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  1. #11
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    Welcome to the family @Vansyckle73
    I was dx on 8/1/16 in Boston after I had 3 months of ear pain, pressure and (once tubes put in) drainage. Nothing could improve my ears so they finally ran inflammation marker labs, then ANCA labs, then CT scan and then lung biopsy. All positive/Weg GPA. I have been on pred and rituximab. Much improved til they started tapering pred. Ear pain has returned and pred brought back up to 30. Only 2 days now, but no improvement. So I'm thinking maybe I have an ear infection instead.
    Like others mentioned, autoimmune disorders like ours fall under the care of a rheumatologist generally. Tho some see nephrologist to coordinate treatment too. I think it's because a specialist, like a pulmonologist, just focus on one body part generally. While the rheumatologist is trained to treat the vasculitis systemically and seek input from specialists. They take all that info and take the lead in the patient's care. I'd think rheumy docs see more Weg GPA patients too and probably are more up-to-date on latest treatments etc. I addition to the pred and ritux I'm on Prilosec to Proctect my stomach, fosomax to protect my bones and bactrim to help fight lung infections. Pred can be rough on stomachs and bones. I'm also told to take calcium w/ vit D. And prescribed ambien to help me sleep.
    Hoping this info helps.
    Wishing you the best as we both are starting our Weg fight together.
    Trust in the Lord with all your heart
    and lean not on your own understanding;
    in all your ways submit to him,
    and he will make your paths straight.
    Proverbs 3: 5-6

  2. #12
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    Quote Originally Posted by Vansyckle73 View Post
    Why is the rheumatologist the right one to manage it? Do they do something specifically different than a pulmonary doctor would? Just curious.



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    I think it is because rheumatologists handle autoimmune conditions, which is what WG is. So we have a rheumatologist oversee the disease, who is more familiar with the immune system than say, a pulmonologist, and then we have the pulmy, ENT, ophthalmologist, etc., as part of the team to monitor the areas that are their specialties. Trouble is, not all rheumies know that much about WG, since it is rare, and many of them mainly treat arthritis and other more common autoimmune diseases. So you need to find one with a fair amount of experience in WG and other autoimmune vasculitis, and preferably, one who is known for this specialty. University teaching hospitals are one place these rheumies might be found, or you can check the Vasculitis Foundation website for lists of specialists.

    I have a confession to make. I am still seeing the pulmonologist who started my treatment 5 1/2 years ago. I was started on the same meds as you and eventually switched to methotrexate as the immunosuppressant. This is pretty standard treatment for someone with sinus, ear, and lung involvement. So even though I'm doing pretty well, and might even be in a medication-maintained remission, I would like to have a rheumatologist with WG experience, for a better overview, more familiarity with the meds, and a better idea of where to go from here, which drugs to taper off of first, and how fast, stuff like that. I have heard of one in my community with at least some WG experience but have procrastinated trying to hook up with him. Your post might help to prod me in that direction.

    Anyway, welcome to the forum! Everything I know about WG I have learned here, and I've made many friends along the way.
    Anne, dx'ed April 2011

  3. #13
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    Quote Originally Posted by Vansyckle73 View Post
    I am on cyclophosphamide and prednisone under the direction of my pulmonary doctor. Next week I am meeting with a rheumatologist to start that relationship.

    I am considerably better but far from the end of this journey. I use SinuPulse machine to assist with my sinuses, looking into ear tubes to drain the fluid and ring my hearing back, and I am trying to figure out how to breathe better. I lose my breath very easily.

    I have noticed bursts of energy more often. Unfortunately they don't last long and I tend to take it too far. I am still learning to manage this.


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    Just a thought... As for the sinupulse... is it sterile? It really important to only put sterile or distilled water/saline solution in your sinuses since you are immune suppressed.
    I use a neilmed sinus bottle, saline packets and distilled water. The bottle itself can be sterilized in the microwave.
    Trust in the Lord with all your heart
    and lean not on your own understanding;
    in all your ways submit to him,
    and he will make your paths straight.
    Proverbs 3: 5-6

  4. #14
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    I clean it after every use and do a special cleaning every week and I do use distilled water with neilmed packets. The ENT saw a huge improvement in my sinuses since the machine.


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  5. #15
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    [QUOTE=Vansyckle73;109333]Why is the rheumatologist the right one to manage it? Do they do something specifically different than a pulmonary doctor would? Just curious.



    Division of Rheumatology


    Dr. Yih Chang Lin
    13330 USF Laurel Dr 6th Floor

    Tampa FL 33612


    Phone: (813) 974-2201
    Fax: (813) 974-5229

    This is the doctor that my husband sees. He's wonderful. We highly recommend him for your GPA treatment. We met him at the Vasculitis Foundation's symposium on June 2015. When you have a moment, please check out the Vasculitis Foundation's website: Vasculitis Foundation.

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