Comments on: CCSVI Webinar

By: mary garner

mary garner — Tue, 17 Jan 2012 21:21:24 +0000

Hi, my name is mary and I was diagnosed in2005. Since then I have lost almost all walking . I live in OK and live alone. I have lost one of my children 9 months ago and eeverything has gotton worse. I ionly have medicaid and no help. PLEASE help me. Thank You, Mary Garner

By: denise vanieris

denise vanieris — Tue, 11 Oct 2011 17:02:00 +0000

I am taking vitamin d3 .I have read your pages that talk about taking the ESSENTIALS ,could you let me know what they are ? Sounds like I should be taking them. Thank you.

By: Debbie Allen-Czerwinski

Debbie Allen-Czerwinski — Fri, 02 Sep 2011 19:52:28 +0000

Hi everyone. I am having my ultrasound done in a couple weeks and the procedure the next day if needed. I’m going to Albany, NY. I am very anxious so glad to have the meditation to help. I’ll keep you posted.
Blessings,
Debbie

By: Debbie Allen-Czerwinski

Debbie Allen-Czerwinski — Tue, 26 Jul 2011 21:09:42 +0000

Hi Paulette,
How are you doing aince your July 12,2011 procedure? Where did you have it done?
Blessings,
Debbie

By: Wanda Donovan

Wanda Donovan — Wed, 20 Jul 2011 16:04:14 +0000

I have had MS for approx. 30 yrs. Last year i don’t remember much of as I was suffering from dementia , loss of bladder conrol, in a wheelchair, etc. After a friend finally got me admitted to a hospital I was given a Cat Scan and MRI among other tests. I was discovered to have Hydroephalus. They also found a tumor between the brain and the skull on the rt. side of the back of my head which was causing my brain to be squashed and too much spinal fluid staying in my head. They operated and put a shunt in my head. It is operated by a pressure valve so when there is too much liquid the valve opens and sends the excess down to my stomache through a small pipe like thingie attached to the bottom of the valve. (I don’t know what it is made of so i call it a drain pipe or thingie, Anyhow it works)

I had been in bed in the hospital for over a month plus in a wheelchair for at least 4 months, and the second day after my surgury was able to walk with a walker. Not very far as my legs were weak. I had the shunt put in Nov. 10th, 2010 and when I went back to see my Neuroligist on Feb. 14th. 2011 I walked in with a cane. He laughed, asked where my wheelchair was and I told him in the basement cupboard. He said are you showing off? I told him YES. He couldn’t believe how many of my symptoms had been the result of the Hydrocephalus and not the MS. My left side is still much weaker, my leg a bit smaller, plus my left arm will not fully straighten. My balance is not good but well enough for me to walk around the house without the cane. I can go outside, feed my 2 horses, minature donkey and goat, plus clean their manure up with the wheelbarrow. Though I am much stronger I would still like to know if I can still be a canadite for CCSVI testing hopefully in Canada. I know I am 67 but I would like for once in my life to be able to get up in the morning not in pain and not stagger around like a drunk.

I know everyone says they can’t beleive how well I am doing when a year ago it was thought I would have to be put in a Nursing home. However there are so many things I want to do that I haven’t been able to do for over half my life, like not be tired so fast, have a little better balance so I can go for a walk in the woods with my dog, and get on my horse by myself.

If you have any advise where to call re. CCSVI I would reatly appreciate it. I do live in Quebec, Canada.

By: Jan Conley

Jan Conley — Fri, 15 Jul 2011 03:32:39 +0000

I have had MS for the last 16 to 18 years with only small signs but in the past 10 years I have had a right sided limp, having to use a cane or a walker and at time, a wheelchair. I have slow movements in talking and use of my bladder. I get tired easily and can sleep for 10-14 hrs a day. My MS is progressing at a slow rate but when I look at the doctors chart it has me at chronic progressive. I am only 56 years old and want to live my life for my children and grandchildren. MS runs in my family starting with my Mother and progressing to my 2 sisters and myself. I didn’t know that it is heiratary? I eat only chicken, pork and fish and eat lots of salads and fruit. I take my essentials and vitamin D3 + Coral Calicum along with fish oils.
Could you let me know what other supplements I should take.

Gratfully yours JC

By: Amie Easley

Amie Easley — Thu, 14 Jul 2011 16:39:27 +0000

@Les(July 3)-I tried the glyconutrients a couple years ago and stayed on them for about a year. They are not cheap as I had to take quite a bit for my MS. I was doing better at the time(as far as my MS) but did not see any big improvements in that year. I then found Dr. Cartwright and take his vitamins and follow his recommendations. I started back on one part of the glyconutrients as well. Nothing has made a difference per se but I don’t know where I would be if I didn’t take them! They are worth a shot I’m sure. They swear they have healed many with MS.
@Lee(JULY11)-I am sorry to hear about your difficulties with the CCSVI procedure. I am scheduled next week but get a little discouraged when I read negative stories. I hope you will see positive results following Dr. Cartwright’s plan!

By: Dixie Baeke

Dixie Baeke — Tue, 12 Jul 2011 23:33:29 +0000

I am new to all of this had an MRI 4 yrs ago, showed white matter spots, had another 2 months ago same spots but not really any other systems besides floating feelings when really stressed doctors dont know if i have ms or not, whats your feeling on this?

By: Lee

Lee — Mon, 11 Jul 2011 19:42:10 +0000

I have had MS for 29 years even before the MRI was available. I went on bataseron 6 months after its release. I believe it slowed my progression but over the pass 5 years I was diagnosed with secondary progressive. I have spent allot of time through the years reading and tried conventional and alternative treatments for my MS. Dr. Cartwright you win the award for the best information and treatment for MS and I’ve tried and listened to quite a bit.
I had the CCSVI procedure done in April, 2011 and had right and left side blockage shown from the ultrasound. For 3 days after the treatment I had 3 noticeable benefits and then back to where I was. It was quite disappointing so I returned for a follow up appointment and the left vein (most of my symptoms affect my left side) once again was blocked the right was good. So with some discussion with the doctor he said he would do it again. Mind you my health insurance paid both times. The second time took a little longer and was more painful than the first time and had no noticeable difference. I just went back for my follow up and the bad news was that my left vein has completely collapsed no surprise to me. I have had worsening blatter problems.
I am unwilling to take the risk of putting a stent in it. Needless to say I need to continue to listen and follow Dr. Cartwright’s information!
Thank you for all your time and information and MS Health Coaching couse!

By: Adamu

Adamu — Fri, 08 Jul 2011 16:14:51 +0000

i’m ready for the CCSVI Procedure no matter how much it will cost because i spent over $10,000 every year for my treatment even though i’m getting better but i think with the CCSVI treatment i’ll feel more better.but my problem is that i want know much about it and how it’s done who are doing it and were,how much it will cost.i’m ready please.