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Experiences with
Dysport
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Walking Speed
I've tried ampyra,
dysport
and I'm still moving like a turtle. My legs still feel very heavy! I'm still hoping to be walking normal again!
I've tried ampyra,
dysport
and I'm still moving like a turtle. My legs still feel very heavy! I'm still hoping to be walking normal again!
Diva1976
in
My MSAA Community
30 days ago
Botox for dystonia
My neurologists injected my neck with
Dysport
which is a form of Botox. After a couple of days I could no longer hold my head up. I call my neurologist and she gave me some medication to help muscles contract. ( which is opposite of the Botox). Since then, I can do very little.
My neurologists injected my neck with
Dysport
which is a form of Botox. After a couple of days I could no longer hold my head up. I call my neurologist and she gave me some medication to help muscles contract. ( which is opposite of the Botox). Since then, I can do very little.
Southernladyla
in
Cure Parkinson's
6 months ago
Dysport and swollen lymph nodes
Has anyone experienced swollen lymph nodes after getting
dysport
? I have one that has popped up in my groin the day after I had cosmetic
dysport
injected and I’m wondering if it is related
Has anyone experienced swollen lymph nodes after getting
dysport
? I have one that has popped up in my groin the day after I had cosmetic
dysport
injected and I’m wondering if it is related
StrengthHopeLove
in
CLL Support
1 year ago
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Artane anyone?
Botox (well actually it was
Dysport
that was given to use due to insurance) has not helped. Movement Specialist recommened Artane. I was wondering if I could have some feedback on people who have tried it. Or, whatever anyone thinks of it. Thank you.
Botox (well actually it was
Dysport
that was given to use due to insurance) has not helped. Movement Specialist recommened Artane. I was wondering if I could have some feedback on people who have tried it. Or, whatever anyone thinks of it. Thank you.
LearningAllICan
in
Cure Parkinson's
4 years ago
Thankful for you...
Except perhaps the toe dystonia, it got really bad - we just tried
Dysport
(Botox), and as a result, it’s a little better - I think - walking is a little better, but sadly he still cannot run. A part of me thinks if he could just run, he would get better.
Except perhaps the toe dystonia, it got really bad - we just tried
Dysport
(Botox), and as a result, it’s a little better - I think - walking is a little better, but sadly he still cannot run. A part of me thinks if he could just run, he would get better.
LearningAllICan
in
Cure Parkinson's
4 years ago
Side effects of Dysport injections for Cervical Dystonia
Hi Everyone, I have just had my second set of 125 units of
Dysport
each, into the left sternomastoid and the right splenius capitis.
Hi Everyone, I have just had my second set of 125 units of
Dysport
each, into the left sternomastoid and the right splenius capitis.
HKAnne
in
Dystonia Society
5 years ago
Dysport
My doctor told me he'd like to try
Dysport
as he'd had some success with some patients feeling faster relief and for a longer time (up to 5 months as opposed to 3). It is now day 2 following the injections and it's working.
My doctor told me he'd like to try
Dysport
as he'd had some success with some patients feeling faster relief and for a longer time (up to 5 months as opposed to 3). It is now day 2 following the injections and it's working.
taihde
in
PSP Association
5 years ago
Am I expecting too much from my first Botox?
Eight weeks ago I had my first Botox injections (150 units of
Dysport
in the right splenius capitis, 50 in the left splenius capitis and 100 in the right sternomastoid).
Eight weeks ago I had my first Botox injections (150 units of
Dysport
in the right splenius capitis, 50 in the left splenius capitis and 100 in the right sternomastoid).
phil999
in
Dystonia Society
6 years ago
Research needs YOU! All UK patients with cervical dystonia who have had botox please consider.
More specifically, we hope to speak to patients who are currently receiving Botox or
Dysport
injections as part of their treatment.
More specifically, we hope to speak to patients who are currently receiving Botox or
Dysport
injections as part of their treatment.
FND_
FND Hope
in
Functional Neurological Disorder - FND Hope
11 years ago
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