Has anyone tried the new inhaled “rescue “ form of levodopa?
Inbrija - Inhaled Levodopa : Has anyone... - Cure Parkinson's
Inbrija - Inhaled Levodopa
I use Sinemet under the tongue for a quick hit of Ldopa
I’ve been in touch with my dr about trying this. He can start prescribing it sometime in April.
I've been using the dissolving type for approx. 10 yrs. I like them because you don't need water to take them. They are called Carbidopa/Levo Odt (orally dissolving tabs). The mfg has them on backorder until. May. My symptoms got a lot worse. My doctor & pharmacist said that can happen. Did your Dr say why he can't prescribe them until April?
I haven't tried it yet but I asked my neurologist about it & she said it works good but it's not the easiest thing to use.
I have been using Inbrija for about 6 weeks and 2-3 times per day. My main symptoms are tremor and left foot dystonia. I also take Rytary 4 times daily.
I use Inbrija when my tremor and left foot start turning inward and my next dose of Rytary is not due. It “kicks in” from 10 to 20 minutes later. I used to feel panic when my Rytary would stop working. My anxiety has diminished so much!
Expensive!! There are patient assistance programs available in USA. I am still figuring out the best timing with my doctor.
I have the Inbrija. I have used it a couple times , in theory I was hoping it would help on my long runs or when my dystonia comes on like crazy and this would help release the muscles faster. But what I found for me , it was like my brain was heavy and when I tried to do something I felt like I had to take a moment and lay my head down. Almost like a hangover. It’s happened every time. I will try again but if that’s my results it’s obviously not for me. And it is very expensive . I was able to get it with the help of script assistance through my dr. I hope it helps others out there but wasn’t right for me , at least not right now , Karen