You can now view "Under Our Skin" on Hulu. A very awesome documentary on Lyme Disease and it's current controversy. Check it out and share the link!! http://www.hulu.com/watch/268761/under-our-skin?c=News-and-Information%2FDocumentary-and-Biography

Please help my friend Elizabeth

Everyone, it does not  matter that you donate only a dollar or a hundred. Even just sharing the link on your page will help Elizabeth get the help she needs. Please do what you can!! http://www.helpelizabeth.net/ Elizabeth is such a kind, generous, giving soul. I don't want to let her down.

Milwaukee Wisconsin Lymewalk

I have been working hard with my new friend Melissa on putting together a Lymewalk. Melissa's mom suffers from Lyme Disease also. It has been really fun and distracting me from my daily aches and pains that Lyme brings on.  Here are the details so far.

Name:   "Lace Up For Lyme
                      

Where:  Milwaukee Zoo 10001 West Blue Mound Road, Milwaukee, Wi 53266

Cost:     Adult $10.25 Children age 3-12 $7.25 at the door, then $20 at the walk for tshirt and walk for
             adult,and $10 for children who want a tshirt.

For more information go to www.facebook.com/laceupforlyme.

All proceeds are going to: http://www.lymesupportnetwork.org/

It would be great to see many of you there!! If you can't go but would like to donate to our cause please go to: http://apps.facebook.com/fundrazr/activity/42746aa5168543fbb190b82786dedcdb

Rifing

So far this is what happened my first months of rifing.

January 15, 2011
Rife Treatment #1
Used Jim's Rife machine
15 seconds of Babesia Frequency
Felt sick for two weeks. It is impossilbe to tell if it was from rife though.
Felt weak and nauseous with bad headache.

January 29, 2011
Rife Treatment #2
Used Doug Coil Machine
Did 5 seconds on 943.3
Chlamydial Pneumonia Frequency
Herxed for a week
Nausea, headache, tight chest

February 5, 2011
Rife Treatment #3
Ran frequency 943.3 for 7 seconds
Chlamydial Pneumonia Frequency
Felt good afterewards, no herxing, had extra energy that night and the next day.

New Diet

Well every person with Lyme I talk to that is doing better at all talks about how they changed their diet. So I am going to follow their lead. This seems to be my hardest area to change for some reason. But last night I went out and bought a bunch of organic, alkalizing, good for my blood type types of food. So we shall see. The beginning of another journey. So far one carrot, pineapple, orange, cilantro, cranberry, spinach slushie down! Wasn't bad actually.

Next journey, to begin rifing again!

Been so busy!!!!

Wow this last week things have really come to fruition. It has been really busy. For as sick as I am, and rarely leaving my little tiny apartment, I feel blessed to have a full time job in Lyme activism. God gives me neverending energy when it comes to this. And I have met the greatest people ever!!

I was happy last night to see Theresa and Donna at our Lyme meeting. Both still very sick but at least out of the hospital. Ready to start their healing now. The support group I go to, started by Kimberly Frank a couple years ago, started out a small little group. Now there's are over thirty members, and they are non profit and doing so much work in activism and supporting other lymies. Check out their website http://www.lymesupportnetwork.org/. There is a letter on there from Dr Maloney, that explains to Drs why they need to diagnose Lyme clinically, print it out and send it to your drs!!

Another thing I've been working on that I blogged about below has been modified. I was working with my friend Robin on a site we were going to call Lymeunited, but she has been really sick and is just not up to it. So I made this website, and am hoping when Robin gets better she can rejoin me. :) Here is the site, if you have any info on support groups or events, please let me know so I can add them. http://lymeevents.webs.com/

The other project I'm so excited about is this group with my freind Kenny & Adi. Please check this out, we need donations of love!!Our goal in this group is to reach out to fellow lymies in need. The website is http://handsforholdinghearts.blogspot.com/ and the facebook group for this is http://www.facebook.com/pages/Hands-for-Holding-Hearts/174955079202037?ref=ts#!/pages/Hands-for-Holding-Hearts/174955079202037

Letters Campaign

Letters For Lyme! Letter Writing Campaign

This campaign in going on now. From Oct 14 until Oct 28, 2011.

The IDSA continues to deny the existence of Chronic Lyme Disease and the severity of the growing Lyme Disease epidemic throughout the world. This letter-writing campaign is about exposing the lies being thrown at the public, putting everyone's health at risk. This is going to be a broad spectrum campaign that will include many different contacts.

Help to bring the ID$A's conflicts of interest and greed-driven $cience to light- let your voice be heard!

As in our previous campaigns we will once again be using a form letter. To access the form letter or to see our list of where to send your letters/emails, go to:

Letters For Lyme Blog Spot

Where To Send The Letters

This event is open to patients as well as family and friends.
For More Information go to these links:

Facebook Group for "Letters For Lyme"