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First of all I just wanted to introduce myself as I haven't been on this site for years.
I've had RRMS since I was 21 and I will be turning 40 in a few months. I would say that the first 13 years my symptoms were pretty mild and I recovered pretty quickly from them. Some I needed prednisone but for most of the symptoms, I recovered on my own.
In 2006, I had a bad attack which effected my whole upper body. Numbness, pins and needles, severe muscle aches, stiffness and severe coordination problems. Treated with prednisone and that lasted two weeks, but I still feel the pins and needles every day of my life for the past six years.
Up until 2010, I had mild symptoms.
2010 - numb from the waist down right down to the bottom of my feet. Severe pain as if I was being tortured. No exaggeration. I was walking like a turtle becuase of the severe stiffness and balance problems. Treated with prednisone. That one lasted 5 weeks. Until this day, I can't walk longer than 10 minutes without feeling tired.
2011 - Whole right arm right down to my hand and fingertips were numb and extremely stiff. I had no control of my arm and hand and had to constantly look for it because I couldn't feel it. I needed help getting dressed and cutting my food, etc. I couldn't use my hand at all. I had to learn how to use my left hand. That one was starting too so I only had 3 good fingers on that hand. I was using one hand for 2 months and I am still recovering. My leg was a little numb too and my balance was off. Couldn't wear heels. Again, I was treated with prednisone.
My fingers are still numb and my arms still feel achy and stiff. I have been on disability since September.
I've been taking Avonex since 2004 and my doctor wants to change my medication.
Anyway, based on the information I provided and in your opinion, does it sound as if my MS has progressed to the next stage and will my symptoms continue to get worse?
Getting info from my doctor is like pulling teeth. He's extremely busy and I am really worried. Can you please help?
Thank you!
JackieView Thread

My fingers are still numb too. I`m making a lot of mistakes right now as I am typing this. I know how you feel.
Thanks for the advice and I am considering firing mine too.
All the best to you.
JackieView Thread

I agree with Kate too. I am getting fed up with my neuro too.
I might make a change very soon.
Thanks for your response.
JackieView Thread

I was on Gabapentin for over a year but my neuro stopped filling my prescription without reason.
When I saw him last November he said he wanted to change my meds to Gilenya. I currently taking Avonex. I have not heard from him since.
I am considering looking for another neuro.
Thanks for your reply Carol and I wish you all the best!
JackieView Thread

Sorry it took me long to respond. I had trouble signing in.
I was thinking of finding another doctor too. He's a great neurologist and works out of the MS Clinic but I'm wondering if he's going to retire soon because he's elderly. He's always been so responsive in the past. He even called me at work once to discuss my symptoms and I was surprised.
My husband doesn't want me taking the drugs either. He said I was doing better without them and he thinks it's poisoning my system.
I personally don't like the flu like symptoms I get from the Avonex.
Thank you so much for your reply Kate! I wish you all the best!View Thread

Thank you so much for your reply. I had an MRI done in January an my doctor hasn't reviewed my results yet. I've followed up a few times and nothing. I feel helpless right now.
I would love to go back to work but can't right now. I'm afraid to go back in fear of another bad flare up which dibilitate me again. It's not fair to my boss to always be calling in sick eventhough she understands and has been very supportive.
I guess all I can do is keep hounding my doctor until I get some answers.
Thanks again!
JackieView Thread
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