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        <title>HEPCnet Forums - A Heppo's Manual</title>
        <description>For tips from others who have lived with Hepatitis C for many years, or if you are newly diagnosed with a lot of quesions</description>
        <link>http://hepcnet.net/boards/phorum/list.php?6</link>
        <lastBuildDate>Thu, 09 Sep 2010 09:10:40 -0700</lastBuildDate>
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            <guid>http://hepcnet.net/boards/phorum/read.php?6,1763,1763#msg-1763</guid>
            <title>Symptoms Known for Hep C (1 reply)</title>
            <link>http://hepcnet.net/boards/phorum/read.php?6,1763,1763#msg-1763</link>
            <description><![CDATA[ Each person may vary in some or all ways.<br />
<br />
1. Fatigue                                    23. Sweating<br />
2. Joint pain                                 24.Hot Flashes<br />
3. Weakness                               25.Cold Flashes<br />
4. Tiredness                                26. Eyesight Problems<br />
5. Muscle Pain                            27.Sensitivity to heat<br />
6. Skin problem                           28.Sensitivity to Cold<br />
7. Memory Loss                          29. Vertigo<br />
8. Mental Confusion                     30. Dizziness<br />
9. Dry                                         31. Coordination<br />
10. Depression                            32.Flu Like Symptoms<br />
11. Anxiety                                 33.Headaches<br />
12. Itchy                                     34. Urinary Problems<br />
13. Irratability                              35.Urinary Odor<br />
 <br />
14. Indigestion                             36.Urinary coloration<br />
15. Rash                                    37. Fever<br />
16. Nausea                                  38. Slow Healing<br />
17. Vomiting                                 39. Slow Recovery<br />
18.Spots                                       40. Suseptibility to Illness<br />
19. Gas                                        41. Suseptibility to Flu<br />
20. Sleep Disturbances                  42. Weight Gain<br />
21. Pain or discomfort in Abdomen     43. Weight loss<br />
22. Chills                                      44. Water Retention<br />
<br />
<br />
   This list does not mean that you will have all these symptoms now or in the future. But the list of known symptoms will validate your feelings, if you have one or more that you are not LOONEY and have these problems whichever they may be.<br />
   Take the first one Fatigue, There is no way possible for anyone not feeling it in understanding the overwhelming state it may be.<br />
   There are people with severe Hep C, that feel great and show no symptoms of the disease. It seems that the counts on the Liver Blood Tests, do not determine the possible symptoms which makes it very hard to know where you are at. In other diseases we look for symptoms to worsen to know that the disease is progressing.<br />
   This is very frustrating for the patient and also for the medical Doctors. This is where the suppoert groups come in because they are just like you struggling to find a goal of feeling better.]]></description>
            <dc:creator>Koreen</dc:creator>
            <category>A Heppo's Manual</category>
            <pubDate>Sun, 04 Jul 2010 14:16:28 -0700</pubDate>
        </item>
        <item>
            <guid>http://hepcnet.net/boards/phorum/read.php?6,1737,1737#msg-1737</guid>
            <title>More Questions to ask Dr. (no replies)</title>
            <link>http://hepcnet.net/boards/phorum/read.php?6,1737,1737#msg-1737</link>
            <description><![CDATA[ 9. Are there any organizations that can provide me with more info about my illness or help with the problems<br />
   that result from my disease? <br />
10. What medications are available to control the disease? Do you ever conduct or can you refer me to someone<br />
    who performs experimental or research trials?<br />
11. What are the risks and benifits of taking the medication at this point in my illness?<br />
12. If I am unable to tolerate this medication or if it is uneffective, are alternative therapies available?<br />
13 How will I know if I am responding to treatment, and how long will I need treatment?<br />
14. Is transplant an alternative at my stage of the illness? would you or when would you recommend it?<br />
15. Are there diet changes or other measures that I can take to lessen the effects of the disease?<br />
16. How often do I need to be seen by a doctor?<br />
17. How do I contact you in an emergency?<br />
18. Can I do any home monitoring of my illnessthat might reduce the need for office visits?<br />
19. Will I beable to continue working?<br />
20. Can I expect to have many sick days?<br />
21. Will this illness affect my ability to obtain life or health insurance?<br />
22. Ask questions about the specific hobbies, sports, family and social activities that the disease<br />
     may have an effect on.<br />
23. Will the drugs I am taking interact withother medications or impair my ability to have sex?<br />
24. What are Your recommendations regarding alcohol, smoking, aspirin/tylenol/motrin, other<br />
     prescription or non prescription drugs?<br />
25. Will the illness or the treatment interfere with my ability to have children?<br />
26. Will the disease or the treatment be disfiguring? (Weight gain/loss, hair loss, ect. )]]></description>
            <dc:creator>Koreen</dc:creator>
            <category>A Heppo's Manual</category>
            <pubDate>Tue, 11 May 2010 13:42:16 -0700</pubDate>
        </item>
        <item>
            <guid>http://hepcnet.net/boards/phorum/read.php?6,1719,1719#msg-1719</guid>
            <title>Questions to ask your Dr. (no replies)</title>
            <link>http://hepcnet.net/boards/phorum/read.php?6,1719,1719#msg-1719</link>
            <description><![CDATA[ <b>SOME QUESTIONS TO ASK YOUR DR:<b></b><br />
<br />
 <br />
1. Is it possible the diagnosis is incorrect? It does happen occasionally<br />
2. Are there any tests (or additional tests) available to confirm the diagnosis or to show<br />
   the severity of of the illnessÉ<br />
3. What organs of my body are involved and in what way. Will the damage to these organs <br />
   be progressive.Be sure to ask the usual time course over which this occurs. Ask for drawings <br />
   and down to earth terms to help you better understand what is going on with your body.<br />
4.What other organs of my body can I expect to become involved due to the illness.<br />
5. What are the possible ways I could have gotten this illness.<br />
6. What are the possibilities of my passing this illness on toothers,and in what ways. Should I <br />
   worry about my family catching it, what about sexual transmission. How can I minimize the risk to others.<br />
7. What complications am I at risk for and at what stage of the disease.<br />
8. What symptoms or change in symptoms should I be concerned about. You need to gain some<br />
   perspective on your illness and not become obsessed with every little ache and pain or change in symptoms.<br />
   Find out which symptoms are important, and which you need to watch out for.<br />
<br />
<br />
More Questions on what to ask to Follow</b>]]></description>
            <dc:creator>Koreen</dc:creator>
            <category>A Heppo's Manual</category>
            <pubDate>Tue, 11 May 2010 09:18:34 -0700</pubDate>
        </item>
        <item>
            <guid>http://hepcnet.net/boards/phorum/read.php?6,1718,1718#msg-1718</guid>
            <title>First Steps (no replies)</title>
            <link>http://hepcnet.net/boards/phorum/read.php?6,1718,1718#msg-1718</link>
            <description><![CDATA[ 1. Start yourself a binder and make a copy of your medical information that lies ahead.<br />
2. When you have BLOOD TEST or LIVER TESTS ask for a copyof the results from the dr. and keep in your binder.<br />
3. Usually they do liver test (blood test) about every 3 months.<br />
4. Have a Hep B test, if it is negative start the vacvine right away, if your dr. says you don't need it, then go to a health unit and do it.<br />
5. Remember to tell anyonethat does a service on you that you have Hep C so that they are aware of it and take precautions...Dentist,<br />
   Denturist, Hairdresser, Barber, Lab techs, anyone who may be in blood to blood contact with you.<br />
6. Find out as much as you can about your condition with this disease, you have it for life, so don't ignore it because it won't get <br />
   better or go away on its own.<br />
7. The reason for this Binder is if you have to see another dr. you then have the test results right there, also you can keep track<br />
   of your ups and downs.<br />
8. Always take a support person with you to your appointments.this way if you miss some imformation they will hear it.<br />
9. Also take a pen and paper with you so you can take notes so you don't miss anything.]]></description>
            <dc:creator>Koreen</dc:creator>
            <category>A Heppo's Manual</category>
            <pubDate>Tue, 11 May 2010 08:44:52 -0700</pubDate>
        </item>
        <item>
            <guid>http://hepcnet.net/boards/phorum/read.php?6,120,120#msg-120</guid>
            <title>The return of a board we tried a few years back (2 replies)</title>
            <link>http://hepcnet.net/boards/phorum/read.php?6,120,120#msg-120</link>
            <description><![CDATA[ Viv had started this board a few years back but we had problems with the software and lost a bunch of wonderful posts.  It was never revived until now.<br />
<br />
For those that remember when it was started before... can you re-post what Viv said what belonged in here?  I set the board description to what she had it set it.]]></description>
            <dc:creator>seok</dc:creator>
            <category>A Heppo's Manual</category>
            <pubDate>Tue, 11 May 2010 08:22:56 -0700</pubDate>
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