Thank you so much for the information. My mom just started INBRIJA for her Parkinson’s off periods and I can’t thank y’all enough. It’s almost like she doesn’t any symptoms of Parkinson’s at all using INBRIJA. Thank you again🙏🏽❤️
I have a friend that was overdosed. She was totally out of it. She also had constipation so bad that she had to be hospitalized. The hospital didn't diagnose the overdose. The rehab center finally realized a month later that she was overdosed, all the time she was totally bedridden. She was begging her husband and her husband was entirely unnerved by the treatment she was getting so he took her home. It was more than one month to get a tentative diagnosis of an overdose but no change was made in medications. We couldn't get it resolved because the first neurologist couldn't be bothered to come in and see her. She had never seen this neurologist who is writing prescriptions without seeing her in person. Now my friend is both bowel and bladder incontinence. And she can't walk, going on four months. All of that was caused by the overdose. The new neurologist said she is supposed to keep the dosage on now and at least she's not doped up all the time. But she does say she going to get up out of the wheelchair. And can't. If she tries she pitches over. She falls out of bed every couple of days.
And that's with constant attention. She will tell me she can walk. We try to help her take a few steps but she quits after a step or two. Her husband can barely move her from bed to wheelchair. Or from wheelchair to couch. She's heavy and it takes all his body strength. We can't hire aids because they don't want to lift a patient. This all happened because of the overdose. She was fine; could walk, reason and had control of all body functions before the increase in dose. The other problem is all the carbidopa/l dopa is that the increase in dopamine makes her unconcerned. She is literally doped, like a drunk or heroin addict. And the illogical doctors in this medical symptom think that if l_opa stops an essential tremor than the patient has Parkinson's. Actually, alcohol will suppress essential tremors. So, you can't diagnose Parkinson's so easily.
Thank you for the information. The only side effect I’ve had is a slight cough, but that’s only if I inhale too quickly. Otherwise if I use the INBRIJA inhaler correctly it gets me out of my off period usually in under 5 minutes. I’ve never seen anything else for Parkinson’s Disease work as effectively and quickly as INBRIJA. Ty for the video.
INBRIJA has changed my Parkinson’s disease and helped me so much. There’s nothing on the market that works better for my Parkinson’s disease than INBRIJA🙏🏽🙏🏽
my father started taking levadopa and has so crazy side effects really so bad he started 1 month ago and has passed out multiple times, he was acting drunk on time etc… he didnt take it for one week and all side effects went away he didnt pass out nothing… but he twitched at night a lot now he started again and now he is pissing blood today and has pain.. I an so concerned he got parkinson last year I think and he has diabetes type 2 what should he do Im so concerened is there a better medication than levadopa because its destroying him
Do you realise how it makes you feel when you have been diagnosed for 10 years and they just talk about early symptoms. It's like w are being forgotten x
I was diagnosed at 40 in 2018. Started off with 2 sinimet per day. Now I am up to 23 per day along with 1 entacopone with every dose. I am fit but off times are bad!! I have been referred for dbs❤
Thank you for the information on INBRIJA. I’ve been hearing great things on this new medication for Parkinson’s Patients. INBRIJA sounds like a game changer against Parkinson’s Disease❤️
Hi Cecilia. Thank you for your comment. We do not go into tremendous detail about this but we do mention that too much Levodopa leads to increased fluctuations and greater involuntary movements. But since this segment is part of a much larger module that answers questions about "what's new?" and "what can someone expect in the future?", we punctuate Dr Stern's comments with information about the new formulations that are either available or about to come to market that deliver the drug in a slower, more regulated way, leading to fewer fears of complications. We will be updating this channel shortly and we'll be sure to add clarity to this module. Thanks again.
If doctors would listen to patients more and stop dismissing our PD symptoms as nothing real or not important, yes we could get diagnosed and treated earlier. I am through with those kind of doctors, especially the ones who think it's all in a woman's mind.
Thank you so much for the information. My mom just started INBRIJA for her Parkinson’s off periods and I can’t thank y’all enough. It’s almost like she doesn’t any symptoms of Parkinson’s at all using INBRIJA. Thank you again🙏🏽❤️
I’ve never seen any medication work as well as INBRIJA for my Parkinson’s. This inhaler has made dealing with my Parkinson’s much more manageable🙏🏽
I have a friend that was overdosed. She was totally out of it. She also had constipation so bad that she had to be hospitalized. The hospital didn't diagnose the overdose. The rehab center finally realized a month later that she was overdosed, all the time she was totally bedridden. She was begging her husband and her husband was entirely unnerved by the treatment she was getting so he took her home. It was more than one month to get a tentative diagnosis of an overdose but no change was made in medications. We couldn't get it resolved because the first neurologist couldn't be bothered to come in and see her. She had never seen this neurologist who is writing prescriptions without seeing her in person. Now my friend is both bowel and bladder incontinence. And she can't walk, going on four months. All of that was caused by the overdose. The new neurologist said she is supposed to keep the dosage on now and at least she's not doped up all the time. But she does say she going to get up out of the wheelchair. And can't. If she tries she pitches over. She falls out of bed every couple of days.
And that's with constant attention. She will tell me she can walk. We try to help her take a few steps but she quits after a step or two. Her husband can barely move her from bed to wheelchair. Or from wheelchair to couch. She's heavy and it takes all his body strength. We can't hire aids because they don't want to lift a patient. This all happened because of the overdose. She was fine; could walk, reason and had control of all body functions before the increase in dose. The other problem is all the carbidopa/l dopa is that the increase in dopamine makes her unconcerned. She is literally doped, like a drunk or heroin addict. And the illogical doctors in this medical symptom think that if l_opa stops an essential tremor than the patient has Parkinson's. Actually, alcohol will suppress essential tremors. So, you can't diagnose Parkinson's so easily.
@@jazztocountry1047 p
@@jazztocountry1047 ❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤
@Jazz To Country no no m
Levodopa works best on an empty stomach. Since it causes nausea it is combined with carbidopa.
Thank you for the information. The only side effect I’ve had is a slight cough, but that’s only if I inhale too quickly. Otherwise if I use the INBRIJA inhaler correctly it gets me out of my off period usually in under 5 minutes. I’ve never seen anything else for Parkinson’s Disease work as effectively and quickly as INBRIJA. Ty for the video.
I hope so too! Diagnosed in November 2021. I’m holding my own but balance is a problem. Thank you!
INBRIJA has changed my Parkinson’s disease and helped me so much. There’s nothing on the market that works better for my Parkinson’s disease than INBRIJA🙏🏽🙏🏽
Really. Ihave not heard of it. Tell me more
How has it helped you?
my father started taking levadopa and has so crazy side effects really so bad
he started 1 month ago and has passed out multiple times, he was acting drunk on time etc… he didnt take it for one week and all side effects went away he didnt pass out nothing… but he twitched at night a lot
now he started again and now he is pissing blood today and has pain.. I an so concerned he got parkinson last year I think and he has diabetes type 2
what should he do Im so concerened is there a better medication than levadopa because its destroying him
A video telling us you don't know? At least it's short.
Do you realise how it makes you feel when you have been diagnosed for 10 years and they just talk about early symptoms. It's like w are being forgotten x
14 years . I hear what you are saying.
I was diagnosed at 40 in 2018. Started off with 2 sinimet per day. Now I am up to 23 per day along with 1 entacopone with every dose. I am fit but off times are bad!! I have been referred for dbs❤
He absolutely refused to answer the man’s simple question.
L
Exactly what I was thinking. How can you trust his therapy when he won't answer a simple question about long-term effects?
INBRIJA is truly the worldwide gold standard for treating Parkinson’s Disease.
You never answered the heading question???
Thank you for the information on INBRIJA. I’ve been hearing great things on this new medication for Parkinson’s Patients. INBRIJA sounds like a game changer against Parkinson’s Disease❤️
He said nothing to answer the question about taking too much Levodopa!!
Hi Cecilia. Thank you for your comment. We do not go into tremendous detail about this but we do mention that too much Levodopa leads to increased fluctuations and greater involuntary movements. But since this segment is part of a much larger module that answers questions about "what's new?" and "what can someone expect in the future?", we punctuate Dr Stern's comments with information about the new formulations that are either available or about to come to market that deliver the drug in a slower, more regulated way, leading to fewer fears of complications. We will be updating this channel shortly and we'll be sure to add clarity to this module. Thanks again.
please stop sending me info, videos, or anything
If doctors would listen to patients more and stop dismissing our PD symptoms as nothing real or not important, yes we could get diagnosed and treated earlier. I am through with those kind of doctors, especially the ones who think it's all in a woman's mind.
@@michelelindseth8250 I agree, 3 doctors told me I just had resting tremors, nothing to worry about. They were wrong!
make focused ultrasound available now for Parkinson's,Whats the problem?
scott tevis it’s available now in Australia but at a cost of $30,000..... so I read.
I understand it's not a permanent fix.
No sound
What is the name of that trial , and is it open?