanks for the welcomes a few weeks ago. My wife and I appreciate knowing there is someone out there.And now a quick question:My wife is fairly newly diagnosed with MS and she really hasn't had a chance to sit down and have her questions answered as far as dealing with symptoms goes.. Her PCP and neurologist are out of town, and that has her wondering about at what times you need to seek more immediate medical attention. With the (of course) caveat that you guys aren't doctors, what kind of symptoms onsetting leads you to head directly for the hospital? What kind do you generally let go and just deal with?Thanks, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2007 Report Share Posted October 18, 2007 Oh that's great! I'm so glad she's found a better Neuro. The otehr Neuro sounds like a real weenie. Hugs, Challis Jim wrote: Thanks for the replies, all...My wife is finally getting going in the right direction with a neurologist, I think. Her previous neuro wouldnt answer any of her questions and basically just repeated 'lose weight' to her over and over again. But as of a few days ago, she's found a neuro that actually wants to spend time explaining everything. BIG IMPROVEMENT! As for me joining her at her appointments, not yet, but I'll start going with her soon. Jim On 10/17/07, Kickin Canes <kickincanescomcast (DOT) net> wrote: Hi, I agree with Pegi, I did IV steroids when first diagnosed with my optic neuritis and falling stuff. I basically uese my neurologist as my GP, since like Clarence brings up, they don't know all of our MS problems and it takes them longer to eventually have you go see your neurologist. Does your wife have a nerologist she feels comfortable with. This is very important that she has a good talking comunication time with him/her including you at time. Do you go with her to her appointments? I used to be able to go myself but can't now. Crazy stuff, I always call my feet as "solid ice" as I feel at time they are very heavy and they are not a normal sensation so I can't drive alot, depends. Take care Darlne Kickin Cane Covers. www.canecovers.org -- Re: dealing with symptoms There are some things that I would call my nerologist about within 24 hours if they happen to me. He said I should call him and he would directly admit me for IV steroids. Double vision or altered vision, worsening of my walk or if my arms/hands noticibly got weaker. I would not go to my GP because frankly she don't know about this stuff in my estimation, but my neurologist knows all about it. This is just me and my doctors though. Pegi%%%%%%%%%%%%%%Hi all,First of all, thanks for the welcomes a few weeks ago. My wife and I appreciate knowing there is someone out there.And now a quick question:My wife is fairly newly diagnosed with MS and she really hasn't had a chance to sit down and have her questions answered as far as dealing with symptoms goes.. Her PCP and neurologist are out of town, and that has her wondering about at what times you need to seek more immediate medical attention. With the (of course) caveat that you guys aren't doctors, what kind of symptoms onsetting leads you to head directly for the hospital? What kind do you generally let go and just deal with?Thanks, __________________________________________________ Quote Link to comment Share on other sites More sharing options...
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