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CBD pills and capsules also deliver a specific dose with each pill. If you have trouble swallowing but want to use the pill form, find one that’s easy to swallow such as CBD softgels. Topicals such as CBD-infused creams and lotions don’t deliver CBD to your bloodstream, but they can soothe pain and stiffness where they’re applied.

Ultimately, the best form of CBD is the one that meets your physical needs and gets you the results you’re after. Whether you know you’re at risk for PD or not, it’s important to only use CBD products made from organically-cultivated hemp. Hemp that isn’t organic may contain high levels of industrial agricultural chemicals such as pesticides.

That said, research studies use dosages of 100 to 600 mg per day.(7) If you’re taking CBD for the first time, you wouldn’t want to go jumping into that 600 mg deep end. Start with a low dose and gradually increase to give your body a chance to acclimate. And if you want consistent results, consistency in your dosage is also important.

With science exploring CBD’s potential to help people with Parkinson’s, we’re on the brink of having a clear understanding of how the cannabinoid best fits in a PD therapy toolkit. Meanwhile, those living with PD are already exploring the benefits of CBD for Parkinson’s tremors, pain management, sleep support, anxiety reduction, and more.

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But with CBD being easily available, it’s accessible to those aiming to be proactive about PD prevention. Thinking about using CBD to manage or prevent Parkinson’s? Find the right form of CBD for your needs, and make sure it’s derived from hemp that was organically grown. Peres, FF, et al.

Cannabis and its derivatives for the use of motor symptoms in Parkinson's disease: a systematic review and meta-analysis - Susan J. Thanabalasingam, Brandan Ranjith, Robyn Jackson, Don Thiwanka Wijeratne, 2021

Cannabidiol as a Promising Strategy to Treat and Prevent Movement Disorders?. Frontiers in pharmacology. (2021). Fox Insight Survey Sheds Light on Cannabis Use and Parkinson's. Michael J. Fox Foundation for Parkinson’s Research. https://www. michaeljfox.org/news/fox-insight-survey-sheds-light-cannabis-use-and-parkinsons Leehey, MA, et al. (2020). Safety and Tolerability of Cannabidiol in Parkinson Disease: An Open Label, Dose-Escalation Study.

https://doi. org/10. 1089/can. 2019.0068 University of Colorado, Denver. (2022). A Study of Tolerability and Efficacy of Cannabidiol on Motor Symptoms in Parkinson's Disease. U.S. National Library of Medicine. https://www. clinicaltrials.gov/ct2/show/NCT03582137 (2022). Can cannabidiol (CBD) treat Parkinson’s symptoms? Parkinson’s UK. https://www. parkinsons.org. uk/get-involved/can-cannabidiol-cbd-treat-parkinsons-symptoms (2022). The Relationship Between Pesticides and Parkinson’s. American Parkinson Disease Association.

apdaparkinson.org/article/the-relationship-between-pesticides-and-parkinsons Millar, SA, et al. (2019). A systematic review of cannabidiol dosing in clinical populations. British journal of clinical pharmacology. https://doi. org/10. 1111/bcp. 14038 .

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BACKGROUND AND OBJECTIVE: Although cannabinoid-based medications are increasingly used by older adults, their safety and tolerability in this age group remain unclear. The purpose of this systematic review was to examine the safety and tolerability of cannabinoid-based medications by conducting a meta-analysis of open-label observational studies of cannabinoid-based medications for all indications in individuals with a mean age of ≥50 years.

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Study quality was assessed using an adapted version of the Grading of Recommendations Assessment, Development and Evaluation criteria and Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines were followed. We included studies that (a) were published from 1990 onwards; (b) included older adults (mean age ≥50 years); and (c) provided data on the safety and tolerability of medical cannabinoids.

Risk of adverse events, serious adverse events and withdrawals was computed as the incidence rate (IR). Separate analyses were conducted by the cannabinoid-based medication used, for delta-9-tetrahydrocannabinol (THC), cannabidiol (CBD) and a combination of THC and CBD (THC:CBD). RESULTS: Thirty-eight studies were identified (THC = 23; CBD = 6; THC:CBD = 9; N = 2341, mean age: 63.

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08 years, men: 53. 86%). THC had a very low incidence of all-cause and treatment-related adverse events (IR: 122. 18, 95% confidence interval [CI] 38. 23-253. 56; IR: 84. 76, 95% CI 0. 13-326. 01, respectively) and negligible serious adverse events (IR = 0). Similar IRs for CBD (all cause, IR: 111.

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24-495. 93; treatment related, IR: 1. 76, 95% CI 4. 63-23. 05) and no serious adverse events (IR = 0). CBD was not associated with a risk of treatment-related withdrawals. THC had a low risk of all-cause and treatment-related withdrawals (IR: 25. 18, 95% CI 12. 35-42. 52; IR: 7.

26-14. 38, respectively). The THC:CBD treatment had a low risk of all-cause and treatment-related adverse events (IR: 100. 72, 95% CI 0. 25-383. 00; IR: 55. 38, 95% CI 8. 61-142. 80, respectively), but reported a risk of all-cause and treatment-related serious adverse events (IR: 21. 32, 95% CI 0.