Sunday, September 7, 2014
Saturday, September 6, 2014
MULTIPLE SCLEROSIS : Day After Day One Hbot Treatment. 09/06/2014
MULTIPLE SCLEROSIS : Day After Day One Hbot Treatment. 09/06/2014: I am sneezing, coughing, and have symptoms of a serious head cold. My neck aches, my head aches, and my throat is irritated. I am feeling v...
Day After Day One Hbot Treatment. 09/06/2014
I am sneezing, coughing, and have symptoms of a serious head cold. My neck aches, my head aches, and my throat is irritated. I am feeling very weak from the non stop coughing attacks. Head pounding exhaustion. And again weary looking and aging from no proper rest since July.I don't know if the Hbot had a viral person inside it before me? Or if I am experiencing a normal reaction?
After the first treatment yesterday, I was a bit loopy and fell asleep for four hours in the afternoon. The adventure out of my house, wore me out and depleted all my energy. I was hoping that after 90 minutes in a Oxygen Chamber I would be feeling amazing. This did not happen.
I have been drinking Ionix Supreme to help my throat feel better, it is not a cough syrup, but it is a healing elixir that has a lot of nutritional ingredients that will help me heal. I have been using Ionix Supreme for eight years to assist me with inflammation and stress.
My right ear and jaw are a concern to me since the pain is still aggressively reminding me that I forgot to tell the Dr. that my ear drum was busted in the summer of 1972 or was it 1973? I really don't remember. But I remember the blood. I remember the flood. I remember some.
I told the Dr I have bouts of PTSD "post traumatic stress disorder'' and not giving him detailed information, but it was from that summer and along with a broken ear drum, I was in my first coma.
I told him 2 weeks but I don't know if it was a month or 8 days? My friend Royce told me I could get the records.. Were talking 40 plus years ago! It always comes back to bite me.
In the intake interview Dr. Matt asked about my fillings and if I had any.. and looked into my pie hole. Seeing my left side has gold crowns.. My right side has extractions. Remember the pain on the right side. Well about 5 years ago I had the dentist remove those molars to ease pain. It didn't work. So if your having tooth ache pain and you have M.S.? Keep your teeth. It is M.S.
But I have to have my gold crowns removed and replaced with porcelain on my left side.
Apparently all metal fillings are taboo. And logic dictates that since my M.S. symptoms are more intense on my right side and those gold crowns are on my left side.. I was bummed too, because I could have had porcelain crowns, but I chose gold. My reasoning is, gold keeps value and when I die my kids can take that gold and cash it in. Dr Matt was laughing out loud when he understood I was serious.
Questions that were asked in the intake.
When did you get your first filling?
How many mercury fillings do you have?
What accidents have you had?
What chemicals and drugs have you been exposed too.
So this all goes back to showing that if you lived in a house built before 1978 you
drank water from lead pipes. Well I lived in Arizona and everything was lead.
So before I even got a chance to run I was toxic.
Working at Rogers Corporation with the MEK "Methyl Ethyl Ketone" this had the Doc shaking his head right and left for at least 30 seconds.
I asked Dr Matt about marijuana and he said it was "SAFE." Wow!
He does not know my history but I almost went to prison for 15 years because I was
associated with pot smokers. Such a different world we live in. There are people in prison
today because they had a rolled joint in their car or burnt little 'roach.'
Ahem, no I do not smoke pot, but I am seriously considering it to help with spasms and migraines.
Normal questions,
How much do you drink? How much do you smoke? When and how often.
How much water do you drink every day? I passed this one with a HAPPY Face.
My SELFIE INSIDE THE HBOT CHAMBER ON SEPTEMBER 5th, 2014
Annihilating Multiple Sclerosis! AMS
Friday, September 5, 2014
SESSION ONE HBOT Annihilate Multiple Sclerosis
I will be posting updates as I move forward and towards completing the 40 Hbot sessions. Some of you may be interested?
I am unable to climb into the chamber without assistance and I walk like a Zombie dragging my right leg and I have drop foot. My whole right side of my body including my tongue is M.S. paralyzed. So yeah, Zombie.
This morning was my first treatment and the pressure hurt my right ear, jaw, neck etc,. and under and over my right eye. I pondered if I could do this? I chose to endure it until I couldn't. Finally the pain subsided and I found a comfortable position inside the chamber and I took this cell phone selfie and I was thinking ''I wish my Mom was alive and with me." Probably not the best thought since I have a fear of feeling trapped. So I psyched my logic in truth. There is a big zipper. A new hashtag #AMS Annihilating Multiple Sclerosis! I like this plan!
After the 90 minute session, I did not notice any major improvement and I did fall into my ritual coma nap after 3 pm today which lasted 4 hours. I have a headache, more painful on my right side and my legs are heavy and feeling the burn. I was expecting to feel amazing and this did not happen.
Today's visit cost $300.00 cash because it was my first visit and there were intake questions. Next week I go back for two 90 minutes Hbot sessions on Monday and Wednesday. Another $300.00 and I should be going every day but it is what I am able to do now.#GRATITUDE
I am unable to climb into the chamber without assistance and I walk like a Zombie dragging my right leg and I have drop foot. My whole right side of my body including my tongue is M.S. paralyzed. So yeah, Zombie.
This morning was my first treatment and the pressure hurt my right ear, jaw, neck etc,. and under and over my right eye. I pondered if I could do this? I chose to endure it until I couldn't. Finally the pain subsided and I found a comfortable position inside the chamber and I took this cell phone selfie and I was thinking ''I wish my Mom was alive and with me." Probably not the best thought since I have a fear of feeling trapped. So I psyched my logic in truth. There is a big zipper. A new hashtag #AMS Annihilating Multiple Sclerosis! I like this plan!
After the 90 minute session, I did not notice any major improvement and I did fall into my ritual coma nap after 3 pm today which lasted 4 hours. I have a headache, more painful on my right side and my legs are heavy and feeling the burn. I was expecting to feel amazing and this did not happen.
Today's visit cost $300.00 cash because it was my first visit and there were intake questions. Next week I go back for two 90 minutes Hbot sessions on Monday and Wednesday. Another $300.00 and I should be going every day but it is what I am able to do now.#GRATITUDE
The weariness of Multiple Sclerosis ..... I am so tired.
BEFORE JULY 2014
This was recorded before the M.S. attacked me I am so glad
I sent a ''Thank you'' Video on my cell phone.
I did not know I would be using it to Fight MS.
Seriously painful
I did not know I would be using it to Fight MS.
Thursday, September 4, 2014
MULTIPLE SCLEROSIS notes
It is 12 noon on Thursday and I am bone tired .. I have done very little to be this fatigued.
There is a t.v. show called EXTANT and it has a robot boy named Ethan.
He runs on batteries and when the bad guy took his energy cell packs out. Ethan looks up and says "My power is low." and he was out.
This is exactly how Multiple Sclerosis is. Only we do not get new cell power packs put into our back.
Every bit of energy in my body is on reserve and when I use any task it takes 5 times more than a healthy person. That is on a good day!
Since I have been in the Flare up, 2 months now. My whole body is showing the stress of no rest.
I just want to scream and hit something hard and crash forward.. I want to break through this ..
I want a CURE.
There is a t.v. show called EXTANT and it has a robot boy named Ethan.
He runs on batteries and when the bad guy took his energy cell packs out. Ethan looks up and says "My power is low." and he was out.
This is exactly how Multiple Sclerosis is. Only we do not get new cell power packs put into our back.
Every bit of energy in my body is on reserve and when I use any task it takes 5 times more than a healthy person. That is on a good day!
Since I have been in the Flare up, 2 months now. My whole body is showing the stress of no rest.
I just want to scream and hit something hard and crash forward.. I want to break through this ..
I want a CURE.
Monday, September 1, 2014
MS Notes Happy Labor Day
Fighting Multiple Sclerosis takes so much energy and quickly. It is the first time that I can remember bringing M.S. Symptoms into September.
"Happy Labor Day Everyone."
I second guess myself all the time. But, I read this article about M.S. medicine and then I remember why I stopped taking Tysabri, Rebif, Copaxone etc., Liver disease and PML and even death is a side effect from taking M.S. drugs.
http://articles.mercola.com/sites/articles/archive/2012/02/09/why-did-ms-drug-kill-eleven-people.aspx
I am tired right now, my energy is used. But I used it wisely. I spent some time with my two youngest grand-babies for a few hours this morning, and while I could not take them to the park, we were very happy to see each other.
The tight burning feelings and spasms in my legs have not stopped. I read that when the legs are the problem then the lesions are on the spine. Not good. Lesion is a dirty word. Admitting the M.S. has tricked me and created new avenues in my nervous system to create havoc is disheartening.
I want to thank you for your prayers and personal notes. And I am praying for you too, whom have been going through challenges.
I discovered today that the 'but' in all of this is learning. Learning to be humble, learning to ask for help, learning to really be open.
GO FUND ME
"Happy Labor Day Everyone."
I second guess myself all the time. But, I read this article about M.S. medicine and then I remember why I stopped taking Tysabri, Rebif, Copaxone etc., Liver disease and PML and even death is a side effect from taking M.S. drugs.
http://articles.mercola.com/sites/articles/archive/2012/02/09/why-did-ms-drug-kill-eleven-people.aspx
I am tired right now, my energy is used. But I used it wisely. I spent some time with my two youngest grand-babies for a few hours this morning, and while I could not take them to the park, we were very happy to see each other.
The tight burning feelings and spasms in my legs have not stopped. I read that when the legs are the problem then the lesions are on the spine. Not good. Lesion is a dirty word. Admitting the M.S. has tricked me and created new avenues in my nervous system to create havoc is disheartening.
I want to thank you for your prayers and personal notes. And I am praying for you too, whom have been going through challenges.
I discovered today that the 'but' in all of this is learning. Learning to be humble, learning to ask for help, learning to really be open.
GO FUND ME
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