Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Hi Debbie, Welcome to the group. I hope you like it here. Margaret A. CoteTo: Group <mserslife >Sent: Fri, December 18, 2009 10:23:30 PMSubject: a NEW MEMBER -- Debbie Comment from new member:Hi, I'm Debbie, newly diagnosed with MS. I have been living with painfor many years, but the MS diagnosis is new and quite scary. Looking forsupport. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member:Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Hi Debbie, I understand the constant headaches. I have had them since childhood. I am still trying to get a dxs. Margaret A. CoteTo: MSersLife Sent: Sat, December 19, 2009 12:28:54 AMSubject: RE: a NEW MEMBER -- Debbie Hi Sharon, Thank you for the welcome. I was actually diagnosed early this month I just got out of the hospital the week before last. The doctor initially thought it possible that I might have had a stroke, but when all is said and done, the diagnosis is MS. I have had a milder form of the symptoms I am having now (eye rolling, being able to see out of only one eye, seeing double, facial numbness, severe headache that feels like my brain is actually being squeezed etc) since I was 17 and they always put it off to migraines. Through the years the symptoms have gotten progressively worse and lengthier until finally I went to bed one Friday night, and Saturday, I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a month later now and the symptoms are still there. There are other things that have occurred that I think now, well yeah that makes sense, I wish someone had investigated further, but they didn’t. I understand that. I have been living with chronic pain and problems since 2001. I fell down a flight of stairs and injured my back. Since then I have had seven back surgeries 6 of them spinal fusions and just before my diagnosis of MS my surgeon said I need another surgery. He wanted me to go to pain management for 3 months first though to see if we could get any kind of improvement because at my last surgery, when I woke up, I couldn’t feel my legs. Now the pain doctor won’t see me until the neurologist clears me and until she sees some kind of progress, she doesn’t really want me to be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of it is the constant headache. My head just pounds and pounds. Today I felt like my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m not really sure what to expect. So I found this group and thought it would be a good one to join J Debbie From: MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of Sharon Sent: Friday, December 18, 2009 10:29 PM To: MSersLife@yahoogrou ps.com Subject: Re: a NEW MEMBER -- Debbie Welcome to the group Debbie. When were you diagnosed? You said you have been living with pain for many years. What kind of pain? It wasn't too many years ago that doctors said there was no pain with MS. Can you believe that?!? lol What other symptoms do you have? I look forward to getting to know you here on the group. Please send an introduction when you feel like it. hugs Sharon join me on Facebook: Sharon Mars wobbletowalk@ yahoo.com This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. From: Sharon <wobbletowalk@ yahoo.com> To: Group <mserslife@yahoogrou ps.com> Sent: Fri, December 18, 2009 9:23:30 PM Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Hi Debbie, I understand the constant headaches. I have had them since childhood. I am still trying to get a dxs. Margaret A. CoteTo: MSersLife Sent: Sat, December 19, 2009 12:28:54 AMSubject: RE: a NEW MEMBER -- Debbie Hi Sharon, Thank you for the welcome. I was actually diagnosed early this month I just got out of the hospital the week before last. The doctor initially thought it possible that I might have had a stroke, but when all is said and done, the diagnosis is MS. I have had a milder form of the symptoms I am having now (eye rolling, being able to see out of only one eye, seeing double, facial numbness, severe headache that feels like my brain is actually being squeezed etc) since I was 17 and they always put it off to migraines. Through the years the symptoms have gotten progressively worse and lengthier until finally I went to bed one Friday night, and Saturday, I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a month later now and the symptoms are still there. There are other things that have occurred that I think now, well yeah that makes sense, I wish someone had investigated further, but they didn’t. I understand that. I have been living with chronic pain and problems since 2001. I fell down a flight of stairs and injured my back. Since then I have had seven back surgeries 6 of them spinal fusions and just before my diagnosis of MS my surgeon said I need another surgery. He wanted me to go to pain management for 3 months first though to see if we could get any kind of improvement because at my last surgery, when I woke up, I couldn’t feel my legs. Now the pain doctor won’t see me until the neurologist clears me and until she sees some kind of progress, she doesn’t really want me to be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of it is the constant headache. My head just pounds and pounds. Today I felt like my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m not really sure what to expect. So I found this group and thought it would be a good one to join J Debbie From: MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of Sharon Sent: Friday, December 18, 2009 10:29 PM To: MSersLife@yahoogrou ps.com Subject: Re: a NEW MEMBER -- Debbie Welcome to the group Debbie. When were you diagnosed? You said you have been living with pain for many years. What kind of pain? It wasn't too many years ago that doctors said there was no pain with MS. Can you believe that?!? lol What other symptoms do you have? I look forward to getting to know you here on the group. Please send an introduction when you feel like it. hugs Sharon join me on Facebook: Sharon Mars wobbletowalk@ yahoo.com This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. From: Sharon <wobbletowalk@ yahoo.com> To: Group <mserslife@yahoogrou ps.com> Sent: Fri, December 18, 2009 9:23:30 PM Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Hi Debbie, I understand the constant headaches. I have had them since childhood. I am still trying to get a dxs. Margaret A. CoteTo: MSersLife Sent: Sat, December 19, 2009 12:28:54 AMSubject: RE: a NEW MEMBER -- Debbie Hi Sharon, Thank you for the welcome. I was actually diagnosed early this month I just got out of the hospital the week before last. The doctor initially thought it possible that I might have had a stroke, but when all is said and done, the diagnosis is MS. I have had a milder form of the symptoms I am having now (eye rolling, being able to see out of only one eye, seeing double, facial numbness, severe headache that feels like my brain is actually being squeezed etc) since I was 17 and they always put it off to migraines. Through the years the symptoms have gotten progressively worse and lengthier until finally I went to bed one Friday night, and Saturday, I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a month later now and the symptoms are still there. There are other things that have occurred that I think now, well yeah that makes sense, I wish someone had investigated further, but they didn’t. I understand that. I have been living with chronic pain and problems since 2001. I fell down a flight of stairs and injured my back. Since then I have had seven back surgeries 6 of them spinal fusions and just before my diagnosis of MS my surgeon said I need another surgery. He wanted me to go to pain management for 3 months first though to see if we could get any kind of improvement because at my last surgery, when I woke up, I couldn’t feel my legs. Now the pain doctor won’t see me until the neurologist clears me and until she sees some kind of progress, she doesn’t really want me to be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of it is the constant headache. My head just pounds and pounds. Today I felt like my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m not really sure what to expect. So I found this group and thought it would be a good one to join J Debbie From: MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of Sharon Sent: Friday, December 18, 2009 10:29 PM To: MSersLife@yahoogrou ps.com Subject: Re: a NEW MEMBER -- Debbie Welcome to the group Debbie. When were you diagnosed? You said you have been living with pain for many years. What kind of pain? It wasn't too many years ago that doctors said there was no pain with MS. Can you believe that?!? lol What other symptoms do you have? I look forward to getting to know you here on the group. Please send an introduction when you feel like it. hugs Sharon join me on Facebook: Sharon Mars wobbletowalk@ yahoo.com This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. From: Sharon <wobbletowalk@ yahoo.com> To: Group <mserslife@yahoogrou ps.com> Sent: Fri, December 18, 2009 9:23:30 PM Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 DebbieI'm glad you found us but I am so sorry you have a need. That said, at least now you know what's wrong with you so hopefully soon your docs will be able to help you feel better. The migraines must be horrible for you. I wish I had a solution for you but I don't. How did they diagnosis you? Sharonjoin me on Facebook:Sharon Mars wobbletowalk@...This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. To: MSersLife Sent: Fri, December 18, 2009 11:28:54 PMSubject: RE: a NEW MEMBER -- Debbie Hi Sharon, Thank you for the welcome. I was actually diagnosed early this month I just got out of the hospital the week before last. The doctor initially thought it possible that I might have had a stroke, but when all is said and done, the diagnosis is MS. I have had a milder form of the symptoms I am having now (eye rolling, being able to see out of only one eye, seeing double, facial numbness, severe headache that feels like my brain is actually being squeezed etc) since I was 17 and they always put it off to migraines. Through the years the symptoms have gotten progressively worse and lengthier until finally I went to bed one Friday night, and Saturday, I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a month later now and the symptoms are still there. There are other things that have occurred that I think now, well yeah that makes sense, I wish someone had investigated further, but they didn’t. I understand that. I have been living with chronic pain and problems since 2001. I fell down a flight of stairs and injured my back. Since then I have had seven back surgeries 6 of them spinal fusions and just before my diagnosis of MS my surgeon said I need another surgery. He wanted me to go to pain management for 3 months first though to see if we could get any kind of improvement because at my last surgery, when I woke up, I couldn’t feel my legs. Now the pain doctor won’t see me until the neurologist clears me and until she sees some kind of progress, she doesn’t really want me to be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of it is the constant headache. My head just pounds and pounds. Today I felt like my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m not really sure what to expect. So I found this group and thought it would be a good one to join J Debbie From: MSersLife [mailto:MSersLife ] On Behalf Of Sharon Sent: Friday, December 18, 2009 10:29 PM To: MSersLife Subject: Re: a NEW MEMBER -- Debbie Welcome to the group Debbie. When were you diagnosed? You said you have been living with pain for many years. What kind of pain? It wasn't too many years ago that doctors said there was no pain with MS. Can you believe that?!? lol What other symptoms do you have? I look forward to getting to know you here on the group. Please send an introduction when you feel like it. hugs Sharon join me on Facebook: Sharon Mars wobbletowalk@... This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. To: Group <mserslife > Sent: Fri, December 18, 2009 9:23:30 PM Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 DebbieI'm glad you found us but I am so sorry you have a need. That said, at least now you know what's wrong with you so hopefully soon your docs will be able to help you feel better. The migraines must be horrible for you. I wish I had a solution for you but I don't. How did they diagnosis you? Sharonjoin me on Facebook:Sharon Mars wobbletowalk@...This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. To: MSersLife Sent: Fri, December 18, 2009 11:28:54 PMSubject: RE: a NEW MEMBER -- Debbie Hi Sharon, Thank you for the welcome. I was actually diagnosed early this month I just got out of the hospital the week before last. The doctor initially thought it possible that I might have had a stroke, but when all is said and done, the diagnosis is MS. I have had a milder form of the symptoms I am having now (eye rolling, being able to see out of only one eye, seeing double, facial numbness, severe headache that feels like my brain is actually being squeezed etc) since I was 17 and they always put it off to migraines. Through the years the symptoms have gotten progressively worse and lengthier until finally I went to bed one Friday night, and Saturday, I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a month later now and the symptoms are still there. There are other things that have occurred that I think now, well yeah that makes sense, I wish someone had investigated further, but they didn’t. I understand that. I have been living with chronic pain and problems since 2001. I fell down a flight of stairs and injured my back. Since then I have had seven back surgeries 6 of them spinal fusions and just before my diagnosis of MS my surgeon said I need another surgery. He wanted me to go to pain management for 3 months first though to see if we could get any kind of improvement because at my last surgery, when I woke up, I couldn’t feel my legs. Now the pain doctor won’t see me until the neurologist clears me and until she sees some kind of progress, she doesn’t really want me to be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of it is the constant headache. My head just pounds and pounds. Today I felt like my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m not really sure what to expect. So I found this group and thought it would be a good one to join J Debbie From: MSersLife [mailto:MSersLife ] On Behalf Of Sharon Sent: Friday, December 18, 2009 10:29 PM To: MSersLife Subject: Re: a NEW MEMBER -- Debbie Welcome to the group Debbie. When were you diagnosed? You said you have been living with pain for many years. What kind of pain? It wasn't too many years ago that doctors said there was no pain with MS. Can you believe that?!? lol What other symptoms do you have? I look forward to getting to know you here on the group. Please send an introduction when you feel like it. hugs Sharon join me on Facebook: Sharon Mars wobbletowalk@... This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. To: Group <mserslife > Sent: Fri, December 18, 2009 9:23:30 PM Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Hi Sharon, It’s good to know the dx and yes, hopefully soon I will get to feeling better. The initial test used was the brain scan and they followed up with the spinal tap to confirm the diagnosis. Another brain scan will be done in 3 months and again in 6 months. The brain scan was compared to one I had a year ago when they claim I had Meningitis but then turned around and said I didn’t….and also a five year medical history with my neurologist was used to make the final dx. The migraines are horrible. They never go away. I’ve been on every medicine she can think of and still, every day my head just kills me. I see the neuro Monday, so hopefully she will have some more answers or something new for me. *HUGS* Deb From: MSersLife [mailto:MSersLife ] On Behalf Of Sharon Sent: Saturday, December 19, 2009 11:52 AM To: MSersLife Subject: Re: a NEW MEMBER -- Debbie Debbie I'm glad you found us but I am so sorry you have a need. That said, at least now you know what's wrong with you so hopefully soon your docs will be able to help you feel better. The migraines must be horrible for you. I wish I had a solution for you but I don't. How did they diagnosis you? Sharon join me on Facebook: Sharon Mars wobbletowalk@... This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. To: MSersLife Sent: Fri, December 18, 2009 11:28:54 PM Subject: RE: a NEW MEMBER -- Debbie Hi Sharon, Thank you for the welcome. I was actually diagnosed early this month I just got out of the hospital the week before last. The doctor initially thought it possible that I might have had a stroke, but when all is said and done, the diagnosis is MS. I have had a milder form of the symptoms I am having now (eye rolling, being able to see out of only one eye, seeing double, facial numbness, severe headache that feels like my brain is actually being squeezed etc) since I was 17 and they always put it off to migraines. Through the years the symptoms have gotten progressively worse and lengthier until finally I went to bed one Friday night, and Saturday, I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a month later now and the symptoms are still there. There are other things that have occurred that I think now, well yeah that makes sense, I wish someone had investigated further, but they didn’t. I understand that. I have been living with chronic pain and problems since 2001. I fell down a flight of stairs and injured my back. Since then I have had seven back surgeries 6 of them spinal fusions and just before my diagnosis of MS my surgeon said I need another surgery. He wanted me to go to pain management for 3 months first though to see if we could get any kind of improvement because at my last surgery, when I woke up, I couldn’t feel my legs. Now the pain doctor won’t see me until the neurologist clears me and until she sees some kind of progress, she doesn’t really want me to be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of it is the constant headache. My head just pounds and pounds. Today I felt like my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m not really sure what to expect. So I found this group and thought it would be a good one to join J Debbie From: MSersLife [mailto:MSersLife ] On Behalf Of Sharon Sent: Friday, December 18, 2009 10:29 PM To: MSersLife Subject: Re: a NEW MEMBER -- Debbie Welcome to the group Debbie. When were you diagnosed? You said you have been living with pain for many years. What kind of pain? It wasn't too many years ago that doctors said there was no pain with MS. Can you believe that?!? lol What other symptoms do you have? I look forward to getting to know you here on the group. Please send an introduction when you feel like it. hugs Sharon join me on Facebook: Sharon Mars wobbletowalk@... This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. From: Sharon To: Group <mserslife > Sent: Fri, December 18, 2009 9:23:30 PM Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Hi Sharon, It’s good to know the dx and yes, hopefully soon I will get to feeling better. The initial test used was the brain scan and they followed up with the spinal tap to confirm the diagnosis. Another brain scan will be done in 3 months and again in 6 months. The brain scan was compared to one I had a year ago when they claim I had Meningitis but then turned around and said I didn’t….and also a five year medical history with my neurologist was used to make the final dx. The migraines are horrible. They never go away. I’ve been on every medicine she can think of and still, every day my head just kills me. I see the neuro Monday, so hopefully she will have some more answers or something new for me. *HUGS* Deb From: MSersLife [mailto:MSersLife ] On Behalf Of Sharon Sent: Saturday, December 19, 2009 11:52 AM To: MSersLife Subject: Re: a NEW MEMBER -- Debbie Debbie I'm glad you found us but I am so sorry you have a need. That said, at least now you know what's wrong with you so hopefully soon your docs will be able to help you feel better. The migraines must be horrible for you. I wish I had a solution for you but I don't. How did they diagnosis you? Sharon join me on Facebook: Sharon Mars wobbletowalk@... This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. To: MSersLife Sent: Fri, December 18, 2009 11:28:54 PM Subject: RE: a NEW MEMBER -- Debbie Hi Sharon, Thank you for the welcome. I was actually diagnosed early this month I just got out of the hospital the week before last. The doctor initially thought it possible that I might have had a stroke, but when all is said and done, the diagnosis is MS. I have had a milder form of the symptoms I am having now (eye rolling, being able to see out of only one eye, seeing double, facial numbness, severe headache that feels like my brain is actually being squeezed etc) since I was 17 and they always put it off to migraines. Through the years the symptoms have gotten progressively worse and lengthier until finally I went to bed one Friday night, and Saturday, I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a month later now and the symptoms are still there. There are other things that have occurred that I think now, well yeah that makes sense, I wish someone had investigated further, but they didn’t. I understand that. I have been living with chronic pain and problems since 2001. I fell down a flight of stairs and injured my back. Since then I have had seven back surgeries 6 of them spinal fusions and just before my diagnosis of MS my surgeon said I need another surgery. He wanted me to go to pain management for 3 months first though to see if we could get any kind of improvement because at my last surgery, when I woke up, I couldn’t feel my legs. Now the pain doctor won’t see me until the neurologist clears me and until she sees some kind of progress, she doesn’t really want me to be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of it is the constant headache. My head just pounds and pounds. Today I felt like my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m not really sure what to expect. So I found this group and thought it would be a good one to join J Debbie From: MSersLife [mailto:MSersLife ] On Behalf Of Sharon Sent: Friday, December 18, 2009 10:29 PM To: MSersLife Subject: Re: a NEW MEMBER -- Debbie Welcome to the group Debbie. When were you diagnosed? You said you have been living with pain for many years. What kind of pain? It wasn't too many years ago that doctors said there was no pain with MS. Can you believe that?!? lol What other symptoms do you have? I look forward to getting to know you here on the group. Please send an introduction when you feel like it. hugs Sharon join me on Facebook: Sharon Mars wobbletowalk@... This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. From: Sharon To: Group <mserslife > Sent: Fri, December 18, 2009 9:23:30 PM Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Hi Sharon, It’s good to know the dx and yes, hopefully soon I will get to feeling better. The initial test used was the brain scan and they followed up with the spinal tap to confirm the diagnosis. Another brain scan will be done in 3 months and again in 6 months. The brain scan was compared to one I had a year ago when they claim I had Meningitis but then turned around and said I didn’t….and also a five year medical history with my neurologist was used to make the final dx. The migraines are horrible. They never go away. I’ve been on every medicine she can think of and still, every day my head just kills me. I see the neuro Monday, so hopefully she will have some more answers or something new for me. *HUGS* Deb From: MSersLife [mailto:MSersLife ] On Behalf Of Sharon Sent: Saturday, December 19, 2009 11:52 AM To: MSersLife Subject: Re: a NEW MEMBER -- Debbie Debbie I'm glad you found us but I am so sorry you have a need. That said, at least now you know what's wrong with you so hopefully soon your docs will be able to help you feel better. The migraines must be horrible for you. I wish I had a solution for you but I don't. How did they diagnosis you? Sharon join me on Facebook: Sharon Mars wobbletowalk@... This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. To: MSersLife Sent: Fri, December 18, 2009 11:28:54 PM Subject: RE: a NEW MEMBER -- Debbie Hi Sharon, Thank you for the welcome. I was actually diagnosed early this month I just got out of the hospital the week before last. The doctor initially thought it possible that I might have had a stroke, but when all is said and done, the diagnosis is MS. I have had a milder form of the symptoms I am having now (eye rolling, being able to see out of only one eye, seeing double, facial numbness, severe headache that feels like my brain is actually being squeezed etc) since I was 17 and they always put it off to migraines. Through the years the symptoms have gotten progressively worse and lengthier until finally I went to bed one Friday night, and Saturday, I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a month later now and the symptoms are still there. There are other things that have occurred that I think now, well yeah that makes sense, I wish someone had investigated further, but they didn’t. I understand that. I have been living with chronic pain and problems since 2001. I fell down a flight of stairs and injured my back. Since then I have had seven back surgeries 6 of them spinal fusions and just before my diagnosis of MS my surgeon said I need another surgery. He wanted me to go to pain management for 3 months first though to see if we could get any kind of improvement because at my last surgery, when I woke up, I couldn’t feel my legs. Now the pain doctor won’t see me until the neurologist clears me and until she sees some kind of progress, she doesn’t really want me to be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of it is the constant headache. My head just pounds and pounds. Today I felt like my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m not really sure what to expect. So I found this group and thought it would be a good one to join J Debbie From: MSersLife [mailto:MSersLife ] On Behalf Of Sharon Sent: Friday, December 18, 2009 10:29 PM To: MSersLife Subject: Re: a NEW MEMBER -- Debbie Welcome to the group Debbie. When were you diagnosed? You said you have been living with pain for many years. What kind of pain? It wasn't too many years ago that doctors said there was no pain with MS. Can you believe that?!? lol What other symptoms do you have? I look forward to getting to know you here on the group. Please send an introduction when you feel like it. hugs Sharon join me on Facebook: Sharon Mars wobbletowalk@... This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. From: Sharon To: Group <mserslife > Sent: Fri, December 18, 2009 9:23:30 PM Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Hi Margaret, I’m sorry you also suffer from constant headaches. They are so terrible Believe me Believe me you ever want to vent to someone who understands, drop me a line…I’ve been living with these since I was seventeen and it’s not easy and I am always here J *HUGS* Deb From: MSersLife [mailto:MSersLife ] On Behalf Of Argaret Cote Sent: Saturday, December 19, 2009 10:24 AM To: MSersLife Subject: Re: a NEW MEMBER -- Debbie Hi Debbie, I understand the constant headaches. I have had them since childhood. I am still trying to get a dxs. Margaret A. Cote From: Cryselle To: MSersLife Sent: Sat, December 19, 2009 12:28:54 AM Subject: RE: a NEW MEMBER -- Debbie Hi Sharon, Thank you for the welcome. I was actually diagnosed early this month I just got out of the hospital the week before last. The doctor initially thought it possible that I might have had a stroke, but when all is said and done, the diagnosis is MS. I have had a milder form of the symptoms I am having now (eye rolling, being able to see out of only one eye, seeing double, facial numbness, severe headache that feels like my brain is actually being squeezed etc) since I was 17 and they always put it off to migraines. Through the years the symptoms have gotten progressively worse and lengthier until finally I went to bed one Friday night, and Saturday, I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a month later now and the symptoms are still there. There are other things that have occurred that I think now, well yeah that makes sense, I wish someone had investigated further, but they didn’t. I understand that. I have been living with chronic pain and problems since 2001. I fell down a flight of stairs and injured my back. Since then I have had seven back surgeries 6 of them spinal fusions and just before my diagnosis of MS my surgeon said I need another surgery. He wanted me to go to pain management for 3 months first though to see if we could get any kind of improvement because at my last surgery, when I woke up, I couldn’t feel my legs. Now the pain doctor won’t see me until the neurologist clears me and until she sees some kind of progress, she doesn’t really want me to be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of it is the constant headache. My head just pounds and pounds. Today I felt like my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m not really sure what to expect. So I found this group and thought it would be a good one to join J Debbie From: MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of Sharon Sent: Friday, December 18, 2009 10:29 PM To: MSersLife@yahoogrou ps.com Subject: Re: a NEW MEMBER -- Debbie Welcome to the group Debbie. When were you diagnosed? You said you have been living with pain for many years. What kind of pain? It wasn't too many years ago that doctors said there was no pain with MS. Can you believe that?!? lol What other symptoms do you have? I look forward to getting to know you here on the group. Please send an introduction when you feel like it. hugs Sharon join me on Facebook: Sharon Mars wobbletowalk@ yahoo.com This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. From: Sharon <wobbletowalk@ yahoo.com> To: Group <mserslife@yahoogrou ps.com> Sent: Fri, December 18, 2009 9:23:30 PM Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Hi Margaret, I’m sorry you also suffer from constant headaches. They are so terrible Believe me Believe me you ever want to vent to someone who understands, drop me a line…I’ve been living with these since I was seventeen and it’s not easy and I am always here J *HUGS* Deb From: MSersLife [mailto:MSersLife ] On Behalf Of Argaret Cote Sent: Saturday, December 19, 2009 10:24 AM To: MSersLife Subject: Re: a NEW MEMBER -- Debbie Hi Debbie, I understand the constant headaches. I have had them since childhood. I am still trying to get a dxs. Margaret A. Cote From: Cryselle To: MSersLife Sent: Sat, December 19, 2009 12:28:54 AM Subject: RE: a NEW MEMBER -- Debbie Hi Sharon, Thank you for the welcome. I was actually diagnosed early this month I just got out of the hospital the week before last. The doctor initially thought it possible that I might have had a stroke, but when all is said and done, the diagnosis is MS. I have had a milder form of the symptoms I am having now (eye rolling, being able to see out of only one eye, seeing double, facial numbness, severe headache that feels like my brain is actually being squeezed etc) since I was 17 and they always put it off to migraines. Through the years the symptoms have gotten progressively worse and lengthier until finally I went to bed one Friday night, and Saturday, I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a month later now and the symptoms are still there. There are other things that have occurred that I think now, well yeah that makes sense, I wish someone had investigated further, but they didn’t. I understand that. I have been living with chronic pain and problems since 2001. I fell down a flight of stairs and injured my back. Since then I have had seven back surgeries 6 of them spinal fusions and just before my diagnosis of MS my surgeon said I need another surgery. He wanted me to go to pain management for 3 months first though to see if we could get any kind of improvement because at my last surgery, when I woke up, I couldn’t feel my legs. Now the pain doctor won’t see me until the neurologist clears me and until she sees some kind of progress, she doesn’t really want me to be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of it is the constant headache. My head just pounds and pounds. Today I felt like my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m not really sure what to expect. So I found this group and thought it would be a good one to join J Debbie From: MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of Sharon Sent: Friday, December 18, 2009 10:29 PM To: MSersLife@yahoogrou ps.com Subject: Re: a NEW MEMBER -- Debbie Welcome to the group Debbie. When were you diagnosed? You said you have been living with pain for many years. What kind of pain? It wasn't too many years ago that doctors said there was no pain with MS. Can you believe that?!? lol What other symptoms do you have? I look forward to getting to know you here on the group. Please send an introduction when you feel like it. hugs Sharon join me on Facebook: Sharon Mars wobbletowalk@ yahoo.com This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. From: Sharon <wobbletowalk@ yahoo.com> To: Group <mserslife@yahoogrou ps.com> Sent: Fri, December 18, 2009 9:23:30 PM Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Hi Margaret, I’m sorry you also suffer from constant headaches. They are so terrible Believe me Believe me you ever want to vent to someone who understands, drop me a line…I’ve been living with these since I was seventeen and it’s not easy and I am always here J *HUGS* Deb From: MSersLife [mailto:MSersLife ] On Behalf Of Argaret Cote Sent: Saturday, December 19, 2009 10:24 AM To: MSersLife Subject: Re: a NEW MEMBER -- Debbie Hi Debbie, I understand the constant headaches. I have had them since childhood. I am still trying to get a dxs. Margaret A. Cote From: Cryselle To: MSersLife Sent: Sat, December 19, 2009 12:28:54 AM Subject: RE: a NEW MEMBER -- Debbie Hi Sharon, Thank you for the welcome. I was actually diagnosed early this month I just got out of the hospital the week before last. The doctor initially thought it possible that I might have had a stroke, but when all is said and done, the diagnosis is MS. I have had a milder form of the symptoms I am having now (eye rolling, being able to see out of only one eye, seeing double, facial numbness, severe headache that feels like my brain is actually being squeezed etc) since I was 17 and they always put it off to migraines. Through the years the symptoms have gotten progressively worse and lengthier until finally I went to bed one Friday night, and Saturday, I woke up and thought oh darn it’s Migraine day. But it never went away. It’s a month later now and the symptoms are still there. There are other things that have occurred that I think now, well yeah that makes sense, I wish someone had investigated further, but they didn’t. I understand that. I have been living with chronic pain and problems since 2001. I fell down a flight of stairs and injured my back. Since then I have had seven back surgeries 6 of them spinal fusions and just before my diagnosis of MS my surgeon said I need another surgery. He wanted me to go to pain management for 3 months first though to see if we could get any kind of improvement because at my last surgery, when I woke up, I couldn’t feel my legs. Now the pain doctor won’t see me until the neurologist clears me and until she sees some kind of progress, she doesn’t really want me to be doing any new or innovative treatments for the back. I am in a lot of pain and exhausted all the time. The worst of it is the constant headache. My head just pounds and pounds. Today I felt like my eye was shaking, and it was going to shake right out of my head I thought. This has all hit me really hard and really fast, and I’m not really sure what to expect. So I found this group and thought it would be a good one to join J Debbie From: MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of Sharon Sent: Friday, December 18, 2009 10:29 PM To: MSersLife@yahoogrou ps.com Subject: Re: a NEW MEMBER -- Debbie Welcome to the group Debbie. When were you diagnosed? You said you have been living with pain for many years. What kind of pain? It wasn't too many years ago that doctors said there was no pain with MS. Can you believe that?!? lol What other symptoms do you have? I look forward to getting to know you here on the group. Please send an introduction when you feel like it. hugs Sharon join me on Facebook: Sharon Mars wobbletowalk@ yahoo.com This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. From: Sharon <wobbletowalk@ yahoo.com> To: Group <mserslife@yahoogrou ps.com> Sent: Fri, December 18, 2009 9:23:30 PM Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Greetings and Welcome, Debbie! in WY " You get a wonderful view from the point of no return... " http://www.flickr.com/photos/liadains_fancies http://practical-blackwork.blogspot.com http://practicalblackwork.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Greetings and Welcome, Debbie! in WY " You get a wonderful view from the point of no return... " http://www.flickr.com/photos/liadains_fancies http://practical-blackwork.blogspot.com http://practicalblackwork.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Thank you , so nice to meet you J Deb From: MSersLife [mailto:MSersLife ] On Behalf Of Thallas Sent: Saturday, December 19, 2009 2:40 PM To: MSersLife Subject: RE: a NEW MEMBER -- Debbie Greetings and Welcome, Debbie! in WY " You get a wonderful view from the point of no return... " http://www.flickr.com/photos/liadains_fancies http://practical-blackwork.blogspot.com http://practicalblackwork.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Thank you , so nice to meet you J Deb From: MSersLife [mailto:MSersLife ] On Behalf Of Thallas Sent: Saturday, December 19, 2009 2:40 PM To: MSersLife Subject: RE: a NEW MEMBER -- Debbie Greetings and Welcome, Debbie! in WY " You get a wonderful view from the point of no return... " http://www.flickr.com/photos/liadains_fancies http://practical-blackwork.blogspot.com http://practicalblackwork.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Cryselle, welcome to life with Multiple Sclerosis!Perhaps, if we all put our MS brains together,plaques notwithstanding, we can be of some helpto you in this long hard battle.Love to you,n Rojas, wMS and a host of other things,including disc disease (no surgeries yet), diagnosedwMS at age 19; I am now 72.5--and life looks good. . .To: MSersLife Sent: Fri, December 18, 2009 10:29:27 PMSubject: RE: a NEW MEMBER -- Debbie Hi , Thanks for the welcome, it’s so nice to meet you J Debbie From: MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of lastinline10@ yahoo.com Sent: Friday, December 18, 2009 10:28 PM To: MSersLife@yahoogrou ps.com Subject: Re: a NEW MEMBER -- Debbie Welcome to the. group. From NE Oklahoma. (with an ie) Sent from my U.S. Cellular BlackBerry® smartphone From: Sharon <wobbletowalk@ yahoo.com> Date: Fri, 18 Dec 2009 20:23:30 -0800 (PST) To: Group<mserslife@yahoogrou ps.com> Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Cryselle, welcome to life with Multiple Sclerosis!Perhaps, if we all put our MS brains together,plaques notwithstanding, we can be of some helpto you in this long hard battle.Love to you,n Rojas, wMS and a host of other things,including disc disease (no surgeries yet), diagnosedwMS at age 19; I am now 72.5--and life looks good. . .To: MSersLife Sent: Fri, December 18, 2009 10:29:27 PMSubject: RE: a NEW MEMBER -- Debbie Hi , Thanks for the welcome, it’s so nice to meet you J Debbie From: MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of lastinline10@ yahoo.com Sent: Friday, December 18, 2009 10:28 PM To: MSersLife@yahoogrou ps.com Subject: Re: a NEW MEMBER -- Debbie Welcome to the. group. From NE Oklahoma. (with an ie) Sent from my U.S. Cellular BlackBerry® smartphone From: Sharon <wobbletowalk@ yahoo.com> Date: Fri, 18 Dec 2009 20:23:30 -0800 (PST) To: Group<mserslife@yahoogrou ps.com> Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 Cryselle, welcome to life with Multiple Sclerosis!Perhaps, if we all put our MS brains together,plaques notwithstanding, we can be of some helpto you in this long hard battle.Love to you,n Rojas, wMS and a host of other things,including disc disease (no surgeries yet), diagnosedwMS at age 19; I am now 72.5--and life looks good. . .To: MSersLife Sent: Fri, December 18, 2009 10:29:27 PMSubject: RE: a NEW MEMBER -- Debbie Hi , Thanks for the welcome, it’s so nice to meet you J Debbie From: MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of lastinline10@ yahoo.com Sent: Friday, December 18, 2009 10:28 PM To: MSersLife@yahoogrou ps.com Subject: Re: a NEW MEMBER -- Debbie Welcome to the. group. From NE Oklahoma. (with an ie) Sent from my U.S. Cellular BlackBerry® smartphone From: Sharon <wobbletowalk@ yahoo.com> Date: Fri, 18 Dec 2009 20:23:30 -0800 (PST) To: Group<mserslife@yahoogrou ps.com> Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 J n, thank you for the welcome, and you all have already been help to me just by letting me know I’m not alone, and that there are resources and friends out there! *HUGS* Deb From: MSersLife [mailto:MSersLife ] On Behalf Of marion j rojas Sent: Saturday, December 19, 2009 5:27 PM To: MSersLife Subject: Re: a NEW MEMBER -- Debbie Cryselle, welcome to life with Multiple Sclerosis! Perhaps, if we all put our MS brains together, plaques notwithstanding, we can be of some help to you in this long hard battle. Love to you, n Rojas, wMS and a host of other things, including disc disease (no surgeries yet), diagnosed wMS at age 19; I am now 72.5--and life looks good. . . From: Cryselle To: MSersLife Sent: Fri, December 18, 2009 10:29:27 PM Subject: RE: a NEW MEMBER -- Debbie Hi , Thanks for the welcome, it’s so nice to meet you J Debbie From: MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of lastinline10@ yahoo.com Sent: Friday, December 18, 2009 10:28 PM To: MSersLife@yahoogrou ps.com Subject: Re: a NEW MEMBER -- Debbie Welcome to the. group. From NE Oklahoma. (with an ie) Sent from my U.S. Cellular BlackBerry® smartphone From: Sharon <wobbletowalk@ yahoo.com> Date: Fri, 18 Dec 2009 20:23:30 -0800 (PST) To: Group<mserslife@yahoogrou ps.com> Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2009 Report Share Posted December 19, 2009 J n, thank you for the welcome, and you all have already been help to me just by letting me know I’m not alone, and that there are resources and friends out there! *HUGS* Deb From: MSersLife [mailto:MSersLife ] On Behalf Of marion j rojas Sent: Saturday, December 19, 2009 5:27 PM To: MSersLife Subject: Re: a NEW MEMBER -- Debbie Cryselle, welcome to life with Multiple Sclerosis! Perhaps, if we all put our MS brains together, plaques notwithstanding, we can be of some help to you in this long hard battle. Love to you, n Rojas, wMS and a host of other things, including disc disease (no surgeries yet), diagnosed wMS at age 19; I am now 72.5--and life looks good. . . From: Cryselle To: MSersLife Sent: Fri, December 18, 2009 10:29:27 PM Subject: RE: a NEW MEMBER -- Debbie Hi , Thanks for the welcome, it’s so nice to meet you J Debbie From: MSersLife@yahoogrou ps.com [mailto:MSersLife@ yahoogroups. com] On Behalf Of lastinline10@ yahoo.com Sent: Friday, December 18, 2009 10:28 PM To: MSersLife@yahoogrou ps.com Subject: Re: a NEW MEMBER -- Debbie Welcome to the. group. From NE Oklahoma. (with an ie) Sent from my U.S. Cellular BlackBerry® smartphone From: Sharon <wobbletowalk@ yahoo.com> Date: Fri, 18 Dec 2009 20:23:30 -0800 (PST) To: Group<mserslife@yahoogrou ps.com> Subject: a NEW MEMBER -- Debbie Comment from new member: Hi, I'm Debbie, newly diagnosed with MS. I have been living with pain for many years, but the MS diagnosis is new and quite scary. Looking for support. Group: please join me in extending a warm welcome to our newest member here at MSersLife! I know we all look forward to getting to know our new member here on the group! New Member: Please feel free to send an introduction as soon as you wish, ask any questions you want, share your experiences with all of us and just jump into the conversations! Sharon (group creator/owner) This email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. Quote Link to comment Share on other sites More sharing options...
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