I dedicate this page to my lovely wife, Teri, whom I love very much.
And this is to those who have just discovered that you or a loved one has the dreaded Hepatitis "C". It's hard to fully understand and comprehend what a family is going thru & enduring. The changes are so suttle that you don't realize what is happening.
Depression is the strongest emotion that you'll have to deal with, b/c they get into low self-esteem, pity, unwanted, unloved, and so on & so on from there, and it's difficult for the person with Hep "C" to see the changes that are impacting their lives.
Below you will see only some of what we have been through. I wish now that I would have kept a diary of what all has happened, b/c it takes awhile to see the pattern that emerges from the behavioral changes..
Hopefully, by reading this others will be able to see & understand these symptoms of Hepatitis C & what radical changes he/she & their families must endure of this disease. There is only one treatment, interferon, which has many severe side-effects, and in my wife's case, dr's are unable to put her on it, due to her medical history of depression caused by a "chemical imbalance" she has...People have been known to commit suicide on this treatment as the side effects can be more severe on the symptoms of the disease.
Alot of times you'll get discouraged & hurt by your loved one with Hep-C, but the best thing to do is try to "always" show love, support & encouragement, as with any disease. Because no one could ever imagine what Hep-C can do to someone's self-esteem, self-assurredness & the heartbreak of feeling inadequate all the time and always sick..until you see it yourself.
Above all, never refuse to talk about it with him/her and never act like "it'll be ok"..Because that only makes him/her feel even worse. After all, they know it will get worse as it is a killing disease.. All the symptoms of this disease add more stress to him/her, which in turns makes the symptoms worse. So the "less stress" environment you can create, the better for him/her. Always be gentle, loving & understanding. I know this sounds like a tall order with all the stress you're having to go thru, too, but always remember--what you have to endure is nothing compared to what the victim of this disease is...especially if him/her has always been so independent & out-going. And you can always walk away from it from time to time. The victim never can..
I truly hope this helps someone, others, going thru this or a loved one.
~HOW MY WIFE'S HEP-"C" HAS CHANGED & AFFECTED OUR LIVES~
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