HELP DALLAS GET A SURGERY
Donation protected
PLEASE HELP ME HAVE A SURGERY FOR MULTIPLE SCLEROSIS.
https://www.youtube.com/watch?v=rRKUcxXS55w
My Story
It was 1999 I was nineteen when I woke up blind one morning. I had been a singer and entertainer for seven years, and had been working in Veterinary Medicine for 3 years as an AHT. I have been doing humanitarian work for years with the homeless and wild life rehabilitation, animal rescues, and even winning 'kindness' awards all over Calgary Alberta in the late 90's. I was changing the world.
I was diagnosed with Multiple Sclerosis at the age of twenty one and it backed me in to a corner and I was forced to make some decisions. I had witnessed what MS did to members of my family in a short period of time previously, so I decided to quit my job in Veterinary Medicine and go on tour with a musical while I still could sing and dance.
Nine months later I found myself existing in a hospital, tied up in a wheel chair with a strap over my forehead, holding my head up to a head strap, not able to speak or swallow. It took a year of daily physiotherapy for me to be able to live similar to a regular person.
For the last 17 years I have been battling to live day to day, minute to minute struggling with extreme severe pain, dead limbs, coordination problems, blindness, confusion, migranes, shooting nervous system pains like lightning bolts going through my skin, bones and body, jerks, tremors, not able to swallow liquids and solids for large chunks of time, waking up every day to something new that was wrong with my body. Only sleep took it away to bring me new disabilities the next day. I have spent fifteen years in bed sleeping as my energy was completely depleted no matter what I did. Every night for years I was so scared that I was going to die in my sleep because of breathtaking pain and my body quickly breaking down.
Now I hadnt left my bed in 2 months and was having some one help me bathe. I have tried every single gimmick, pill or suggestion, diet, acupuncture, water pressure beds or any possibility in the journey of this disease. No feeling in my arm or leg on my entire left side, cognitive apprehension dificulties and I didn't know what was going on half the time. I experienced extreme killing pain to where I would lose my hearing. All clothing and even the slightest wind breeze would hurt my skin. I also experienced maddening migranes that would last for weeks at a time where I was curled in a ball on the floor beside my bed holding my head, vomiting, going blind.
I was dying.
I travelled to Tuscon Arizona, in 2010 to have the controversial surgery CCSVI or as its called "the Liberation procedure" for MS and it radically changed my life to health again. Just as the procedure was taking place, I got really hot and started to sweat, my body was humming and pulsating with new blood flow and adrenaline.
I didn't sleep for three days in a row as I finally had energy to be awake. My legs got so sore during that time from using those muscles which hadn't been used in years.
My confusion completely disappeared as I could finally count out my change at a store and I was able to dial a phone number. I gave away my canes, wheel chair, walker and little red scooter. I was well again.
Tremors and jerks were completely gone as if they had never happened, and my extremities didn't go dead any more for days and weeks at a time. The migrane headaches instantly disappeared.
I began volunteering again as I had not been able to work any more for years by then and I was only able to volunteer once in a while. I started singing and dancing again professionally. I was finally living again. I have worked with every animal rescue under the sun in three different provinces and ran my own animal rescue. It lasted three precious years, where I could start volunteering again, and become a real person, having a life.
Currently, I have been progressively gettting sick again as it has been six years since the surgery. I am now back to a low quality of life and live with extreme pain constantly. I cannot stay awake for more than four and a half hours, and am in constant pain and discomfort.
I have experienced several accidental overdoses because I am in so much pain, I cant breathe. I was franctically trying every pill in the house, losing track of time and what pills I have taken. I would crawl from room to room on my hands and knees and collapse like I had narcolepsy, falling asleep every few paces.
The pain is back in the front of my neck, like I am being choked by invisible hands.
The tremors, jerks and shakes have come back worse and they are worse than ever.
The shooting pains like lightning bolts slam through my skin in to my bones and it makes me scream or fall and are so much worse than before. The itching sensations I get are usually at night and make me scratch so hard that I bleed. There are scars all over me now. It is hard to wear socks or any clothing because my skin hurts and crawls so much. It is like having a particle in my eye that is so irritating and painful, so relentless all throught my body, but there's nothing I can do about it. The other night I began to feel a real hot burn on the side of my lower leg. After an hour, I was in so much pain I couldn't breathe in. My flesh was burning off from what felt like acid. I sat on my kitchen floor holding an ice pack at 2 in the morning while I was grabbed the stove handle and tried to hide my wimpers from my sleeping room mate. You can be strong and a fighter for only so long before you become a little child bawling for your mummy.
I am getti ng sicker and the ugly monster that hides and does whatever it wants to, no matter how hard I try to heal is progessing quickly and attacking my body, the disease is eating me alive.
People with MS have narrowed and twisted deformed main jugular and veins that only allow blood flow up to the brain but does not allow it to drain back down. It creates blood pools on the brain that results in lesions and black holes in the brain. The CCSVI surgery opens those jugular veins with a balloon simular to angioplasty.
CCSVI name has changed to 'TVAM', basically because the FDA has stopped drs licences for doing this simple surgery that they do every day all over the world but because the word MULTIPLE SCLEROSIS is involved it is illegal. TVAM surgery is being done now in replacement as it works better and longer lasting. They open all of your veins and even the ones that are not deformed through your entire body and open valves. I have a left bundle branch blockage in my heart and a mostly closed valve that the TVAM will open.
This TVAM procedure is being done in New Port Beach California by DR ARATA, very highly recommended! This is more promising and works better than my first procedure CCSVI .
They also do stem cell replacement there which tricks your body in to forgetting it has a disease, the cleaned purified good stem cells are put back in your body and attack the sick ones, reproducing healthy ones from now on. I need this STEM CELL procedure as well to help me live. The TVAM VASCULAR OPENS DEFORMED VEINS. The STEM CELL PROCEDURE CHANGES YOUR ENTIRE SYSTEM TO WORK PROPERLY AGAIN. It is a permanent fix with no side effects.. Also cures PARKINSON'S, ALS EXCT.
It is hard to smile again. I am asking for donations so I can get another surgery to prolong my life and existence so I can help change the world again.
I have help and financial help besides my uncle, some family members and a few friends. I am desperate. I am OVERWHELMED and feel HOPELESS.
Please help me overcome this nightmare.
TVAM PROCEDURE-$7, 050
STEM CELL PROCEDURE - $6,950
= $14,000
ain.
Please help me end what is a neverending nightmare. Please donate to the cost of my new surgery at the same clinic, and the travel and lodging while I am there.
PLEASE HELP ME HAVE A BETTER QUALITY OF LIFE.
: Donations can be made here on http://www.gofundme.com/r53ks3z8
or
: PAYPAL - DALLAS GRAMLICK, - [email redacted]
THROUGH EMAIL TRANSFER TO [email redacted]
The limit of this account is $3000 per day, per person, any larger amounts can go to your bank and you can give my account information to transfer larger amounts : this is my MS trust account at
SCOTIA BANK
DALLAS GRAMLICK
TRANSIT # - 70979
INSTITUTION # - 002
ACCOUNT # -0247626
THANK YOU EARNESTLY FROM THE BOTTOM OF MY HEART!
https://www.youtube.com/watch?v=rRKUcxXS55w
My Story
It was 1999 I was nineteen when I woke up blind one morning. I had been a singer and entertainer for seven years, and had been working in Veterinary Medicine for 3 years as an AHT. I have been doing humanitarian work for years with the homeless and wild life rehabilitation, animal rescues, and even winning 'kindness' awards all over Calgary Alberta in the late 90's. I was changing the world.
I was diagnosed with Multiple Sclerosis at the age of twenty one and it backed me in to a corner and I was forced to make some decisions. I had witnessed what MS did to members of my family in a short period of time previously, so I decided to quit my job in Veterinary Medicine and go on tour with a musical while I still could sing and dance.
Nine months later I found myself existing in a hospital, tied up in a wheel chair with a strap over my forehead, holding my head up to a head strap, not able to speak or swallow. It took a year of daily physiotherapy for me to be able to live similar to a regular person.
For the last 17 years I have been battling to live day to day, minute to minute struggling with extreme severe pain, dead limbs, coordination problems, blindness, confusion, migranes, shooting nervous system pains like lightning bolts going through my skin, bones and body, jerks, tremors, not able to swallow liquids and solids for large chunks of time, waking up every day to something new that was wrong with my body. Only sleep took it away to bring me new disabilities the next day. I have spent fifteen years in bed sleeping as my energy was completely depleted no matter what I did. Every night for years I was so scared that I was going to die in my sleep because of breathtaking pain and my body quickly breaking down.
Now I hadnt left my bed in 2 months and was having some one help me bathe. I have tried every single gimmick, pill or suggestion, diet, acupuncture, water pressure beds or any possibility in the journey of this disease. No feeling in my arm or leg on my entire left side, cognitive apprehension dificulties and I didn't know what was going on half the time. I experienced extreme killing pain to where I would lose my hearing. All clothing and even the slightest wind breeze would hurt my skin. I also experienced maddening migranes that would last for weeks at a time where I was curled in a ball on the floor beside my bed holding my head, vomiting, going blind.
I was dying.
I travelled to Tuscon Arizona, in 2010 to have the controversial surgery CCSVI or as its called "the Liberation procedure" for MS and it radically changed my life to health again. Just as the procedure was taking place, I got really hot and started to sweat, my body was humming and pulsating with new blood flow and adrenaline.
I didn't sleep for three days in a row as I finally had energy to be awake. My legs got so sore during that time from using those muscles which hadn't been used in years.
My confusion completely disappeared as I could finally count out my change at a store and I was able to dial a phone number. I gave away my canes, wheel chair, walker and little red scooter. I was well again.
Tremors and jerks were completely gone as if they had never happened, and my extremities didn't go dead any more for days and weeks at a time. The migrane headaches instantly disappeared.
I began volunteering again as I had not been able to work any more for years by then and I was only able to volunteer once in a while. I started singing and dancing again professionally. I was finally living again. I have worked with every animal rescue under the sun in three different provinces and ran my own animal rescue. It lasted three precious years, where I could start volunteering again, and become a real person, having a life.
Currently, I have been progressively gettting sick again as it has been six years since the surgery. I am now back to a low quality of life and live with extreme pain constantly. I cannot stay awake for more than four and a half hours, and am in constant pain and discomfort.
I have experienced several accidental overdoses because I am in so much pain, I cant breathe. I was franctically trying every pill in the house, losing track of time and what pills I have taken. I would crawl from room to room on my hands and knees and collapse like I had narcolepsy, falling asleep every few paces.
The pain is back in the front of my neck, like I am being choked by invisible hands.
The tremors, jerks and shakes have come back worse and they are worse than ever.
The shooting pains like lightning bolts slam through my skin in to my bones and it makes me scream or fall and are so much worse than before. The itching sensations I get are usually at night and make me scratch so hard that I bleed. There are scars all over me now. It is hard to wear socks or any clothing because my skin hurts and crawls so much. It is like having a particle in my eye that is so irritating and painful, so relentless all throught my body, but there's nothing I can do about it. The other night I began to feel a real hot burn on the side of my lower leg. After an hour, I was in so much pain I couldn't breathe in. My flesh was burning off from what felt like acid. I sat on my kitchen floor holding an ice pack at 2 in the morning while I was grabbed the stove handle and tried to hide my wimpers from my sleeping room mate. You can be strong and a fighter for only so long before you become a little child bawling for your mummy.
I am getti ng sicker and the ugly monster that hides and does whatever it wants to, no matter how hard I try to heal is progessing quickly and attacking my body, the disease is eating me alive.
People with MS have narrowed and twisted deformed main jugular and veins that only allow blood flow up to the brain but does not allow it to drain back down. It creates blood pools on the brain that results in lesions and black holes in the brain. The CCSVI surgery opens those jugular veins with a balloon simular to angioplasty.
CCSVI name has changed to 'TVAM', basically because the FDA has stopped drs licences for doing this simple surgery that they do every day all over the world but because the word MULTIPLE SCLEROSIS is involved it is illegal. TVAM surgery is being done now in replacement as it works better and longer lasting. They open all of your veins and even the ones that are not deformed through your entire body and open valves. I have a left bundle branch blockage in my heart and a mostly closed valve that the TVAM will open.
This TVAM procedure is being done in New Port Beach California by DR ARATA, very highly recommended! This is more promising and works better than my first procedure CCSVI .
They also do stem cell replacement there which tricks your body in to forgetting it has a disease, the cleaned purified good stem cells are put back in your body and attack the sick ones, reproducing healthy ones from now on. I need this STEM CELL procedure as well to help me live. The TVAM VASCULAR OPENS DEFORMED VEINS. The STEM CELL PROCEDURE CHANGES YOUR ENTIRE SYSTEM TO WORK PROPERLY AGAIN. It is a permanent fix with no side effects.. Also cures PARKINSON'S, ALS EXCT.
It is hard to smile again. I am asking for donations so I can get another surgery to prolong my life and existence so I can help change the world again.
I have help and financial help besides my uncle, some family members and a few friends. I am desperate. I am OVERWHELMED and feel HOPELESS.
Please help me overcome this nightmare.
TVAM PROCEDURE-$7, 050
STEM CELL PROCEDURE - $6,950
= $14,000
ain.
Please help me end what is a neverending nightmare. Please donate to the cost of my new surgery at the same clinic, and the travel and lodging while I am there.
PLEASE HELP ME HAVE A BETTER QUALITY OF LIFE.
: Donations can be made here on http://www.gofundme.com/r53ks3z8
or
: PAYPAL - DALLAS GRAMLICK, - [email redacted]
THROUGH EMAIL TRANSFER TO [email redacted]
The limit of this account is $3000 per day, per person, any larger amounts can go to your bank and you can give my account information to transfer larger amounts : this is my MS trust account at
SCOTIA BANK
DALLAS GRAMLICK
TRANSIT # - 70979
INSTITUTION # - 002
ACCOUNT # -0247626
THANK YOU EARNESTLY FROM THE BOTTOM OF MY HEART!
Organizer
Dallas Gramlick
Organizer
Calgary, AB