We are a member of the Fund Raising Standards Board

 

We are all volunteers and the advice we receive is also given freely.

 

All donations are used to further the work we do.

 

Please Donate

 

Join Us

 

Provide Support

Buy At

 

UK Charity

No 1131517

 

Copyright © Proventus 2010

 

Terms & Conditions

 

Help-Line 01233 334879

 

Proventus

Making Life Fairer

 

Working Together to Make a Difference

UK Charity No 1131517

Peoples Stories

Working together to make a difference

Find Us Here

You tube
Follow Provpeter on Twitter
You Tube
twitter

Secondary Progressive MS

 

Paul’s first symptoms appeared in 1991 with loss of balance, dizziness, pains in legs and double vision. First diagnosed with multiple sclerosis in 1996 following a MRI scan. Paul has been unable to walk (even a couple of steps) and therefore has been totally dependant on his wheelchair for the last 4-5 years. He is still able to stand by pulling himself up with the use of support rails.

 

Paul suffers from muscle spasms and uncontrollable shaking of both legs every morning and occasionally during the day. His left leg is still capable of exerting forward pressure though his right leg cannot exert any pressure. He suffers from regular back pains.He has almost no manual dexterity with his right hand (Paul is right handed) therefore cannot write (sign his name) eat, shave etc with that hand.

 

Paul uses his left hand to eat with though cannot write with it. Shaking in his left hand is evident when lifting food from plate to mouth etc.

 

He suffers from headaches/migraines every couple of days (relieved with gentle massage to back of head). His speech has slowed a little though is mainly unaffected though has been slurred during relapses but has so far always recovered. Paul can no longer read a book, in his right eye his vision is clouded, left eye vision is also clouded in the morning, but clears towards the end of the day, he suffers from double vision when tired.

 

Has a permanent catheter connected  directly into bladder.

 

Paul has taken three forms of  beta interferon the first was discontinued after a relapse (first/second year after diagnosis). The second one was Avonex a weekly intra-muscular injection, these injections drained him of what energy he had, taking 2 days to recover from each injection, this treatment was discontinued after a few months. The third one was Rebif a 3 times a week injection into the stomach for 10 months discontinued treatment after a relapse had occurred.

 

He now takes Baclofen (muscle relaxant) 7-10 10mg tablets per day, Coproximal (pain killer) 7 tablets a day and a monthly B12 Injection.

 

Notes

Source - Personal story submission - Paul Burton Told by Paul’s brother, Steven...

Top of Page