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Support, help, advice and information for Multiple Sclerosis. Ask questions and share experiences with people affected by MS.
colmmc

foot drop

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colmmc

Hi

I want to let you all know about a device I have had for about 2 weeks,

and its great!I first came across it at MS life in Manchester in the summer

and after a lot of phone calls, visits to my GP ,Physio ,hosp trust,ect

I have got it through the NHS. Well its wonderfull, ive not tripped since i got it

well worth a look if Footdrop is a problem for you.heres the web site.

http://www.odstockmedical.com/PatientsSite/Home.html

keep on walking!!!!!!!!!!!

Colm

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Michelle

A bit like a tens machine.

All the best Colm

 

Michelle :bdayflames:

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goonasi

Interesting, I was supposed to have a Botox injection last week to help correct the over-activity in my calf muscle and help correct the foot drop caused but it was deemed that I would not benefit from this treatment.

 

I have signed up for an information pack.


[b]Keep Well
Simon x[/b]

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rachy

Do you stilll use this? Do it actually work? I was told I would have to pay for one and dont know if it would even work for me .. x


.....................................

 

Rachy xx

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colmmc
Do you stilll use this? Do it actually work? I was told I would have to pay for one and dont know if it would even work for me .. x

 

 

Yes it works , But since liberation I don't use it anymore. I'm trying to retrain my brain.

 

Colmmc

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KateB

Colm you are really lucky to get this on NHS. I borrowed one from my Neuro Physio and it was wonderful - couldn't believe the difference it made. However, it is not available on NHS in my area, so needs to be bought privately - nearly

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debzsanderson

KateB - are you a member of the MS Society? They may possibly be able to help financially. The other alternative is your local Lions Club - Mark got a motorised exercise bike bought in full by them a few years ago and they are lovely people. It makes me so angry that equipment that can make someones life better is not supplied on the NHS!!

 

Good luck

 

debz xx


Mark has PP MS but I am his partner and do the posts as he cant use the computer!!

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colmmc

I don't know why your NHS hospital won't supply it it's approved by NICE ?

 

Colmmc.

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KateB

:moonieman: Great News! :cheerleader:

The "Friends" of my GP practice are funding the machine for me. I am getting it on Wednesday - great Christmas present.

Have a good Christmas everyone - I know I will with my new "gadget" :lolbash:

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debzsanderson

I'm so pleased for you-enjoy your "christmas present"!!

 

debz xx


Mark has PP MS but I am his partner and do the posts as he cant use the computer!!

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