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Lionel -- I really have no specific advice, just my sympathy and caring
wishes. You both have been going thru hell and I empathize. Hope everything
turns out as well as it can.
Ann Gibbons

-----Original Message-----
From: Lionel Modra <[log in to unmask]>
To: [log in to unmask] <[log in to unmask]>
Date: Friday, August 24, 2001 6:37 AM
Subject: Epidural for PWP ???


>My wife, who is the PWP in this family, is scheduled for surgery
>(Proctectomy, Sigmoid Colostomy. Cystectomy, Urostomy) on Sept 5, and we
>were advised yesterday that the usual procedure is to insert an epidural
>catheter (prior to surgery) to introduce pain relieving medication post
>operatively.
>Does anyone know if there are any undesirable side effects of this
>procedure in PWPs?
>We are aware of the Pethidine / Selegiline reaction, and have ensured
>that all involved in her treatment are also aware of that interaction.
>She fell and fractured her 3rd sacral vertebra, damaging the S3 nerves,
>in Feb '99. The nerve damage resulted in dysfunction  of both bladder
>and bowel (retention), and continuous pain in the pelvic area,
>increasing in intensity as the bladder and rectum fill. No improvement
>in the nerve function has occurred, hence the move to surgical
>intervention. She has tried all the available medications, and nerve
>stimulation (Medtronic), but unfortunately without success. Life for her
>revolves around self-catheterisation and enemas at present.
>The stress of this problem has accelerated her PD (she has gone from
>good control with 450 mg levodopa per day, to on/off control with 1,100
>to 1,200 mg per day. She also takes 2 x 5 mg Selegiline / day. She has
>not been able to take any of the agonists because of their constipating
>effect, and the effect of reducing blood pressure.
>We would appreciate any comments or advise regarding the epidural, or
>other PD related matters.
>Lionel Modra, c/g for Win (71\67\??)
>
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