Guest guest Posted June 2, 2010 Report Share Posted June 2, 2010 Diane, I saw your post and just wanted to throw in my 2c lol. Don't know how old you are or the extent of your issues, but after you get turned down once it is time to at least consult an attorney. I had one and it still took 3 years to go through. Anyways, are you familiar with the " blue book? " It tells about disabilities and what qualifies as " disabled " for various conditions. That is what SS uses to decide if you are or are not disabled. It is more about what the SS doctors say than what your own do also. I would urge you to at least consult with an attorney - there is normally no cost if they take your case they only get paid if they win. Otherwise, there are a couple good yahoo groups dealing with SS/SSDI etc. Might check in to them as well, lots of good info from people who have been through the whole system a time or three. I found a wealth of stuff there. Such as if you are over 50 your chances go up on getting it esp. if you have anything on paper saying you cannot go back to doing what your career was before. good luck, chris in IN ps-one thing tho, if you go back to work, it generally means you are telling the world " I am not disabled because yes I can still work. " So if you work more than a few months it means starting all over again plus it looks really bad for your disability case when you do it. Because for SS disability means " Nope cannot work. " > > Hi Jena, > > No Social Security - I've been denied 3 times. But I haven't used a lawyer > yet. I really need all of my doctors to get on the same page as far as what > I can and can't do. My podiatrist tells me I can't work, but pain > management doesn't fully agree. He feels that I can work at least part time > if it's primarily a desk job, but those are really hard to find around here. > So, if my doctors don't fully support me, then there is no use applying > again yet. > > > > I realize that having any other diagnosis isn't going to change the way the > medicine works, but it could help to find which medicine would be most > effective instead of trying everything out there until something works well > and consistently. I'm currently on MS Contin and Neurontin with Percocet > for breakthrough pain. Well, the breakthrough pain is almost constant, so > I'm taking the Percocet every 6 hours every day. When storms come in, or I > do too much, the pain gets worse, but I don't have anything else to take, > and just have to suffer through it. So, at my next appointment, I'll be > asking for something else, or an increase in the PRN Percocet. > > > > Diane - in NJ ~0) (my never ending cup of coffee, lol) > > > > Photography <http://dianef.deviantart.com/> http://dianef.deviantart.com/ > > Handmade Necklaces <http://www.angelfire.com/kitsune-kreations/index.html> > http://www.angelfire.com/kitsune-kreations/index.html > > Family and Pets <http://community.webshots.com/user/njwitch> > http://community.webshots.com/user/njwitch > > Facebook <http://www.facebook.com/dflemings66> > http://www.facebook.com/dflemings66 > > > > " Until one has loved an animal, a part of one's soul remains unawakened. " - > Anatole France > > ---------------------------------------------------------------------------- > -------------- > > > > From: Hugs-N-Pain [mailto:Hugs-N-Pain ] On > Behalf Of *~*Jena*~* > Sent: Monday, May 31, 2010 12:24 PM > To: Hugs-N-Pain > Subject: Re: OT- My Cat > > > > > > Diane, do you have your Social Security? if not I don't blame you for > wanting all your diagnosis. my SIL has hers and she was telling me the other > day she wanted a full body MRI. I ask did she realize what that would cost > even with Ins. my 20% on my back was 1,000.00 so why would she want to spend > that kind of money so she can grip about every little thing that is wrong > with her. not throwing that at you Diane. but it just didn't make sense to > me. she has Fibro. and the ones of us that has that knows oh gosh, the pain. > we have had thunderstorms for the last 3 days and have more coming for the > rest of the week. and of the pain. > Jena > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2010 Report Share Posted June 2, 2010 you are much like me. how in the world am I going to pass a drug test. taking these meds. I was on what you are taking but about a 1.5 years ago my dr. increased me to 40mg OpanaER and Roxicodone15mg for breakthrough pain every 6 hrs and like you I take them just about every 6 hrs to control my pain. who is going to hire me. I can't pass a drug test. no way. to me that should be enough for disability on its own Re: OT- My Cat Diane, do you have your Social Security? if not I don't blame you for wanting all your diagnosis. my SIL has hers and she was telling me the other day she wanted a full body MRI. I ask did she realize what that would cost even with Ins. my 20% on my back was 1,000.00 so why would she want to spend that kind of money so she can grip about every little thing that is wrong with her. not throwing that at you Diane. but it just didn't make sense to me. she has Fibro. and the ones of us that has that knows oh gosh, the pain. we have had thunderstorms for the last 3 days and have more coming for the rest of the week. and of the pain. Jena Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2010 Report Share Posted June 2, 2010 I my social security has been ongoing since Nov,06. I was turned down 2 x's so I hired a law firm that only took cases that were sure things and they only charge if you win. I have been to a appeal Feb. 09. it took until Oct. 09 to get my answer and I was turned down. that judge basically talked to me like a dog in my letter. and said because my daughter graduated I decided to apply for social security. I had dr. records were I had fractured the worst place in my back one week before school was out and I had been under a dr's care for other problems and because of the way my lawyer questioned me as I have said before my appeal was a complete flop. so now the firm has 2 federal attorney's in Atlanta that works for them with cases such as mine. and at this present time one of the attorneys has my case going on it with a fine tooth comb. if I ever get back in front of that judge again he will know exactly what my life is like. it just so happened that day my husband could not go with me that day. but hell or high water he will go with me. I have been through to much. he lives with me. he knows my life. me misery. it will be much different. Re: OT- My Cat > > > > > > Diane, do you have your Social Security? if not I don't blame you for > wanting all your diagnosis. my SIL has hers and she was telling me the other > day she wanted a full body MRI. I ask did she realize what that would cost > even with Ins. my 20% on my back was 1,000.00 so why would she want to spend > that kind of money so she can grip about every little thing that is wrong > with her. not throwing that at you Diane. but it just didn't make sense to > me. she has Fibro. and the ones of us that has that knows oh gosh, the pain. > we have had thunderstorms for the last 3 days and have more coming for the > rest of the week. and of the pain. > Jena > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2010 Report Share Posted June 2, 2010 Hi...Diane again. Again, i have RA, and neropathy, plus some other stuff. I got a buch of stuff am cujrntl;y struggling with a bunch of stuff but thank god the struggle I went through awhile back, with no money, no place to live, being un relapse because I was self-medicating, etc..... (and we all know how everyone just loves a self-medicator.....right......wrong!!! )...We are usually misunderstood, hatred and abused..... " She is just drug-seeking " was my favorite one.....I used to think, I'd like to see you with this kind of pain ans wha you can handle. But anyway my point in all this is that pain, pain mgt. pain meds, all of it has alwys been a bit of a bone of contenion for me and it feels so nice when I can get a reprival from it all. I started asking some of my Dr's about break through medicines afrer hearing about it , and once again I was met with resistance. so when I hear alof o yu share what you are taking, I sometimes feel a bit jealous, or something. so let me ask you all somwthing. For thoseof you that are taking any kind of strong meds, like oxycotin....or whatever, are you able to get this because you never had a problem with it, from the addiction point of view. do you know whAT i mean....see part of my struggle is because i am also a recovering addicti, so it complcates things, and sometimes I hear you all sharing about some liberal pain mt. but than I think, well maybe it is okay bcause they have never had trouble with adiction, or with alochol, etc and I have. Lots of trouble, so it gets tricfky, but I am getting more honest, and since I beong to several different groups I could see memanipulation myself inot a situation thT I muight not get ouit of so it is sometimwa better fofr me to get honest with it all at this level, do you know what I mean. Thhis is not to say I cant have anything at all because thEN i COULD GET IN TROUBLE TOO, THE PAIN GETTING SO BAD AND ME GOING OVERGBOARD TO RELIEVE IT, IT IS A TOUCH THING, BUT so what nobody ever said any of this would be easy. I want a life though. and I cant or wont be a martyr. So I just sont know why i get ao much resitance from people like my RA Dr. you would think ohim of all pople. He knows I am on methdone but he wont prescribv it and he wqont give me any back up medinine....stuff like that. I just have so much to untangle and figure out and work thorujgh right now with all my medical stuff and of course issue saround pain and pain mgt. are some of the worse issuea I have to deL WITH. So any thoughts would be appreciated, otherwise thankyou for listening.....love diane To: Hugs-N-Pain From: dianeflemings@... Date: Wed, 2 Jun 2010 09:06:41 -0400 Subject: Jena /RE: OT- My Cat Hi Jena, No Social Security - I've been denied 3 times. But I haven't used a lawyer yet. I really need all of my doctors to get on the same page as far as what I can and can't do. My podiatrist tells me I can't work, but pain management doesn't fully agree. He feels that I can work at least part time if it's primarily a desk job, but those are really hard to find around here. So, if my doctors don't fully support me, then there is no use applying again yet. I realize that having any other diagnosis isn't going to change the way the medicine works, but it could help to find which medicine would be most effective instead of trying everything out there until something works well and consistently. I'm currently on MS Contin and Neurontin with Percocet for breakthrough pain. Well, the breakthrough pain is almost constant, so I'm taking the Percocet every 6 hours every day. When storms come in, or I do too much, the pain gets worse, but I don't have anything else to take, and just have to suffer through it. So, at my next appointment, I'll be asking for something else, or an increase in the PRN Percocet. Diane - in NJ ~0) (my never ending cup of coffee, lol) Photography <http://dianef.deviantart.com/> http://dianef.deviantart.com/ Handmade Necklaces <http://www.angelfire.com/kitsune-kreations/index.html> http://www.angelfire.com/kitsune-kreations/index.html Family and Pets <http://community.webshots.com/user/njwitch> http://community.webshots.com/user/njwitch Facebook <http://www.facebook.com/dflemings66> http://www.facebook.com/dflemings66 " Until one has loved an animal, a part of one's soul remains unawakened. " - Anatole France ---------------------------------------------------------- -------------- From: Hugs-N-Pain [mailto:Hugs-N-Pain ] On Behalf Of *~*Jena*~* Sent: Monday, May 31, 2010 12:24 PM To: Hugs-N-Pain Subject: Re: OT- My Cat Diane, do you have your Social Security? if not I don't blame you for wanting all your diagnosis. my SIL has hers and she was telling me the other day she wanted a full body MRI. I ask did she realize what that would cost even with Ins. my 20% on my back was 1,000.00 so why would she want to spend that kind of money so she can grip about every little thing that is wrong with her. not throwing that at you Diane. but it just didn't make sense to me. she has Fibro. and the ones of us that has that knows oh gosh, the pain. we have had thunderstorms for the last 3 days and have more coming for the rest of the week. and of the pain. Jena Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2010 Report Share Posted June 2, 2010 Hi...One more thing Imeant to say..... I do have my Social swecurity Disability thNKJ God and one thing is you can work parttime and still get it. so is it [ossible thay your Dr. sAYING you may be able towork parttime at the right kind of job, that may not be such a conflisct after all.....do you know what I am saying? d > To: hugs-n-pain > From: Franco775@... > Date: Wed, 2 Jun 2010 21:56:04 -0400 > Subject: RE: Jena /RE: OT- My Cat > > > Hi...Diane again. Again, i have RA, and neropathy, plus some other stuff. I got a buch of stuff am cujrntl;y struggling with a bunch of stuff but thank god the struggle I went through awhile back, with no money, no place to live, being un relapse because I was self-medicating, etc..... (and we all know how everyone just loves a self-medicator.....right......wrong!!! )...We are usually misunderstood, hatred and abused..... " She is just drug-seeking " was my favorite one.....I used to think, I'd like to see you with this kind of pain ans wha you can handle. But anyway my point in all this is that pain, pain mgt. pain meds, all of it has alwys been a bit of a bone of contenion for me and it feels so nice when I can get a reprival from it all. I started asking some of my Dr's about break through medicines afrer hearing about it , and once again I was met with resistance. so when I hear alof o yu share what you are taking, I sometimes feel a bit jealous, or something. so let me ask you all somwthing. For thoseof you that are taking any kind of strong meds, like oxycotin....or whatever, are you able to get this because you never had a problem with it, from the addiction point of view. do you know whAT i mean....see part of my struggle is because i am also a recovering addicti, so it complcates things, and sometimes I hear you all sharing about some liberal pain mt. but than I think, well maybe it is okay bcause they have never had trouble with adiction, or with alochol, etc and I have. Lots of trouble, so it gets tricfky, but I am getting more honest, and since I beong to several different groups I could see memanipulation myself inot a situation thT I muight not get ouit of so it is sometimwa better fofr me to get honest with it all at this level, do you know what I mean. Thhis is not to say I cant have anything at all because thEN i COULD GET IN TROUBLE TOO, THE PAIN GETTING SO BAD AND ME GOING OVERGBOARD TO RELIEVE IT, IT IS A TOUCH THING, BUT so what nobody ever said any of this would be easy. I want a life though. and I cant or wont be a martyr. So I just sont know why i get ao much resitance from people like my RA Dr. you would think ohim of all pople. He knows I am on methdone but he wont prescribv it and he wqont give me any back up medinine....stuff like that. I just have so much to untangle and figure out and work thorujgh right now with all my medical stuff and of course issue saround pain and pain mgt. are some of the worse issuea I have to deL WITH. So any thoughts would be appreciated, otherwise thankyou for listening.....love diane > > > To: Hugs-N-Pain > From: dianeflemings@... > Date: Wed, 2 Jun 2010 09:06:41 -0400 > Subject: Jena /RE: OT- My Cat > > > > > > Hi Jena, > > No Social Security - I've been denied 3 times. But I haven't used a lawyer > yet. I really need all of my doctors to get on the same page as far as what > I can and can't do. My podiatrist tells me I can't work, but pain > management doesn't fully agree. He feels that I can work at least part time > if it's primarily a desk job, but those are really hard to find around here. > So, if my doctors don't fully support me, then there is no use applying > again yet. > > I realize that having any other diagnosis isn't going to change the way the > medicine works, but it could help to find which medicine would be most > effective instead of trying everything out there until something works well > and consistently. I'm currently on MS Contin and Neurontin with Percocet > for breakthrough pain. Well, the breakthrough pain is almost constant, so > I'm taking the Percocet every 6 hours every day. When storms come in, or I > do too much, the pain gets worse, but I don't have anything else to take, > and just have to suffer through it. So, at my next appointment, I'll be > asking for something else, or an increase in the PRN Percocet. > > Diane - in NJ ~0) (my never ending cup of coffee, lol) > > Photography <http://dianef.deviantart.com/> http://dianef.deviantart.com/ > > Handmade Necklaces <http://www.angelfire.com/kitsune-kreations/index.html> > http://www.angelfire.com/kitsune-kreations/index.html > > Family and Pets <http://community.webshots.com/user/njwitch> > http://community.webshots.com/user/njwitch > > Facebook <http://www.facebook.com/dflemings66> > http://www.facebook.com/dflemings66 > > " Until one has loved an animal, a part of one's soul remains unawakened. " - > Anatole France > > ---------------------------------------------------------- > -------------- > > From: Hugs-N-Pain [mailto:Hugs-N-Pain ] On > Behalf Of *~*Jena*~* > Sent: Monday, May 31, 2010 12:24 PM > To: Hugs-N-Pain > Subject: Re: OT- My Cat > > Diane, do you have your Social Security? if not I don't blame you for > wanting all your diagnosis. my SIL has hers and she was telling me the other > day she wanted a full body MRI. I ask did she realize what that would cost > even with Ins. my 20% on my back was 1,000.00 so why would she want to spend > that kind of money so she can grip about every little thing that is wrong > with her. not throwing that at you Diane. but it just didn't make sense to > me. she has Fibro. and the ones of us that has that knows oh gosh, the pain. > we have had thunderstorms for the last 3 days and have more coming for the > rest of the week. and of the pain. > Jena > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 3, 2010 Report Share Posted June 3, 2010 Diane, your Rheumatologist is probably the last person that is going to give you anything. When I first went to mine, I was already see my pain management Dr. so the Rhuenmy told me I had osteoporosis, osteoarthritis in my hips, then wonderful fibro along with the CFS, my hips give me fits. 6 weeks before my last appt with my pain management dr he put a trigger point injection in my hip and it was instant relief. I mean wonderful. but he is so busy it is almost impossible to get a appt with him so I called and got a appt with my now ex-Rhuemy. He was so rude to me. he told me I had a pain management dr why did I not go to him. I told him he was the one that diagnosis me with osteoarthritis in my hips and I wanted him to do something to make them stop hurting and if he thought I was there for drugs he was wrong I wanted a trigger point injection. and that was it. he was soooo rude. He says you have many tender areas all over your body. I told him if he would check his records he would see he also diagnosis me with fibro. I told him I also needed a new script for Celebrex. he told me he never gave me any Celebrex and once again. I ask him to please take a few minutes to read his notes that he had made on me. I was not there for dope. I wanted nothing but a steroid shot in my hip if he would please and a refill for my Celebrex. and he told me he gave me a script for a year for my Celebrex. And he made it look and me fill like I am standing on the street corner selling Celebrex like anybody would want any. My husband had driven 50 miles to see this quake. I am suppose to go back and see him next month., but unless I change my mind because of my social security he will not get a dime from me. He just jab the injection in my hip just where he thought it should go. and that was that. my pain management dr. had me to stand up pull down my pants and he gentle poked around till I almost kicked him and he said " I found it " ! LOL my suggestion is to find you a good pain management DR. you can search them out now on the computer and read their credentials and everything. I was referred by my MD> And was very fortunate to find him. my husband does not like him. Hubby thought when I fractured my back and I had the vertebroplasty I would be fixed and he could work me like a mule for at least another 20-25 years. but it just didn't work that way. I also ruptured the disc below the vertebrae. so I have constant pain. at times I feel someone took a 2x4 and hit me across the back with it. If it wasn't for my pain meds. I don't even want to think about it. You were talking about addiction. yes they are very addicting. and I am addicted I have been on them since 06. but after you find that good pain management Dr. you have to just keep going back don't put on your make-up let him see your pain. and if he is good he will finally get you up there where it will at least halfway control your pain. at least that has been my experience. also the most important thing. DO NOT HID ANYTHING FROM, BE UP FRONT AND STRAIGHT WITH HIM, HE HAS TO BE ABLE TO TRUST YOU AS YOU HIM. Mine had a tech that tried to get me in trouble, it turn out my appt was early the girl at the appt desk made the appt I didn't. and this tech really lower the boom on me to him until he got in the room and seen it was me. HE KNEW ME. I TRIED TO TELL THE TECH UP FRONT BUT SHE HAD A REALLY BAD ATITTUDE PROBLEM, THANK GOD SHE IS GONE. SO THAT IS WHY IT IS SOOO IMPORTANT THAT HE CAN TRUST YOU. BECAUSE OF THE MONEY SITUATION. HE GIVES ME MY SCRIPTS FOR 3 MONTHS AT A TIME. My mama had fibro too. she was seeing another pain management dr. and she had to go monthly and had to do a drug test each time. that was his rules. THE LAST TIME I WENT IT WAS TIME FOR MY DRUG TEST HE HAS ME DO ONE A YEAR. I HAD A BAD UTI. AND I COULD NOT EVEN PEE ENOUGH TO GET ENOUGH FOR THE TEST. AND I ASK HIM CAN'T YALL JUST DRAW SOME BLOOD OR SOMETHING. AND HE SAID HE WASN'T THE POLICE. IT WAS JUST SOMETHING THE LAW MADE HIM DO. SO AFTER DRINKING A 1\2 GALLON WATER. I FINALLY TRICKLED OUT A LITTLE BIT. AND HE TOLD ME NOT TO WORRY ABOUT IT AND GO ON HOME.. Sorry didn't mean to write a book. but just wanted to stress the importance of getting a good pain management dr. because there are some bad ones out there. and you really got to check them out. hope this hopes Jena in GA. Re: OT- My Cat > > Diane, do you have your Social Security? if not I don't blame you for > wanting all your diagnosis. my SIL has hers and she was telling me the > other > day she wanted a full body MRI. I ask did she realize what that would cost > even with Ins. my 20% on my back was 1,000.00 so why would she want to > spend > that kind of money so she can grip about every little thing that is wrong > with her. not throwing that at you Diane. but it just didn't make sense to > me. she has Fibro. and the ones of us that has that knows oh gosh, the > pain. > we have had thunderstorms for the last 3 days and have more coming for the > rest of the week. and of the pain. > Jena > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 10, 2010 Report Share Posted June 10, 2010 It's almost impossible to win without a disability advocate/disability lawyer.  If you get one, make sure it's someone that actually works with disability.  I used a non lawyer advocate and won with her.  They will tell your chances.  They don't get paid until you do.  You may want to reconsider going it alone. Lotacats “I love cats because I enjoy my home; and little by little, they become its visible soul.†Twitter_follow me http://twitter.com/LotacatsFunPix Express Chronic Pain Awareness http://www.cafepress.com/lotacatspix/5815010 Lotacatsfunpix.com http://www.lotacatsfunpix.com/ Deviantart http://lotacats05.deviantart.com/ Facebook http://www.facebook.com/#/profile.php?ref=name & id=1030129414 Subject: Jena /RE: OT- My Cat To: Hugs-N-Pain Date: Wednesday, June 2, 2010, 6:06 AM  Hi Jena, No Social Security - I've been denied 3 times. But I haven't used a lawyer yet. I really need all of my doctors to get on the same page as far as what I can and can't do. My podiatrist tells me I can't work, but pain management doesn't fully agree. He feels that I can work at least part time if it's primarily a desk job, but those are really hard to find around here. So, if my doctors don't fully support me, then there is no use applying again yet. I realize that having any other diagnosis isn't going to change the way the medicine works, but it could help to find which medicine would be most effective instead of trying everything out there until something works well and consistently. I'm currently on MS Contin and Neurontin with Percocet for breakthrough pain. Well, the breakthrough pain is almost constant, so I'm taking the Percocet every 6 hours every day. When storms come in, or I do too much, the pain gets worse, but I don't have anything else to take, and just have to suffer through it. So, at my next appointment, I'll be asking for something else, or an increase in the PRN Percocet. Diane - in NJ ~0) (my never ending cup of coffee, lol) Photography <http://dianef.deviantart.com/> http://dianef.deviantart.com/ Handmade Necklaces <http://www.angelfire.com/kitsune-kreations/index.html> http://www.angelfire.com/kitsune-kreations/index.html Family and Pets <http://community.webshots.com/user/njwitch> http://community.webshots.com/user/njwitch Facebook <http://www.facebook.com/dflemings66> http://www.facebook.com/dflemings66 " Until one has loved an animal, a part of one's soul remains unawakened. " - Anatole France ---------------------------------------------------------- -------------- From: Hugs-N-Pain [mailto:Hugs-N-Pain ] On Behalf Of *~*Jena*~* Sent: Monday, May 31, 2010 12:24 PM To: Hugs-N-Pain Subject: Re: OT- My Cat Diane, do you have your Social Security? if not I don't blame you for wanting all your diagnosis. my SIL has hers and she was telling me the other day she wanted a full body MRI. I ask did she realize what that would cost even with Ins. my 20% on my back was 1,000.00 so why would she want to spend that kind of money so she can grip about every little thing that is wrong with her. not throwing that at you Diane. but it just didn't make sense to me. she has Fibro. and the ones of us that has that knows oh gosh, the pain. we have had thunderstorms for the last 3 days and have more coming for the rest of the week. and of the pain. Jena Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 10, 2010 Report Share Posted June 10, 2010 I have a lawyer cats. I hired him this summer 3 years ago. he screwed me at my hearing. he told me he was going one way with it and then when we got in there with the judge. he questioned me like I was on trial for murder. I knew before I left that room I had lost. I was so confused. That judge contradicted everything I said and my lawyer didn't help me out. and I let him have when we got outside. but he has been working for 3 years and he hasn't gotten a penny either. I just keep thinking how nice my back pay will be if I ever do get it. the firm that has my case has 2 federal lawyers in Atlanta that work for them when the cases turn out like this. and they turn the cases over to them. They have had mine now about 6 weeks. they said, if he was able to do what he is suppose to I will have another hearing. and you can bet your sweet bippy I will convince the judge this time. and that (^ & * lawyer and me will be working together and not against each other. I don't know about the rest of you but since I got this FM the further you push me the worse confused I get. and I am more or less like a scared puppy and I can't think. I talk in circles. and nothing I say makes any sense and it is just like I an lying but I don't mean to be it just I can't help it. This is one of the things my husband and me have had some of our worse fights over. he accuses me of being on dope. But, if he is on me hot and heavy I don't care if I just balanced the checkbook. I have to go look to see what the balance was because I can't remember. my mind just goes flying out the window. anybody know what I am talking about? Jena in GA. Re: OT- My Cat Diane, do you have your Social Security? if not I don't blame you for wanting all your diagnosis. my SIL has hers and she was telling me the other day she wanted a full body MRI. I ask did she realize what that would cost even with Ins. my 20% on my back was 1,000.00 so why would she want to spend that kind of money so she can grip about every little thing that is wrong with her. not throwing that at you Diane. but it just didn't make sense to me. she has Fibro. and the ones of us that has that knows oh gosh, the pain. we have had thunderstorms for the last 3 days and have more coming for the rest of the week. and of the pain. Jena Quote Link to comment Share on other sites More sharing options...
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