Archive for the ‘Treatment’ 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.

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**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.

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.

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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.

Adirondack Researcher Raises the Alarm on Tick Invasion

https://www.wcax.com/content/news/Adirondack-researcher-raises-the-alarm-on-tick-incursion-511909882.html?ref=882

Adirondack researcher raises the alarm on tick invasion

PLATTSBURGH, N.Y. (WCAX) Ticks are gaining ground in the Adirondacks like never seen before and experts are trying to get the word out.

Courtesy: Adirondack Watershed Institute

They want to make sure people living there including visitors and medical providers know how to spot and treat ticks.

Paul Smith’s College tick researcher Lee Ann Sporn helped organize a panel this week — “A Ticking Time Bomb: The Tick Crisis in the Adirondacks” — and is traveling around different parts of the North Country presenting her latest research.

“The lore, the common lore is still that there isn’t ticks and there are no risk of tick borne diseases here in the North Country. Physicians are still failing to treat people with tick bites because they say this is a no risk, or low risk tick borne disease area, which now is really untrue, so we’re really trying to get that word out,” Sporn said.

The best way to protect yourself from ticks includes covering your skin by wearing light and bright colors, use an insecticide like pyrethrin, and do a tick check from head-to-toe when you get home.

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**Comment**

At this point, any doctor who fails to treat people with tick bites should be turned into the medical board.
Ticks are everywhere.

https://madisonarealymesupportgroup.com/2019/03/09/danish-study-shows-migrating-birds-are-spreading-ticks-their-pathogens-including-places-without-sustainable-tick-populations/

https://madisonarealymesupportgroup.com/2019/04/03/ticks-lyme-are-in-cities-too/

https://madisonarealymesupportgroup.com/2019/06/07/ny-tick-study-challenges-belief-that-tickborne-disease-risk-is-only-in-natural-settings/

Please watch this video of how ticks were found in the cracks of sidewalks in CA:  https://madisonarealymesupportgroup.com/2019/05/17/video-showing-questing-ticks-in-the-middle-of-the-sidewalk/

Ticks have been found in caves, on rocks, underneath picnic benches, and have fallen from trees onto patios:  https://madisonarealymesupportgroup.com/2018/06/07/ticks-on-beaches/

Ticks found on eyeball, butt, and penis:  https://madisonarealymesupportgroup.com/2017/07/30/ticks-found-on-eyeball-buttocks-and-penis/

https://madisonarealymesupportgroup.com/2019/06/19/a-creepy-bed-time-story-from-stephen-king/ (Tick on eye)

Tick in ear had to be surgically removed:  https://madisonarealymesupportgroup.com/2019/05/02/tick-in-boys-ear-had-to-be-surgically-removed/

It’s a good thing they don’t fly.  But, they do blow in the wind. Advocates have told me stories of ticks blowing into their swimming pools. My neighbor with a farm field mowed his lawn, blowing the grass toward my house. I found ticks crawling on my basement screens and a few found their way inside the house on the walls.

The tick maps should be thrown into the trash.

For far too long patients have been denied diagnosis and treatment based on a piece of paper telling them where ticks are supposed to be.

This is STILL happening as this is being written:  https://madisonarealymesupportgroup.com/2019/04/22/its-just-crazy-why-is-lyme-disease-treatment-so-difficult-to-find-in-mississippi/

 

 

 

 

Touched By Lyme: Singing From the IDSA Lyme Hymnal

https://www.lymedisease.org/mandavilli-response/

TOUCHED BY LYME: Singing from the IDSA Lyme hymnal

 

 

 

Doctors at Many Stem-Cell Clinics Don’t Have Relevant Training

https://www.nature.com/articles/d41586-019-01999-6?

Doctors at many stem-cell clinics don’t have relevant training

Few US clinics offering unproven treatments employ physicians with expertise in all the conditions they offer to treat, finds survey.
Photo of a syringe containing cells prepared for stem cell therapies for a patient

A clinician prepares a syringe containing stem cells used for therapy.Credit: Patrick T. Fallon/Getty

Many companies offering unproven stem-cell therapies in the United States do not employ clinicians with relevant medical training, an analysis has found.

Fewer than half of the 166 businesses analysed in the study employed physicians whose formal medical training covered the conditions the company claimed to treat, according to the paper, which was published on 25 June in JAMA1.

“This study highlights that patients need to be aware that many physicians who advertise stem-cell treatments are not only operating outside the bounds of scientific evidence, but outside their own professional qualifications,” says Douglas Sipp, a researcher at the RIKEN Center for Biosystems Dynamics Research in Kobe, Japan.

The only stem-cell-based products that are approved by the US Food and Drug Administration (FDA) as medical treatments are blood-forming cells used to treat certain blood and immune-system disorders. Stem cells taken from healthy bone marrow are also used in transplants to treat some cancers. Yet in the past decade or so, hundreds of clinics have sprung up in the country offering stem-cell treatments for a wide range of other conditions, including muscular dystrophy, Alzheimer’s disease and vision loss.

In the United States, stem cells can be extracted and reinjected into people without FDA approval as long as the cells have been only “minimally manipulated”. Companies have argued that their procedures therefore do not need approval — but many bioethicists disagree, claiming that many of the procedures they offer should be classified as drugs, biologics or medical devices, which the FDA must approve for use.

Background checks

The analysis looked at the websites of 166 companies that were advertising their services in January 2018 and that listed their clinical staff online.

Nine companies did not list any physicians. Five of these were staffed entirely by podiatrists; two by naturopaths, who use interventions such as homeopathy and acupuncture; and one by dentists.

Of the companies that employed doctors, just 81 listed physicians who had medical training that the researchers deemed was necessary to cover all of the conditions the firms’ clinics offered to treat (see ‘Stem-cell doctors’).

Source: Ref. 1

Businesses offering unproven stem-cell treatments for orthopaedic conditions — among the most common conditions for which such therapies are offered — were more likely to employ trained doctors: 77% listed one or more physicians with formal training in orthopaedics. But only 19% of practices offering to treat non-orthopaedic conditions employed physicians with relevant specialist training.

“Patients need to ensure they look at trusted sources of information and consider the backgrounds of physicians when considering medical care, including regenerative care,” says Zubin Master, a bioethicist at the Mayo Clinic in Rochester, Minnesota, who led the study.

Master acknowledges that some of the physicians employed by the companies might have gained relevant further qualifications beyond their formal medical training.

doi: 10.1038/d41586-019-01999-6

References

  1. Fu, W. et al. J. Am. Med. Assoc. 321, 2463–2464 (2019)

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**Comment**

As always, “Buyer Beware,” when it comes to treatments.

https://www.treatlyme.net/guide/stem-cell-therapy-lyme  Great article by Dr. Ross.  Excerpt:

What The Data Says

However, most with Lyme disease do not appear to benefit from stem cell therapy as it is currently practiced. My Lyme Data, an ongoing research project of lymedisease.org, shows only three percent of patients receiving stem cell therapy report improvements. For more information about this study see: What Alternative Treatments Work for Lyme Disease? What Are Their Side Effects? at lymedisease.org

On the other hand, there are some case reports in the literature which show marked improvement in Lyme disease by people who undergo stem cell therapy using human embryonic stem cells (HESC).

My Lyme Data’s findings are instructive, but could be limited by the small number of people who have had stem cell therapy. Also, not all stem cell therapies are equal. And My Lyme Data does not indicate what type of stem cell therapy people received.

My Observation

Before stopping my Seattle clinical practice in late 2018, I did not observe major improvements in most of my patients who tried stem cell therapy either before or after having treatment with me. I did not have any of my active patients pursue this type of therapy while they were under my care.

https://www.publichealthalert.org/stem-cell-therapy-for-lyme-disease.html

https://lymediseaseguide.net/stem-cell-treatment-for-lyme-disease

I know few who have used stem cell therapy for Lyme disease, but it’s expensive and make sure if you are considering it ask many, many questions. Patients can spend thousands and not be informed up front of the lengthy & costly follow up treatments that were not included in the original price.

Unfortunately, those I know did not improve.