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!
Thursday, January 13, 2011
Thursday, January 6, 2011
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
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
Tuesday, January 4, 2011
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"
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