Top Tweets for #ResearchForAlex
One of the toughest Lyme fighters we know is also one of our most cherished friends, and today we are proud to share her story. (Found in the link below.) π
#ResearchForAlex
https://t.co/hEurmlusBg

Good news, friends! The CDC has updated their website to address the issue of maternal-fetal transmission of Lyme disease, from an infected mother to her fetus/baby.
Learn more by visiting the link below!
#ResearchForAlex
https://t.co/FEVwDPTcpX
With a new year comes a new look, and we are so excited to share with you our updated website for AHLF! Special thanks to Adrian Alvarado who spent months creating the perfect website that would capture Alexβs story and our mission. ππ
#ResearchForAlex
https://t.co/cQ6yQ1fM9W

The Kay Hagan TICK Act, designed to improve the governmentβs response to Lyme and other tick-borne diseases, was signed into effect on Friday, December 20th (Alex's birthday). π
#ResearchForAlex
https://t.co/SBltZh46bI
A special message of gratitude from AHLF Founder Jody Hudson can be found by visiting the link below. Be sure to read it and subscribe to our newsletter to stay updated on what's coming our way in 2020! π
#ResearchForAlex
https://t.co/Ow3X4UAv7H

Every lady pictured below have volunteered their time, efforts & skills to help make AHLF what it is today. We're so grateful for each of them, & with Thanksgiving right around the corner, we'd be remiss not to note their contributions to this organization. π
#ResearchForAlex

"Remission is hard sometimes. Life is hard sometimes. But itβs all absolutely worth it." - Savannah Marcum
Read more about Savannah's journey with Lyme disease, MCAS and life in remission by visiting the link below. π
#ResearchForAlex
https://t.co/KHhQrxk3aa
It's not always easy to share your story, but by doing so, we are creating a safer, more positive environment for those living with Lyme. Thank you, Chloe, for sharing your journey. We are so proud of you and are here to support you. ππ
#ResearchForAlex
https://t.co/PQMfPw4buO
The AHLF team is taking our fight against Lyme disease all the way to Sacramento. Click on the link below to learn how! ππͺπ½
#ResearchForAlex
https://t.co/nfYHo7sRyQ
2019 has been an absolute whirlwind, but in the best way possible. Thank you to all those who have supported our journey thus far; we love all of you. π
Watch our recap video here: https://t.co/CcLhiTWnrn
#ResearchForAlex

Our hearts are filled with joy. Thank you to all of those who joined us for today's "Tea for Alex" event; we are so grateful for each and every one of you. π
#ResearchForAlex
https://t.co/CcLhiTWnrn

Yesterday, Assemblyman @JimPatterson559 presented us with a proclamation stating that May is officially Lyme Disease Awareness Month. We are so honored and excited to continue on our advocacy journey, and we're thankful for your support!
#ResearchForAlex
https://t.co/qs9Jj519Vi

"Much of the controversy surrounding Lyme disease could be settled with an accurate test. One that could detect 100% of infectionβand determine when the infection has been cleared." (Via @Lymenews)
#ResearchForAlex
https://t.co/zkPP00tetc
Curious to learn about our event speakers, Olivia and Holiday Goodreau? Head on over to our Facebook page to read a bit more about these amazing trailblazers in the Lyme community!
#ResearchForAlex
https://t.co/CcLhiTWnrn

"Researchers are seeking answers and the biomedical tools to bring sick patients back from the brink. These scientists need our support, not our scorn."
A great read by Aeon Health and Psychology Editor Pamela Weintraub.
#ResearchForAlex
https://t.co/FqIZe52veb
On Saturday, October 26, AHLF is partnering with Lyme disease advocate, designer and writer Ally Hilfiger for a book signing event at Fresno's Barnes & Noble! She will be signing copies of her book, βBite Me,β which details her 19 year battle with Lyme disease.
#ResearchForAlex

Can you believe that our "Tea for Alex" fundraiser is only a few weeks away?! How many of you will be there?? π
#ResearchForAlex

Psychiatrist Robert Bransfield calls for more research, and attention, to the ties between Lyme disease and psychiatric ailments.
#ResearchForAlex
https://t.co/fw39GfVUbM
This past weekend, AHLF Founder Jody Hudson attended The LivLyme Foundation's annual Lyme Summit.This educational conference brought together clinicians, patients and advocates from all over the country to discuss numerous matters pertaining to Lyme disease.
#ResearchForAlex

βOne tick-check can make all the difference,β said Senator Sue Serino. βWe know from experience that a simple reminder can go a long way in helping people stay tick-free and thatβs what this bill is all about.β
#ResearchForAlex
https://t.co/NAUmnjmnc5
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