Watch my friend Donna, who I went to india with, take her first steps in ten years, the day after the liberation treatment. She is now regressing but still hopeful. See full interview: http://www.edmontonjournal.com/videos/Health/video.html?embedCode=E0YmZnMjr9WxntkpmFzvKnSVnXf1hvec
Posts Tagged ‘Crystal Phillips’
One year ago today, the urge to treat my MS 100% naturally had built up enough for me to get off the daily injectable I was on for 5 years!
At this time last year, I also lost vision in my left eye so the decision made a few friends and family members a little nervous and my doctors very nervous.
My neurologists wanted me to go on steroids and a new injectable drug that may cause liver damage. One of my neurologists even painted me this pretty picture: “You’re disease is very serious, it’s progressing and it only takes one lesion to flare up and ruin your life. I don’t want you wheeling in here in a wheel chair next year and tell me that you wish you did everything you could. I strongly suggest you try these new drugs.” hmmm some encouragement that was! The thought of pumping my body full of poisons that will give me flu-like symptoms for months, possibly destroy my liver and trusting this negative neurologist who was chugging diet pop throughout our entire meeting was WAY scarier than the “risk” of going drug-free. My diecision was made.
With only a minor relapse in the winter (double vision for 4 days), this last year has been my healthiest year since my diagnosis 6 years ago AND my MRI in January showed no disease progression. It has been win-win for both my health and my career. Working as a Natural Nutritionist and continuing my studies in herbal medicine have really helped me stay encouraged and confident to stay drug free and the fact that I feel better doing my natural thing keeps me encouraged to stay on this same career path.
I would also like to add that my “natural thing” does not not include some magic supplement or secret diet plan. It is simply enjoying a fresh, wholesome diet and thinking healthy thoughts.
So the only wheeling I’m going to be doing this year is on my road bike in Panorama for the Branch Out Bike Tour ;) https://www.2mevents.com/pledge/249
Cheers to a healthy future!
You would think after skating season finished a few weeks ago, I would be less busy not having to train 4-6 hrs a day. I worried about that since I seem to be more stressed out when my plate is not full. Thankfully, The Branch Out Bike Tour project (www.branchoutfoundation.com), working as a sports nutritionist at Athletes-Nation, continuing my herbal medicine studies at the Wild Rose College, moving, and getting a million medical tests done by Dr. Bruce Hoffman is keeping my plate full
Since going drug-free last May, I decided to continue my healing path, the natural way. I was referred to a private medical doctor, Dr. Bruce Hoffman (http://www.hoffmancentre.com/), who just happens to also use herbology, nutrition, homeopathy, meditation, vitamin/mineral therapy, aromatherapy and energy healing in his practice. Surprised I chose him ?
The good news is that Dr Hoffman is a Doctor who is open-minded……crazy right!!? The bad news is the price tag. As holistic as Dr. Hoffman is, he is still very scientific and, therefore, has his patients (especially me) get a million tests done here and ships the samples of, well, you name it and I gave it, to some of the top labs in the world.
By million tests, I mean 16, but still.
Here is the list of tests I got and the hefty price tag that comes along with them. Not exactly your regular GP tests….
Physical Exam and CLS Review- $150-$300
Calgary laboratory Services tests (blood, urine, ECG)
Heart Rate Variability
Heart Rate Variability/Valsava Test-$120
Body Composition Analysis-$60
MRT- Food Allergy Testing-120 foods and 30 chemicals (blood) $550
Hair Toxic Elements Exposure Profile-20 (hair) $275
Individual Optimal Nutritional Profile-20 amino acids (blood and urine)
GI Effects- gastrointestinal Function Profile (stool) $690
Full Panel-E2, t, D&C 1-4 (saliva) $475 (hormone testing)
Neuro screen basic (urine) $495
Stimulated Comprehensive Cytokine Profile with PHA-LPS-Candida (blood) $110 (check for yeast overgrowth)
Complete Lyme- Western Blot IgG&IgM, IgG/IgM/IgA IFA and PCR (blood) $800
*It is very common that MS patients are misdiagnosed when they actually have Lyme’s*
Methylation Test (blood) $625
A couple visits with Dr. Hoffman- $500
This comes to a grand total of $5200 + tax, and that is before treatment!
Thanks to continued support through the Crystal patches campaign, I was able to cover all these costs and finished getting all these tests done last week. On one testing day, I filled 18 vials of blood after food fasting for 13 hrs prior and was only able to drink two cups of water! No fainting, but close.
I am now waiting for my results and treatment plan which I am hoping I’ll get in the next month or so. As for my health right now, I am feeling great with just a little numbness/burning sensation in my left leg.
Cheers to a healthy future!
On January 3rd 2011, I went in for my 8th MRI since my diagnosis in 2005. This was also my first MRI since going off drugs in May 2010. All of my previous MRI results leading up to this one have either shown progression (new lesions in my brain and spinal chord) or inflammation on the original lesions.
Lesions or “plaque” found in the brain and/or spinal chord in MS patients represent damage to the myelin sheath. This damage is what slows or delays message transmission causing a large variety of symptoms. My most severe symptoms to date have been numbness/burning/tingles/weakness in my left leg, loss of bladder control, fatigue and loss of vision in my left eye (most recent). The only symptoms I am experiencing and have been for the past year is some vision loss in my left eye and minor numbness/burning sensation in my left leg. The fascinating thing about this disease is that no two MS patients are ever the same.
I am very happy to announce to you today that after 9 months drug free and 6 yrs since my diagnosis, my MRI showed no inflammation in my current lesions and no newly formed lesions. This is my best result so far and I’m sure you can guess my answer when my neurologist asked if I wanted to go onto Rebif, an interferon injection with a risk of liver damage.
What an MRI looks like:
On May 1st 2010,
I decided to go off “Copaxone” AKA “Glatiramer Acetate”, a daily injection that I was on for 5 yrs to help reduce the severity and frequency of MS attacks by 20-30%… maybe. There is no real way of knowing if the drug is working since all MS patients are different.
As I am sure most of you know, I lost vision in my left eye (optic neuritis) due to my MS which spawned the Crystal Patches campaign to help me raise money to get tested for CCSVI, a controversial new finding by Dr. Zamboni from Italy, linking a vascular disorder with MS. Losing vision was actually a push for me to follow through with my goal to go drug free. My neurologist, Luanne Metz, would probably be disapointed to know that she is a big reason why I decided to finally make this scary and lonely choice.
Why did I go drug free?
I went drug free for several reasons. If I sound a bit bitter, it is because I am….
Since my diagnosis, my neurologists have often made it seem like an MS patient has no control over this disease as it is completely unpredictable. They focus on how serious this disease is and how ugly an MS patients’ future can look like, especially if you do not go on the drugs prescribed.
Now remember, I am not saying this because my profession is in the natural health field nor am against ALL pharmaceutical drugs and medical doctors. I am speaking through my personal experience as an MS patient who cried many tears after hearing the fear tactics that my Canadian neurologists have instilled in me and after taking a daily injection for 5 yrs with little to no improvements with my disease (i.e.- new lesions in my brain and spinal chord were still appearing on MRI scans and I was still experiencing minor relapses and many symptoms).
In MS, you CAN take control and be proactive in aiding your body to heal itself. You DO have red flags that your body screams at you before going into relapse. You do NOT have to rely on drugs and expect to sit back and do nothing other than cross your fingers in hopes that they work.
When Dr. Zamboni’s publishings on CCSVI became public, you could not even call the MS Society OR the MS doctors or MS nurses to ask questions about it, even though stories of MS patients going from wheelchairs to walking post-Liberation Treatment became more and more prevalent (Donna, the lady who went to India with me had amazing results).
When I saw my neurologist, Luanne Metz, to talk about my optic neuritis, I asked her opinion about CCSVI and the “liberation treatment”. She immediately shut the idea down with excuses like “there is a strong psycho-somatic effect with the Liberation Treatment”, “I do not reccomend it and do not see any point in researching it further.”
Well, maybe it is a psycho somatic effect and not the final answer or cure for MS, but is it not worth pursuing when results seem to be so amazing? And if Luanne Metz, the other neurologists and MS pharmaceutical reps really believe that the liberation treatment is an effective placebo, then why are they trying to get me on liver toxic drugs (“Rebif” specifically, a drug that you have to take monthly blood tests because of potential liver damage shown in the clinical trials)? versus prescribing me an unharmful sugar pill? Or better yet become a psychologist to enhance the psycho-somatic placebo effect? The point is, after that appointment I decided to not only get tested for CCSVI but to also go against what Luanne prescribed and go off all drugs.
After my diagnosis , it was not until I started eating and thinking healthier that I really noticed huge improvements with my disease. I was able to train full time again and even qualified to race in the 2010 Olympic trials, finishing 10th in the 1000m long track. I give no credit to Copaxone, and 100% credit to diet, lifestyle and my friends and family who have given me so much support along the way!
Copaxone costs about $1500 a month! I know this sounds pessimistic but what pharmaceutical company who is making that kind of money wants to find a cure? Especially since you do not necessarily die from MS, meaning you could be taking those drugs for a LONG time.
Taking a daily injection that causes pain, bruising, swelling and hard lumps…sucks.
Going off drugs will force me to be extra proactive and keen on finding alternative remedies for multiple sclerosis and overall health
How Am I feeling 6 months drug free?
I am relapse free since going off drugs!
I am back training full time with lots of energy, strength and working on getting my endurance back (started training later than normal this year so have a bit of catching up to do).
I lost vision in my left eye while on Copaxone and it has not fully come back and may never. I still find it very interesting, though, that I have 80% vision when my heart rate is under 100bpm but within seconds of exercising and my heart rate goes above 100bpm, I lose almost 100% vision again. This occurence is what still has my hopes up that there is something vascular going on and that I may still be eligible to get the liberation treatment in the near future. My tests in India showed that my left jugular vein is half the size of my right….maybe this IS the cause. I’m determined to find out.
My next MRI is in January 2011 and will be the real test to see whether my disease is progressing, staying the same or dissapearing since going off drugs.
Would I Ever go back on Drugs?
I am not ruling that possibility out, but for now I am happy and feeling healthy off of drugs. There is still a lot of great research going on and new promising drug therapies but obviously my guard is up so it will have to be a pretty convincing study for me to go back on.
How do I treat my MS naturally?
I do not think there is one treatment for all MS patients which is why I do individual nutritional consultations with all of my clients (do not only work with MS patients). However, Dr. Ashton Embry has done amazing work and has had very successful results with his dietary and supplemental reccomendations for MS patients. My diet is similar to his reccomendations that can be found at direct-ms.org. If you or someone you know is interested in an individual nutritional consultation or to have me to a nutrition seminar you can contact me at email@example.com or 403.200.0494.
Cheers to a healthy future!
Oopsies…. 4 months and not 3 months off medication (at the time of the speech).
Thank you to all those who watched my videos. I definetely bounced all over the place throughout the talk but look forward to continueing and improving my public speaking skills and hope I was still able to get my message across. Any constructive critisism is more than welcome!
Cheers to a healthy future!
On August 28th, I was asked to do an inspirational talk at the “Skate Like a Girl” camp at the Olympic Oval, Calgary. I had a whole hour and decided to tell my story on how I managed to overcome many obstacles in sport and with my MS and what lessons I learned along the way. It was such a rewarding experience and I look forward to learning from and improving my public speaking skills as I do more. I hope my message can be taken and applied to anyone’s life hurdles in some way or another….
The following video is part 1 of 6. I will post a new video each week as the presentation is quite long.
-Numbness and tingles in muscles not ligaments
-I was actually 18, not 17, when I first lost feeling from my chest to my toes.
-Named Laura not called Laura
It’s been about three weeks since I got back from India and it has taken a long time to get back into a routine and a different routine then I have ever had before. In the past, my typical summer day consists of waking up and eating, training, eating, napping, training, eating, sleeping. ahhh so simple!
Things are a little different now for a few reasons. A) I just started training this week in comparison to starting in May. Because of my last relapse of losing vision and sensation in my left leg I have had to take a much longer off season. B) I am trying to find a new path to healing, starting with finding a neurologist/doctor/naturopath or healer of any sort with a scientific yet wholistic background and approach. C) I am living in Edmonton for the summer with my parents and working in a big kid job in St. Albert as a performance nutritionist. (more…)
In a few hours I will finally be discharged from the hospital and free to see India for the first time. I can just imagine how grounding it will be to see what the majority of the population lives like.
Donna is doing really well with noticeably more feeling in her hands and feet. This is a good sign and I have a feeling that it is only the beginning of her improvements. I only got to see her briefly yesterday but will, of course continue updating on her progress. (more…)