Jump to content
The MS PEOPLE UK Forum
Support, help, advice and information for Multiple Sclerosis. Ask questions and share experiences with people affected by MS.
Elle-N

A survey into the treatment of spasticity

8 posts in this topic Last Reply

Recommended Posts

Elle-N

Hello,

 

My name is Elicia and I am currently on an access course on the nursing pathway. I am basing my end of year essay on the treatment of spasticity for those who have MS and any first hand input would be a great help. All details are kept anonymous and the results will not be used for any other purpose.

 

https://www.surveymonkey.com/s/GJ2C8DQ

Share this post


Link to post
Sleepy
Scully

All done

Scully


They are not brain lesions..........they are just bright ideas

 

"The truth is out there"

Share this post


Link to post
Elle-N

Thank you so much!

Share this post


Link to post
Nindancer

Also done :wink2:

Sonia x

Share this post


Link to post
Nick

Anything to help, all completed.

 

Nick


Just another Warrior...........

Share this post


Link to post
Elle-N

Thank you, all of your reponses will help me alot!

Share this post


Link to post
Skippysprite

Sorry to be late, but I have done it now.

 

Pam x


Live for today.......never have regrets

Share this post


Link to post
Elle-N

Your response was not too late and thank you!

Share this post


Link to post

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

About Us

Founded in 2004, MS People UK is a community website and discussion forum by and for people with Multiple Sclerosis as well as for friends, families, supporters and those interested in this disabling condition.

If you’re newly diagnosed or want to ask about possible first symptoms, or if you’ve had Relapse Remit, Secondary or Primary Progressive MS for some time, a welcoming group of fellow MS sufferers is here to chat with you about MS symptoms, diagnosis and treatments.

The atmosphere is friendly whilst being compassionate, supportive and caring. Members also post about a variety of subjects not related to MS, as well as share jokes, talk about their hobbies, have fun, and more.


The MS People Forum is not responsible for advice or information supplied by members. We suggest you seek medical advice before trying anything.
×