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  • Dr. Chang & Meridian Medical

    Posted by Bronkmommy on March 1, 2008 at 4:48 pm

    We went to Dr Chang last evening. As you know we are grasping at straws. At the meeting were both my parents, my sister & I. We all left the meeting feeling like Dr Chang was great. He is clearly very intelligent, he was very personable. He went through his philosphy of treatment which is primarily do no harm, do what make logical and scientific sense and do everything possible to help. He DID NOT push herbs etc. He perscribed for her 3 medications that are used for totally different diseases but that have shown to attack bladder cancer in studies. The thought being that you never know what is going to push you over the edge into survival. (My mothers tumor is HUGE – 17 cm, on her liver, she was given only 3 months.) The three drugs are Cipro (the antibiotic), Celebrex and an anti diabetes drug. None sound like they will help to me but he showed us the studies on them. He was very careful to tell her to take one drug for 5 days then add the next, then the next 5 days later – thought being that if she takes all three at once and has a bad reaction then he needs to take her off all three so he wants her to wean herself into them.

    As far as the Xeloda that her Oncologist & Dr Barjoin want her to start taking he was very surprised that they were suggesting it. After we told him her history he understood that Xeloda is a last ditch option that her dr’s are trying. He is concered with how it will effect her blood levels because she has a VERY hard time with her platelet levels. Right now she is at 30,000 which for her is high. He gave her (don’t laugh) a supplement made from Peanut Husks that he says will help her build her platelets back quickly. Apparently used by the chinese to build blood for years. He told us about an FDA approval that is coming for a drug to improve platelets in next few months. The chinese have already approved the drug and have found that you can become refractory to that drug if it is applied under the skin but seems to have less of a chance to become refractory if put directly into a vein or through a port…but all that said he wants to try the peanut husks before he would recomend the chinese version of the drug. The thought behind this is only to support her abilty to take the xeloda as per its protocal so that it has the best chance of working.

    On Monday mom is going to see his partner to look at what she is eating and what she should be eating. Dr Chang asked her to keep track of everything she puts in her mouth…water, drugs, food. She needs to bring that for Dr Yee ( I think that is her name.)

    Dr Chang gave us a script for blood work in two weeks to have a study done and then we will go back to him in the 3rd week.

    Dr Chang is going to make contact with both of her oncologists via a letter to let them know what he is doing to help support them in the Xeloda. Dr Bajorin from Sloane spoke of Dr Chang on a first name basis and said that he was not sure exactally what he was up to these days but that he respected him and thought highly of his abilities. We have also made an appointment for 3/19 with the alternative medicine folks at Sloan to compare what Dr Chang thinks to what they think.

    We are INCREDIBLY interested to see if the peanut husks help the platelets. In my mothers words..”If it works I will think he is a God.”

    the long and the short…We as a family felt for the $750 it costs to see him…if anything he offers her works… is more then worth the money. I will let you know.


    Jane & Crew
    Bronkmommy replied 17 years, 1 month ago 4 Members · 6 Replies
  • 6 Replies
  • bronkmommy's avatar

    bronkmommy

    Member
    March 6, 2008 at 2:09 pm

    Good news & Bad…

    First the good. My mothers platelet count more then doubled in 4 days. She went from a 29 to a 61 count. During those 4 days she was taking the peanut husk supplement from Dr Chang at Meridian. This is the largest jump in platelet count she has ever had. Unbelieveable. Her counts are almost to the point where they will start her on the Xeloda.

    Bad new is we got the platelet count last night becasue she is in the hospital with dehydration from vomitting. The Oncologist is saying he thinks she has a virus but is not ruling out that it can be from the tumor. Personally, as much as I hope it is a virus, I think it is from the tumor too. I am not surprised to see your posts to look out for unexplained vomiting.


    Jane & Crew
  • wsilberstein's avatar

    wsilberstein

    Member
    March 5, 2008 at 9:43 pm

    I don’t know about metastatic disease of the liver, but I do know that vomiting is a symptom of hepatitis, so apparently inflammation of the liver can lead to vomiting.


    -Warren
    TaG3 + CIS 12/2000. TURB + Mitomycin C (No BCG)
    Urethral stricture, urethroplasty 10/2009
    CIS 11/2010 treated with BCG. CIS 5/2012 treated with BCG/interferon
    T1G3 1/2013. Radical Cystectomy 3/5/2013, No invasive cancer. CIS in right ureter.
    Incontinent. AUS implant 2/2014. AUS explant 5/2014
    Pediatrician
  • mssmr's avatar

    mssmr

    Member
    March 5, 2008 at 7:15 pm

    I take your posting as a sincere request for information. I have liver mets and
    one of the things my doctor told me to look out for is “vomiting with no apparent reason.” That hasn’t happened yet, but I was told to report it if it did. I was not told, now that I think of it exactly why. I hope this distress passes quickly for your mother — Susan

  • bronkmommy's avatar

    bronkmommy

    Member
    March 5, 2008 at 7:08 pm

    Today was the day that we were supposed to have our first look to see if the supplements were helping my mothers blood counts but… she is throwing up so badly today that she did not go to the doctor to get the counts done. :(

    Any thoughts on why she would be getting so sick now? Anyone who has mets/tumors on the liver experience this?

    I will keep you posted on Dr. Chang etc as we know more info.


    Jane & Crew
  • clara's avatar

    clara

    Member
    March 4, 2008 at 1:29 pm

    Please do keep us posted on all of this, I find it very interesting and do believe in many of the remedies that people try.

    Clara


    Caretaker of husband, Bob.
    Stage IV
    Diagnosed Jan, 2007
  • mssmr's avatar

    mssmr

    Member
    March 3, 2008 at 10:09 pm

    Thank you for sharing this information. Please keep in touch with the list.
    I certainly wish your mother the best. (My mets are lung, liver and possibly bone —
    and, so far, unresponsive to chemotherapy — but I’m feeling well.) Of course, I hope for breakthroughs that can help us — in support — Susan (mssmr)

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