The “Doing” that I am going to Keep Doing

 

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The doctor was so very pleased with my progress and the “life choices” I have made to thrive that she told me “keep doing what you are doing”. If you didn’t see the update from my latest MRI you can read it here. In this blog I am going to share with you all of my not-so-secret tips.

The first decision I made to thrust me into thriving was to guard my mind.  I have been in the trenches and teetered on depression many times but choosing to stand on truth and to live each moment with a heart of thanksgiving enabled me to pull up and out victoriously. Journaling thanksgivings in the mundane moments and times of struggling and choosing to see the gifts in every day has helped me pull through. Thanksgiving has been a life source.

Second, I chose to keep moving. When  I could barely walk unassisted, I said, “Look I can walk!”. Then I said, “Look I can take these steps without assistance” and then I kept moving. I used a stair stepper exercise machine. I would hold onto the wall or couch to balance and I could barely do it for three minutes before I wanted to break into a tear stained mess but I did it and then I worked up to four minutes, then five and then up to nine. A friend blessed me with a stationary bike and I found that to be much easier on my legs. I pushed my body to pedal, pedal, pedal and then I would cool myself down with ice packs. I found a way so that I could keep moving. Each day I strengthened my legs more and more. Pilates was also a wonderful tool I utilized to get a low strain exercise. It has been four years and I am still riding the stationary bike, stretching and strengthening my core with Pilates and light free weights. With each relapse I recovered better because my legs and arms were stronger. Ice packs are vital to cooling my body so that I can keep functioning after a workout.

Third,  I changed my diet. I know this is a hard one for a lot of people. I get it. We had slowly purged sugar long before my diagnosis but this was a step towards being healthier. My diet at the time of diagnosis was far from antioxidant and phytonutrient rich. A month after diagnosis and much research we chose a diet that was 99% Vegan for the first year. We chose to go on the diet as a family because we knew it would help all of us and it sure did. Even the children got a good body cleanse. We flushed out toxins and filled ourselves with healthy, vitamin rich foods. Since that first year, we have incorporated fish into our diet once a week and we take fish oil pills daily. The DHA and EPA is so very important for the brain. The fats we eat are from nuts, seeds, avocados, coconut oil, and coconut milk. We still enjoy a good quality dairy free dark chocolate. We don’t feel like we are missing out. There are lots of great tasting foods in our diet.

Fourth, I began taking Low Dose Naltrexone last year. This medicine is a natural route  in the medicine world. I was really struggling last year. I was having issues with bowel movements (due to numbness), dependent on walker with a seat so I could sit if  I had to do anything in the kitchen for more than five minutes  and I was battling other issues causing hindrances to my day to day enjoyment of life. It took the right pharmacy making the medicine, a few months of regularly taking it and I began to regain my abilities and experience a calm in pain. I am beyond thankful for this medicine. I recommend McGuff Pharmacy in Santa Ana, CA. They deliver within a few days. This medicine is a God-send.  Check out the research! It was also recently approved for M.S. You can click here and here to read more info. on LDN.

Last and just as important as the rest of these are the supplements I take. I took Juice Plus consistently for three years and I value this product immensely. These capsules allowed me to flush my body and fill it with phytonutrients and antioxidants effectively without the expense, time and work of juicing. I have been off of it for about six months as I take some time to try some other products but I have a feeling we will go back to JP eventually.

Here is the bulk of  supplements I am currently taking: B12, Turmeric Curcumin, Fish Oil, Vitamin D (6K), Plexus Probio (it has probiotics and digestive enzymes in one), Plexus Bio Cleanse (Vitamin C, Magnesium, Sodium Bicarbonate and Bioflavenoid complex- this helps me have regular bowel movements. Pro Biotics seem to stop me up. Sorry if this is TMI.)

And the two supplements that I recently realized are helping me to have WAY less pain are Plexus Ease (New Zealand green lipped mussel powder, bromelain, serrapeptase, turmeric extract) and Plexus Nerve (Thiamin, riboflavin, niacin, vitamin B6, folic acid, Vitamin B12, Biotin, magnesium, zinc, copper and a mix of amino acids, horse chestnut  extract 20%, butcher’s  broom root and quercitin).  I did not realize they were working as well as they were until I got off of them for a few short weeks. I  suddenly remembered what pain I usually experience during these hot summer months. Oh my. My nerves began going nuts again. I went back to not being able to turn clothes right side out and turn socks the right way. Owie! My feet hurt just walking on the carpet and my nerves frazzled. I just got my newest shipment and now my nerves are on the mend.  I don’t ever want to go off of these products again! When I shared with Dr. Neurologist she was amazed at how much these natural products are helping me. She knows where my damage is and where I should be having issues. It isn’t that my issues are gone. It is that the pain, lack of control and so many repercussions  that come from my damage are not as severe due to the products I am using.

I also use Essential Oils to ease discomforts and promote healing. I may have to do a seperate post on oils that I love!   ;^)

I am beyond thankful for God’s guiding hand and His grace that upholds me daily.

“He also brought me up out of a horrible pit, out of the miry clay, and set my feet upon a rock, and established my steps. He has put a new song in my mouth-praise to our God!”Psalm 40:2-3

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