Re: [TMIC] : Today is my 7 year anniversary
Kim, I agree we need to give constant thanks to our supporters.What would we do without them!This is my 4th year with TM and the adjustment has been hard, but I just read an article about a woman with ALS. I immediately was thankful I only had TM after reading the article, but after a while I go back to thinking what it was like before TM. I guess that is only human. Janice From: kimharrison...@comcast.net Sent: Thursday, October 06, 2011 5:00 AM To: tmic-list@eskimo.com Subject: [TMIC] : Today is my 7 year anniversary Today is my 7 year anniversary that TM, (transverse myelitis) came into my life. I never would have imagined one morning I would wake up, my right foot be asleep and in less than 8 hours be paralyzed on the right side of my body from the waist down, changing my life forever. I have tried to welcome the challenges and have crossed many hurdles this spinal cord disease thrown at me. I would like to thank my family, friends and especially Brian for the love and support I have been given. Sometimes I fail to say Thank You as often as I should to everyone who has supported me. I would not be where I am today without all of you. As I do not see a “cure” for this disease in my life time, the journey will continue and life as I know it will “roll on” http://www.christopherreeve.org/site/c.mtKZKgMWKwG/b.6357597/k.3480/Living_Life_to_the_Fullest_with_TM.htm
Re: [TMIC] : Today is my 7 year anniversary
Janice I agree with you. When I start feeling sorry for myself, I think about all those who have it much worse and then I realize how lucky I am that I can walk after a fashion and can get around. Patti - Wisconsin On Sat, Oct 8, 2011 at 10:19 AM, Janice Nichols jan...@centurytel.netwrote: Kim, I agree we need to give constant thanks to our supporters.What would we do without them!This is my 4th year with TM and the adjustment has been hard, but I just read an article about a woman with ALS. I immediately was thankful I only had TM after reading the article, but after a while I go back to thinking what it was like before TM. I guess that is only human. Janice *From:* kimharrison...@comcast.net *Sent:* Thursday, October 06, 2011 5:00 AM *To:* tmic-list@eskimo.com *Subject:* [TMIC] : Today is my 7 year anniversary Today is my 7 year anniversary that TM, (transverse myelitis) came into my life. I never would have imagined one morning I would wake up, my right foot be asleep and in less than 8 hours be paralyzed on the right side of my body from the waist down, changing my life forever. I have tried to welcome the challenges and have crossed many hurdles this spinal cord disease thrown at me. I would like to thank my family, friends and especially Brian for the love and support I have been given. Sometimes I fail to say Thank You as often as I should to everyone who has supported me. I would not be where I am today without all of you. As I do not see a “cure” for this disease in my life time, the journey will continue and life as I know it will “roll on” http://www.christopherreeve.org/site/c.mtKZKgMWKwG/b.6357597/k.3480/Living_Life_to_the_Fullest_with_TM.htm
Re: [TMIC] : Today is my 7 year anniversary
keep your chin up! From: kimharrison...@comcast.net kimharrison...@comcast.net To: tmic-list@eskimo.com Sent: Thursday, October 6, 2011 6:00 AM Subject: [TMIC] : Today is my 7 year anniversary Today is my 7 year anniversary that TM, (transverse myelitis) came into my life. I never would have imagined one morning I would wake up, my right foot be asleep and in less than 8 hours be paralyzed on the right side of my body from the waist down, changing my life forever. I have tried to welcome the challenges and have crossed many hurdles this spinal cord disease thrown at me. I would like to thank my family, friends and especially Brian for the love and support I have been given. Sometimes I fail to say Thank You as often as I should to everyone who has supported me. I would not be where I am today without all of you. As I do not see a “cure” for this disease in my life time, the journey will continue and life as I know it will “roll on” http://www.christopherreeve.org/site/c.mtKZKgMWKwG/b.6357597/k.3480/Living_Life_to_the_Fullest_with_TM.htm
