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A Visit to Dr. Peterson V: Tests and the CFS/ME Bond by Corinne (conclusion)

Discussion in 'ME/CFS Doctors' started by Cort, Feb 14, 2010.

  1. Cort

    Cort Phoenix Rising Founder

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    Raleigh, NC
    CorrineBeach.jpg Allow me to share one final experience before I close. As you're probably already aware, the bond between those of us with this illness is strong. If you’re like me, you’re best friends are PWC’s/ME. They're the ones I contact when I really need support from someone who truly understands and vice versa. Our relationships with one another are special and, I believe, quite unique in that not only do our friends and families have difficulty understanding us but so does the medical community. This tends to present itself as a sort of intense loneliness that would be difficult to explain to anyone, even someone who is suffering from another illness. This bond resulted in me finding myself drawn to observing other patients of Dr. P.'s.

    As soon as we set up “camp” in the parking lot I would gaze out the window and wonder if that person entering the building was his patient are not. One, in particular, was quite obvious. I saw her emerge from the car and handicapped parking space adjacent to ours. The man who had driven, held her hand as they walked slowly down the walkway to the elevator. She had that walk, you know the one... wide stance for balance, slow, deliberate gait…and the look on both of their faces was a bit sad and a bit worn out.

    As I sat in the waiting room the following day they sat across from me. Even though Dr. P sees patients without CFS/ME I knew she was one of us. The man who accompanied her arose to get the papers she needed to sign and then returned them to the receptionist for her. My husband did the same for me.

    The following day when I saw them once more, I noticed her hair was obviously unwashed. I understood. In a couple of days, I'd be in the same boat... appointments to make, tests to take…. the ponytail would have to do for now. When my eyes met hers I could “see” the spaciness. I smiled but didn't think she could focus enough to see it.

    Back home, when I'm in my GP’s waiting room I’ll often glance at the other patients. One coughs, another sniffles and the others seem perfectly healthy; none of them have CFS/ME. There is no connection, only a brief wish to trade places with any one of them if only for a day or two.

    But this place was different. There was no desire to trade places. We were all fighting the same fight. One of the rooms in the office seemed to be used for those receiving IVs. One day while parked in my wheelchair directly across from that room, I caught glimpse of a young woman seated in a chair, I.V. slowly dripping into her arm.

    Our eyes met and though we weren't close enough to speak I felt I knew almost everything about her. Her eyes mirrored mine …that glassiness that says “I’m exhausted and I'm sick “. Her hair was disheveled and she sat up with that slump that says “I’m too weak to sit up straight “. Off and on she would put her head into her hand, rubbing her forehead . Perhaps she had a headache, or perhaps her head was just too heavy to support … either way I'd been there and done that.

    I had the urge to give her a hug and might have if I'd had the strength to get up, walk across the room and introduce myself. For now a silent prayer would have to do. It had been quite a while since I was able to attend a CFS/ME support group meeting so for me it was quite touching to be reminded of how powerful this bond is between us.

    Thank you for allowing me to share what I consider a very privileged experience. Perhaps if you are one of the close to 1,000 names on Dr. P.'s waiting list this can help you in your decision to persevere or not.

    I would like to send a special thanks to Cort Johnson who graciously transcribed my scribbles into electronic type and literally spared me many painful migraines! “Thank you, Cort!” And thank all of you for allowing me to share my experience.

    Feel Well,
    Corrine (aka 'The Queen of Questions')


    Corinne’s Early Test Results

    Virology -
    • active EBV
    • enterovirus (evidence of active infection)
    • HHV-6 (evidence of active infection)

    Immunology -
    • Extremely low function and number of NK cells
    • Low IgG subclass 3
    • Very high Interleukin-8 (pro-inflammatory cytokine)
    • High levels of fragmented (Low Molecular Weigh) RNase L (protein quantification)

    Neurological
    • Abnormally high spinal fluid pressure
    • abnormal brain MRI (UBO’s)

    Vascular
    • orthostatic intolerance (low BP, low HR)
    • low blood red blood cell volume

    Metabolic
    • very low VO2 max

    Digestive
    • High levels of citrobacter braaki (“ bad” gut bacteria)
    • very low levels bifido and Lactobacillus (“good” gut bacteria)

    Corinne’s Tests

    • Lumbar puncture
    • Bicycle exercise/stress test
    • MRI brain with and without contrast
    • Brain Spect scan
    • 24 hour EKG monitor
    • 24 hour blood pressure monitor

    Pathogen Tests by Real-Time PCR
    • Chlamydia tarchomatis
    • Mycoplasma hominis
    • Chlamydolphia pneumonia
    • Mycoplasma penetrans
    • Mycoplasma pneumonia
    • Chlamydia species
    • Lyme, Borrelia burgdorferi

    Other Pathogen Tests

    • HHV-7 DNA (plasma
    • Rapid HHV-6 culture and antigenemia
    • Nested HHV-6 PCR
    • Nested cytomegalovirus (HCMV) PCR
    • Rapid HCMV Culture and antigenemia
    • Epstein-Barr virus chronic/active infection
    • HTLV - 1/II antibodies, Qual
    • Enterovirus antibodies profile

    Endocrine

    • ACTH, plasma
    • Cortisol a.m. and p.m.
    • FSH and LH
    • IGF-1 (insulin like growth factor)
    • Thyroxine (T4), free, direct, S
    • Testosterone, serum
    • Thyroid panel with TSH

    Immune

    • RNase L Panel (activity assay and protein quantitation)
    • Immunobilan
    • Immunoglobulin, M.,Qn, serum
    • Immunoglobulin a, Qn, serum
    • Cytokine profile (interferon-y, interleukin's, etc)
    • C. reactive protein, Quant
    • Natural killer cell (total T cells)
    • TNF alpha, circulating levels
    • T and B gene rearrangement, PCR
    • IgG, subclasses (1-4)
    • HCV Ab w Rflx, to RIBA

    Others

    • Complete metabolic panel (14)
    • Lipid panel with Chol/HDL ratio
    • Lactic acid, plasma
    • Heavy metals (Pb, As, U-Hg, U)
    • Heavy metals sensitivity tests
    • Ferritin, Serum
    • Creatine kinase, total serum
    • CBC with Diff/platelet
    • Nitric oxide synthase assay
    • Amino Acid Prof. Qn (random urinalysis)
    • Amino Acid Prof. Qn, Plasma
    • UA/M w reflex culture (urinalysis)
    • Prothrombin Time (PT)
    • Narcolepsy evaluation
    • Iron and TIBC
    • D- lactate, plasma

    Cerebrospinal Fluid Tests

    • Cerebr+MBP+Oligoc+Pr+CSF (includes total protein, IgG, albumin, IgG Index, IgG/? Ratio, immunoglobulin G., myelin basic protein, illegal clonal bands)
    • Lyme PCR, CSF
    • Meningoenceph reflex (West Nile virus ab IgG; herpes simplex virus type 1 and 2 antibodies, IgG)
    • Cell count, CSF
    • Glucose, CSF
    • Epstein-Barr virus PCR, CSF
    • Lactic acid, CSF
    • Nested HHV-6 DNA PCR
    • HHV-7 DNA PCR

    Tests to take at Home



    • CDSA w/ parasitology (purge/random still analysis)
    • Intestinal permeability
  2. KC22

    KC22 Senior Member

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    Ohio
    Hi Corrine,

    I really related to your post. Yes, I have many CFS friends and they are the ones I can talk to about this disease. They get it!!!

    I hope you will share your journey with Dr. P. and what he is going to do about all of your problems.

    Again, thanks for sharing your story.

    Peace and blessings....
  3. Kelvin Lord

    Kelvin Lord Ampligen Journalist

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    Colorado
    Just like veterans in the armed services, who can recognize each other across the room without a room, we are veterans of another kind of war that share a bond. You've described this connection beautifully, Corinne. Please keep writing, and "scribbling!"
  4. anne

    anne Guest

    Corinne, please let us know what Dr. P suggests for you.
  5. Cort

    Cort Phoenix Rising Founder

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    Raleigh, NC
    I believe Corinne is going to see Dr. Peterson in the next week or two. She has the very unfortunate problem of being unable to be on the internet only for very brief periods before she becomes ill. I hope she can continue to inform us how it all goes with her.
  6. Sue C

    Sue C Sue C

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    NJ
    thanks for sharing

    As one who has been through similar experiences with dx testing, I am grateful to Corrine for all the info from her doctor visits.

    It is a huge effort especially travel, to get there! After I became ill in 1994, I went to the Cheney clinic for dx tests and tx.

    It is empowering to sit with those who know our illness, have dedicated years to research and treatment (and be moved by their

    patience and kindness .)

    Although not able to continue going to the clinic for a few years now, it gives me strength and courage to follow Corrine's journey.

    Thanks to you, Cort, for transcribing her visits, being the instrument for the rest to be informed. Sue C
  7. creekfeet

    creekfeet Sockfeet

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    Eastern High Sierra
    I didn't find "A Visit to Dr. Peterson V." Is one installment missing?

    Thanks so much, Corinne, for your wonderful recounting of the entire experience---and thank you for going through it all! And thank you, Cort, for transcribing and posting.
  8. Cort

    Cort Phoenix Rising Founder

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    Raleigh, NC
    My mistake - today - I flaked when the numbers got too high; there were only five. I fixed the title. She said she would be reporting on her latest visit.
  9. glenp

    glenp "and this too shall pass"

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    Vancouver Canada suburbs
    ty Corrine

    Thank you so much Corrine for taking the time to do all of this for us. And thank you too Cort for all that you do.

    glenp
  10. ldhunter

    ldhunter

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    TY Corrine and Cort for putting this all together. I could relate with everything you went through-even the lumbar puncture and walking with my head hanging between my legs :), but I could never put it in to words like you! Thanks for sharing the gift of your story, and please give us an update when you are well enough to do so.
    Prayers for your improved health,
    L.

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