Hyperthermia advancements

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FloridaLady
FloridaLady Member Posts: 2,155
edited June 2014 in Complementary and Holistic Medicine and Treatment

http://www.freecollegevideos.com/college_videos_view/interview_with_md_explaining_hyperthermia_cancer_treatment_213222

Read up on this protocol. I may be one of the rats for this research. I will know in a few months. This has been around for 2,000 years.  The medical industry has been researching on and off for about twenty years.  Another case of they just don't know.  A lot of naturopathic recommend whole body hyperthermia.

Flalady

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  • Binney4
    Binney4 Member Posts: 8,609
    edited March 2009

    Hi, Flalady!

    Do get your LE therapist on board with this, as you'll need to do some extra LE maintenance due to the accumulation of lymph fluid caused by heat. Will you be doing rads/chemo along with it? "Cornfieldheiress" here has done this (with rads, I believe). Hopefully she'll be along soon. Or PM her for her experience.

    Hugs!
    Binney

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  • FloridaLady
    FloridaLady Member Posts: 2,155
    edited March 2009

    Hi Binney, (just love you lady!)

    I had so many issues right now I'm still have not found a LE therapist.  My disease is coming thought the chest wall again and I have a tumor through the skin just above the arm on my shoulder. They do not want me to massage at all right now.  I'm really miserable with this.  I now back to taking pain meds because of the backed up fluid in these areas. At some point I will have to try and move this to my back to see if I can get drainage.  This is the worst my arm has ever been.  I did mention to the trial person on the phone I do have LE and she did note it on my file.  I'm just running out of options right now...

    I glad you noted this...I did think about this and have concerns...I can't imagine heat or rads on the area. Yuck!

    Love you

    Flalady

    I want to do rads but they feel I've ready had my limit.  If I can get in I will be doing Adrmin in a lipsome(sp?) fats.  I really don't want more chemo with my neuropathy but I might be down to this or nothing unless I travel again.

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  • Estepp
    Estepp Member Posts: 6,416
    edited March 2009

    I just wanna say GOOD LUCK to you! I have reading your posts in soooo many threads for a long time now... can I just say.. I really look up to you. God Bless you and Keep fighting... fight for you.. and fight for us. You inspire me. Thank you!.. I am sorry you are in pain.. I just am!

     I pray for you... I wish your pain was GONE! I actually would like the opportunity to meet you someday. Anyway... I just did not want another day to go by without telling you that I admired you and you give me hope... I will keep doing research like you do.

    God Bless and His Love to you! Laura

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  • FloridaLady
    FloridaLady Member Posts: 2,155
    edited March 2009

    Thank you so much Laura.  Mostly thank you for your prayers, the most valuable treatment of all!  I do seem to get around don't I?  I hope to never stop learning how to help myself in others.  It does give me hope that others will want to learn more about their disease and take charge. And just maybe we will find a way to beat this thing.

    God Bless

    Flalady

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  • suegeyer
    suegeyer Member Posts: 14
    edited March 2009

    Hi Flalady,

    I am sooo sorry you are in pain again!   This disease sucks!  Sending up more prayers!  You are such a great support to everyone here!

    Sue

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