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LEADER 00000cim a22006373a 4500 
001    kwgtjw75h9txddz0 
003    SE-LIBR 
007    cr |||   ||||| 
008    200729s2020    dk | |||o||||||ma | eng|d 
020    9788711673935 
024 7  |5MoE|a9788711673935|2Distributör: WeDoBooks 
041    eng 
082 04 920.7|222 (machine generated) 
084    Lz Chambers, Sue, 1956/DR|2kssb/8 
084    Vef/DR|2kssb/8 
084    Lz Chambers, Sue, 1956|2kssb/8 
084    Vef|2kssb/8 
100 1  Chambers, Sue,|d1956-|4aut|4nrt 
245 12 A magical sense 
264  1 Köpenhamn :|bSaga Egmont,|c2020 
300    4 tim., 31 min 
336    spoken word|bspw|2rdacontent 
337    audio|bs|2rdamedia 
500    E-ljudbok (strömmande) 
500    |5MoE|aNedladdningsbar MP3, krypteringsskyddad (227.98 MB)
520    Sue has been living with MS (Multiple Sclerosis) since 
       1985. In this very personal audiobook, she explores how MS
       has affected her, physically and mentally, and provides 
       valuable advice for others in the same position. 
       Throughout the book, Sue's humour comes through making it 
       a life affirming read. It is a must read for anyone 
       affected by MS. A diagnosis of MS was the start of a 
       journey for Sue. This book tells of that journey, from the
       initial shock of the diagnosis through the education 
       process (and the periods of denial) to an understanding of
       what it takes to survive and live with MS. No one in the 
       medical team can tell it from the position of the person 
       with MS. Sue can and she does so with personal candor and 
       incredible humour. The initial diagnosis was hard to 
       accept. As Sue puts it, "Once I ran out of things to blame,
       the shock really took over. My husband, bless him, has a 
       great ability to make people laugh. When I was with him, 
       it wasn't too bad. But when I was alone, the pain of 
       feeling hard done by and victimized really hurt. Like a 
       physical thump in the guts and literally an ache in the 
       heart. And really, even many, many years on, there are 
       still times when I seek out company, so I can't dwell on 
       how hurt I feel."Sue handles a difficult subject 
       sensitively. There is a large body of information in this 
       book which will be useful to everyone affected by MS, 
       whatever their role. Medical staff will find it useful to 
       gain the perspective of one of their "users" (as Sue 
       describes herself). Sue's sister was diagnosed with MS in 
       1989, four years after Sue's own diagnosis and died in 
       2001. It was only then that Sue realised that MS could be 
       fatal. It was the trigger that started the writing of this
       book ...[WeDoBooks] 
520    Sue has been living with MS (Multiple Sclerosis) since 
       1985. In this very personal audiobook, she explores how MS
       has affected her, physically and mentally, and provides 
       valuable advice for others in the same position. 
       Throughout the book, Sue's humour comes through making it 
       a life affirming read. It is a must read for anyone 
       affected by MS. A diagnosis of MS was the start of a 
       journey for Sue. This book tells of that journey, from the
       initial shock of the diagnosis through the education 
       process (and the periods of denial) to an understanding of
       what it takes to survive and live with MS. No one in the 
       medical team can tell it from the position of the person 
       with MS. Sue can and she does so with personal candor and 
       incredible humour. The initial diagnosis was hard to 
       accept. As Sue puts it, "Once I ran out of things to blame,
       the shock really took over. My husband, bless him, has a 
       great ability to make people laugh. When I was with him, 
       it wasn't too bad. But when I was alone, the pain of 
       feeling hard done by and victimized really hurt. Like a 
       physical thump in the guts and literally an ache in the 
       heart. And really, even many, many years on, there are 
       still times when I seek out company, so I can't dwell on 
       how hurt I feel."Sue handles a difficult subject 
       sensitively. There is a large body of information in this 
       book which will be useful to everyone affected by MS, 
       whatever their role. Medical staff will find it useful to 
       gain the perspective of one of their "users" (as Sue 
       describes herself). Sue's sister was diagnosed with MS in 
       1989, four years after Sue's own diagnosis and died in 
       2001. It was only then that Sue realised that MS could be 
       fatal. It was the trigger that started the writing of this
       book ... [Elib] 
650  7 Multipel skleros|0https://id.kb.se/term/sao/
       Multipel%20skleros|2sao 
653    E-bok 
653    eLib 
655  7 Självbiografier|2saogf 
655  7 Sjukdomsskildringar|2saogf 
655  7 Ljudböcker|2saogf 
852    |5MoE|bMoE|cLjudbok|zNedladdningsbar MP3, 
       krypteringsskyddad (227.98 MB) 
856 42 |uhttps://biblio.app/material/9788711673935