Re: RE: [TMIC]
Hello all! 1. I seem to always "overheat". My first thought was menopause was hitting. I never even thought it might be TM related! I call them solar flares. I have also found that I don't tolerate the heat as well as I used to. Sitting in the hot sun used to be enjoyable, but now I find it hard to tolerate and that type of heat makes me feel weak. Even a hot shower or a hot tub that is extremely warm will drain any energy I had. The cold does not seem to affect me. 2. My banding is when I run (or attempt to run). Like when I need to catch the bus or something. To me it feels like someone has wrapped a large and thick elastic band around my torso and is pulling both ends tight. I am guessing that everyone may feel it differently. For me the banding has decreased quite a bit. It does seem that someone who has TM has varying degrees of these symptoms for the most part. Everyone is different though. Have a great day! MargaretFrom: Janice [mailto:jan...@centurytel.net] Sent: Thursday, June 11, 2009 8:41 PMTo: transverse myelitisSubject: [TMIC] This is Janice,I have 2 questions:1. With hot weather coming, do any of you have a problem with all of a sudden being really hot? I know someof you had a problem with the cold last winter, but does your body change in summer and you get hit with being hot insteadof cold? I really have a problem with heat - especially with humidity. I get hot, then weak. Not good.2. Several of you have mentioned the tight "band" around your body. I am not sure this band is in the same place foreveryone. Also, has there been any change in the band with those of you who have had TM for a long time?
RE: [TMIC] misc
Thank you for sharing. And well said. From: Robert Pall [mailto:rp...@neillsupply.com] Sent: April-24-09 12:24 PM To: tmic Subject: [TMIC] misc I tried sending this with an attachment and it did not go thru.I am trying it again with a cut and paste and hopefully the group will receive it! I have been reading all of the many posts many of which are heartbreaking. I can only relate to my own personal experiences. First of all living in a large urban area where access to excellent medical facilities are in abunbdance helped me. Within 24 hours I was taking 1000 mg per day of prednisone (steroids) which I believe limited the damage to my spine. After going to numerous Drs, physical therapists and even chiropractors I came to realize that after passing the one year mark I would not get much better. Ten years ago I started seeing Dr. Kerr and have done so once annually since then. He gives me very little hope of a cure in the near future but he does treat my symptoms (banding,hot/cold,numbness etc,)I therefore view my condition as one requiring pain managemnt vs a cure. I think acceptance of our condition is imperative...I try every day to not let TM dictate my life. TM has not reduced my bucket list it has simply made me make some adjustments due to what I am capable of doing physically. What make this group (as well as my New Jersey support group) so special is that we are discussing our problems and limitations with people who understand and are eager to pass on their own sucesses in order to help all of us. It appears that recently this site is doing exactly what it is meant to do...post questions,get answers and help us to all remember we are not alone. I recently posted an essay I wrote (for no reason except I wanted to put down on paper what I could not or would not speak aloud). The title of the essay is normal. I am attaching it to this email for the new members and the ones who have not previously read it. I encourage all of you to put down on paper your feelings regarding TM...and hopefully by doing that it helps put our head in the right direction. Life is short...do everything you can to live it to its fullest...TM is a challenge and the ones that handle it best I believe have acquired some acceptance. OK that is more than enough for one writing! All the best! Rob in New Jersey NORMAL Normal..what a simple word! This is a word I took for granted until one week past my 50th birthday. What did normal mean to me? Normal meant being like everyone else..it was being able to run, walk, exercise, climb up stairs, play sports.basically being able to do everything that normal people do without giving it a thought. I guess I figured as I got older I would slow down a little.maybe replace basketball with golf. Perhaps I would have to exercise a little longer to stay in shape.no big deal.this was normal. Sure like all normal people I would get sick from time to time and maybe break a bone or two..but I always knew that I would get better.and until one week after my 50th birthday that was just how life was.normal. Now let us go back 11 or so years where in a period of several hours I went from normal to cripple. In a few hours I had zero feeling from my waist down..that can't be possible.I had played ball all weekend.there had to be a simple answer. Maybe a pinched nerve or something like that...the idea that I would never be normal again never crossed my mind.I was sure it would be just a matter of time until I was all better.and normal again . Even after 3 MRI's and 2 Lumbar Punctures I was certain that Dr. House would figure out the problem, give me some medicine and I would be all better.I would be normal again.just like everybody else I knew. Three weeks after being crippled from the waist down I was told what I have...Transverse Myelitis..what the heck is that.I never heard the words before and had no idea of their meaning. The Neurologist at the top New York City hospital explained it to me.he said he was sure I would eventually walk again.but he could not say for sure what assistance I would need. Perhaps a walker (how embarrassing), maybe a quad cane (better but not great) and if I was lucky perhaps I could graduate to a straight cane (better but not normal) After spending 3 weeks in the hospital I was transferred to the Kessler Rehabilitation facility in West Orange, New Jersey (same place Christopher Reeves rehabbed in). Slowly over a period of 3 months I started getting a little better.I went from a walker to a quad cane to upon leaving the rehab center a straight cane..I was surely getting better. I would prove all of the doctors wrong...oh just one little side note.while it was true that I was learning to walk better there also came some small side effects. When I first came down with TM I had no feeling and therefore I had no pain or discomfort..but.as some feeling came back these feelings were so so bad. Where previously I
RE: [TMIC] testing
Yes you are! From: jrushton [mailto:jrush...@columbiaenergyllc.com] Sent: April-21-09 11:56 AM To: tmic Subject: [TMIC] testing Just checking to see if I'm still 'alive' on tmic???
RE: [TMIC] transverse myelitis
I don't have the banding. I did at the onset of TM but not any longer. From: alle...@aol.com [mailto:alle...@aol.com] Sent: April-19-09 1:58 PM To: tmic-list@eskimo.com Subject: Re: [TMIC] transverse myelitis Welcome Betty, One symptom I'd say we all have is definitely the banding yet other symptoms do vary. I'm a paraplegic since 9/2000, lesion T6-10. I don't have the numbness but a buzzing feeling that is uncomfortable without meds. Ask us anything you wish and you will get an answer. Have you talked with anyone since 2004 with TM? You have a group of friends here. Ella in Ohio _ A Good Credit Score is 700 or Above. See http://pr.atwola.com/promoclk/100126575x1220814852x1201410738/aol?redir=htt p:%2F%2Fwww.freecreditreport.com%2Fpm%2Fdefault.aspx%3Fsc%3D668072%26hmpgID% 3D62%26bcd%3DAprilfooter419NO62 yours in just 2 easy steps!
RE: [TMIC] Hello Jude!
Thank you for your note, Patti. The recover is moving along slowly. Part of my problem is that I have so much scar tissue from 14 previous surgeries that it is limiting my movement quite a bit. I am working hard on it every day and I am sure that once the zipper (staples) are removed, it will be much easier. Margaret From: Patricia Cooley [mailto:patticoo...@wi.rr.com] Sent: April-03-09 8:39 AM To: 'Margaret Monson'; tmic-list@eskimo.com Subject: RE: [TMIC] Hello Jude! MARGARET: I WISH YOU A SPEEDY RECOVERY FROM YOUR KNEE REPLACEMENT. MY HUSBAND HAD BOTH KNEES REPLACED ABOUT 3 YEARS AGO. HIS RECOVERY WAS TERRIFIC. OF COURSE, THERE IS A LOT OF PAIN WITH P.T., BUT IT IS TO YOUR BEST INTEREST TO TRY AS HARD AS YOU CAN. HE WAS VERY FAITHFULL DOING HIS PRE-SURGERY EXERCISES WHICH I THINK HELPED HIM RECOVER SO FAST. YOU WOULD NEVER KNOW THAT HE HAS NEW KNEEWS. HE CAN DO EVERYTHING, EVEN KNEEL IN HIS GARDEN. THE ONE PLUS SIDE IS HE IS NO LONGER BOWLEGGED. WE USE TO TEASE HIM THAT A CAR COULD DRIVE THROUGH AND HE WOULDN'T KNOW IT. NOW HE WISHES HE HAD DONE IT YEARS AGO. GOOD LUCK IN YOUR RECOVERY. PATTI - WISCONSIN From: Margaret Monson [mailto:mag...@telus.net] Sent: Thursday, April 02, 2009 1:31 PM To: heyjude48...@aol.com Cc: tmic-list@eskimo.com; tmic-digest-requ...@eskimo.com Subject: [TMIC] Hello Jude! I am glad to hear that you are home and healing. I hope that all is going well. You were and are in my thoughts. Although we have never personally met or talked with each other, I welcome your emails to the list. You always seem to have such a positive outlook on things no matter what is thrown at you. You always have a kind word and offer advice based on your experience. Jude, you are a gem. I am at home recuperating from a partial knee replacement done on March 26. I am healing well but know this will be a slow recovery. I was amazed at the number of doctors and people who actually think you can fully recover from TM. One doctor was surprised when I told him that you never fully recover and will always have TM. You only recover to the best that your body can. Do take care Jude and I hope you are able to post soon! I miss your emails! Margaret Edmonton AB Canada
RE: [TMIC] FROM JUDE
Thank you for posting for Jude. She can't post but is she receiving our emails to the site? Margaret From: alle...@aol.com [mailto:alle...@aol.com] Sent: April-02-09 11:35 AM To: tmic-list@eskimo.com Subject: [TMIC] FROM JUDE She can't post for some reason and asked that I send this for her: Hello there...anybody out there? Boy, I go into the hospital for a couple of weeks and this is what I come home to. I've heard about two sites where y'all might be hanging out, One is Yahoo and the other is a different type of site that I know nothing about, not even the name. Are there any new people with TM waiting around for some activity? My name is Jude; I am a T3 paraplegic, totally paralyzed from the nipple-line on down to my toes. I don't begin to say that I know everything, in fact, I know next to nothing...just like the doctors. If you have any questions or simply need someone to talk to send me an email and we will work it out. Try to keep it Positive! Jude _ Worried about job security? Check http://jobs.aol.com/gallery/growing-job-industries?ncid=emlcntuscare000 3 out the 5 safest jobs in a recession.
[TMIC] Hello Jude!
I am glad to hear that you are home and healing. I hope that all is going well. You were and are in my thoughts. Although we have never personally met or talked with each other, I welcome your emails to the list. You always seem to have such a positive outlook on things no matter what is thrown at you. You always have a kind word and offer advice based on your experience. Jude, you are a gem. I am at home recuperating from a partial knee replacement done on March 26. I am healing well but know this will be a slow recovery. I was amazed at the number of doctors and people who actually think you can fully recover from TM. One doctor was surprised when I told him that you never fully recover and will always have TM. You only recover to the best that your body can. Do take care Jude and I hope you are able to post soon! I miss your emails! Margaret Edmonton AB Canada
RE: [TMIC] blood, tissue, organ donation
I, too, donate blood through the Red Cross in Canada with no problems. Margaret From: gor...@earthlink.net [mailto:gor...@earthlink.net] Sent: March-25-09 6:59 PM To: Lawrence King; tmic-list@eskimo.com Subject: Re: [TMIC] blood, tissue, organ donation Re: I donate blood (4 gallons), gave a sample to the bone marrow registry. I am interested that you give blood and bone marrow. I was told I could no longer donate because, although my TM was considered idiopathic (don't know what caused it), the possibility that it was an autoimmune factor led them to nix me as a blood donor as well as concerns about tissue and organ donation - with the exception of the corneas I believe. I haven't explored it since then and it has been ten years. Maybe things have changed. Can you enlighten me to the discussions you may have had concerning allowed donation? Thanks. - Original Message - From: Lawrence King mailto:we4king...@verizon.net To: tmic-list@eskimo.com Cc: Lawrence mailto:we4king...@verizon.net King Sent: Wednesday, March 25, 2009 8:25 PM Subject: Re: [TMIC] stem cell (OT?) Re: I donate blood (4 gallons), gave a sample to the bone marrow registry.
RE: [TMIC]
Hello Janice! I too had the hot/cold sensitivity you speak of. I actually gave myself a 2nd degree burn without realizing. The sense of hot and cold has returned for me and did so after about a year. What I find now is that I cannot handle really hot showers and sometimes have issues with hot tubs. The hot water makes my skin tingle and makes me feel nauseous. As to the buzzing, I think I also know what you mean but many may call it something else. My Neuro told me that what I was feeling was my nerves firing. It made sense. Mine diminished after a few years but my body still tingles when I push things. It's my body's way of letting me know that it has had enough. My concern is that I have lived with the symptoms of TM for coming up 8 years that I believe I have gotten used to all the things it throws at you. I do not know what normal is anymore. Maybe that is a good thing? That way I don't know what I am missing! Margaret From: Janice [mailto:jan...@centurytel.net] Sent: March-21-09 3:15 PM To: transverse myelitis Subject: [TMIC] This is Janice - yet again with another question. It has been 2 years since the onset of TM. From the top of my ribs to my toes I can not tell water temperature on my skin. I have to be very careful with taking my showers.Do any of you have that? I am wondering if it is something that will eventually go away or if it is something I will live with. Also, one improvement I have just noticed lately is the constant buzzing that I had in my legs as soon as feeling started coming back. Did you all have that and have any of you also lost it? Thanks again, Janice
RE: [TMIC] My TM experience
Hello Deb, Thank you for sharing your story. From everything I have been told and read, there is never a full recovery. I am estimating that I am at about 90% of what I was. But then my TM is not as severe as most. Over doing it is all based on each person and their own limits. Just as every healthy person has limits as to how much they can do, so do we. Our limits are now lower than they were before. When I over do it, my body tells me by giving me more tingles than normal and being exhausted which comes on quicker than it did before. That is what I have found. I am sure everyone with TM has their own things to tell you about limits and recover as we are all different. Margaret -Original Message- From: Deb Monteleone [mailto:aiki...@optonline.net] Sent: March-08-09 6:33 PM To: tmic-list@eskimo.com Subject: [TMIC] My TM experience Hi, my name is Deb. I am glad some of you are giving the history of your experience with TM. I am fairly new to it and I am still trying to deal with it and figure things out. I have been part of this group since about August 2008 but have not participated much. I am still hopeful of making a good recovery and I sensed that this group is mostly, if not all, comprised of people who have not recovered fully. When first joining I had asked the question, does anyone know what the stages of recovery are and no one answered. My episode started June 2008, five days after my 52nd birthday. I woke up one morning and noticed my feet were numb. I tried wiggling my toes but nothing happened, I jumped out of bed thinking my feet would be blue from lack of circulation. To my surprise, they looked fine. I walked around and nothing changed, so I went to work with numb feet. In the next five days, the numbness progressed up to my waist. I could still walk but I started using a cane. Within the 1st two weeks (can't remember exact times anymore) I woke up in the middle of the night with an excruciating pain on my side. I couldn't even move. My husband (my hero) called 911; I thought maybe my appendix burst. The emergency room ignored the fact that I was numb and had to walk with a cane, they were just focusing on the pain in my side. They found nothing, next day I went to my primary care doctor; they took one look at me and called a Neurologist, who saw me that day. The Neurologist took one look at me and told me I had TM and I would be having a lifestyle change (boy, I had no idea what he was really referring to). He said the pain in the side was a referred pain from the TM (it happened again the next weekend, off to the hospital for morphine). I went on IV steroids for three days, then oral ones for seven days. Three days after the end of the steroids I couldn't walk (left leg went limp), bladder shut down as did bowels. Went to hospital for 5 days of IV steroids, then off to Rehab for 2 ½ weeks. Then home to deal with my new lifestyle. It took me about a month to accept that my life was really changing and this was not something that would be better in a month or two. I had the support and help of my 75 year old mother (she moved in with us for two months) and my husband. At this time I was using a walker and trying to learn how to walk again and get balance back. I feel I am still making progress, although very slowly. I now walk with a cane, drive with hand controls and work full time which is tiring and hard to concentrate with the baclofen, neurontin, cymbalta and klonopen. I still have questions and am trying to learn how my body now reacts to things. I was always active and still do not really understand how you judge what 'overdoing' it is. One of the emails explained that paying for it means that the burning gets really bad. I do have bad days with the burning, stinging and spasticity but I didn't think I overdid anything; this is where I fall short of knowing my new limits. Also, is it possible to build up stamina or will that never happen? Any input on these questions would be appreciated. Deb Long Island, NY
RE: [TMIC]
And now my turn. . . My name is Margaret and I live in Edmonton Alberta Canada. I was 40 years old when I was diagnosed in April 2001. My TM is not nearly as severe or bad as many others. I am one of the walking wounded. I woke up on a Saturday morning and had a dull ache in my right elbow. Carried on through the day only to wake up on Sunday with tingling hands. I went to work at my part time job at a coffee shop and all through the day I kept wringing my hands to try to get the tingling to stop. I didn't think much of it until my boss asked me what was wrong and I told him about the tingling. He was concerned that I may be having a stroke. I laughed it off but it stayed in the back of my mind. So I went home and started searching for answers on the internet. I read about TM and all my symptoms seemed to point to TM with the exception that I hadn't been sick or had a virus for at least the last 4 years. My husband at the time told me that if it was still there on Monday, I needed to see my doctor. Monday morning I awoke and the tingling hands were still there and now my feet were tingling. I went to work and made an appointment to see my family doctor that afternoon. Off to the doctor I went. She was totally dumbfounded and said she would get me in to a Neurologist. She left the office and I figured Okay, I'll see the Neuro in a few months. When my GP came in she had an appointment for me the next day! Tuesday I woke up and my hands and feet were tingling and now my legs were too. I couldn't hold a pen without having a death grip on it! I could barely write my name because I couldn't feel the pen. I went to work for the morning and then went to the Neuro in the afternoon. She asked many questions, did many coordination tests and pin prick tests and decided that I had either TM or MS. She was going to book me for blood tests and a MRI. She was sure it was TM and told me all the nasty things that I had read . . . that TM is usually a precursor to MS, I would never be 100% again and it was going to get worse. WOW! Un-freaking-believable! How the heck did I get something like this??? Wednesday came and I went to work. I was trying to come to grips with what the doctor told me and I think I was trying to convince myself that she was wrong and that it was just a pinched nerve. All along, I am getting worse. The tingles are crawling their way up my body. When I had to run to catch the bus, I felt like there was this elastic band around my torso tightening itself as if to choke me. Thursday, reality hit with a vengeance and I realized the severity of what I had contracted and what it meant to me and the rest of my life. I spent the day in bed mentally and emotionally exhausted. It really struck home when my husband was standing at the side of the bed and my 90 pound dog was sitting on me and he told her to get off me. I told him she wasn't on me and when I looked I saw she was literally sitting on me and I could not feel her. It was then that I realized just how bad I was. It was also then that I realized I could do one of two things - I could lay there and feel sorry for myself and give in to this thing or I could fight it and get out of bed and try to keep going with all that I had. I got out of bed. Within six weeks it hit the worse and then slowly started to get better. At it's worse, I was numb from the armpits down. My arms were always okay but my hands always tingled. My feet were numb and I had a hard time walking because I couldn't feel what was under them. I had to watch my step so that I would catch the edge of a side walk or curb and end up twisting my ankle. One Sunday I was making a roast and was draining the dripping into a pot when the pan slipped out of my hands and hit the stove. I didn't realize it but I had splashed the hot liquid on my tummy and ended up with a second degree burn. I didn't feel a thing and didn't have a clue what I had done until a 6 inch long blister developed on my tummy the next day! Another realization! I eventually started to see my symptoms get better and over 3 years I healed the best that I could and ever would. I still don't have all the feeling in my hands. Because of that I have had to give up needlework like cross stitch. I find it difficult to fasten necklaces or buttons or deal with small things. I still get the tight elastic band feeling if I run or jog. I cannot over do it or get stressed because then I get tired and the tingles hit with a vengeance. I find it hard to walk fast or for long distances without many breaks. When I bend my head and then lift it up, I get the tingles and a wave of nausea. When I do push it and the tingles hit, I get nauseous. My life has changed and I have had to give up many things. But my attitude and my outlook has changed for the better. I don't sweat the small stuff any more. I have more patience. I
RE: [TMIC] T-2 Lesions
I have two lesions and have TM with no signs at all of MS. Margaret From: Regina Rummel [mailto:regina...@sbcglobal.net] Sent: February-11-09 3:15 PM To: tmic-list@eskimo.com Subject: [TMIC] T-2 Lesions Am going over the MRI report of the brain before seeing the neurologist. One notation in particular concerns me and I quote The FLAIR study demonstrates multiple bright T-2 lesions in the deep white tracts of both cerebral hemispheres, etc... Frank explained at one time that 1 lesion is TM, more than 1 is MS. I'm scared. What do you think? Many thanks for your comments. R
RE: [TMIC] Any news on Jude?
So happy to hear you are back home and on the mend, so to speak. My thoughts are with you, Jude! Margaret From: heyjude48...@aol.com [mailto:heyjude48...@aol.com] Sent: January-24-09 12:52 AM To: kimr1...@bellsouth.net; TMIC-LIST@eskimo.com Subject: Re: [TMIC] Any news on Jude? Yes, I have an update on myself. But first, thank you all for the love and prayers sent my way. I am sure I could feel the warmth of all of your arms around me and the prayers have worked, because I am now home. The doctors still do not know the names of the bacteria that has invaded my body. They have sent cultures out to U of M in Ann Arbor (A2), but no one can figure out what kind of bacteria they are. I now have several new ones and all the docs say is that the bacteria is colonic in nature, meaning they come from the colon, but they have not been seen before so no one knows how to treat them. There is no problem with sending me to Ann Arbor, but so far it has been sufficient to send the labs, and I agree with that. I am just a tad septic, with an attack of autonomicdysreflexia that caused my blood pressure to plummet. I was talking to Gunny at the time, so it is his fault!!! LOL... My home nurse had just arrived so when she got in the house, Gunny hung up, but he waited online for me, not wanting to leave me alone. The nurse took vitals and my blood pressure was 85/54 and she immediately called 911. I remember nothing after that, but woke up in the hospital later on. They didn't do a whole lot for me in the hospital because the drugs they were giving me were making me feel sick. Each time they tried a new med I would throw it back up at them and so they quit that after a while. The wounds, (pressure sores) are what are infected and now the bones in that vicinity are dx'd as being diseased too, so treatment it very difficult. This time, before sending me home, they took deep biopsies and lots of blood to send to the various labs in the area, including A2. Umm, I have not had much energy. All blood levels are low, except for the ones that are supposed to be low...those are high! Well, folks, I am getting tired and sleepy. So will go for now and catch you up on the rest later. I love and appreciate you all. Jude,
RE: [TMIC] Don't Worry About Me
Thanx for what you have said, Jude. I am one of the lucky TM'ers. But I know that there are many many TM'ers out there that have it much more difficult than I do. Although I will not say that I can understand or relate to what you are going through (because no one can as each person is different), I will offer any support that I possibly can. I do not read all the emails nor do I reply to many. My thoughts are that if you feel you have something to say to a fellow TM'er, than have at it with the understanding that you respect that person and everybody else. If you are concerned about getting a ton of emails, then set up a different email account strictly for TMIC. Everyone in this world need support, TM or not. If people find that support and some solace in chatting on line, then so be it. It is their way of coping and communicating. Who knows? You may even find a friend or two or three while chatting. To those who wish to email, I say please feel free to jam up my inbox! To those that do not like it . . . well you can leave the support and friendship of the group by your choice. But do not condemn anyone else! Sorry, but just had to give you my two cents worth. Margaret From: heyjude48...@aol.com [mailto:heyjude48...@aol.com] Sent: January-10-09 7:13 PM To: tmic-list@eskimo.com Subject: [TMIC] Don't Worry About Me First, let me thank those of you who have taken the time to email me and lend me your support. Those of you who have been on the List for some time know how I feel about every one of you. If you don't, you haven't been reading my email! I am a mature woman, a lover of people and yet I have the ability to take care of myself. I do not go out of my way to make strife on the List and I think that Jim knows that or he would have asked me to leave long before this. What I may be, is somewhat naive, and tend to write before I think at times. I will do my best not to email so often when the topics are not specific to TM. I think that having TM and being bedridden has made me rather jaded on the subject. I feel resigned to my fate and tend to forget that there are so many of you with TM who walk and get around quite well on your own. Why is it that there is so much diversity when it comes to managing TM by the medical field? There are all types of medications...none of us are on the same drugs, are we? There are all types of therapies available but depending upon insurance companies many Tm'ers are unable to take advantage of them. Since my time on the List I have read emails by some of the most uplifting persons I know. I have read my share of emails written by those with no hope, only to be turned around by the List group. And, I have had the sobering emails about those of us who simply can't take it any more. Those TM'ers we will never hear from again. And then there are those ungrateful people who criticize whatever is written on this List that might not exactly fit the criteria of the Rules. If we belong to this List...if we have TM...then as long as we write in a respectable manner, we ought to be able to say what we need to say as long as it will help another person with TM. HELP ANOTHER PERSON WITH TM... Those are the words that are important here. And that is what I will continue to try to do. As other's have done for me. (that sounds somewhat familiar, aye?) As a die-hard Beatle fan, I must say, ALL WE NEED IS LOVE, LOVE IS ALL WE NEED. Jude o _ A Good Credit Score is 700 or Above. See http://pr.atwola.com/promoclk/10075x1215855013x1201028747/aol?redir=htt p://www.freecreditreport.com/pm/default.aspx?sc=668072%26hmpgID=62%26bcd=Dec emailfooterNO62 yours in just 2 easy steps!
[TMIC] November Birthday Addition
Margaret Monson - November 6, 1961 I am fairly new to the group but read every posting. I seem to have one of the milder cases compared to some of the posts I have read! Thanx for all the info I have gleaned from the many posts. Margaret
