At the end of my hospital stay, I was confident in two things:
After my second relapse I was diagnosed officially and at the moment my doctor was watching at me with so much pity, that I wanted to punch him. Only once I was weak enough that I could pity myself. I noticed that and thought that it will never happen again!
I knew nothing about MS and tried to be in a good mood. I was told many times that MS must be treated as soon as possible, but I didn't have enough money for Interferons. I guess you know the costs of them: from $900 to $2700 per month and they should be taken for at least 2-3 years. I earn $300 per month and live with my mother and my younger brother. Unfortunately, I am the main source of money in the house.
When my MS got worse to the point that I couldn't walk more than 200-300 meters, I had to stay home and work at home. Of course my job as a technician had to end, but I could still work at home, so my boss gave me the possibility to work at home. I am still working, despite the fact that I'm feeling worse.
From the very first relapse and till now I've lost some of my friends and my ability to walk outside without help, but I gained much more. Now I have my beloved girlfriend, a true friend with a unique sense of humor that is helping me to get through this and a chance to get my life back.
About 1.5 years ago I've learned about a new procedure (called 'The Liberation Procedure' among people with MS). The condition for the procedure has the official name of CCSVI, which in fact means that a person has blocked veins in neck and upper torso. I got interested and tried to found out a lot more about it.
After a huge amount of time I got very confident that I have CCSVI too and it can maybe even cure me completely. Unfortunately it is not a cure at all, but the effect that this procedure makes is amazing. I wanted to do this procedure in America, but my closest ones convinced me to find another place, that will be cheaper... They succeeded. I found the cheapest variant of this procedure, which was in Bulgaria. My boss helped me with the money and all I had to do is go to Bulgaria and have this done.
Now I understand, that I shouldn't have listened to my family, get some more money and get this all done in America.
To be continued...
- I will get trough everything, because I have a lot of planes undone.
- There is someone that is watching and helping me.
After my second relapse I was diagnosed officially and at the moment my doctor was watching at me with so much pity, that I wanted to punch him. Only once I was weak enough that I could pity myself. I noticed that and thought that it will never happen again!
I knew nothing about MS and tried to be in a good mood. I was told many times that MS must be treated as soon as possible, but I didn't have enough money for Interferons. I guess you know the costs of them: from $900 to $2700 per month and they should be taken for at least 2-3 years. I earn $300 per month and live with my mother and my younger brother. Unfortunately, I am the main source of money in the house.
When my MS got worse to the point that I couldn't walk more than 200-300 meters, I had to stay home and work at home. Of course my job as a technician had to end, but I could still work at home, so my boss gave me the possibility to work at home. I am still working, despite the fact that I'm feeling worse.
From the very first relapse and till now I've lost some of my friends and my ability to walk outside without help, but I gained much more. Now I have my beloved girlfriend, a true friend with a unique sense of humor that is helping me to get through this and a chance to get my life back.
About 1.5 years ago I've learned about a new procedure (called 'The Liberation Procedure' among people with MS). The condition for the procedure has the official name of CCSVI, which in fact means that a person has blocked veins in neck and upper torso. I got interested and tried to found out a lot more about it.
After a huge amount of time I got very confident that I have CCSVI too and it can maybe even cure me completely. Unfortunately it is not a cure at all, but the effect that this procedure makes is amazing. I wanted to do this procedure in America, but my closest ones convinced me to find another place, that will be cheaper... They succeeded. I found the cheapest variant of this procedure, which was in Bulgaria. My boss helped me with the money and all I had to do is go to Bulgaria and have this done.
Now I understand, that I shouldn't have listened to my family, get some more money and get this all done in America.
To be continued...
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