Experiences with Azilect (Rasagiline) as a monotherapy

Posted by tptully @tptully, Apr 1, 2023

Hi! I’m new to this group. I was recently diagnosed with early stage Parkinson’s (tremor dominant). I have left side tremors in my hand/arm and leg; mild bradykinesia of my left hand and some mild left arm/shoulder/hand rigidity. My mobility and balance are excellent and I exercise daily with a variety of exercises (Rock Steady Boxing, fast walking on a treadmill, Smoovey vibrating rings, weight lifting, and exercise/stretches with physical therapy resistance bands).

My PD/movement disorder specialist does not think I need any medication at this time, but he suggested that I consider taking Azilect (alone) since it MIGHT have some disease modifying properties. Generally, I like to avoid medications, but if I can find people who truly believe that Azilect as a monotherapy has slowed or stabilized their progression I would love to hear their stories But I would also love to hear the stories of those who have taken Azilect as a monotherapy and have experienced no stabilizing or improvement of their PD.

I have searched through all of the existing posts on Azilect, and I am looking for new information/experiences.

Thanks and God bless you all!

Interested in more discussions like this? Go to the Parkinson's Disease Support Group.

Profile picture for impossiblefuture @impossiblefuture

My Brother has stage 3 Parkinson, along with Addisons and long covid, not a great outlook for a person barely in his 60s, many meds you find others rave about are usually only those almost uniquely for their singular issues.

Battling one issue with one med is fine, battling more than one, well let's say not much hope. My brother's timeline has been reduced by least 15 years due to Addisons.

Jump to this post

🫂 🤗

REPLY
Profile picture for impossiblefuture @impossiblefuture

My Brother has stage 3 Parkinson, along with Addisons and long covid, not a great outlook for a person barely in his 60s, many meds you find others rave about are usually only those almost uniquely for their singular issues.

Battling one issue with one med is fine, battling more than one, well let's say not much hope. My brother's timeline has been reduced by least 15 years due to Addisons.

Jump to this post

Hello @impossiblefuture and welcome to the Parkinson's support group on Mayo Connect. I appreciate you posting about your brother. He certainly has a lot of health issues to deal with. How long ago was he diagnosed with these disorders?

REPLY
Profile picture for Teresa, Volunteer Mentor @hopeful33250

Hello @impossiblefuture and welcome to the Parkinson's support group on Mayo Connect. I appreciate you posting about your brother. He certainly has a lot of health issues to deal with. How long ago was he diagnosed with these disorders?

Jump to this post

Long Covid about 2 years now, Parkinsons about a year.
The Addisons nearly 6 years now.

REPLY
Profile picture for Teresa, Volunteer Mentor @hopeful33250

Hello @impossiblefuture and welcome to the Parkinson's support group on Mayo Connect. I appreciate you posting about your brother. He certainly has a lot of health issues to deal with. How long ago was he diagnosed with these disorders?

Jump to this post

My fear however is if he has it my chances of getting it increases especially as I get full body vibrations nearly every night and have had for over 40+ years, it's not like shaking, it's like my whole body is vibrating inside on a smooth but consistent wave length, lasts anything from 5 minutes to 3 hours.

REPLY
Please sign in or register to post a reply.