Wednesday, July 27, 2011

6 Months Post Angio Update

Hi all, A little note to show my progress to date. Video to follow on YouTube soon!

Someone mentioned to me the other day that I could sit outside in this heat wave now without my cooling bands. We rarely put the air conditioner on in the house. It is truly a miracle from God and I am very blessed. Thank God we have a pool to keep cool in though as well.

PHYSIO:
I have spent the last couple of months getting my strength and muscles built up through physiotherapy, swimming, walking and hiking. It is not going as fast as I had hoped it would and I am still finding issues with the muscles not responding as I thought they would by now. My feet and lower legs do go numb a bit after about 30 minutes of walking but not nearly as much as before procedure as they would be numb right up to my thighs within 15 minutes. . I go for a walk most days with my puppy Jasper (we share him with our daughter Lisa). After going head on into hiking on the beach with my walking sticks I injured a tendon and strained muscle in my arm which is still healing. I must learn to take things slowly which I am now doing so with guidance from my physiotherapist. We are hoping to know more about my muscle strength in another month. My physiotherapist holds out hope though, as he has seen progress made after one year where nerves and muscles respond after continued efforts, so we are not giving up. Riding a bicycle and golfing are my ultimate goals for this winter in Florida and this is what we are working towards at physio.

BLOODWORK & Physical Checkup:
Looking very good in all departments! My family doctor is very happy with my progress. No Babinsky's reflex, blood pressure great, losing weight for the first time in 12 years at two pounds per month so far. I can walk, stand, sit, twirl, dance etc...Bladder medication:Oxybutinchloride (Ditropan) was 3xday now 0. Except for the Interferon Beta 1A I take which is suppressing my immune system the way it is supposed to I would have a perfect blood workup! Energy is high and very little fatigue (only on the days after my needle).


NATOROPATHIC DR. TERI JAKLIN:Teri Jaklin in Costa Rica
I am being treated by Teri and I am following her plan for MS patients. This plan can be found here Nutritional Management of MS and also some great videos she has made with Dr. Mark Hacke, Dr. Bill Code & Dr. Joseph Hewett. CCSVI Videos (this will lead you to all 5 videos). They are all collaborating together to help us out with aftercare for angioplasty for CCSVI and have much good advice to follow. I was tested for food and metal sensitivities and have been found to have heavy metals more lead, aresenic and cadmium than anything else so am being chelated with drops for the next two months. (Air pollution, chemicals from my husband's workplace, years of smoking, my past work as a plumbers daughter and sister exposed me to a lot of lead solder, pipes etc.) My metabolism is basically zero which is no surprise to me. I am taking Dr. Jaklin's Neuroform B complex, multi strain probiotics, using castor oil packs and eating basically rice, salads, vegetables and fruit. Protein is powder, hemp hearts fish, eggs, chicken. Found some new recipes so I have been trying out a few. I do not like quinoi which is a powerhouse of protein so must use other things instead. I have just found some I can tolerate in my favourite breakfast cereal mix from  ECO Planet Organics Instant Hot Cereal Apples and Cinnamon which I use as a topping for my fruit bowl along with some goat yogurt and molasses. I am now taking 4000 Vitamin D-3  and sitting in the sunshine as much as possible. Because I do not eat fish I take Fish Oil Omega-3, 1000 mg with epa 1200, Natrol Green Tea Capsules Milk Thistle to help my liver,  and I take Natural Calm with calcium and zinc. Kale, Romaine lettuce, spinach, napa cabbage are my greens of choice along with parsley, time, oregano, cilantro, basil from my garden. Squash, broccoli, zuchinni, Organic Tahini ,Almond Butter., Organic Texmati Brown Rice, Himalayan Red Rice,  Tinkyada Brown Rice Penne Pasta are now staples in my cupboards. Sheep and goats cheese and yogurt and almond or rice milk for cooking and blending. I use honey and mollasses for sweetening and baking. I did not have egg sensitivity so for that I am most grateful as I do like to use eggs in my cooking and baking. I must say here that I am no longer burning from pain in stomach and colon. There is a noticeable improvement in bowel function. I am not totally gluten, wheat or meat free but am dairy free now, I am getting there, as it is very hard.

EMOTIONS:
Depression has lifted about 75% I still feel down a few days but find it does not linger on like before. I have not cried in over six months. My husband would say this is the miracle as I cried all the time before procedure. (He is a saint!) I am happy and smiling a lot. People tell me I am glowing!

NEUROLOGICAL CHECKUP:
August 2-Good checkup. Because I am not in inflammation at this time and I am doing so well I have decided to go off of my Interferon. The side effects are taking a toll on me and I would just like to see if my body can clear the after effects and come to some sort of balance again. Please say a prayer for me that all goes well and that my healing continues. I have two very good doctors supporting me and a lot of peace from the Lord as well. We will be doing an MRI comparison of before and after in December so I will keep everyone posted.

Thursday, July 21, 2011

Videos Posted by Barbara Iglesias Garcia: Pop Up Video (8)

Fabulous Dr. Bulent Arslan in a great video message with my friend Barbara Garcia.

Videos Posted by Barbara Iglesias Garcia: Pop Up Video (8)

Saturday, July 16, 2011

Dr. Bulent Arslan Interview re:CCSVI Angioplasty Treatment

Here is a wonderful article from an interview with my fabulous Dr. Bulent Arslan from Moffitt Cancer Center in Tampa Florida discussing CCSVI angioplasty treatment.

MS Controversy: Inflating Veins, Deflating Symptoms - Health News Story - KSAT San Antonio

Wednesday, July 13, 2011

Blood Thinners & Supplements Pre & Post Angioplasty

A very important note from Linda Roussey about blood thinners before and after angioplasty. I would also add: regular or low dose Aspirin & FIsh Oil should not be taken before angioplasty as well. I stopped 7 days before and resumed after Plavix (or your prescribed blood thinner) was finished.

Here is the link:

Blood Thinners FYI (411)

Monday, June 27, 2011

BREAKING NEWS! SENATOR JANE CORDY TABLES CCSVI BILL S-204 in SENATE

Here is the link to:

BREAKING NEWS! SENATOR JANE CORDY TABLES CCSVI BILL S-204 in SENATE

5 Month Post Angio Update

Today I am 5 months old in my newly transformed body and I am doing fabulously well! I have been doing lots of walking, shopping, Nordic pole walking along the beach and hiking. I am doing everything I have been dreaming about for a while now and I feel wonderful. This weekend we went to the Pinery Flea Market and walked all around the whole place with Meridsy. We watched a magic card trick lady demonstrate all morning, bought a pink flamingo, fudge and popcorn, sat on an amazing wooden garden set and had a good time on a beautiful Sunday. I am a little sore from my old muscles being used for the first time in a good way for a long time but with the help of Dr. Teri Jaklin and trying to follow her good nutritional and healing advice to keep my blood flowing and giving my muscles the nutrition and energy they need to function properly, it seems to be working. I am getting stronger and am trying to adjust my whole being (Spirit, Soul & Body) to this new paradigm shift. I am reading a book without any pain or cog fog it is wonderful and a wonderful book it is” CCSVI as the Cause of Multiple Sclerosis by Marie A. Rhodes: The Science Behind the Controversial Theory. Going to try riding a bike soon, booking tickets for Jesus Christ Superstar at the Avon theatre in August and WWE wrestling is coming to London in September and I am going! Whoo Hoo! If Josh Groban is anywhere between Detroit and Toronto I am gonna go to that too! Sign Me Up! I’m In!
Love and Blessings to all
Wendy
PS my friend Tim Donovan is going to be in London & Sarnia to rally support for CCSVI Treatment in Canada. Please support him and stop by to see him and if anyone you know with MS and wants to learn about CCSVI treatment come on out and hear his amazing story. You can find out more at http://www.newhopeforms.ca

Friday, June 24, 2011

EGCG (green tea) - an iron chelator, anti-inflammatory and super anti-oxidant

Why Green Tea Extract EGCG should be used by people with MS & CCSVI. Drinking green tea is also a plus as it is full of antioxidents, polyphenols and good for our whole body as well. Here is an article about it by Joan Beal:

EGCG (green tea) - an iron chelator, anti-inflammatory and super anti-oxidant

Monday, June 6, 2011

Two Month Update

Sunday - two months post angio - too busy having fun to post - I will try and write something soon!

Three month Doppler Ultrasound & Update

‎3 month doppler test done! Results: 0/5 criteria for CCSVI. I am 100% flowing free! I feel wonderful. I have had a great miracle from the Lord and I am very grateful to all who have prayed for me and supported me! Thanks Be To God for sending Dr. Arslan to us. Blessings to all who are on this journey to the truth about MS & CCSVI. For more results please see my note:What I can do today. Blessings Wendy

What I can do today...

What I can do today...

by CCSVI Treatment for Wendy on Tuesday, May 3, 2011 at 7:03pm
Today I can go for a walk, shop, attend pro sports events, dance, swim, sit in the hot sun all day long, carry my own groceries, push my own shopping cart, unpack them all and put them away, wash and dry and style my hair, stand up and have a shower, bend over and touch my toes more than once, walk without assistance and not fall into the bushes or walls, bend my toes, feel a ladybug land on my leg, feel a bee sting, feel my husband's skin, feel his mustache tickle me when he kisses me and more, I do not cry and have not cried except for tears of happiness since January 27, 2011, I can sweat, I can feel the sand under my feet, I can feel that the patio stones are hot and have crevices and cracks in them, my feet do not burn when I put them into the water, I have no more hypersensitvity in my feet, I do not have hot flashes, I have good blood flow, I know my brain is healing. Today I can do anything!

Four Months Post Angio Update

CCSVI Treatment for Wendy
Today is my birthday! Four months old as a new woman! Yesterday I shopped alone for four hours! Bought and carried all my own stuff including three ceiling fans, drove all over town, walked around and window shopped. For the past three weeks I have been doing spring cleaning and organizing my house. Today is more cleaning upstairs -has to be done before the weekend. The only two days a week I am down is when I get my Avonex needle. This is for all you naysayers, keep the placebo effect going! I am living my life and lovin it happy and healthy and whole again! Thanks Be To God who gave me this wonderful miracle through Dr. Arslan's skillful hands. Blessings to all. Wendys.

Saturday, June 4, 2011

POST ANGIO:Nutrition, Vitamins & Supplements for Vein Health

I have recently attended Dr. Teri Jaklin's wonderful Naturopathic Health Clinic in Waterdown Ontario and am starting a new way of living. I will keep you posted as of next month on the new way of eating, exercising and supplements I am now taking. I wasn't too far off the mark along the way I was taking so I don't feel bad and realize because I was trying to do the right things - my health improved and the success of my procedure is proof! More to come...

Pre-treatment Diet, Nutrition, Vitamins & Supplements & Exercise

This is an outline of what I have been doing for the past ten years before treatment for CCSVI in order to create an environment for my body to heal and become stronger from a devestating attack of MS. You can find out more, get some great recipes and read excerpts from my journey through MS by purchasing my cookbook "Recipes From The Heart Complete". This book is filled with wonderful recipes, hints and tips using organic, fair trade products from Blessings Coffee Break.

The Diet: 

I had a very compromised digestive system after my MS attack and could only eat mashed potatoes for weeks after, then the first meat I could eat was of all things a hot dog! (I still enjoy a hot dog about once a month with vegetarian chili!). I now follow a diet utilizing low Fat, no saturated or trans fat ingredients.I cleaned out my cupboards and try not to use any processed food. My baking supplies and spices are organic and whole whole grain & gluten free, organic fair trade cocoa and dark chocolate.  I use Extra Virgin Olive Oil to dress salads, and cook with. Eggs three times a week or more. Organic, Fresh fruits and vegetables from the Farmer's Market in season and frozen vegetables in winter,  local honey, apple cider vinegar, organic whole grains, rice & oats. I recently started going less dairy & more gluten free using rice and almond milk for cereal and drinking. I  have a probiotic capsule every morning.  I eat mostly chicken, fish, and seafood instead of beef or pork (harder to digest) except in spagetti sauce - a small amount of ground beef in the sauce does not seem to bother me and I do substitute ground chicken or turkey in my sauce and chili as well. I make my own french fries coating the potatoes with spices and olive oil spray then baking in the oven. Sweet potato fries are great this way as well. For Poutine (a family favourite) I usually use pork & beans for the gravy and shredded low fat cheese to melt on top! Delicious! I drink lots of organic, fair trade green tea, white tea and black tea, & coffee because we sell it! Blessings Coffee Break carries Numi, Choice & Equita Organic Fair Trade teas and Level Ground Trading Ltd. Organic Fair Trade Coffees from around the world!

The Supplements:
ECGC-Green Tea Extract I take one/day.

The Vitamins:
Multi Vitamin I take 1 day

Vitamin D3 I take 2000/day in summer and 4000/day in winter
Vitamin C I take one or two per day summer and winter
Vitamin B12 sublingual I take 1 day 

CCSVI Treatment for Wendy

CCSVI Treatment for Wendy
May 27, 2011
Today is my birthday! Four months old as a new woman! Yesterday I shopped alone for four hours! Bought and carried all my own stuff including three ceiling fans, drove all over town, walked around and window shopped. For the past three weeks I have been doing spring cleaning and organizing my house. Today is more cleaning upstairs -has to be done before the weekend. The only two days a week I am down is when I get my Avonex needle. This is for all you naysayers, keep the placebo effect going! I am living my life and lovin it happy and healthy and whole again! Thanks Be To God who gave me this wonderful miracle through Dr. Arslan's skillful hands. Blessings to all. Wendys.

I am not a particularly brave person... - CCSVI Locator

I am not a particularly brave person... - CCSVI Locator

that is for sure. I am a big suck when it comes to pain consequently my hubby rushes to bring me sweets and ice cream when I am feeling pain. I was in pain most days. I found a great  over the counter medicine to take which helped me a lot and I found that  heating pads, prayer, meditation and music also soothed my pain. I never quite understood all the pain I was in.   I was told it was caused by the deterioration of the myelin sheath covering my nerves. I was told some of it was just "sensation" and it would not hurt me... but i did hurt. I was told not to worry and to just  carry on when I had chest pains so bad I thought I was having a heart attack many times. I could hardly breathe or move some days it hurt so bad. I was told that my muscles would heal and work better if I used them more, I did, but it hurt so much. Epsom salts baths would help a lot with muscle pain and heating pads as well. I was told to do deep breathing exercises and sing. It hurt but I did it anyways. I smiled even though it hurt. I tried to learn new things to keep my brain working and to think clearly even though that hurt. January 27, 2011 my IR Dr. Bulent Arslan performed simple angioplasty for CCSVI, opening my blocked azygous vein, and right jugular vein valve and upper vein. Today the only thing that hurts is my heart and that is breaking for all of those suffering with Multiple Sclerosis whose hope is to be diagnosed and treated for CCSVI and have some of thier symptoms releived in Canada.

RESEARCH:

The following research is how I made my decision to have treatment. I spent over two years reading and researching before booking my treatment with Dr. Arslan. At times I had to read two three and four times and ask people to help explain it to me. I have made some wonderful friends on facebook including doctors and nurses who know how to turn medical jargon into plain English. Many thanks to my facebook friends Joan Beal, Sief Hart and Dr. Bill Code .

Must Read: All of the notes from Joan Beal's Facebook Page:CCSVI-in-Multiple-Sclerosis. Also the whole CCSVI Alliance website including videos.

Great research links can also be found on Facebook:Denise Manley Facebook:All notes & papers links in one place

If you have not read this research it is not a good idea to book treatment. If you find it too difficult to read and understand the research please ask someone to help you.

CCSVI Treatment One Month Post Angioplasty

This has been such an exciting month for us. New changes every day. My vision and hearing are so much better and we notice things every day are different. I have so much energy it is astonishing! Meeting our new neighbours in our park in Florida I am very surprised how easily I can remember all their names and introduce them to others as well! My Sudoku puzzles are getting easier to do and I have more "I won"s than "I lost" than ever before in my book. My dry mouth is definitely diminishing and my bladder and bowel function is vastly improved. Heat intolerance is somewhat better but not so dangerous as before treatment. Pain is minimal...still no neck pain or need to prop up my neck with pillows and flax wraps. Life is Good!