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#1 | ||
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Junior Member
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First, hello to everyone who knows me from other places.
![]() Just thought I would ask here if anyone else is having problems with dystonia in their feet. I've recently received this diagnosis from my neuro and have started Mirapex. My right foot which is usually numb and tingly feeling is starting to twist and it is beginning to get more difficult to walk. |
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#2 | |||
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Grand Magnate
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sorry, i don't know.
is there any physical therapy that could help? welcome to NT btw.
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Judy trying to be New Skinny Butt ______________________ You are a child of the universe, no less than the trees and the stars; you have a right to be here. And whether or not it is clear to you, no doubt the universe is unfolding as it should. -------------------------------------- "DESIDERATA" by Max Ehrmann |
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#3 | ||
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Junior Member
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Quote:
I'm hoping that it goes away, but in the meantime I'm taking Mirapex which hasn't started working, yet. Thanks for the welcome. |
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#4 | |||
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Elder
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Hi Jalee! Nice to have you back! Have missed you!
![]() I suffer from much the same thing as you but haven't been dx'd with dystonia just severe muscle spasms and cramping in my feet and calves. I take Sinemet and it works very well. The other drugs (Requip, etc) didn't work at all. I also get weekly massages and my therapist focuses on my calf muscles. She also taught me a technique for releasing the "charlie horse" type cramping I get in my feet that cause them to twist. I also take Klonopin/clonazepam which helps as well. The two drugs work together to keep the muscles from twitching all the time. Sinemet comes in a couple different dose strengths and for me this drug has virtually no side effects! That's a plus! Good luck finding something that works! I hate the middle of the night spasms that in my feet! Yeow!
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Cheryl Dx: MS 2001 CRPS 2009 “When everything seems to be going against you, remember that the airplane takes off against the wind, not with it.” - Henry Ford |
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#5 | ||
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Junior Member
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I've been titrating my dose of Mirapex for a month now. I take a single dose in the morning, then a double at night. I've had some nausea off and on, hence the slow escalation. I can see that if I don't get this under control, it could be quite disabling. I've missed you too. ![]() I've been trying to concentrate on RL and staying well. Most of the time I can't stand to talk. It is difficult to find the words I want to say. It is easier not to. ![]() |
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"Thanks for this!" says: | tovaxin_lab_rat (01-12-2009) |
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#6 | |||
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In Remembrance
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So sorry or your pain, Jalee.
![]() I hope you find something soon, that helps. ![]()
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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#7 | |||
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Wisest Elder Ever
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Welcome to NeuroTalk! I'm sorry for the pain you're experiencing. Cramps in the legs, especially at night, are awful. I hate being awakened like that. I hope the meds start working for you. Massage might be helpful although I've never tried it.
__________________
These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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#8 | ||
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Junior Member
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"Thanks for this!" says: | SallyC (01-11-2009) |
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#9 | ||
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Junior Member
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![]() It gets sore after awhile of constant spasm. It is so strange. I hope the med works. |
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#10 | ||
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Member
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I hope the Mirapex works too,Jalee.
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"Thanks for this!" says: | Jalee (01-13-2009) |
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