<?xml version="1.0" encoding="UTF-8" standalone="yes"?><oembed><version><![CDATA[1.0]]></version><provider_name><![CDATA[PSSD LAB]]></provider_name><provider_url><![CDATA[https://pssdlab.wordpress.com]]></provider_url><author_name><![CDATA[ghostpssd]]></author_name><author_url><![CDATA[https://pssdlab.wordpress.com/author/ghostpssd/]]></author_url><title><![CDATA[Physical Diagnostics]]></title><type><![CDATA[link]]></type><html><![CDATA[<p>For the other categories, I don&#8217;t give specific references to practitioners. For this, I will. He is far and away the best PSSD doctor in the world, and he&#8217;ll make sure that you check off most of the boxes I mention in the other sections (Less time is spent on your mental health with him).</p>
<p>Dr. Irwin Goldstein is the doctor you want to see. He&#8217;ll take care of everything. He is wonderful, caring, and very intelligent. He cares about PSSD and wants to help. I say all of this with absolutely nothing to gain personally from recommending him. However, expect to pay around $2,000 + cost of hormone tests + costs of flights to San Diego + assorted costs. Overall, expect $3-4k for this trip.</p>
<p>If you have that money, find <a href="http://www.sandiegosexualmedicine.com/">San Diego Sexual Medicine</a> and go. The rest of this page will won&#8217;t matter until you get back from your appointment in a month or so.</p>
<p>If you don&#8217;t, or aren&#8217;t yet sure you have PSSD, I want to create a platform that allows you to do much of this work yourself.</p>
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<p><strong>See a Urologist</strong></p>
<p>First, you need to rule out physical problems. There are many things that can cause physical ED. A urologist will be helpful with that. Don&#8217;t go to any urologist. Go to one at a big university hospital or other large clinic. If you need help finding one in your area, don&#8217;t hesitate to <a href="https://pssdlab.wordpress.com/contact/" target="_blank" rel="noopener">contact me</a>.</p>
<p>You&#8217;re going to want to get a doppler ultrasound to look for fibrosis. Dr. Goldstein sees this in a lot of PSSD patients. I&#8217;ll eventually be writing more about this in the research section of this site when time permits. If insurance doesn&#8217;t cover this for you (which you obviously should check before), I suggest just eating the cost of visiting Dr. Goldstein. Why pay out of pocket for someone other than the best PSSD doctor to look for fibrosis?</p>
<p>If you have fibrosis, there are some new treatments that may be available. Again, email me after you have this positive diagnosis and I&#8217;ll try to help the best I can.</p>
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<p><strong>See a Physical Therapist / Pelvic Floor Dysfunction specialist</strong></p>
<p>Get to a PT who specializes in Pelvic Floor Dysfunction of your gender. I wasted 3.5 years not doing this. My strongest recovery to date came after a PT session where my trigger points were released.</p>
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<p>Read over this thread, it&#8217;s the best piece of info we currently have:</p>
<p><a href="http://www.pssdforum.com/viewtopic.php?f=20&amp;t=183" target="_blank" rel="noopener">PSSD Pelvic Floor Thread</a></p>
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<p>I&#8217;m in the process of putting together a <a href="https://pssdlab.wordpress.com/physical-therapy-protocol/" target="_blank" rel="noopener">PT protocol for PSSD/PFS/HF</a>. This is information that every person should have.</p>
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