Archive for the ‘Uncategorized’ Category

Tony Evers Signs Two Lyme Bills

https://www.lymedisease.org/wisconsin-two-lyme-bills/

Wisconsin governor signs two Lyme bills related to state parks

 

 

 

Dear Lyme Warrior…Help!

https://globallymealliance.org/dear-lyme-warriorhelp-10/

lyme warrior

by Jennifer Crystal

Every few months, Jennifer Crystal devotes a column to answering your questions. Below she answers some that she’s recently received. Do you have a question for Jennifer? If so, email her at lymewarriorjennifercrystal@gmail.com.

How can I keep anxiety under control while waiting for test results?

Waiting is one of the hardest parts of being sick. You are waiting for results, waiting for medication to work, waiting to get your life back on track. Despite the label “patient,” it can be very hard to practice patience when you have a complex illness such as Lyme.

The important thing to remember with tick-borne illness is that testing is faulty and cannot be fully relied upon as the sole indicator of whether you have Lyme disease. Specialized testing can help support clinical diagnosis, but that’s a judgment call made by your doctor, who needs to take your symptoms and full medical history into account. Tests for inflammatory and immune markers can help your doctor make an accurate assessment. If you are seeing a good Lyme Literate Medical Doctor (LLMD) and feel comfortable with their diagnosis, don’t hang too much on test results.

It’s also critical to face the fact that tick-borne illness can physiologically cause anxiety. The Lyme bacteria can get into your brain and cause symptoms of anxiety on top of the natural worries you may already be having about how your illness is affecting you. Be sure to tell your doctor if you are experiencing psychological symptoms (including depression, confusion, an inability to concentrate) that may affect your treatment plan. I also highly recommend talking to a therapist who understands chronic illness. Doing so really helped me manage my own anxiety.

How can I help someone who has severe anxiety about treatment, and is resisting it?

As hard as it is for Lyme patients to deal with anxiety, it can be just as hard for caregivers to watch their loved ones become fearful and, at times, irrational. Lyme can cause inflammation in the brain, which can lead to all sorts of out-of-character behavior. Patients who were once calm and cheerful may become nervous, obsessive, angry, and confused. They may not be able to make sense of treatment options and may feel overwhelmed by all the conflicting information being thrown at them from health care professionals and the internet.

It’s important for Lyme patients to know that they are not alone. First and foremost, reassure your loved one that you are on their team. Validate their feelings and concerns rather than arguing against them. For example, instead of saying, “You just need to do x,” tell someone, “I hear your fears about treatment. I have fears, too.”

Then, demonstrate that you understand the risks and benefits of treatment options by showing insight into their suffering. In order to do this, read books and articles about the lived experience of tick-borne disease. This way the patient will know your advice is coming from a well-informed place. Offer to accompany the patient to one or more doctor’s appointments, so that you can help them make sense of what’s being said.

Finally, you may need to be direct with the patient, though in a loving way. If someone had said to me,

“I think the illness is affecting your ability to make this decision, and I want to help you because I want you to get well,” that would have really reassured me.

You might even bring up the patient’s anxiety when you’re together at the appointment, to get the doctor’s advice—just make sure you ask the patient about whether he or she is alright with this. You could also offer to go to therapy appointments with them to talk about both of your concerns and the best methods for communication.

Do all Lyme symptoms go away if you kill off the bacteria, or do some symptoms remain?

The answer to this question is different for every patient. It depends on how quickly you’re diagnosed, how well you respond to treatment, whether you are also battling co-infections, and whether the bacteria has crossed into the central nervous system. Many patients who are diagnosed immediately after a tick bite and take a standard course of antibiotics get fully well. Some 20%, though, develop Post Treatment Lyme Disease Syndrome (PTLDS) which means symptoms persist after treatment. Still others enjoy remission with periods of flare-up.

All it takes is one dormant Lyme bacterium (spirochete) to start replicating for the infection to return. This is more likely in long-term, complex cases like my own, which took eight years to diagnose. I have Lyme plus two tick-borne co-infections. My Ehrlichia seems to have gone away completely, while Lyme and babesia still flare-up. It’s babesia that still gives me the most trouble. However, all of my symptoms are greatly decreased and are far more manageable than they once were.

Since no two cases of tick-borne illness are alike, the fact that some of my symptoms have persisted doesn’t mean that yours will. Here is what I can tell you for sure: under the care of a good LLMD, you may not be cured, but your life can get much, much better.


jennifer crystal_2

Opinions expressed by contributors are their own.

Jennifer Crystal is a writer and educator in Boston. Her memoir about her medical journey is forthcoming. Contact her at lymewarriorjennifercrystal@gmail.com.

 

 

Dr. Jemsek Vindicated!

https://www.facebook.com/JemsekSpecialtyClinic/videos/827014311079433/  Video Here

One of the physicians featured on the documentary “Under or Skin” has just made a major announcement:

Dr. Jemsek announces the action by the North Carolina Medical Board to overturn their 2006 decision to restrict Dr. Jemsek’s medical license by rescinding and abolishing that wrongful decision.

He was disciplined for prescribing long term antibiotics to treat chronic Lyme disease.
This is vindication for patients suffering from this disease.

 

WI – Amazing Testimonies on AB546 – Now Email Health Committee

THANK YOU, Wisconsin Citizens for

Amazing Testimonies Last Week on AB546!

Now Let’s Ask for the VOTE in the Assembly Executive Committee!

Support the Bill to Protect Complementary and Alternative Healthcare

We need your help NOW to contact your legislators to support Wisconsin’s “Safe Harbor” Practitioner Exemption bill, A546, a bill that will protect the right of homeopaths, traditional naturopaths, herbalist, energy healers and many more to offer their services to consumers in Wisconsin.  Help Wisconsin become the twelfth state to have a health freedom law protecting these practitioners!

How YOU Can Help:

1. Click Here to Email the Health Committee members and your personal legislators to ask for their support of AB546 and for it to be heard in an Executive session.  They heard the bill in Committee on January 7th and now, in order to VOTE it out of Committee, they have to hear it in an Executive meeting in order to move it and pass it out of the Committee.

2. Use this simple form to send WIHFC your testimony and we’ll submit it to the committee for you. See below for an example.  Sharing your story – in person or in writing – is crucial to the success of this bill!  Legislators love personal stories and your positive experience using complementary health could sway committee members to vote yes.

Example Message for Legislators: “Members of the Committee, my name is [insert name].  I live in [city].  I support AB546 and I want you to please VOTE YES on AB546, the “Consumer Protection for Complementary Healthcare” bill.  This bill is important to me because [insert your own brief reason why you support access to complementary and alternative health care]. Thank you.”

[i.e.,

– I depend on complementary and alternative health care for myself and my family and I want Wisconsin law to protect my rights as a consumer to a free and educated choice in health care providers.

OR

– I am a practitioner of complementary healthcare and a small business owner in Wisconsin. I want to serve my clients without the fear that my state’s laws could be used to treat me as a criminal.  Please update WI law to reflect what is happening in our state.]

Thanks in advance for helping pass AB546 into law.  Together, with your help, we can convince Wisconsin legislators to protect WI residents’ health freedom rights to access the healing modalities and practitioners they want.

For more about what this WI bill does for complementary and alternative health practitioners and their clients, see our website here (bill originally introduced as LRB-1960/1).  Read the bill here.  Read about Safe Harbor bills here.

_________________

**Comment**

I know a lot of bills are coming out and it can be very confusing.  Please know the bill in this email has to do with protecting complimentary and alternative health care like homeopathy.  It is NOT the WI bill (AB313) about the 16 member panel that we are trying to squash as it is huge government overreach and could affect the way our Lyme docs treat us here in the state of WI.

 

 

 

 

 

Reminder: WI Lyme Patients Contact Legislators to Stop AB313

This is a plea from Jeannette Wheat the former head of the Madison Group and an experienced medical professional.

Hello All People with Lyme,

I have written before about this bill, AB313, but now it is becoming urgent.

The WI Senate has already passed this bill and it will likely be passed in the Assembly if people don’t get active and contact their state Assembly people right now!

This bill will essentially create a new IDSA Lyme Guidelines committee, Infectious Disease Society of America, except that it will be WI based.

I am attaching the bill to this email, but just to give you a glimpse into it, a couple of the tasks assigned to this committee are to make recommendations to the legislature to make policy (ie law) about diagnosis and treatment of Lyme disease in Wisconsin and the Insurance Commissioner of the State of WI will be one of the committee members!  Just think for a moment how that will work against people with Lyme.

We all know how damaging the IDSA Guidelines are and how opposed to the ILADS, International Lyme and Associated Diseases Society, Guidelines they are. We just can’t let that happen in WI! Please contact your WI Assembly person NOW!!! This is likely to voted on in the next week or two.

The Senate has already passed this. So don’t bother to contact your state Senator about this now. If you don’t know who your representative is or how to contact them, here is a link to a page where you can input your address and it will find him/her for you.

https://legis.wisconsin.gov/ It says “Who are my legislators?” On my browser this shows up on the lower, right side of the page.

Tell your representative that the diagnosis and treatment of Lyme disease is not a state issue and that the insurance commisioner should not be involved in deciding how to diagnose or treat Lyme disease.  Tell them this committee thing has already been done with disasterous outcomes by the IDSA.  Tell them to vote NO on this bill- AB313!

Please take action now!  Your ability to be diagnosed and receive treatment for Lyme disease in WI is at risk!

Thank you, Jeanette Wheat, RPh MBA, and long time Lyme sufferer, support group leader (in days gone by)  and advocate..

For more:  https://madisonarealymesupportgroup.com/2019/11/06/wisconsinites-a-reminder-to-please-write-oppose-assembly-bill-ab313-today/

Exact wording of the bill: Assembly Bill 313

AB 313, previously LRBs 1652 and 3362Establishes a sixteen-member Tick-Borne Disease Study Committee to create a report for the legislature on consensus-based recommendations for policy changes on awareness, prevention, surveillance, diagnosis, reporting, and treatment of Lyme Disease.

This bill would allow Governor Evers to appoint a 16 member advisory panelto offer recommendations on how doctors diagnose and treat Lyme disease.

Many of us have explained to our representatives about the potential for that bill to go side-ways since nothing about Lyme/MSIDS is agreed upon in the medical community as well as the fact that appropriate Lyme guidelines already exist.

This bill is huge government overreach – telling doctors how to diagnose and treat patients.

All of the Lyme literate doctors I spoke with oppose this bill for numerous reasons – one of which is the fact this bill could seriously interfere with the way they currently treat patients as well as could increase scrutiny of their medical practice. They are already under severe scrutiny with many having to pay fines to the state medical board:  https://madisonarealymesupportgroup.com/2012/03/04/dr-hoffmann-updated/  My own doctor spent over 50K to protect his practice against such a witch hunt.

All we have to do is look across the state border to see problems in Minnesota:  https://madisonarealymesupportgroup.com/2019/11/17/minnesota-medical-board-reinstates-sanctions-on-controversial-lyme-disease-treatment/