Monday, September 20, 2010
life after ccsvi
so i woke this morning...thats good right lol. what a ride this b has been...a life experience lol. as most of you know vince and i went to cabo san lucs aug 26 for ccsvi treTMENT. I HAD SIMPLE ANGIOPLASTY AUG 27 AND WOW IS QALL I CAN SAY LOL THAT FIRST NIGHT WAS SO COOL I WAS SHOWING IOFF LOL MY HUSBAND CALLED ME HIS LITTLE CHICKEN LOL I WAS UP MAND DOWN WALKING DOWN THE HOTEL HALL WITHN HANDS ON HIPS NOT HOLDONG WALLS...I WAS A RUNWAY MODEL LOL....VINCE TOLD ME TO TAKE IT RASY BUT I WAS AMAZED AT ALL THAT WAS DIFFERENT I WANT THAT AGAIN...AFTER ONLY A COUPLE HRS HOW CAN THIS SHIT HAPPEN LOL THEN I CRASHED AND BURNRD LOL BUT NI WAS TIRED...NOT THE FATIGUE TIRED HARD TO EXPLAIN BUT DIFFERENT MANY OF YOU KNOW WHAT I MEAN 3 TO 4 DAYS LATER I STARTED TO FEEL CRAPPY AGAINN BUT THOUGHT IT WAS THE HEAT...IUTWAS HOT THERE LOL...I THOUGHT ONCE I GOT HME TO MY CLIMATEand all things wouold be good...boy was i wrong lol....got home and all tjhat was good went aweay ND GOT WORSE UGH!! now the doc who i have kept in contact with thinks i have restenosised and have thrombosis....who knows wtf that is...i aint looking...just more to worry about lool....so it looks like we may be going back to cabo ugh i hate mexico niot my first choice for a hol;iday!! i did meet really great people there some there for the same reason as me some mexicans...and i cant wait to hear from you nall!! so once we figure out what is up i wiu;ll let all thanks for all the welol wishes and ttys!!
Thursday, July 29, 2010
ccsvi help
ABOUT ME:
Heyyy. My name is Roxane, i am 35 yrs old.Wife to Vince and mother to Tessa 16 and Brianna 12. I was diagnosed(dx) with multiple sclerosis in 2006...wow coming up 5 yrs already lol. I have been legally blind for almost 4 yrs i have had double vision all of those years.I have no balance whaat so ever and i am always dizzy and nauseaous. My hands and feet go numb and just lately i am so itchy i want to rip my own skin off.My hands and feet are always cold and i dont walk so well. Years earlier i had another run in with ms IN 1993 MY DAD STARTED SHOWING SIGNS OF ms WITH TINGLING FINGERS A FEW YRS LATER HE WASDX WITH ms...IT WAS A FAST STEADY PROGRESSION AND went downhill fast and my dad died in 1999 from complications to his MS i see that happening to me and its scary!! Everyday seems to get worse...is that possible??lol
ABOUT MY QUEST:
In November 2009 i saw this clip on w5 about ccsvi and how it may relieve MS symptoms(sx)at the time i remember thinking that the MSS would have my back on this...in the coming months i would see how this was not to be lol. i have friended a few on FBK who have had the ccsvi treatment and wow they are doing so much better.This is something Canada will not pay for and doesnt seem to recognize as helpful. In the past few days i have seen brad wall on the news tryong to bring this to SK but i dont have the time to wait so i have contacted a place in Mexico and have scheduled a flight there on august 26th i am still waiting for confirmed dates from them. Like most people i dont just have 10 k sitting around sooo here i am trying to raise momey for the procedure. I am asking anyone that wants to help me in my quest to get this simple procedure...ask your friends nboss heck even your neighbours lol. I just want some of my life back!! If you can help i have many ways
RBC banking:07218-5055090
air miles: 8403 281 8099
paypal:vincegarland@sasktel.net
or snail mail...does anyone do that anymore lol i dont even know how much a stamp is lol Roxane Garland
27 Cavendish st
Regina, sk
s4n1p1
Heyyy. My name is Roxane, i am 35 yrs old.Wife to Vince and mother to Tessa 16 and Brianna 12. I was diagnosed(dx) with multiple sclerosis in 2006...wow coming up 5 yrs already lol. I have been legally blind for almost 4 yrs i have had double vision all of those years.I have no balance whaat so ever and i am always dizzy and nauseaous. My hands and feet go numb and just lately i am so itchy i want to rip my own skin off.My hands and feet are always cold and i dont walk so well. Years earlier i had another run in with ms IN 1993 MY DAD STARTED SHOWING SIGNS OF ms WITH TINGLING FINGERS A FEW YRS LATER HE WASDX WITH ms...IT WAS A FAST STEADY PROGRESSION AND went downhill fast and my dad died in 1999 from complications to his MS i see that happening to me and its scary!! Everyday seems to get worse...is that possible??lol
ABOUT MY QUEST:
In November 2009 i saw this clip on w5 about ccsvi and how it may relieve MS symptoms(sx)at the time i remember thinking that the MSS would have my back on this...in the coming months i would see how this was not to be lol. i have friended a few on FBK who have had the ccsvi treatment and wow they are doing so much better.This is something Canada will not pay for and doesnt seem to recognize as helpful. In the past few days i have seen brad wall on the news tryong to bring this to SK but i dont have the time to wait so i have contacted a place in Mexico and have scheduled a flight there on august 26th i am still waiting for confirmed dates from them. Like most people i dont just have 10 k sitting around sooo here i am trying to raise momey for the procedure. I am asking anyone that wants to help me in my quest to get this simple procedure...ask your friends nboss heck even your neighbours lol. I just want some of my life back!! If you can help i have many ways
RBC banking:07218-5055090
air miles: 8403 281 8099
paypal:vincegarland@sasktel.net
or snail mail...does anyone do that anymore lol i dont even know how much a stamp is lol Roxane Garland
27 Cavendish st
Regina, sk
s4n1p1
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