Hi there. Just about all of us. My suggestion would be to go to all the related posts on this question....there's a whole library of questions and discussions around just about everything related to PD. You'll find all you need to know.
It's understandable to be concerned about your wife's experiences with levodopa. While it is regarded as the "gold standard" in the early stages of PD, this sentiment may be overshadowed by various HU discussions. Open communication with her neurologist is crucial; if there are side effects or issues, it’s important to address them so that adjustments can be made accordingly.
As a partner, you can play a vital role by creating a supportive environment, collaborating on healthy lifestyle choices, and being attentive to your wife's emotional needs.
The fear of addiction to levodopa is unfounded. However, it is wise—especially for women—to aim for a minimal dosage. Research has shown that women can often manage with half the usual dose of carbidopa/levodopa, which is why they tend to experience side effects more frequently.
Moreover, delaying the initiation of medication is unnecessary, as demonstrated in research. The LEAP randomized trial found no differences in outcomes five years later between those who started levodopa immediately versus those who delayed treatment for 40 weeks.
By staying informed and engaged, you can help navigate this journey together, ensuring that your wife receives the most effective care while addressing her concerns.
Thank you for your well thought out and easily understood reply.She has a scheduled session in a couple of months with her neurologist. We'll ask if a reduction is appropriate in her case.
It may also help to vary the times when your wife takes her meds, try a slow-release dose at bedtime, etc. Every PD patient is an individual!Best wishes to you both.
Melatonin for sleep, Restoralax for constipation, nicotine gum for anxiety/mood. Any kind of exercise will also help. A strict sleep/wake schedule also helpful. Check with doc.
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