Anonymous wrote:I have two emotional connections to this story. One, I was desperate enough to save my life from treatment resistant depression that I sought out IV ketamine about 6 years ago before it was commonplace. It was miraculously efficacious and hen nothing else was, and I met dozens of people in waiting rooms who had similar experiences, as well as with CRPS and fibromyalgia…not surprisingly, also diagnoses where women’s self-reporting of their own pain is often dismissed as exaggerated or hysterical. Just as ketamine seems to successfully “reset” many of a patient’s default neural pathways in a way that changes thought patterns in depression, so it can also “reset” the brain’s pain perception system that has gone haywire.
It is not surprising to me at all that ketamine is a successful treatment for CRPS. It *was* surprising that she was in such high dosages, as it is certainly also addictive at high doses, so some of the pain Maya might have been suffering in the hospital was likely withdrawal.
Even so, the removal of her child from her care and presence is so over the top cruel that I can’t fathom the level of pain the child and her mother were in. Beata was pushy and confident in her knowledge and expertise. It seemed more like the doctors and nurses were offended that she questioned their God-given authority.
The second way that it hit me emotionally was the memory of being separated from my son when he was in the NICU and I was recovering from pre-eclampsia and an emergency C section. Hospital staff wouldn’t let me see the baby until I brought my blood pressure down, which I felt I couldn’t do until could touch my baby. I felt so enraged and helpless and loooked down upon. I can’t imagine how much more magnified Beata’s stress was. That poor woman.
Anonymous wrote:Anonymous wrote:Anonymous wrote:Anonymous wrote:The doctor is the one who suggested and gave ketamine to Maya, not Beata. They saw her dramatically improve with freedom of pain. So Beata wanted to continue with the treatment that seemed to have helped her daughter. I dont see how that’s abuse from Beata.
Bc you can find a doctor anywhere to say anything. Let’s say you go to a doctor who tells you your chemo needing child can instead eat a raw food diet and get sunlight daily. Can you shrug and say it’s on the doctor bc I trusted what he said?
It's not that clear, as there aren't that many doctors who specialize in CRPS. In addition, the approach to CRPS has shifted since the events in the documentary to an approach that focuses on therapy and physical therapy and not medications. The documentary does not offer a clear timeline, but it does reflect that the family tried other things, including lower doses of ketamine, before going to Mexico for treatment.
The timeline seemed pretty clear to me?? Maya started presenting with pain in July 2015 and they flew to Mexico for the ketamine coma in November 2015. IDK, that seems like a pretty short amount of time to decide to fly your kid to Mexico for a treatment that isn't legal in the US...
Anonymous wrote:Anonymous wrote:Anonymous wrote:So did they eventually give her high dose ketamine? Or did she improve on her own like they said she would?
Seems crazy the mom gave up after less than 3 months. That’s not that long.
I don't think that Maya "improved on her own." It took her several years of treatment before she started walking again. Treatment for CRPS usually involves a multi-disciplinary approach that includes counseling, intensive physical therapy, and sometimes pain management. It also involves educating the family.
It's not accurate that the mother gave up after three months. She had been trying to help her daughter for years when the cruel treatment at the hands of Dr. Smith and the hospital put her over the edge. It's hard to imagine what it feels like to have a chronically ill child. My guess is that Beata thought that after the ketamine coma, they were on the right path, so having what seems like a major setback hit her hard.
The difficult thing about CRPS is that not all doctors agree on what to do. An older generation of doctors, which it seems like Dr. Kirkpatrick was a part of, believe that you need to address a patient's pain (calm it down) before you start PT to regain function. The newer approach is to immediately start intensive PT, regardless of the pain level. If, as a parent, you are hearing two different voices, one that appears to be addressing your child's pain and another that is going to cause pain, which one would you choose? It's a huge leap of faith to accept that your child, who is in terrible pain, will get better if you force them to endure even more pain.
It can't be stated enough how unfamiliar with CRPS many healthcare providers are. One of the things mentioned in the documentary (or maybe it was an article) was that Beata was concerned about the nurses causing pain by taking Maya's blood pressure. If your child has a condition where even a light touch causes pain, dealing with providers who don't understand or don't seem willing to understand undermines your confidence in their professional judgment.
Still, it seems horrible that she took her own life because she “couldn’t take it anymore” but her daughter had been through it all herself and was still coping and still needed her mother. I could never have abandoned my child. Never.
Anonymous wrote:Anonymous wrote:Anonymous wrote:The doctor is the one who suggested and gave ketamine to Maya, not Beata. They saw her dramatically improve with freedom of pain. So Beata wanted to continue with the treatment that seemed to have helped her daughter. I dont see how that’s abuse from Beata.
Bc you can find a doctor anywhere to say anything. Let’s say you go to a doctor who tells you your chemo needing child can instead eat a raw food diet and get sunlight daily. Can you shrug and say it’s on the doctor bc I trusted what he said?
It's not that clear, as there aren't that many doctors who specialize in CRPS. In addition, the approach to CRPS has shifted since the events in the documentary to an approach that focuses on therapy and physical therapy and not medications. The documentary does not offer a clear timeline, but it does reflect that the family tried other things, including lower doses of ketamine, before going to Mexico for treatment.
Anonymous wrote:Anonymous wrote:I might trust a doctor who used an extreme therapy if it helped my child and freed her from pain,
Exactly. That's what makes this case so difficult. We aren't talking about a parent rejecting conventional treatment for a disease. It sounds like they tried other things that did not help.
Also, in response to the link about the family that didn't want chemo for their son, the state did not take the son away from the parents because of this disagreement about treatment.
I've posted several times in this thread offering my opinion as a parent of a child with CRPS. Unless you have been through an experience like Maya's, you can't understand the desperation a parent feels trying to help a child experiencing extreme pain. The level of stress and desperation is ratcheted up when you have to deal with uninformed healthcare providers who seem to understand nothing about your child's condition. Body parts that are affected by CRPS are extremely painful even when touched lightly. For some, even a shower or the touch of a blanket brings intense pain, so imagine how Beata felt seeing nurses put a blood pressure cuff on Maya's arm without any regard for her pain.
Anonymous wrote:I might trust a doctor who used an extreme therapy if it helped my child and freed her from pain,
Anonymous wrote:Anonymous wrote:Anonymous wrote:The doctor is the one who suggested and gave ketamine to Maya, not Beata. They saw her dramatically improve with freedom of pain. So Beata wanted to continue with the treatment that seemed to have helped her daughter. I dont see how that’s abuse from Beata.
Bc you can find a doctor anywhere to say anything. Let’s say you go to a doctor who tells you your chemo needing child can instead eat a raw food diet and get sunlight daily. Can you shrug and say it’s on the doctor bc I trusted what he said?
Um, yes, yes you can!
Anonymous wrote:Anonymous wrote:The doctor is the one who suggested and gave ketamine to Maya, not Beata. They saw her dramatically improve with freedom of pain. So Beata wanted to continue with the treatment that seemed to have helped her daughter. I dont see how that’s abuse from Beata.
Bc you can find a doctor anywhere to say anything. Let’s say you go to a doctor who tells you your chemo needing child can instead eat a raw food diet and get sunlight daily. Can you shrug and say it’s on the doctor bc I trusted what he said?
Anonymous wrote:Anonymous wrote:The doctor is the one who suggested and gave ketamine to Maya, not Beata. They saw her dramatically improve with freedom of pain. So Beata wanted to continue with the treatment that seemed to have helped her daughter. I dont see how that’s abuse from Beata.
Bc you can find a doctor anywhere to say anything. Let’s say you go to a doctor who tells you your chemo needing child can instead eat a raw food diet and get sunlight daily. Can you shrug and say it’s on the doctor bc I trusted what he said?