Dedicated to raising awareness of ALL tick borne diseases, offering support, and providing referrals for information, research, and healthcare choices.

Meet us at Starbucks, 2507 Richmond Rd, Texarkana, TX at 10:30 AM. Saturday, June 25th.

We’ll be giving out free information as well as informing the general public about the dangers of Lyme Disease. There needs to be an emphasis on prevention and protecting our children. Wear Lyme green, bring a Lyme green sign. We are going to make a visual presence in this community. Contact me with any questions. Hope to see you guys there!

 

I’m scheduling a very informal “meet and greet meeting” :
Saturday, June 4th @ 5:PM.
Subies Deli
4833 Texas Blvd
Texarkana, TX.

For those of you who may not be familiar with Texarkana, here are the Directions:

From I-30, take the State Line Ave exit. Go south (towards town) on State Line Ave. Stay on State Line until you reach the intersection of AR and TX Blvd. (This won’t be very far) Turn right onto TX Blvd. Go approximately 1- 2 blocks. Subies Deli is located on the right. This is a small establishment, very quiet and comfortable. I informed then that there will be a group coming for an informal meeting and they will happy to accommodate. .You are under no obligation to purchase a meal, but you may want a beverage while there.

Remember, this is very casual, we just want to get to know each other. It’s very important to know that you have moral support right now. That’s why it’s important that we come together and hold each other up. We are facing, or have already faced, a devastating illness. Let’s link arms and join the fight for good health, proper treatment, encouragement, and resources.

I hope to see you guys there. You can email me if you have a question. Arklatexlyme@yahoo.com. I’ll try to get around to calling ALL of you as soon as possible.

Guys, I got back from the Lyme disease rally and I’m pumped up. There were people there from all over: Connecticut, Maryland, New York, Michigan, Ohio, West Virginia, Virginia, North Carolina, Florida…..and of course, Arkansas! I’ll post the pictures and videos as soon as I can download them all. I just got my computer out of the hospital and it got a clean bill of health, so I’ll work on posting the rally information ASAP.

Note: I want to have a our first informal meetup the first weekend after Memorial Day….that would be June either June 6, 7, or 8th. I’ll let you know as soon as I arrange a meeting place, but it will be in a public location in Texarkana for sure. Later friends!

I’m announcing the listings of when the talk show will air this week.

Heart To Heart talk show is on channel 10, if you have Cable, in the Arklatex.

Listings are as follows: May 6 @ 9:pm, May 7 @ 8:pm, May 8 @ 9:pm, May 9 @ 12:am, 5:am, 12:pm, & 9:pm.

It will possibly air more times than this, but this is the information I have presently.

Arklatexlyme support group is getting closer to setting a place and time to meet. We plan to have a kick-off rally in June with everyone coming together to meet in Texarkana. In the meantime, I’ve connected with another comrade. We taped a televised interview today with KLFI TV35 in Texarkana on the talk show ‘Heart to Heart’. It will air Friday, May 7 at 9:pm, then will be shown several more times.

Look for the Health Beat insert in the Texarkana Gazette soon. I gave an interview explaining my story and they plan on putting it in the next issue. Every story we tell, each bit of information we put out there will further our cause and help us to connect to others who are fighting this dreaded disease. Remember, the purpose of Arklatexlyme is to offer resources, support, and information.

If you have a friend who wishes to join us, just send them a link to the website or email us here. I know there are others in the area who were meeting before I came onto the scene. I’d very much like to hear from you guys and add you to the list.

I’m headed to Washington D.C. for Mayday Lyme support rally on May 21st. Wish me luck, as I’m going solo and plan to brave the Metro alone. I have my Lyme green attire ready and plan to document the event. Hopefully I’ll hook up with you guys when I get back.

Email me with any ideas or suggestions on where we can meet.

God bless you all and here’s to getting your health back, maintaining it, and revealing the hushed truth about Lyme disease to our community!

          Hello everyone.  If you read about this website in one of the newspapers, then you already know I want to start a local support group.  Right now, as of April 5, 2011, I am completely Solo!  I am the only group member.

        It’s very impportant to raise Lyme Disease awareness, especially with the summer months approaching.  We also need to know that we have each other to lean on.   That’s why organizing a face to face meeting with local folks is so important.  We need the support and the acknowledgement!  That’s why standing together is so important.

      Right now, I don’t know where we will meet.   I need folks who really want to be involved…..don’t worry, I won’t ask anyone to do something you don’t want to do!   WE NEED NUMBERS!

     Contact me.  Click the link here on the site at the top.  I want to get a head count on how many are interested.  Then we’ll figure out where we can all meet each other, probably in Texarkana.   I need your help. 

   Remember, we are all kindrid spirits, fighting Lyme Disease in some way or another.  Let’s team up in this area!

Sincerly,

The Staff of Arklatexlyme.com

Hey everybody in the Lyme community and all support groups!! Stand with us as we demand a complete revision of Lyme disease diagnostic and treatment guidelines. We will meet on the lawn between the Whitehouse and the Washington monument on the north side of the Ellipse in Washington DC at 11:30 AM on Saturday, May 21, 2011.

Bring signs, bring banners, bring your VOICE!!! We have been encouraged to remain silent for far too long. We must raise our voices to a level that can no longer be ignored. We must GET LOUD!!! STAY LOUD!!!!!

This demonstration of awareness is held in conjunction with other actions throughout the country and the world as a part of Lyme Disease Awareness month. Please, do what you can to make a difference.

This event will be needing volunteers and people to help coordinate.

For more information and to volunteer for the event call please contact lymeday2011@gmail.com

 
 

 Dedicated to the prevention of Lyme Disese and it’s coinfections and the support of individuals suffering from the illness.   

 If you are suffering from this disease or have a loved one who is sick or suspect you may have Lyme Disease, please explore this site for vital information.  You are not alone!