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Transcripts for BBCNEWS BBC 100 Women in Conversation 20240604 20:34:00

that it s psychosomatic and you would feel better if you got a boyfriend? i cannot say how many times my fatigue and my speech disturbances, even in my 20s, the speech would come out when i developed tics from some flares and things, that would say, ok, what kind of trauma have you had? we do think this is psychosomatic. but without any real neurological tests. it was just talking to me. and taking a case history, so i did just believe that. iwas like, wow, i m really depressive, i cannot get to the bottom of how to ignite some life force in me. and i took it. ever since i was 12 i was told that it was just depression. how did you feel when you finally got the diagnosis and the doctor said to you the you have ms? how did that feel?

Transcripts for BBCNEWS BBC 100 Women in Conversation 20240604 05:35:00

it s psychosomatic and you might feel better if you got a boyfriend? i can t say how many times. my fatigue and my speech disturbances even in my 20s, the speech would come out when i developed tics from some flares and things that would say, ok, what kind of trauma have you had? we do think this is psychosomatic, but without any real neurological tests. it was just talking to me and taking a case history. so, i did just believe that. i was like, wow, i m really depressive. i can t get to the bottom of how to ignite some life force in me. and i took it. ever since i was 12, i was told that it was just depression. how did you feel when you finally got that diagnosis? when the doctor said to you you ve got ms, how did that feel? when the doctor told me the night of the mri that i had ms, i cried, that it had a name.

Transcripts for BBCNEWS BBC 100 Women in Conversation 20240604 14:37:00

it because i was ashamed and concerned i would not work again. and when the diagnosis came, it really took the lid off a lot for me and unburdened me. is it true that somewhere along the line, a doctor said to you that it s psychosomatic and you would feel better if you got a boyfriend? i cannot say how many times my fatigue and my speech disturbances, even in my 20s, the speech would come out when i developed tics from some flares and things, that would say, ok, what kind of trauma have you had? we do think this is psychosomatic. but without any real neurological tests. it was just talking to me. and taking case history, so i did just believe that. iwas like, wow, i m really depressive, i cannot get to the bottom of how to ignite some life force in me.

Transcripts for BBCNEWS BBC 100 Women in Conversation 20240604 13:35:00

i developed tics from some flares and things, that would say, ok, what kind of trauma have you had? we do think this is psychosomatic. but without any real neurological tests. it was just talking to me. and taking case history, so i did just believe that. iwas like, wow, i m really depressive, i cannot get to the bottom of how to ignite some life force in me. and i took it. ever since i was 12 i was told that it was just depression. how did you feel when you finally got the diagnosis and the doctor said to you the you have ms/ how did that feel? when the doctor told me the night of the mri that i had ms, i cried, that it had a name, and it was an amazing, comforting feeling, even though i don t wish disease on anyone,

Transcripts for BBCNEWS BBC 100 Women in Conversation 20240604 17:35:00

what kind of trauma have you had? we do think this is psychosomatic. but without any real neurological tests. it was just talking to me. and taking a case history. so i did just believe that. iwas like, wow, i m really depressive, i cannot get to the bottom of how to ignite some life force in me. and i took it. ever since i was 12 i was told that it was just depression. how did you feel when you finally got that diagnosis and the doctor said to you the you have ms? how did that feel? when the doctor told me the night of the mri that i had ms, i cried, that it had a name, and it was an amazing, comforting feeling, even though i don t wish disease on anyone, but it was a huge, comforting feeling to know there s a whole community of chronic illness, or ms patients. and so, i always felt 0k.

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