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Joan aka MSBunny

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In Jan. 1986 I had my first mini stroke. Feb. saw ENT doctor (don’t know his name). Mar. had second mini stroke and saw an intern doctor (still don’t know his name either). Went to see my sister, Kim, in Boston and had a seizure. June had third mini stroke. July stopped driving and saw one doctor (still don’t know his name either) in Columbus, MD and one MS doctor (still don’t know his name either) in Towson, MD and ATH in St. Joseph Hospital. Sept. we decide to see Dr. Johnson, a MS specialist. He said it could be MS but more likely strokes. Oct. stayed at University of Maryland for 3 weeks saw Dr. Price, had a lot test, had another seizure, and because of bad test result had penasine. In August 1987 had symptoms of a seizure and went back to UofM and another test found a hole in my heart. Sept. saw a cardiologist and surgeon at St. Joseph Hospital and had open-heart surgery. In 1993 MS showed its ugly head. Dx with relasing progression. In April 1999 started Beta. August started Detrol LA. Sept. did not sleep for 3 weeks, depress, went to St. Joseph Hospital Mental Section for help. Stopped Beta (made me worse). Dec. got an E/W/C . In August 2001 started Novantrone. In May 2003 stopped Novantrone. 
In October I started LDN. I truly believe EVERYONE SHOULD BE ON LDN! LDN IS LOW DOSE NALTREXONE AND ONE SHOULD READ ABOUT IT WWW.LOWDOSENALTREXONE.ORG. IT IS NOT A CURE BUT IT IS THE BEST AND CLOSEST THING WE HAVE TO ONE. A PERSON CAN TAKE LDN BY ITSELF OR WITH ANOTHER TREATMENT BUT ONE CAN’T TAKE LDN WITH ANOTHER CONTROL SUBSTANCE. LDN IS A PRESCRIBED MEDICATION. IF YOU CANNOT FIND A DOCTOR WHO WILL GIVE YOU THE PRESCRIPTION, YOU CAN HAVE A TELEPHONE CONSULTATION WITH ONE OF THE DOCTORS LISTED AT THE YAHOOGROUP SITE. TO LEARN MORE GO TO WWW.YAHOOGROUP.COM. LDN DOES NOT COST ALOT; APPROXIMATELY $30.00 PER MONTH. THE PRESCRIPTION HAS TO BE FILLED AT A COMPOUNDING PHARMACY. IN ONLY 6 WEEKS LDN WILL IMPROVE YOU AND IT HAS BEEN 2 WEEKS I SEE A DIFFERENCE. LDN IS NOT PERFECT BUT IT DOES HELP. I DON’T KNOW WHY THE NATIONAL MS SOCIETY HAS NOT SAID ANYTHING MORE ABOUT IT. I DON’T KNOW EVERYTHING ABOUT IT, BUT I KNOW SOME. I WILL CONTINUE TO UPDATE MY PROGRESS. IF YOU WISH TO CONTACT ME ABOUT THIS YOU MAY AND MY E-MAIL ADDRESS IS: JMARCHILDON@PEOPLEPC.COM.

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