Guest guest Posted February 20, 2008 Report Share Posted February 20, 2008 I JUST WANTED TO SAY IF IT WASN'T FOR ME GOING TO THE RHUMIE DR. I DID AND DO, I DON'T KNOW WHERE I WOULD BE, SHE DOES TREAT, AND TREATS WELL, PEOPLE COME FROM 2 SURROUNDING STATES TO SEE HER, AND EVERY TIME I HAVE BEEN IN WAIT RM THERE HAVE BEEN AT LEAST 2 OTHER FIBRO SUFFERS BESIDES ME, WHO PRAISE HER FOR HER KNOWLEDGE. SO ANYONE WHO WANTS TO COME TO THE EAST COAST I WILL PASS HER ON, SHE IS VERY PASSIONATE WITH HER PT'S ALSO. WE DO ALL BRING A BOOK ON APPT DAY AS WE WAIT BUT SO WORTH IT. I ALSO HAVE BEEN LUCKY WITH MY PRIMARY THEY HAVE THE SAME COMPASSION SHE DOES AND HAVE NEVER DOUBTED MY SYMPTOMS, AND CONTINUED TO DIG FOR 2YRS BEFORE SENDING ME TO RHUMIE, BUT DID HAVE ANOTHER ONE IN MIND WHO ALSO WAS RECOMMENDED WITH DEALING AND BEING GOOD AT DIAGNOISING FIBRO, BUT MY MOM HAD BEEN SEEING THE ONE I SEE, AND HAD FOUND THE WEIRD TYPE OF AUTO IMMUNE ARTHRITIS SHE HAS THAT NO ONE ELSE WAS ABLE TO FIND AFTER BEING TAKEN BY AMBULANCE FOR SEVERE PAIN AND HOSPITALIZED 4 DAYS. SO FOR THOSE OUT THERE DON'T GIVE UP AND IT IS WHAT I HAVE BEEN TOLD THE RHUMIE WHO IS ABLE TO DO THE PROPER TESTING TO MAKE THE DIAGNOIS. BETTER DAYS TO ALL AHEAD I HOPE. SHARON CJ wrote: , I would be the first to say you probably do have fibromyalgia syndrome! The C6 and C7 you speak of causes the tingling down the arm and fingers - I have this too. It can get really bad! Sometimes I lose functioning of my entire arm. DDD can cause this as well - and there is most likely not a surgery to fix it as you have probably found out. The pain you speak of is VERY common among fibromyalgia patients. The strangests things keep happening to us - so the knuckles with the skin problem is not at all something I would rule out as a fibromyalgia symptom. Sometimes we have in my case many syndrome problems as well - dry skin, dry eyes, dry mouth, dry nose etc... With fibromyalgia every day is a new challenge as it moves from here to there. Sometimes lingering in one place for a long time and never going away and sometimes new places. Nothing suprises me with this monster! Rheumy docs don't seem to be dealing much with fibromyalgia anymore. They may be able to quickly diagnose it - but probably won't treat it. You will be extremely fortunate to find one that does, so I wish you the best. Just don't let docs tell you it is stress or all in your head! It is not! It is physical, and not always all so invisible! Good luck and thanks for joining. Welcome!!! mncjl > > > Been here.done that. and DO NOT WANT TO GO THERE AGAIN! > > > > > > Since I went into the hospital for back surgery on Feb I have slowly > > > been sliding into depression. My church has been wonderful in > > helping > > > with food, but NO and I mean NO ONE has come to visit me since I got > > > home. I feel like I have been cut off from civilization and am > > slowing > > > going down hill. I have not gotten out of bed today and was crying > > > earlier due to being lonely and depressed. I go back to the doctor > > > tomorrow for a check up and I am so hoping that he will release > > me to > > > go back to work as I do not know how much more of being trapped > > inside > > > all the time and alone. I am losing my mind. All I do is lay in bed > > > and watch tv. I really have no idea what or why I am writing here, > > > guess I am just trying to connect and figure out why I am so > > alone. I > > > need to go back to work so that I at least have people connection. > > > Thanks for listening/reading my ramblings. > > > > > > Christi in Waxahachie TX > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 20, 2008 Report Share Posted February 20, 2008 I JUST WANTED TO SAY IF IT WASN'T FOR ME GOING TO THE RHUMIE DR. I DID AND DO, I DON'T KNOW WHERE I WOULD BE, SHE DOES TREAT, AND TREATS WELL, PEOPLE COME FROM 2 SURROUNDING STATES TO SEE HER, AND EVERY TIME I HAVE BEEN IN WAIT RM THERE HAVE BEEN AT LEAST 2 OTHER FIBRO SUFFERS BESIDES ME, WHO PRAISE HER FOR HER KNOWLEDGE. SO ANYONE WHO WANTS TO COME TO THE EAST COAST I WILL PASS HER ON, SHE IS VERY PASSIONATE WITH HER PT'S ALSO. WE DO ALL BRING A BOOK ON APPT DAY AS WE WAIT BUT SO WORTH IT. I ALSO HAVE BEEN LUCKY WITH MY PRIMARY THEY HAVE THE SAME COMPASSION SHE DOES AND HAVE NEVER DOUBTED MY SYMPTOMS, AND CONTINUED TO DIG FOR 2YRS BEFORE SENDING ME TO RHUMIE, BUT DID HAVE ANOTHER ONE IN MIND WHO ALSO WAS RECOMMENDED WITH DEALING AND BEING GOOD AT DIAGNOISING FIBRO, BUT MY MOM HAD BEEN SEEING THE ONE I SEE, AND HAD FOUND THE WEIRD TYPE OF AUTO IMMUNE ARTHRITIS SHE HAS THAT NO ONE ELSE WAS ABLE TO FIND AFTER BEING TAKEN BY AMBULANCE FOR SEVERE PAIN AND HOSPITALIZED 4 DAYS. SO FOR THOSE OUT THERE DON'T GIVE UP AND IT IS WHAT I HAVE BEEN TOLD THE RHUMIE WHO IS ABLE TO DO THE PROPER TESTING TO MAKE THE DIAGNOIS. BETTER DAYS TO ALL AHEAD I HOPE. SHARON CJ wrote: , I would be the first to say you probably do have fibromyalgia syndrome! The C6 and C7 you speak of causes the tingling down the arm and fingers - I have this too. It can get really bad! Sometimes I lose functioning of my entire arm. DDD can cause this as well - and there is most likely not a surgery to fix it as you have probably found out. The pain you speak of is VERY common among fibromyalgia patients. The strangests things keep happening to us - so the knuckles with the skin problem is not at all something I would rule out as a fibromyalgia symptom. Sometimes we have in my case many syndrome problems as well - dry skin, dry eyes, dry mouth, dry nose etc... With fibromyalgia every day is a new challenge as it moves from here to there. Sometimes lingering in one place for a long time and never going away and sometimes new places. Nothing suprises me with this monster! Rheumy docs don't seem to be dealing much with fibromyalgia anymore. They may be able to quickly diagnose it - but probably won't treat it. You will be extremely fortunate to find one that does, so I wish you the best. Just don't let docs tell you it is stress or all in your head! It is not! It is physical, and not always all so invisible! Good luck and thanks for joining. Welcome!!! mncjl > > > Been here.done that. and DO NOT WANT TO GO THERE AGAIN! > > > > > > Since I went into the hospital for back surgery on Feb I have slowly > > > been sliding into depression. My church has been wonderful in > > helping > > > with food, but NO and I mean NO ONE has come to visit me since I got > > > home. I feel like I have been cut off from civilization and am > > slowing > > > going down hill. I have not gotten out of bed today and was crying > > > earlier due to being lonely and depressed. I go back to the doctor > > > tomorrow for a check up and I am so hoping that he will release > > me to > > > go back to work as I do not know how much more of being trapped > > inside > > > all the time and alone. I am losing my mind. All I do is lay in bed > > > and watch tv. I really have no idea what or why I am writing here, > > > guess I am just trying to connect and figure out why I am so > > alone. I > > > need to go back to work so that I at least have people connection. > > > Thanks for listening/reading my ramblings. > > > > > > Christi in Waxahachie TX > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 20, 2008 Report Share Posted February 20, 2008 I JUST WANTED TO SAY IF IT WASN'T FOR ME GOING TO THE RHUMIE DR. I DID AND DO, I DON'T KNOW WHERE I WOULD BE, SHE DOES TREAT, AND TREATS WELL, PEOPLE COME FROM 2 SURROUNDING STATES TO SEE HER, AND EVERY TIME I HAVE BEEN IN WAIT RM THERE HAVE BEEN AT LEAST 2 OTHER FIBRO SUFFERS BESIDES ME, WHO PRAISE HER FOR HER KNOWLEDGE. SO ANYONE WHO WANTS TO COME TO THE EAST COAST I WILL PASS HER ON, SHE IS VERY PASSIONATE WITH HER PT'S ALSO. WE DO ALL BRING A BOOK ON APPT DAY AS WE WAIT BUT SO WORTH IT. I ALSO HAVE BEEN LUCKY WITH MY PRIMARY THEY HAVE THE SAME COMPASSION SHE DOES AND HAVE NEVER DOUBTED MY SYMPTOMS, AND CONTINUED TO DIG FOR 2YRS BEFORE SENDING ME TO RHUMIE, BUT DID HAVE ANOTHER ONE IN MIND WHO ALSO WAS RECOMMENDED WITH DEALING AND BEING GOOD AT DIAGNOISING FIBRO, BUT MY MOM HAD BEEN SEEING THE ONE I SEE, AND HAD FOUND THE WEIRD TYPE OF AUTO IMMUNE ARTHRITIS SHE HAS THAT NO ONE ELSE WAS ABLE TO FIND AFTER BEING TAKEN BY AMBULANCE FOR SEVERE PAIN AND HOSPITALIZED 4 DAYS. SO FOR THOSE OUT THERE DON'T GIVE UP AND IT IS WHAT I HAVE BEEN TOLD THE RHUMIE WHO IS ABLE TO DO THE PROPER TESTING TO MAKE THE DIAGNOIS. BETTER DAYS TO ALL AHEAD I HOPE. SHARON CJ wrote: , I would be the first to say you probably do have fibromyalgia syndrome! The C6 and C7 you speak of causes the tingling down the arm and fingers - I have this too. It can get really bad! Sometimes I lose functioning of my entire arm. DDD can cause this as well - and there is most likely not a surgery to fix it as you have probably found out. The pain you speak of is VERY common among fibromyalgia patients. The strangests things keep happening to us - so the knuckles with the skin problem is not at all something I would rule out as a fibromyalgia symptom. Sometimes we have in my case many syndrome problems as well - dry skin, dry eyes, dry mouth, dry nose etc... With fibromyalgia every day is a new challenge as it moves from here to there. Sometimes lingering in one place for a long time and never going away and sometimes new places. Nothing suprises me with this monster! Rheumy docs don't seem to be dealing much with fibromyalgia anymore. They may be able to quickly diagnose it - but probably won't treat it. You will be extremely fortunate to find one that does, so I wish you the best. Just don't let docs tell you it is stress or all in your head! It is not! It is physical, and not always all so invisible! Good luck and thanks for joining. Welcome!!! mncjl > > > Been here.done that. and DO NOT WANT TO GO THERE AGAIN! > > > > > > Since I went into the hospital for back surgery on Feb I have slowly > > > been sliding into depression. My church has been wonderful in > > helping > > > with food, but NO and I mean NO ONE has come to visit me since I got > > > home. I feel like I have been cut off from civilization and am > > slowing > > > going down hill. I have not gotten out of bed today and was crying > > > earlier due to being lonely and depressed. I go back to the doctor > > > tomorrow for a check up and I am so hoping that he will release > > me to > > > go back to work as I do not know how much more of being trapped > > inside > > > all the time and alone. I am losing my mind. All I do is lay in bed > > > and watch tv. I really have no idea what or why I am writing here, > > > guess I am just trying to connect and figure out why I am so > > alone. I > > > need to go back to work so that I at least have people connection. > > > Thanks for listening/reading my ramblings. > > > > > > Christi in Waxahachie TX > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 20, 2008 Report Share Posted February 20, 2008 I JUST WANTED TO SAY IF IT WASN'T FOR ME GOING TO THE RHUMIE DR. I DID AND DO, I DON'T KNOW WHERE I WOULD BE, SHE DOES TREAT, AND TREATS WELL, PEOPLE COME FROM 2 SURROUNDING STATES TO SEE HER, AND EVERY TIME I HAVE BEEN IN WAIT RM THERE HAVE BEEN AT LEAST 2 OTHER FIBRO SUFFERS BESIDES ME, WHO PRAISE HER FOR HER KNOWLEDGE. SO ANYONE WHO WANTS TO COME TO THE EAST COAST I WILL PASS HER ON, SHE IS VERY PASSIONATE WITH HER PT'S ALSO. WE DO ALL BRING A BOOK ON APPT DAY AS WE WAIT BUT SO WORTH IT. I ALSO HAVE BEEN LUCKY WITH MY PRIMARY THEY HAVE THE SAME COMPASSION SHE DOES AND HAVE NEVER DOUBTED MY SYMPTOMS, AND CONTINUED TO DIG FOR 2YRS BEFORE SENDING ME TO RHUMIE, BUT DID HAVE ANOTHER ONE IN MIND WHO ALSO WAS RECOMMENDED WITH DEALING AND BEING GOOD AT DIAGNOISING FIBRO, BUT MY MOM HAD BEEN SEEING THE ONE I SEE, AND HAD FOUND THE WEIRD TYPE OF AUTO IMMUNE ARTHRITIS SHE HAS THAT NO ONE ELSE WAS ABLE TO FIND AFTER BEING TAKEN BY AMBULANCE FOR SEVERE PAIN AND HOSPITALIZED 4 DAYS. SO FOR THOSE OUT THERE DON'T GIVE UP AND IT IS WHAT I HAVE BEEN TOLD THE RHUMIE WHO IS ABLE TO DO THE PROPER TESTING TO MAKE THE DIAGNOIS. BETTER DAYS TO ALL AHEAD I HOPE. SHARON CJ wrote: , I would be the first to say you probably do have fibromyalgia syndrome! The C6 and C7 you speak of causes the tingling down the arm and fingers - I have this too. It can get really bad! Sometimes I lose functioning of my entire arm. DDD can cause this as well - and there is most likely not a surgery to fix it as you have probably found out. The pain you speak of is VERY common among fibromyalgia patients. The strangests things keep happening to us - so the knuckles with the skin problem is not at all something I would rule out as a fibromyalgia symptom. Sometimes we have in my case many syndrome problems as well - dry skin, dry eyes, dry mouth, dry nose etc... With fibromyalgia every day is a new challenge as it moves from here to there. Sometimes lingering in one place for a long time and never going away and sometimes new places. Nothing suprises me with this monster! Rheumy docs don't seem to be dealing much with fibromyalgia anymore. They may be able to quickly diagnose it - but probably won't treat it. You will be extremely fortunate to find one that does, so I wish you the best. Just don't let docs tell you it is stress or all in your head! It is not! It is physical, and not always all so invisible! Good luck and thanks for joining. Welcome!!! mncjl > > > Been here.done that. and DO NOT WANT TO GO THERE AGAIN! > > > > > > Since I went into the hospital for back surgery on Feb I have slowly > > > been sliding into depression. My church has been wonderful in > > helping > > > with food, but NO and I mean NO ONE has come to visit me since I got > > > home. I feel like I have been cut off from civilization and am > > slowing > > > going down hill. I have not gotten out of bed today and was crying > > > earlier due to being lonely and depressed. I go back to the doctor > > > tomorrow for a check up and I am so hoping that he will release > > me to > > > go back to work as I do not know how much more of being trapped > > inside > > > all the time and alone. I am losing my mind. All I do is lay in bed > > > and watch tv. I really have no idea what or why I am writing here, > > > guess I am just trying to connect and figure out why I am so > > alone. I > > > need to go back to work so that I at least have people connection. > > > Thanks for listening/reading my ramblings. > > > > > > Christi in Waxahachie TX > > > > > > > Quote Link to comment Share on other sites More sharing options...
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