Archive for the ‘Activism’ Category

Psychosis and PANS Meet Plasmapheresis – Our Final Slam Dunk

https://pandamoniumblog.com/psychosis-and-pans-meet-plasmapheresis/

Psychosis and PANS meet Plasmapheresis – Our Final Slam Dunk

PANS and PANDAS often mimic mental illness, presenting as psychosis. The day after Aidan’s worst night in the psychiatric hospital three years ago, he sat in the corner of the hallway picking at his red hospital socks and said to his nurse, Ms. English,

“Nobody knows how I feel.”

Our son, Aidan, was psychotic – there, I said it. Nurse English was the one psyche nurse with whom Aidan connected. She was ultra compassionate and took the time to meet Aidan where he was – in the corner, in the hallway, on the floor. Picking, picking, picking at his one-size-too-big, floppy hospital socks – the ones with the no-slip bottoms. Interestingly enough, he still has those socks tucked away in his top dresser drawer. I think they were the highlight of his stay.

Yes, I saw it with my own eyes. Aidan was psychotic because of PANS. Pyschotic because of a illness that was almost diagnosed during his inpatient stay in 2016.

Unlike many children diagnosed with PANS or PANDAS, Aidan’s onset was not overnight; I believe that he had a misdirected immune system from infancy. However, I can recall what illness in what month of what year and how many weeks after he ‘recovered’ from that illness when we noticed increased rages and aggression, decreased motor skills and an onset of tics. In short, the bottom fell out. We did not know what to do or where to go.

We ended up in a pediatric psyche ward and came out with more diagnoses: a movement disorder for the tics and imbalance, and a second-time mood disorder NOS (not otherwise specified) for the rages, aggression and psychosis. He was also labeled a fall risk (rightfully so) and was emotionally liable upon discharge.

Game Changer #1: Proper Diagnosis

Three weeks after Aidan’s discharge from the hospital, he had an appointment with the developmental pediatrician who diagnosed him with autism. It was a follow-up appointment that was scheduled one year prior.

The exam room had a mat on the floor, and for that I was thankful. All Aidan had done since coming home from the hospital was roll around on the floor, from one side of the family room to the other.

I remember saying to the doctor, “Is this Aidan with autism but on different medications?” I explained life since the bottom fell out until now, looking up from the mat where I was trying to keep Aidan somewhat calm. I wasn’t very successful, nor was I ready for what the doctor had to say:

“This isn’t autism, Mrs. Keatts. This is PANDAS or PANS, and the most successful treatments are not covered by medical insurance.”

By the end of this appointment, my head was spinning. Aidan had been seen by more than 10 doctors during his inpateint stay, and at an appointment that I made one year prior for an unrelated diagnosis, we discover the root cause of Aidan’s symptoms that were holding him hostage in his own body.

Game Changer #2: Proper Intervention

If and when our children are properly diagnosed and a proper treatment plan is implemented, parents and doctors try to counter PANS and PANDAS with antibiotics, anti-inflamatories, steroids, supplements, IVIG and antibody therapy. Sometimes, one of these interventions or a combination thereof provides long-term relief. For us, however, they did not.

Our last resort was plasmapheresis, which in its simplest terms is a way to cleanse the blood system of the antibodies that are attacking our children’s brains. This is how I can best explain how plasmapheresis works:

  1. Blood has three parts: plasma, red cells and white cells. Antibodies are found in the plasma part of the blood.
  2. Plasmapheresis takes blood from the strongest source, the heart, and separates the plasma from the red and white blood cells.
  3. The red and white bloods cells are stored together and kept safe during the treatment, while the old plasma is collected separately and disposed of later.
  4. Then the red and white blood cells are put back into the blood stream with the new donor plasma.
  5. Plasmapheresis therapy takes place over the course of two weeks – three days each week, with at least one day in between each session.

Some kids, like Aidan, respond immediately to plasmapheresis – also called PEX. Others, progress slowly over weeks, even months. And still others require additional treatment modalities ranging from IVIG to cognitive behavioral therapy and intensive exposure therapy to further recover from the damage done by a misdirected immune system.

Regardless of the pace at which the child progresses following PEX, for many children this ‘blood cleaning’ process opens the pathway to healing and recovery.

On the Rebound

We are coming up on the two-year anniversary of Aidan’s plasmapheresis treatments, and since then I have spoken to several moms before their child began PEX. While their children’s onset stories and symptoms vary, one constant prevails — each mom is understandably apprehensive about plasmapheresis. It is invasive – a surgery is required to place a port into the aorta, and there is risk of infection.

Every time I share our experience with plasmapheresis, I speak from my heart. PEX opened a door to Aidan’s healing that I truly thought we would never find. In complete transparency, Aidan’s illness tested my faith far beyond any other struggle in my life.

Nearly two years later, I realize that there are four intentions that I subcouncioulsy set, yet mindfully observed during Aidan’s PEX. When I fully saw how the Divine’s healing hand was there all along, I gained clarity that is unique to Aidan’s journey. And so, I share with you my insights with a heart not only of gratidude for Aidan’s healing, but a fierce hope that your child will too find healing.

  • Be brave. Your child and family have gone through hell and back because of PANS or PANDAS. You are all warriors in your own right. You have been courageous and resilient from the beginning – even if you have fallen apart and cried yourself to sleep more times than you can count. You made it to this point, and that’s what matters.
  • Be bold. Let your spirit lead you. Let your worries drift away. Believe that your child will heal, and that healing begins this day. Sacrifice and intention preempt healing. Your child and your family have sacrificed much and suffered terribly. Now, set your intention. A mindset of clarity and healing is the next step. Each day leading up to the procedure claim your intention – to heal your child.
  • Be open. Your child will be just as anxious and afraid as you are, yet neither of you will tell the other. You have both learned how to be stoic throughout this journey. I welcome you to share Aidan’s story with your child and explain that other kids with PANS / PANDAS have begun to heal after the ‘bad guys’ were removed from their bodies.
  • Be watchful. Sometimes healing begins almost immediately. Other times it progresses slowly. Every child is different, and every story of healing is unique. The smallest signs of healing are blessings and are meant to encourage hope. Although Aidan’s signs of healings began just one day after his first plasmapheresis treatment, his full path to remission lasted more than a year. Healing occurs in stages as the body is able to respond and process various interventions. Be patient, and remain watchful.

After years of flagrant fouls and air balls in our journey to heal Aidan, PEX allowed us to score the winning shot in a game that ran into overtime for years. Reflecting on my fears, frustrations, desperation, and even my loss of faith, I now see twists and turns in Aidan’s illness through a new lens – a courtside view of Nurse English rebounding the ball for Aidan during open play in the hospital gymnasium, and a box seat view of the Divine palming the ball, guiding my next pivot and lifting us up for the final slam dunk.

MJ Keatts is a mom of three – one of whom inspired her to start this blog. A journalist by trade, minimalist at heart, and a stunt girl in her dreams, MJ proudly admits that she’s learned more from her kids and husband than she could ever teach them herself. She loves to laugh – especially at herself – and one day hopes to amaze her husband and be ready on time.

_______________

**Comment**

Click on the author’s name at beginning of article for other articles she’s written.

For more:  https://madisonarealymesupportgroup.com/2019/03/16/brain-under-attack-pans-pandas-related-developmental-disorders/

https://madisonarealymesupportgroup.com/2017/10/01/panspandas-steroids-autoimmune-disease-lymemsids-the-need-for-medical-collaboration/

https://madisonarealymesupportgroup.com/2017/10/08/misdiagnosed-how-children-with-treatable-medical-issues-are-mistakenly-labeled-as-mentally-ill/

https://madisonarealymesupportgroup.com/2017/12/01/guidelines-for-treating-pans-its-real/

https://madisonarealymesupportgroup.com/2018/10/29/neuropsych-disorders-in-kids-an-interview-with-co-founder-of-the-stanford-pans-clinic-dr-kiki-chang/

https://madisonarealymesupportgroup.com/2018/09/05/pans-autism-the-immune-system-an-interview-with-expert-neurologist-dr-richard-frye/

https://madisonarealymesupportgroup.com/2019/01/02/pans-pandas-a-survivors-story/

FYI: Lyme/MSIDS can often be a part of the PANS/PANDAS picture.

Volunteers Needed For Research – ME/CFS, MS, RA, & Post Cancer Fatigue

The Open Medicine Institute that is setting up the Lyme Clinic at Howard Young Medical Center in Woodruff, WI. is looking for children with lyme, ages 10-17 to participate in a study. The institute is paying $75 per-participant. They’re looking for adult lyme patients as well. You can contact Open Medicine as per-below. I believe they’ll mail kits to those out of the area.

Volunteers for Medical Study

Re: Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS)

Looking for patients diagnosed with Multiple Sclerosis, Post-Cancer Fatigue, or Rheumatoid Arthritis

Dear Volunteer,

The Open Medicine Institute (OMI) and the Centers for Disease Control (CDC) are running a study of “ill” individuals compared to CFS patients and “normal” healthy patients.

  • Eligible individuals may be asked to re-participate;
  • will be paid $75 for completing the study

We are asking for your help to ask anyone that you know between 18 and 70 years of age with one of the aforementioned diagnoses to help millions of ME/CFS individuals and loved ones.  Interested parties can sign up by emailing research123@openmedicineinstitute.org along with your contact information and availability to come into the OMI office at

319 North Bernardo Ave.

Mountain View, CA 94043

Volunteers are asked to do the following (at no cost):
  1. Fill out a set of online questionnaires via a secure patient portal (this can be used as your own electronic medical record and is yours for free to use on-going);
  2. visit the OMI Office for a physical exam;
  3. have a blood draw;
  4. collect saliva swabs done at home the day before the exam (home kit shipped upon appointment scheduled).
  5. Incentive payment will be mailed upon completion.

If you have any additional questions, please contact the research team at
research123@openmedicineinstitute.org or call (650) 433-8930 x 4005

 

 

NY Senator Helming: Bill to Study Lyme Disease Coverage Clears Legislature

https://www.nysenate.gov/newsroom/press-releases/pamela-helming/senator-helming-bill-study-lyme-disease-coverage-clears

Senator Helming: Bill to Study Lyme Disease Coverage Clears Legislature

GENEVA – Senator Pam Helming today announced that legislation she co-sponsored to review insurance coverage for the treatment of Lyme and tick-borne diseases has passed both the Senate and the Assembly unanimously. As a member of the Senate Task Force on Lyme and Tick-Borne Diseases, Senator Helming has been a strong advocate for those suffering from Lyme and tick-borne diseases and their loved ones and has fought for measures aimed at prevention, treatment, and awareness of these illnesses. Currently, health insurance companies are not required to cover long-term treatment for those who suffer from chronic Lyme and tick-borne diseases. This bill (S.4571/A.6146) calls for a study and report on the adequacy of such insurance coverage. The data gained through the study will help lawmakers make informed decisions about insurance.

“Lyme and other tick-borne diseases continue to be a prevalent threat across our region and around our state. Since taking office as State Senator, I have proudly advocated on behalf of those suffering from these illnesses as well as the medical and public health professionals working with them. Those suffering from chronic Lyme and tick-borne diseases can experience serious symptoms such as extreme and long-term fatigue, nausea, depression, and joint pain. However, insurance coverage is insufficient when it comes to helping patients pay for the treatments related to these illnesses and their related symptoms. That can be devastating to people who are already battling these debilitating diseases. This study will give us the data and facts we need to address this problem. As State Senator, I will keep working with my colleagues on both sides of the aisle as well as local grassroots organizations to work toward better prevention, treatment, and awareness of Lyme and tick-borne diseases. This legislation is a major step forward in this regard, and I thank the Senate and Assembly for supporting it in a bipartisan, unanimous manner. I am hopeful the Governor will sign it into law soon,” Senator Helming said.

The legislation directs the New York State Department of Financial Services, in consultation with the commissioner of the Department of Health, to study and report upon the adequacy of insurance coverage for the treatment of Lyme disease and other tick-borne related diseases. The study will provide insight into the current state of insurance coverage as it relates to Lyme and tick-borne diseases and recommend solutions to ensure all New Yorkers are adequately protected. Many areas of New York suffer from high incidence of Lyme and other tick-borne diseases, yet insufficient insurance coverage impacts many seeking care. Rhode Island and Connecticut are among the states that have recognized the toll these diseases take on victims by passing legislation that requires insurance to cover these diseases.

___________________

Bill S4571: https://legislation.nysenate.gov/pdf/bills/2019/S4571

According to this 2014 article on the Massachusetts State Center for Health Information and Analysis, the cost of long-term Lyme disease care would only increase insurance polities by 13 cents: https://www.telegram.com/article/20140525/NEWS/305259757/1116.  The Bill would require insurance carriers to provide coverage for antibiotic treatment lasting beyond 28 days when it is determined by a physician to be medically necessary as well as insurance coverage for diagnostic testing for the tick-borne disease.

Response From Dr. Paul Auwaerter Regarding the IDSA Grant (Part 2)

https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/u/24788664?

Response from Dr. Paul Auwaerter regarding the IDSA grant (Part 2)

JUL 5, 2019 — 

Please see today’s letter to the TBDWG…….

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: tickbornedisease@hhs.gov, chris.smith@mail.house.gov
Cc: (98 Undisclosed recipients)
Date: July 5, 2019 at 9:07 AM
Subject: NEW: Response from Dr. Paul Auwaerter regarding the IDSA grant to search for an infectious cause of Alzheimer’s disease.

July 5, 2019

The IDSA Foundation
1300 Wilson Boulevard Suite 300
Arlington, VA 22209
Attn:  Paul Auwaerter, vice chair of the IDSA Foundation

Dear Dr. Auwaerter,

Lyme disease is recognized as the fastest growing vector-borne infectious disease in the United States with an estimate of over 300,000 new cases yearly. [i] It is imperative that at least one (or more) of those $100,000 IDSA Foundation grants is earmarked for research related to Borrelia infections and possible connection to Alzheimer’s disease.

Rheumatic fever as you know is a consequence of untreated strep throat leading to irreversible heart disease. We have evidence that untreated Lyme is just as destructive as Dr. Neil Spector’s untreated Lyme infection required a heart transplant.[ii]  Kris Kristofferson’s untreated Lyme led to a misdiagnosis of Alzheimer’s disease [iii] and Dr. Vincent M. Tedone has identified Lyme in his daughter’s neurodegenerative ALS diagnosis. [iv]

Personal Health; When Lyme invades the brain and spinal system.

By  JANE E. BRODY FEB. 15, 1995

https://www.nytimes.com/1995/02/15/us/personal-health-when-lyme-invades-the-brain-and-spinal-system.html

——————-

Focusing on the acute stage of Lyme disease after early treatment misses the horribly disabled who have gone months, years or decades before diagnosis and it’s time to recognize this fault in the science.

Subjective symptoms after treatment of early Lyme disease.
https://www.ncbi.nlm.nih.gov/pubmed/20102996
Gary Wormser, New York Medical College Jan 2010

It is common knowledge that Dr. Allen Steere has had a career long fixation on the swollen arthritic knee presentation of Lyme disease.

“Charting the scope of Lyme disease”
Marisa Venegas, New York Times 1988 Accession number 30957138

Quote from Dr. Raymond Dattwyler:

“This disease can involve virtually every organ system of the body, Dr. Dattwyler said. It makes sense to look at this as a whole-body disease, rather than narrowly. In syphilis, which is a similar spirochetal illness in some ways, there is also arthritis. If I concentrated on that aspect of syphilis, it would be ludicrous….”

And then there is this paper from Dr. Robert Bransfield…..

Aggressiveness, violence, homicidality, homicide, and Lyme disease  Oct 2017
https://www.dovepress.com/aggressiveness-violence-homicidality-homicide-and-lyme-disease-peer-reviewed-fulltext-article-NDT

_________________________

Dr. Auwaerter,

It is imperative that research continues in the area of Borrelia infections and possible connection to Alzheimer’s disease and I must insist that funding be restricted from the researchers who are identified as defendants in the racketeering lawsuit as these individuals clearly have a conflict of interest.

The following list of additional references was recently brought to my attention:

Alzheimer’s disease, dementia, Parkinson’s disease, brain atrophy caused by spirochetes and other pathogens of infectious diseases

http://www.erlebnishaft.de/alzheimerspirochaetosis.pdf

Respectfully submitted,

Carl Tuttle

Lyme Endemic Hudson, NH

Cc: Tick-Borne Disease Working Group

References:

[i] Data and Surveillance

https://www.cdc.gov/lyme/datasurveillance/index.html
[ii] Doctor Hopes His Medical Journey Inspires Others

https://www.dukehealth.org/blog/doctor-hopes-his-medical-journey-inspires-others
[iii] “A Slow Slipping Away”— Kris Kristofferson’s Long-Undiagnosed Battle with Lyme Disease

https://www.huffpost.com/entry/a-slow-slipping-away-kris-kristoffersons-long_b_577c047be4b00a3ae4ce6609
[iv] A Revolutionary Idea: Bacteria Causes Neurodegenerative Conditions

https://www.winningthefight.org/bacteria–nerve-disease.html

_______________________________________

On July 3, 2019 at 8:12 AM Paul Auwaerter <pauwaert@jhmi.edu> wrote:

Dear Mr. Tuttle,

The grants for research are evaluated by an independent scientific review board. I do not sit on this board, and I cannot speak for them. The IDSA Foundation encourages applications, and we do not exclude any pathogen.  I expect the grant awards to be highly competitive.

Sincerely,

Paul G. Auwaerter, MD

Vice Chair, IDSA Foundation
Sherrilyn and Ken Fisher Professor of Medicine
Clinical Director, Division of Infectious Diseases
Johns Hopkins University School of Medicine
Baltimore, Maryland USA

Assistant: Stephanie Knight

Email: sknigh22@jhmi.edu

T: 443-287-4800

F: 410-502-7029

Personal Health; When Lyme invades the brain and spinal system.
Meanwhile, within weeks of entering the body, the spirochete, a bacterium that resembles the organism that causes syphilis, can…

Steven & Alexandra Cohen Foundation Appalled By Misleading New York Times Piece That Rejects Chronic Lyme Disease

https://www.businesswire.com/news/home/20190702005596/en

Steven & Alexandra Cohen Foundation Appalled by Misleading New York Times Piece that Rejects Chronic Lyme Disease

President Alex Cohen, a Chronic Lyme Sufferer, Lends Voice to Other Patients

STAMFORD, Conn.–(BUSINESS WIRE)–The Steven & Alexandra Cohen Foundation, the largest private donor of Lyme and tickborne disease research in the United States, is deeply dismayed by a recent New York Times opinion piece that denies the existence of chronic Lyme disease.

In “My Son Got Lyme Disease. He’s Totally Fine,” published in the Voices column of the New York Times Well section on June 27, the writer recounts her son’s short-lived bout with Lyme disease. She quotes pediatricians who support the hotly debated idea that Lyme is easily cured with a single course of antibiotics—and does not include counterviews.

“We find that the misinformed comments run contrary to current research and all the work that our Foundation is doing to bring light and awareness to this insidious disease,” said Alex Cohen, president, Steven & Alexandra Cohen Foundation. “I personally take offense to this article because I myself am a chronic sufferer. It is a disservice to so many who are truly suffering.”

Every year across the country, Lyme disease affects over 300,000 people, an estimated 10 to 20 percent of whom suffer from chronic symptoms after receiving antibiotic therapy. According to the Tick-borne Disease Working Group’s 2018 Report to Congress, these persistent symptoms can be disabling, though their exact cause is still unknown. The report also points to research that has found antibiotics to be ineffective in fighting “persister” bacterial cells and reiterates the limitations of current diagnostic testing.

Lyme disease has often been called “The Great Imitator”; it manifests differently in each patient, making it difficult to diagnose and treat. The writer’s son was fortunate to receive a timely and accurate diagnosis. However, his journey toward recovery may not reflect that of others. Many patients struggle to pinpoint the root cause of their symptoms, either due to flawed testing or limited access to Lyme-competent clinicians. Still others go on to develop chronic Lyme despite treatment.

In light of these complex issues, the Foundation launched the Cohen Lyme & Tickborne Disease Initiative in 2015 and since then has committed $60 million toward research focusing on new methods of prevention, diagnosis, and treatment. Having been diagnosed with Lyme disease, Mrs. Cohen has made it her personal mission to combat the spread of all tickborne diseases.

For more information and resources, visit the Johns Hopkins Lyme Disease Research Center directed by Dr. John Aucott, a renowned Lyme expert and a Foundation grant recipient. Or, read the Cohen Lyme & Tickborne Initiative’s latest newsletter.

About Steven & Alexandra Cohen Foundation

The Steven & Alexandra Cohen Foundation is committed to inspiring philanthropy and community service by creating awareness, offering guidance and leading by example to show the world what giving can do. Since launching the Foundation in 2001, Steven and Alexandra Cohen have generously funded local and national nonprofit organizations that uplift the communities in which they serve. The Cohens’ giving reflects their personal connection with the causes that inspire them. To learn more, please visit steveandalex.org or follow the Foundation on Facebook, Twitter, and Instagram.