Hello, I am the person on the Facebook Parkinson’s Disease page that told about my Son who had grand mal seizures for 18 years and after 80 dives at Dr. Paul Harch’s place in New Orleans has been seizure free for 13 years. Here is what I DIDN’T share on that page: I just did a 40 dive 2 atmospheres pressure at Dr. Harch’s from April 1st until May 28th of this year. I am in Stage 3 but just diagnosed in March 2024. It’s a long story, I kept ignoring and making excuses for my symptoms for almost a decade.🙄🙄😕😞 Anyway when I first did my first dive my feet were red and purple because I am a busy woman. I cook, I clean. I do lots of Mom and Wife stuff. Anyway my circulation in my feet was horrible. Dr. Harch was appalled but said hyperbaric would fix me up.💪🏼. He was right. In less than 5 dives, my feet were turning a normal pink color. My circulation had dramatically improved.💪🏼. I found I was sleeping better with less REM bad nightmare sleep. 👍🏼. My mood was improved-I wasn’t crying just watching a commercial or seeing a bird fly.🙄👍🏼. I am walking without a cane and gave not fallen since I started this, and I was falling often before treatment. I have learned that increased oxygenation in the blood can do amazing things to telomere length and can actually cause neurogenesis in neuronal synapses in the brain. Did that happen for me? I do not know yet. Time will reveal all. I DO know that it was a very positive experience. My feet are still a pink normal color. I am still in a happier mood. My sleep is so much better. We plan on doing this again next year if we need to (my Husband is the one who drove me to and fro). I will keep you posted on this and thank you for covering this topic. It is paid out of our own pocket which is why I didn’t me it on that Facebook page. It seemed cruel to mention something great that the majority of people could not afford.😞.
This is amazing testimony! I understand your hesitancy to mention all of that in that group. I hope to see you more in the comments section Julie! I appreciate your feedback here and on Facebook.
Many would say this is too good to be true, I must say this real quick that it is very good and very true how Dr Madida Sam on UA-cam cured my Parkinson Disease with their PD treatment protocol🌱
My mom had been getting HBOT treatments in a soft sided chamber. She said it felt like her brain fog decreased somewhat; it also seemed to calm her tremors a bit. However, now I’m wondering if a hard chamber would be better as the ata would be higher? I believe the soft chambers have an ata of about 1.3.? What are your thoughts on this?
Great question! I think it would be better as I’ve heard that they can do treatments of up to 2-3 atmospheres in the hard chambers. I know a PwP who has done this
My father went through interferon therapy trials around 23 years ago...a couple of years later he was diagnosed with Parkinsons. I’ve read that toxins like interferon can trigger Parkinsons...and thoughts?
Consider specialized pro resolving Mediators and Palmitoylethanolamide Role of Specialized Pro-resolving Mediators in Reducing Neuroinflammation in Neurodegenerative Disorders
Hello, I am the person on the Facebook Parkinson’s Disease page that told about my Son who had grand mal seizures for 18 years and after 80 dives at Dr. Paul Harch’s place in New Orleans has been seizure free for 13 years. Here is what I DIDN’T share on that page: I just did a 40 dive 2 atmospheres pressure at Dr. Harch’s from April 1st until May 28th of this year. I am in Stage 3 but just diagnosed in March 2024. It’s a long story, I kept ignoring and making excuses for my symptoms for almost a decade.🙄🙄😕😞
Anyway when I first did my first dive my feet were red and purple because I am a busy woman. I cook, I clean. I do lots of Mom and Wife stuff. Anyway my circulation in my feet was horrible. Dr. Harch was appalled but said hyperbaric would fix me up.💪🏼. He was right. In less than 5 dives, my feet were turning a normal pink color. My circulation had dramatically improved.💪🏼. I found I was sleeping better with less REM bad nightmare sleep. 👍🏼. My mood was improved-I wasn’t crying just watching a commercial or seeing a bird fly.🙄👍🏼. I am walking without a cane and gave not fallen since I started this, and I was falling often before treatment.
I have learned that increased oxygenation in the blood can do amazing things to telomere length and can actually cause neurogenesis in neuronal synapses in the brain. Did that happen for me? I do not know yet. Time will reveal all. I DO know that it was a very positive experience. My feet are still a pink normal color. I am still in a happier mood. My sleep is so much better. We plan on doing this again next year if we need to (my Husband is the one who drove me to and fro). I will keep you posted on this and thank you for covering this topic. It is paid out of our own pocket which is why I didn’t me it on that Facebook page. It seemed cruel to mention something great that the majority of people could not afford.😞.
This is amazing testimony! I understand your hesitancy to mention all of that in that group. I hope to see you more in the comments section Julie! I appreciate your feedback here and on Facebook.
Many would say this is too good to be true, I must say this real quick that it is very good and very true how Dr Madida Sam on UA-cam cured my Parkinson Disease with their PD treatment protocol🌱
Bonjour, merci pour cette vidéo. Comment contacter la clinique de oxford pour des renseignements ? Merci
Mais oui! Voici le lien: theoxfordcenter.com
My mom had been getting HBOT treatments in a soft sided chamber. She said it felt like her brain fog decreased somewhat; it also seemed to calm her tremors a bit. However, now I’m wondering if a hard chamber would be better as the ata would be higher? I believe the soft chambers have an ata of about 1.3.? What are your thoughts on this?
Great question! I think it would be better as I’ve heard that they can do treatments of up to 2-3 atmospheres in the hard chambers. I know a PwP who has done this
My father went through interferon therapy trials around 23 years ago...a couple of years later he was diagnosed with Parkinsons. I’ve read that toxins like interferon can trigger Parkinsons...and thoughts?
I have no idea if there is a connection. Interferon is often used in autoimmune conditions if I remember correctly.
Consider specialized pro resolving Mediators and Palmitoylethanolamide
Role of Specialized Pro-resolving Mediators in Reducing Neuroinflammation in Neurodegenerative Disorders
Thank you, is this the title of a journal article?
@@parkinsonsdiseaseeducation Yes, it's one, there are many more with reference to MS, ALS, ALZ, etc.
@@parkinsonsdiseaseeducation Same holds for PEA.
This is great, much appreciated!
@@parkinsonsdiseaseeducation You are so welcome, we need this sort of info to permeate society, my sub has this sort of stuff in spades.
Prolonged excessive masturbation daily per day upto 8 years cause Parkinson disease yes or no
No, there is no connection between sexual activity of any kind that would cause Parkinson’s.