Hi, i was wondering if anyone has experience of this treatment for urinary incontinence? It’s been proposed for a family member (c 30 years after PD diagnosis at age 40) if dual drug treatment doesn’t help - mirabegron & solfenacin - and our experience is that the drugs don’t seem to be effective after some encouraging early results. We’ve been warned that botox runs a risk of being too effective, which would be a similar nightmare, but, as I said it’d be interesting to know of anyone here who had been through it/know of others who have.
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Hi Nuno64,
Thank you for contributing to the forum. We’re sure someone who has had experiences with this will be able to give their opinions soon. In the meantime you may find the information on this page helpful.
If you do need any further information out helpline is always there. Please do give us a call on 0808 800 0303. We also always recommend raising this with your doctor or healthcare professional.
All the best,
Parkinson’s UK Moderation Team
I’ve been diving into health topics, and while exploring anti-pollution skincare for environmental stressors, it struck me how essential tailoring solutions is - just like considering Botox for unique cases
Making connections between treatments can sometimes spark new angles to discuss with healthcare professionals
If you’re speaking with doctors, perhaps mentioning related avenues of individual care, like skincare, could open up different perspectives on patient care
Bringing this one back up because I’m curious to know if anyone’s had an update on how Botox has worked for Parkinson’s-related urinary issues recently. I’ve heard mixed results and would love to hear more personal experiences or insights. Also, has anyone explored complementary therapies alongside Botox that seemed to help?