Imagine you are blind. You get a cut on your foot because you tripped and landed on a sharp edged stone cause you did'nt see it! Now imagine you go to your local Canadian emergency department because you are bleeding and need a stitch or two to stop it. They say sorry about your luck we cannot treat you because you are blind! Now what would you do. I would take the money out of my piggy bank and take a little trip over the border to get a stitch put in by the helpful doctors in the good ole USofA.

Now imagine your problem is a vascular one. You have a swollen, red face, your hearing and sight is compromised. You are in extreme pain in your neck and muscles. You have swollen hands and feet. You are turning an ugly shade of yellowy gray. Your feet are blue and purple. Your mind no longer functions and your head is so fuzzy you think there is a dark black cloud taking over in there. Your brain is mush and you cannot read, think or comprehend anymore. You will need a specialized ultrasound, MRV and venogram angioplasty procedure to diagnose CCSVI and correct it. You see your doctor in Canada and he says sorry my hands are tied because you have Multiple Sclerosis. Go see your neurologist about this problem. You see your neuro who says your vascular problem is normal for people with MS. Your blocked veins have nothing to do with your Multiple Sclerosis. After ten years we will give you an MRI to check out what's happening with your brain. There is nothing we can do for you. Do not go off your $1800.00/month meds (which make you sick for two days out of seven each week and have compromised your immune system). See you next year!  There is no response from the neuro about the MRI results. I don't get it! We cannot be treated for a venous insufficiency because we have Multiple Sclerosis?

I see on facebook people with the same symptoms as me going to Poland, Costa Rica and USA for CCSVI treatment coming back to say they could now function like a normal person. What would you do?  Well I went to the good ole USofA where compassionate doctors are treating people with CCSVI. (Chronic Cerebral Spinal Venous Insufficiency). I have a Canadian diagnosis from a Canadian Doppler Ultrasound and a Canadian doctor which states I had 3/5 criteria for CCSVI (which, by the way, no Canadian doctor told me this it was the American doctor). Canadian Phlebologists agree that CCSVI is a known vascular disorder. Canadian Interventional Radiologists treat CCSVI in kidney, cancer and heart patients among others everyday in Canadian hospitals. 50% of patients USA doctors are treating for CCSVI are Canadians! What is this saying about our health care system.

This Canadian has now been Liberated by a simple angioplasty procedure from a compassionate doctor in the USA. I can now walk with no pain, sit with no pain, think with no pain, sing with no pain, swollen face - gone, pink and healthy face, feet, brain. Weight of at least 25 lbs on each arm and leg -gone. MS Hug and breathing problems - gone! Extreme fatigue and overheating - gone! Dry mouth, Tongue and throat-gone! Bladder and bowel funcion much improved! Hearing and eyesight improvements and much more as I am getting better each day.

Discrimination is just wrong. Discrimination against people with disabilities is much more wrong. Stop the discrimination against people with MS. We support the charter challenge for discrimination against people with MS. Please help our cause. The sooner we can file this challenge the sooner we will see CSSVI testing and treatment for Canadians. http://angioplastyforall.com/ anything else is unacceptable!

Dr. Arslan shares success story with us all!