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Global Lyme & Invisible Illness Organisation

ILADS announces next Tick Borne Conference to be held in Finland

6/2/2016

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Save the Date: 10 - 11 June, 2016
Where: Paasitorni, Helsinki, Finland
What: Physician and Researcher Training
If you are interested in learning more about International Lyme and Associated Disease Association and registering for their conference please visit:  ILADS6thEuropeanConference
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News on the Blanket Fort Party and Holiday Wishlist

7/11/2015

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For Christmas and the holiday season this year - Global Lyme & Invisible Illness Organisation will again be hosting the Blanket Fort Party for fun, games, and to have a place for laughs for those unable to leave home for Christmas..

We are also going to incorporate Co-Founder Lisa Hilton's, Christmas Wish-list into the "Holiday Seasons" Events.

This will involve:
1. Compiling a List of Children / Families who  may not receive anything this Christmas as they (or their caregivers) live with Lyme & Co., and there is limited funds.

2. Compiling a
List of Adults Wishes / Fundraisers  they may have going for treatment / Living Expenses

3. Listing / Providing Links to patients selling art and craft for their treatment and living expenses.

4. Matching up people with those that may need items with those that have items to
Give away.


5. Asking people to donate goods (wishes) or money / gift cards that will go to children / families that may have otherwise not receive anything.

We will be adding a page and making events for the Blanket Fort Party soon so stay tuned and check back please!




6 Comments

Di Ellis battled Lyme2surf again Plz vote4CV Sportsperson of Year

7/11/2015

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Australian (NSW), Di Ellis, is in the running for sportsperson for the Clarence Valley Sportsperson of the Year.  Di is a wonderful lady whose strong spirit has seen her raising awareness for Lyme, helping others get through the journey, and re-gaining her life back. Di overcame many years of illness to Place 3rd in the over 35's woman's group for the Aussie Longboard Titles earlier this year.
Please get behind Di - to say what a remarkable achievement - and in addition raise more awareness of Lyme.

Vote by going to the following Link:
http://www.dailyexaminer.com.au/news/two-weeks-until-sports-awards-sports-awards/2823876/

And click on Di's Name Nomination (Shown in small picture below), about 3/4's of the way down the page.
THREE VOTES PER PERSON are allowed - Simply refresh the page - and use all three votes at once :) Thank you in advance for the support!!

Voting ends: 5pm Wednesday, 11th November. Australian Time.

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Sweet Video made from a Father for a Son with Lyme Disease

28/10/2015

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UK Lyme in the News: Interview with Adelle Huckins

10/10/2015

1 Comment

 
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UK Lyme in the News

Adelle Huckins speaks about her families situation with Lyme disease, how hard it was to choose who gets treatment, and the guilt of passing it down to your children. 

Read the article from The Telegraph Below

'Like the Caudwells, our family also has Lyme disease'​

If you are looking for Lyme Disease information in the UK please visit here.



1 Comment

New Hope in the Lyme community as John Caudwell wants to help bring Lyme to the light.

2/10/2015

2 Comments

 
Money can buy you a lot of things but if you don't have your health, it cannot buy you happiness. John Cauldwell speaks in this video about his son and his psychiatric symptoms that develops after being infected with Lyme disease. He talks about how hard it was to get a diagnosed and how he plans to help the Lyme community in the future.
Also See Article:
Phones4U billionaire John Caudwell ‘devastated’ after whole family diagnosed with Lyme disease
2 Comments

"Global Faces of Lyme" video

1/10/2015

4 Comments

 
Global Faces of Lyme was a fourth in a series of videos called "Faces of Lyme." This video was made to show the world that Lyme disease is a pandemic. It has spread across the world, and patients are suffering everywhere. Because of the IDSA/CDC Lyme disease treatment guidelines, the world is not getting proper care, as many countries' medical systems are based on these guidelines.  

​But there has a been a turn in the tide and patients are all uniting together to make this terrible disease public. We are not going to sweep it under the rug. Together as the world unites in this battle to expose and raise a cure for Lyme disease, we can win this fight. Stay strong warriors. 
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