Guest guest Posted March 28, 2001 Report Share Posted March 28, 2001 > I would like to join the support group if someone could please email > me. My address is bratzaj@a... My name is Bruce and I have had > this disease for three years now. I have so many questions to ask > others about it. Could any one please email me on how to get to the > chat group and what day and time they meet. > Hi Bruce, and welcome. And welcome to all the other new members, too! My name is Tull, and I'm a friend/primary care-giver of Karyn's, who created this group about a year and a half ago. She's not able to get on the computer herself very much these days, so I kind of try and " fill in " for her in the meantime. As far as looking for a place to ask questions about this disease, you've definitely come to the right place! That's one of the main purposes of this this group. While none of us are doctors, most have direct experience in dealing with this condition, and are more than willing to share that with others. So go ahead and start posting any/all questions you may have ..... maybe one or 2 at a time! ;-) As far as the chat group goes, folks are still kind of evaluating different options for that, so it's still kind of in a state of " flux " . The Chat room supplied for this purpose from the Yahoo groups web site seems to be too slow, and some of the other options that have been tried don't allow enough folks to join simultaneously. When that gets sorted out, I'll update the " calendar " section of the website, and everyone will get an e-mail reminder each week with the time and URL for the chat. I believe one of our newer members (Mark?) has graciously provided a link to his web site, and folks will be trying that out tonight, Wednesday, March 28, starting at 5:30 pm Pacific Standard Time (which I think is 8:30 Eastern Standard time????). Here's the URL: http://www.top5plus5.com/Chat%20Rooms.htm In the meantime, feel free to start asking questions via e-mail! Cheers to all, --Tull Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2001 Report Share Posted March 28, 2001 Hi Bruce, Welcome, my friend. It is still kinda sketchy what we are doing with the chat group yet. We have been having big fun chatting every night, and last night I think there was a great big confusion where we were suppose to meet. When someone, or everyone, figures out what we are doing, someone will let us all know. I am on the AOL IM - Kru20Laws............and also the MSN IM Kru20Law@... if you have either of these services, please add my name, and when you see me on, IM me & we can chat that way until everything else gets straightened out. Thanks, and again, WELCOME! Lots of Hugs, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 17, 2001 Report Share Posted April 17, 2001 Dear I can certainly understand your frustration with Chrissie's problems. If she is not eating it is important that she is getting some kind of nutrition. Possibly in liquid form so it will not give her any pain swallowing. I can only imagine what you are going through. Make sure you get breaks from caretaking as this is so important in your own well being. You are doing a wonderful Job. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 13, 2001 Report Share Posted May 13, 2001 Hi, , and welcome. What you describe sounds very similar to something my Mom had. Has your mother's thyroid levels been checked? My mom has been on Synthroid for years, but then the bumps and itching started on her back. She finally got it checked out, and the same thing - doctors had no clue. I told her to go back and ask them to re-check her thyroid levels. Sure enough, they were down a wee bit, and upping her Synthroid dose cleared her up. Hope this helps. Air hugs, Jackie _________________________________________________________________ Get your FREE download of MSN Explorer at http://explorer.msn.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 13, 2001 Report Share Posted May 13, 2001 Hi, , and welcome. What you describe sounds very similar to something my Mom had. Has your mother's thyroid levels been checked? My mom has been on Synthroid for years, but then the bumps and itching started on her back. She finally got it checked out, and the same thing - doctors had no clue. I told her to go back and ask them to re-check her thyroid levels. Sure enough, they were down a wee bit, and upping her Synthroid dose cleared her up. Hope this helps. Air hugs, Jackie _________________________________________________________________ Get your FREE download of MSN Explorer at http://explorer.msn.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2001 Report Share Posted May 14, 2001 hmmm...Your description sort of sounds like scabies. But with scabies you will see some " tunneling " marks on her skin, too Scabies seems to be seen quite intensely in the armpits and folds of the elbows...and the warm places on the body (usually not the scalp, though)...but can occur on back, etc. Might your Mom have a fungal infection? Have your Dr. check for that. Poor baby, my heart goes out to her. Love, Suzanne in Juneau, Alaska > >Reply-To: urticaria >To: urticaria >Subject: Help >Date: Mon, 14 May 2001 14:52:18 -0700 > >Hi All - > >A friend just told me about this list, so I'm giving it a shot and hope >you'll be able to help. My mother has " something " - the dermatologist >and her doctors have not been able to diagnose it. She has small red >bumps all over, especially her back, lower back, legs, arms, a bit on >her feet, and shoulders. Sometimes they appear red, sometimes they >don't. She also has some areas with a rash. Sometimes the bumps drain >(if she scrathes), then forms a little scab. Some will bleed if she >scratches too much. > >She has a lot of itching. The dermatologist even took a biopsy and he >still doesn't know what it is. She's had it for six months; my final >frustration came the other day when he suggested it might be scabies, >because he didn't know what ele to say. Well, obviously, if that is >what the problem is, we would all have it. Plus that's not at all what >it looks like. > >Using Sea Breeze followed by the anti-itching lotion they give her >helps. She's also taking methylprednisolone, (generic for Medrol) 4mg. > >Anyone have any thoughts? Anything specific on the FAQ you can suggest? > >Thanks. You can email me privately if you like. > > > > > _________________________________________________________________ Get your FREE download of MSN Explorer at http://explorer.msn.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2001 Report Share Posted May 14, 2001 hmmm...Your description sort of sounds like scabies. But with scabies you will see some " tunneling " marks on her skin, too Scabies seems to be seen quite intensely in the armpits and folds of the elbows...and the warm places on the body (usually not the scalp, though)...but can occur on back, etc. Might your Mom have a fungal infection? Have your Dr. check for that. Poor baby, my heart goes out to her. Love, Suzanne in Juneau, Alaska > >Reply-To: urticaria >To: urticaria >Subject: Help >Date: Mon, 14 May 2001 14:52:18 -0700 > >Hi All - > >A friend just told me about this list, so I'm giving it a shot and hope >you'll be able to help. My mother has " something " - the dermatologist >and her doctors have not been able to diagnose it. She has small red >bumps all over, especially her back, lower back, legs, arms, a bit on >her feet, and shoulders. Sometimes they appear red, sometimes they >don't. She also has some areas with a rash. Sometimes the bumps drain >(if she scrathes), then forms a little scab. Some will bleed if she >scratches too much. > >She has a lot of itching. The dermatologist even took a biopsy and he >still doesn't know what it is. She's had it for six months; my final >frustration came the other day when he suggested it might be scabies, >because he didn't know what ele to say. Well, obviously, if that is >what the problem is, we would all have it. Plus that's not at all what >it looks like. > >Using Sea Breeze followed by the anti-itching lotion they give her >helps. She's also taking methylprednisolone, (generic for Medrol) 4mg. > >Anyone have any thoughts? Anything specific on the FAQ you can suggest? > >Thanks. You can email me privately if you like. > > > > > _________________________________________________________________ Get your FREE download of MSN Explorer at http://explorer.msn.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2001 Report Share Posted May 14, 2001 hmmm...Your description sort of sounds like scabies. But with scabies you will see some " tunneling " marks on her skin, too Scabies seems to be seen quite intensely in the armpits and folds of the elbows...and the warm places on the body (usually not the scalp, though)...but can occur on back, etc. Might your Mom have a fungal infection? Have your Dr. check for that. Poor baby, my heart goes out to her. Love, Suzanne in Juneau, Alaska > >Reply-To: urticaria >To: urticaria >Subject: Help >Date: Mon, 14 May 2001 14:52:18 -0700 > >Hi All - > >A friend just told me about this list, so I'm giving it a shot and hope >you'll be able to help. My mother has " something " - the dermatologist >and her doctors have not been able to diagnose it. She has small red >bumps all over, especially her back, lower back, legs, arms, a bit on >her feet, and shoulders. Sometimes they appear red, sometimes they >don't. She also has some areas with a rash. Sometimes the bumps drain >(if she scrathes), then forms a little scab. Some will bleed if she >scratches too much. > >She has a lot of itching. The dermatologist even took a biopsy and he >still doesn't know what it is. She's had it for six months; my final >frustration came the other day when he suggested it might be scabies, >because he didn't know what ele to say. Well, obviously, if that is >what the problem is, we would all have it. Plus that's not at all what >it looks like. > >Using Sea Breeze followed by the anti-itching lotion they give her >helps. She's also taking methylprednisolone, (generic for Medrol) 4mg. > >Anyone have any thoughts? Anything specific on the FAQ you can suggest? > >Thanks. You can email me privately if you like. > > > > > _________________________________________________________________ Get your FREE download of MSN Explorer at http://explorer.msn.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2001 Report Share Posted May 14, 2001 , Hello and welcome to the group!!! I am sorry to hear that your Mom has been suffering. It is so hard to figure this unique puzzle out. This website might be worth checking out and maybe a picture on it will help http://tray.dermatology.uiowa.edu/DermImag.htm I hope this helps in some way. Hang in there!! ~Alena's Mom Help > Hi All - > > A friend just told me about this list, so I'm giving it a shot and hope > you'll be able to help. My mother has " something " - the dermatologist > and her doctors have not been able to diagnose it. She has small red > bumps all over, especially her back, lower back, legs, arms, a bit on > her feet, and shoulders. Sometimes they appear red, sometimes they > don't. She also has some areas with a rash. Sometimes the bumps drain > (if she scrathes), then forms a little scab. Some will bleed if she > scratches too much. > > She has a lot of itching. The dermatologist even took a biopsy and he > still doesn't know what it is. She's had it for six months; my final > frustration came the other day when he suggested it might be scabies, > because he didn't know what ele to say. Well, obviously, if that is > what the problem is, we would all have it. Plus that's not at all what > it looks like. > > Using Sea Breeze followed by the anti-itching lotion they give her > helps. She's also taking methylprednisolone, (generic for Medrol) 4mg. > > Anyone have any thoughts? Anything specific on the FAQ you can suggest? > > Thanks. You can email me privately if you like. > > > > > > > ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ > If you do wish to unsubscribe then you can click on the following link: > urticaria-unsubscribeegroups > ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ > > This list is in the service of those who suffer from Chronic Urticaria (hives). We strive to support and lift each other as a worldwide cyber-family. > > We share whatever needs to be shared to help one another in our struggle with Chronic Urticria. Information provided in this forum is not to be taken as medical advice. Always consult your health professional before trying anything new. > > Any posting that is off the main topic of Chronic Urticaria, we post with a prefix of NCU -. This is done out of respect for those who do not wish to read such postings. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2001 Report Share Posted May 14, 2001 , Hello and welcome to the group!!! I am sorry to hear that your Mom has been suffering. It is so hard to figure this unique puzzle out. This website might be worth checking out and maybe a picture on it will help http://tray.dermatology.uiowa.edu/DermImag.htm I hope this helps in some way. Hang in there!! ~Alena's Mom Help > Hi All - > > A friend just told me about this list, so I'm giving it a shot and hope > you'll be able to help. My mother has " something " - the dermatologist > and her doctors have not been able to diagnose it. She has small red > bumps all over, especially her back, lower back, legs, arms, a bit on > her feet, and shoulders. Sometimes they appear red, sometimes they > don't. She also has some areas with a rash. Sometimes the bumps drain > (if she scrathes), then forms a little scab. Some will bleed if she > scratches too much. > > She has a lot of itching. The dermatologist even took a biopsy and he > still doesn't know what it is. She's had it for six months; my final > frustration came the other day when he suggested it might be scabies, > because he didn't know what ele to say. Well, obviously, if that is > what the problem is, we would all have it. Plus that's not at all what > it looks like. > > Using Sea Breeze followed by the anti-itching lotion they give her > helps. She's also taking methylprednisolone, (generic for Medrol) 4mg. > > Anyone have any thoughts? Anything specific on the FAQ you can suggest? > > Thanks. You can email me privately if you like. > > > > > > > ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ > If you do wish to unsubscribe then you can click on the following link: > urticaria-unsubscribeegroups > ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ > > This list is in the service of those who suffer from Chronic Urticaria (hives). We strive to support and lift each other as a worldwide cyber-family. > > We share whatever needs to be shared to help one another in our struggle with Chronic Urticria. Information provided in this forum is not to be taken as medical advice. Always consult your health professional before trying anything new. > > Any posting that is off the main topic of Chronic Urticaria, we post with a prefix of NCU -. This is done out of respect for those who do not wish to read such postings. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2001 Report Share Posted May 14, 2001 , Hello and welcome to the group!!! I am sorry to hear that your Mom has been suffering. It is so hard to figure this unique puzzle out. This website might be worth checking out and maybe a picture on it will help http://tray.dermatology.uiowa.edu/DermImag.htm I hope this helps in some way. Hang in there!! ~Alena's Mom Help > Hi All - > > A friend just told me about this list, so I'm giving it a shot and hope > you'll be able to help. My mother has " something " - the dermatologist > and her doctors have not been able to diagnose it. She has small red > bumps all over, especially her back, lower back, legs, arms, a bit on > her feet, and shoulders. Sometimes they appear red, sometimes they > don't. She also has some areas with a rash. Sometimes the bumps drain > (if she scrathes), then forms a little scab. Some will bleed if she > scratches too much. > > She has a lot of itching. The dermatologist even took a biopsy and he > still doesn't know what it is. She's had it for six months; my final > frustration came the other day when he suggested it might be scabies, > because he didn't know what ele to say. Well, obviously, if that is > what the problem is, we would all have it. Plus that's not at all what > it looks like. > > Using Sea Breeze followed by the anti-itching lotion they give her > helps. She's also taking methylprednisolone, (generic for Medrol) 4mg. > > Anyone have any thoughts? Anything specific on the FAQ you can suggest? > > Thanks. You can email me privately if you like. > > > > > > > ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ > If you do wish to unsubscribe then you can click on the following link: > urticaria-unsubscribeegroups > ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ > > This list is in the service of those who suffer from Chronic Urticaria (hives). We strive to support and lift each other as a worldwide cyber-family. > > We share whatever needs to be shared to help one another in our struggle with Chronic Urticria. Information provided in this forum is not to be taken as medical advice. Always consult your health professional before trying anything new. > > Any posting that is off the main topic of Chronic Urticaria, we post with a prefix of NCU -. This is done out of respect for those who do not wish to read such postings. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 16, 2002 Report Share Posted May 16, 2002 Hello,I was wondering If anyone out there knows what to do for extreme back pain and leg pain!I have good days and bad days,but today is really bad.I take neurontin 100 mg,Ithelps with my head and gazing,but it does not help with my back and legs.I have poor balance and coordination at times I feel like I'm going to fall but luckily I catch myself.If anyone has any info I would greatly appreciate it! Thanks Tiff,mom of ally and ariel all 3 of us have mitochondrial encephalomyopathy! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 16, 2002 Report Share Posted May 16, 2002 Tiff I am the mother of Colby, COX IV< LCHAD, I too suffer from back pain. I was on ms contin for awhile, neurotin did nothing for me. I had 3 series of epidural blocks in my back last year, it worked for a year, and I am ready to go back again. Look in your yellow pages for pain management. Hope this helps. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 16, 2002 Report Share Posted May 16, 2002 Tiff I am the mother of Colby, COX IV< LCHAD, I too suffer from back pain. I was on ms contin for awhile, neurotin did nothing for me. I had 3 series of epidural blocks in my back last year, it worked for a year, and I am ready to go back again. Look in your yellow pages for pain management. Hope this helps. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 16, 2002 Report Share Posted May 16, 2002 Tiff I am the mother of Colby, COX IV< LCHAD, I too suffer from back pain. I was on ms contin for awhile, neurotin did nothing for me. I had 3 series of epidural blocks in my back last year, it worked for a year, and I am ready to go back again. Look in your yellow pages for pain management. Hope this helps. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 17, 2002 Report Share Posted May 17, 2002 Thanks ,I can use all the help I can get,My neurologist doesn't tell us anything.he once told me a couple years back,that i would have good days and bad days.but,he did not tell us what would be a bad day was!I found out what a bad day was about.god bless.Tiff Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 17, 2002 Report Share Posted May 17, 2002 Thanks ,I can use all the help I can get,My neurologist doesn't tell us anything.he once told me a couple years back,that i would have good days and bad days.but,he did not tell us what would be a bad day was!I found out what a bad day was about.god bless.Tiff Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 17, 2002 Report Share Posted May 17, 2002 I have no advice but we sure know all about neurontin not working for leg pains! It hasn't made one bit of difference in our son's leg pain. We are going to ask for something else when we go back in June. Maybe I can let you know what we get. Hopefully something that works! re:help Hello,I was wondering If anyone out there knows what to do for extreme back pain and leg pain!I have good days and bad days,but today is really bad.I take neurontin 100 mg,Ithelps with my head and gazing,but it does not help with my back and legs.I have poor balance and coordination at times I feel like I'm going to fall but luckily I catch myself.If anyone has any info I would greatly appreciate it!Thanks Tiff,mom of ally and ariel all 3 of us have mitochondrial encephalomyopathy!Please contact mito-owner with any problems or questions. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 17, 2002 Report Share Posted May 17, 2002 I have no advice but we sure know all about neurontin not working for leg pains! It hasn't made one bit of difference in our son's leg pain. We are going to ask for something else when we go back in June. Maybe I can let you know what we get. Hopefully something that works! re:help Hello,I was wondering If anyone out there knows what to do for extreme back pain and leg pain!I have good days and bad days,but today is really bad.I take neurontin 100 mg,Ithelps with my head and gazing,but it does not help with my back and legs.I have poor balance and coordination at times I feel like I'm going to fall but luckily I catch myself.If anyone has any info I would greatly appreciate it!Thanks Tiff,mom of ally and ariel all 3 of us have mitochondrial encephalomyopathy!Please contact mito-owner with any problems or questions. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 17, 2002 Report Share Posted May 17, 2002 I have no advice but we sure know all about neurontin not working for leg pains! It hasn't made one bit of difference in our son's leg pain. We are going to ask for something else when we go back in June. Maybe I can let you know what we get. Hopefully something that works! re:help Hello,I was wondering If anyone out there knows what to do for extreme back pain and leg pain!I have good days and bad days,but today is really bad.I take neurontin 100 mg,Ithelps with my head and gazing,but it does not help with my back and legs.I have poor balance and coordination at times I feel like I'm going to fall but luckily I catch myself.If anyone has any info I would greatly appreciate it!Thanks Tiff,mom of ally and ariel all 3 of us have mitochondrial encephalomyopathy!Please contact mito-owner with any problems or questions. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 24, 2003 Report Share Posted December 24, 2003 I do have some cards missing. I found my list and I had at least 8 missing. I bought more cards and finally got them addressed and put where the cats cannot get to them. Sharon HELP My cats messed up my cards and I have some of them missing. I went to see if I had the list and for some dumb reason I deleted it. I need pages 1 through 4. I have 5 through 10. My cards will be late this year because of all the craziness going on. I hope you forgive me and I promise next year I will get them out a lot earlier. Sharon ~~~~ *** ~~~ *** ~~~ *** ~~~~The Neurosarcoidosis CommunityLive Group Chat:-Mondays & Fridays 10pm EST USAhttp://www.elderwyn.com/neurosarcoidosis/chat.phpMessage Archives:-http://groups.yahoo.com/group/Neurosarcoidosis/messagesMembers Database:-Listings of locations, phone numbers, and instant messengers.http://groups.yahoo.com/group/Neurosarcoidosis/database Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 24, 2003 Report Share Posted December 24, 2003 I do have some cards missing. I found my list and I had at least 8 missing. I bought more cards and finally got them addressed and put where the cats cannot get to them. Sharon HELP My cats messed up my cards and I have some of them missing. I went to see if I had the list and for some dumb reason I deleted it. I need pages 1 through 4. I have 5 through 10. My cards will be late this year because of all the craziness going on. I hope you forgive me and I promise next year I will get them out a lot earlier. Sharon ~~~~ *** ~~~ *** ~~~ *** ~~~~The Neurosarcoidosis CommunityLive Group Chat:-Mondays & Fridays 10pm EST USAhttp://www.elderwyn.com/neurosarcoidosis/chat.phpMessage Archives:-http://groups.yahoo.com/group/Neurosarcoidosis/messagesMembers Database:-Listings of locations, phone numbers, and instant messengers.http://groups.yahoo.com/group/Neurosarcoidosis/database Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 27, 2004 Report Share Posted August 27, 2004 Hi! My name is Tina and I'm new to this group. I've started the process with Kaiser to get approval for this surgery. So far, things have not gone very smoothly. My doctor had no problem referring me initially. I attended the class at Pt. West given by a nutrition person and a behavioral medicine person. According to the teachers of the class, the next step was paperwork being sent to SSF for approval and that it should take approximately 2 months to find out. Well, 1 month after I took the class, I called SSF (Marina) to make sure she had my paperwork. Low and beyond, NO PAPERWORK! I've called and left messages with my PCP and have tried to talk to various people at Kaiser to find out the process but no luck. Any help would be greatly appreciated. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 29, 2004 Report Share Posted August 29, 2004 Hi Tina, Welcome to the group. I hope you brought lots of patience with you too. Kaiser hasn't been the fastest route for obtaining WLS but they do provide some highly skilled surgeons who do the surgery. I wish I could tell you that the road to surgery will be a smooth one. It has been for a few Kaiser patients. From a patient's point of view I can only tell you that there are a lot of people here who share your frustration, and we help each other through the processes for WLS with Kaiser. You didn't mention specificly when you started the process for WLS. I started the process for approval of a gastric by-pass in August of 2003. I received approval in June of 2004. I am scheduled for orientation at the new Fremont site next month, September 28th 2004. I know I will have another month's wait for my visit with the surgeron, anesteologist, 2nd psych eval & 2 nutritionist. Some people have a shorter process than I have had others have had longer. One year is about the norm for most patients. BTW, my PCP supposedly sent in my file for approval to SSF the first week of March. It wasn't until the first week of April that I found out is wasn't submitted. Then it took another month for my file to accutally be compiled and sent to SSF....hence the June approval. Hang in there. We are here to listen and support you in the process. In the mean time, don't give up on calling your PCP. Keep on her. (and whomever is compiling your file for submission to SSF). The squeaky wheel definitely gets things in motion where Kaiser is concerned. Best of luck, D > Hi! My name is Tina and I'm new to this group. I've started the > process with Kaiser to get approval for this surgery. So far, things > have not gone very smoothly. My doctor had no problem referring me > initially. I attended the class at Pt. West given by a nutrition > person and a behavioral medicine person. According to the teachers of > the class, the next step was paperwork being sent to SSF for approval > and that it should take approximately 2 months to find out. Well, 1 > month after I took the class, I called SSF (Marina) to make sure she > had my paperwork. Low and beyond, NO PAPERWORK! I've called and left > messages with my PCP and have tried to talk to various people at > Kaiser to find out the process but no luck. Any help would be greatly > appreciated. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 30, 2004 Report Share Posted August 30, 2004 Welcome to the group Tina...I see you found it....Hope you find all the answers in this wonderful group. Shirley (near Sacramento) Dr. 281.5/184/150 Quote Link to comment Share on other sites More sharing options...
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