HepC 

                        
                                                    Regina Chapter

New update in the Rant section 12/17/2006 
Compensation update: http://www.northernlife.ca/News/LocalNews/2006/11-24-06-zivnyTOP.asp?NLStory=11-24-06-zivnyTOP 

No Compensation Money Received yet, read interview above link.!!!

Government sets the amount at $100 million. Now going through the courts is the next step.
More to come later.

To Those we lost from this disease, families and Loved ones.
"Love is always patient and  kind. It is never jealous. Love is never boastful nor conceited. It is never rude or selfish. It does not take offence and is not resentful.  Love takes no pleasure in other peoples sins... But delights in the truth. It is always ready to excuse, to trust, to hope... AND ENDURE WHAT EVER COMES."

Thinking of starting a group in SK or Canada. See the daily rant section.

 I will help as best I can "health permitting", anyone to get a Chapter up and running if you feel there is a need and commit. Funding is up to those starting the chapters. I can not help you there as I am needing support as well and have funded out of my own everything to keep this site up and running 110% worth at times, plus the Sponsors if it wasn't for them this wouldn't be possible and appreciated greatly.
 I am always looking for help as well, now my health is failing me. Any Doctors  and Nurses and Professional Health Mediators, Lawyer or Politician wanting to commit to the cause, please e-mail me. I am also looking for a Psychologist as well to better help the families in need of counseling. I am always looking for information as well to keep updated so a heads up if you have any and would like to make it aware to me I would appreciate it as well.
Follow The Link mail@hepatitiscsociety.com

I made some changes and added a Daily Rant Section for those who want to know a few things about HCV from my own perspective. Grass Roots stuff. I'm not a Doctor and don't give out medical information just personal experiences in this department. I would appreciate some feed back and some communication with all of Canada HCV groups. Please and Thank You. I will update some medical information as I catch up on the new programs and experimental one/s as well. CURRENT UPDATED and as SOON as possible.
  I myself will be doing more current site updates and medical requirement procedures about each province of Canada or as a whole; universal liver transplant protocol/s, by province to province. If you have any information you are willing to share or  link to your site for your hard work will be appreciated. Time consuming but also it's immediate answers and information now is what we need. That pertinent direction and fulfillment of the goals towards a new liver and prolonging lives for now till a cure is found.
   
I would like to know if there have been any changes in telephone numbers and Groups that are new and contact/s from Saskatchewan GROUPS wishing to communicate together for Saskatchewan's betterment and perhaps exchange ideas and work together towards said goals. This will help Canada as a whole I feel. 
  If it wasn't for ideas and suggestions we wouldn't be where we are at to date. 
Look how far we have come and look at all the hard work others are doing and recognition to what they have achieved in a very short time even though it seems very long. To the people who have participated in collecting information I say, "THANK YOU" it is a wonderful gift. This group is willing to work with others to achieve this goal in the future and look at this as a gift as well for all Canadians and people world wide to become informed possibly cured. 
  Lives can be saved and individuals can attain some kind of knowledge as well towards the betterment of their lives as a whole, if the correct updated materials are there for us to use in a positive and productive way. Share the education information please.
  I am humbled by the magnificent work others have done for this HCV cause. I feel proud to be part of, and able to still help as my health fails me now, like many others doing the work. To this I say "Thank you" for being their for each other. I know very little but I do have faith and hope and participate as best I can.
 So for now over. 
  But never out. 
  (by my friend Monika).

NOTE: In the future please let me know if you have anything pertaining to HCV.
hep-c.regina@accesscomm.ca

Thanks to all the people involved to make this site possible.

As time rolls on we will be expanding this site to cover other  HepC issues. Please visit us often to keep up with the changes. We also have an e-mail link to reply to if you have questions.

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