Just a note to say I am alive. Currently trying to figure out what I want to be when I grow up!!!
Hugs to All
Posted on Saturday, July 16th, 2011
Under: And so it goes | No Comments »
Hello All,
Just wanted to post that I have been extremely busy. Trying to recover my life after my little adventure the last couple of years has been exciting.
Posted on Thursday, April 14th, 2011
Under: And so it goes | No Comments »
Hello Friends and Family,
I am doing well. As most of you know I have been fighting Viral Meningitis for the last 13 months. It has been an adventure!! As of Sept 1st I have been ungrounded cautiosly by the Doctor. He said that I need to be careful not to set off a major event as it could cause me to back slide. So I am going forth. I will let all of you know how my job search and recover continue to go!
As some of you know I had 2 very special people in my life. Thier names are Bill Gill and Bryant Ante.
Bryant was an amazing 8 year old that battled Lymphoma for 2 years before he unfortunately lost his battle and passed way July of 2009. He will be missed by all who knew him.
Bill was a truely awe inspiring 80 year old that managed to turn a 4 month diagnosis of Luekemia into almost 10 years!!!! Bill passed away May of this year.
In memory of these 2 amazing people myself and the boys will be participating in the Luekemia and Lymphoma Society Light the night walk this Saturday September 11th in Anchorage. Each of the 3 of us have a goal of raising $100.00 to help fight blood cancers and help current surviors of blood cancers have a better quality of life!! If you can make a donation of any size towards our goals we would really appieciate it!! Thanks!!
We are on the Team Bill Says: in honor of Bill and his continuing legacy of Bill says signs that are posted on the different Team in Training marathon corses to help give the participants a boost on thier big day of completing a truely life changing event in thier life. Only 3 percent of the US population and 1% of the world population will ever complete a marathon in thier lifetime.
Here is some of the things that the donations go towards:
A donation of $25 provides patients and their loved ones with FREE booklets that contain up-to-date information on their disease and help them make informed decisions about their treatment options.
A donation of $50 makes possible a Family Support group with a trained facilitator where comfort can be found and experiences can be shared among patients and family members.
A donation of $100 helps supply laboratory researchers with supplies and materials critical to carrying out their search for cures.
A donation of $1,000 makes possible one- on-one conversations with health care specialists who provide patients with information about their disease, treatment options, and helps prepare them with questions for their health care team.
For more information about The Leukemia and Lymphoma Society please go to http://lls.org/
Donations are taken below at the secure webpages each of us have our own webpage for donations.
Here are the links to our pages. Any amount donated will go a long way to helping those people that are currently fighting blood cancers.
Sorry for the short notice, with my Meningitis it has been hard to predict what I will be able to do in the future. That should be behind me now!!!
Hugs,
Gene Looman
Posted on Tuesday, September 7th, 2010
Under: TNT/LLS/Light the Night | No Comments »
Not back to 100% yet about 60% though!!!! I am doing Ok. The Dr is extremely happy with my progress and so am I in 20 days it makes a year with this crap!!! Yucky!!!
Hugs to all.
Will post more I promise!
Gene
Posted on Wednesday, July 7th, 2010
Under: And so it goes | No Comments »
Hello!
I am doing OK. Not as great as I would like. I have been increasing my activity level hoping to get my “normal” life back when I go back to the Dr on the 22nd. It is not going as well as I would like. Would not say it is going bad just not as fabulous as I would like.
With the meds the Neurologist has me on it has mitigated about 90% of my headaches and other neurological symptoms. However that was if I only stay about at a 25% normal activity level. When I increase my activity level to 50% to 75% of normal activity the meds effectiveness drops to about 50%! So I am going to call tomorrow and schedule a visit with my Neurologist this week instead of waiting for another almost 2 weeks.
Not sure what he will say but I will post and update!
Hugs to all!!
Gene, aka aksewinman
Posted on Sunday, January 10th, 2010
Under: And so it goes | 1 Comment »