The Time is Coming

Well I think its time for an update post.

I got back to the Hansa Center for visit 2 in less than a month. I stop all of the remedies I started in January in just a few days, March 14.
Before I go back I will have to repeat the initial bloodwork and I will also repeat my hair heavy metals test. I am hoping to see high levels of metal dumping out into my hair because its leaving from my body(finally!!).

I had my last ND appt. in December. It has been so nice to get off all of the supplements they had me taking!  Most of these did very little for me, I had to add in herbs to treat my infections. Since changing to the Hansa Center from the ND I have noticed an enormous difference in how I feel.
The ND used SCIO biofeedback that is capable of testing supplements with my body to see what kind of reaction. The HC uses BioResonance Scanning, which is a form of muscle testing, that also checks my body's reaction to the remedies.

The ND had a very similar technology, just not the same resources and know how behind it. Its amazing how much the doctor themselves will affect the patients outcome just by the supplements and treatment methods they prefer. My ND had many of the same supplements and even some of the same training, but its taken the strong detoxing and specific remedies to make a difference in my health.

Anyway, I think I have proved my point that I really do love how the doctors at Hansa treat their patients. It saddens me when I see people like Parker Goertzen fail...
with LLMD's you typically pick your favorite most convenient doctor. They will all try the same group of antibiotics, IV's, and herbs. The HC is different, they have about 3k remedies to pick from, not 100-200 the better LLMD's have.

------Back to me------

My current symptoms are Insomnia, fatigue, exercise intolerance, and no concentration.
Overall I don't have the sick feeling I used to have, the sauna keeps my muscles fairly loose, I have had very little dizziness or pain. At this point I just need to get my resistant symptoms knocked out. This will hopefully be finished up after the next visit.

I have managed two long and strenuous school fieldtrips in the last month and the flu since coming back from my last HC visit. Beforehand all of this would have knocked me down significantly.
All that has happened since these things is extra fatigue, its a problem but I am not stuck in bed!

Now I just need to get back to my juices and smoothies....I have ingested more junk food in the last month than I care to admit to! They sure do make a difference.

I Would Like to Ask for Something

As you all have seen I follow many blogs, at some point I think I've mentioned most of them. A few months ago I posted about one blog in particular, Ticks and Trust. This blog is written by a Canadian mom who also battles Lyme disease and several co-infections. Several years ago her son Parker was also bitten. Shannon has since been able to better than when she had a full blown set of infections constantly. Parker however has not been able to become assymptomatic. He reached remission once, but the pain never fully went away. Now he is doing worse and nothing seems to be making him well.

The faith and confidance in of this family has been challenged so hard. I think many of the people who read my blog understand what it's like to he chronically ill because most of them probably are. But this family, nearly all of them have been Lyme positive at some point. Nearly all of them have been through Lyme treatment. They have all had to deal with trying to find a doctor to treat them, which has turned into multiple doctors and multiple treatments. Shannon's oldest and youngest are doing well how, but her middle child Parker only knows suffering at this point.

I would like to ask for prayers for the Goertzen family. I know what it's like to be the sick kid whose just held back by everything, thinking about other kids like Parker who are much worse than I ever was just makes my heart break.
I wish I had some other way to help them in addition to our prayers, but this time all I have to offer is my own hope in God that one day he will he ok. Parker will be a new person and when he comes out of this darkness he lives under he will be able to look back and find the positive things that happened in his long journey.
I am personally praying he will never lose faith that he will be okay and all of this happens for a reason, it's not God trying to torture him in any way.

Here is a link to the most recent post.

Psalm 23:4
Even though I walk through the valley of the shadow of death, I fear no evil, for You are with me; Your rod and Your staff, they comfort me.

Luke the Lyme and Ticks and Trust blog, seen them??

As I have mentioned a few times on this blog, I like reading. One thing I enjoy reading (all the time) is blogs written by other people suffering with lyme disease. I mentioned several weeks ago I was reading Ticks and Trust, I finally finished it a few days ago.

Ticks and Trust is written by a Canadian mom who contracted lyme disease and several co-infections. Throughout her journey that began in 2006 all three of her kids have tested positive for lyme disease, with her youngest son hit the hardest. Her son Parker went from being a normal boy to not being able to walk in 6 weeks.
Can you imagine that?? Suffering for years with lyme disease travelling to another country to be treated, then your child being knocked out of his reality into a wheelchair and a new life. That's mind boggling. I am not a parent, so I cannot even remotely understand what Shannon went through. They did it though, it took years and some crazy, God sent perseverance . Parker is still sick, she hasn't updated on him in a few months but he has not reached remission as far as I know.

Here is where their journey began.

Lukes blog, Luke the Lyme is still a work in progress. Luke only found his diagnoses a few months ago.  He is just in the beginning of his fight.
His symptoms originally started as face pain, then began to disseminate around his body into the more common Lyme symptoms. He is still suffering from this disease everyday.
I found Lukes blog through twitter, often times we are both tweeting about our symptoms of the day.

Both of these blogs have something in common. Something you may find surprising...but only if you are not educated on lyme disease. Shannon and Luke both live in Canada.
Lyme disease "doesn't exist" in Canada! Says those who believe ticks need a passport to cross the border.
If there was no lyme disease, bartonella, babesia, in Canada I wouldn't have made this post. Neither of those blogs would have ever been created, because they wouldn't be infected!!
Shannons family and Luke have Lyme disease. In Canada.
Shannon and her children have positive blood tests to prove it.
If Lyme didn't exist in Canada, why are their bodys producing antibodies to it? Its not because they were bored in their spare time ill tell you that!

Here is the Canadian Lyme website for more information