What type of MS do you have?

I've been told I now have SPMS after 15 years of slow progressive decline, when initially told it was sensory benign!

I have rrms

 I have spms, diagnosed 3 years ago my balance is getting worse than it has ever been. 

Falling 2/3 times a week at the moment.

Jamielee1916@gmail.com

Makes me wonder what is next.

@jamie

Know the feeling Jamie, have just had to give mine up

Thanks for your message Ian I've had MS for 17 years now and not walked for about a year,but I can stand for about a 90 seconds at the moment.

But for most of the time I'm in a wheelchair.

What do you mean " give mine up" driving?

I'm suprised that I'm still not fed up yet,but I do know it will only get worse now.

The clock is ticking faster now!

@Michelle47 I also have severe headaches/migraines for up to 5 days which don’t seem to go with drugs all of them time and then only taking the edge of.  May not be MS related but my gut tells me they are.  I’ve found that cutting diary out has helped, and avoiding too much sugar and definitely no aspartame.  Hope they get better for you! 

Thank you 

have been really bad this week having a steroid drip for 3 days tomorrow be interesting to c if this helps yes i have tried cutting out diary and gluten it does make a difference, i feel diet really makes a difference hard to find a variety off food which dont contain some off these, i found a lady on you tube who controls her ms with diet her name is Pam bartha very interesting. 

@Michelle47 

Thankyou 

i have tried cutting out diary n gluten yes it makes a difference hard to find a variety off foods on this diet, I'm having to have steroid infusion at the min my main symptom is headache be interesting to c does the headache disappear, i found an interesting ladies story on you tube how she controls her ms symptoms totally through diet her name is Pam Bartha, 

I was told I have sensory benign ms then that it wasn't ms at all so I don't know where I am at but been ongoing for 30 years now. 

Hi guys,  im new to this site.i was diagnosed RRMS in 2014.  Just wanted to pick your brains!! I was told ive just had spinal relapse in Oct last year, had MRI 2 weeks ago and they have said no new lesions. I have been struggling with walking as right leg is weak with horrific spasms and now same in right arm. I have a tremor in left leg. Im soooo confused to what is going on, havent got a follow up app till 17th March. I feel so fed up. Feel like I'm imagining all these symptoms. 

Can there be decline with no lesions????

Jackie.