Pudendal Neuralgia (PNE)

Per my testimony: I was on Letrozole for 1 1/2 months and was very drug sensitive to it and had to stop. Letrozole Aromatase Hormone Inhibitor was far too detrimental to my cardiopulmonary limitations amongst other extremely harsh side effects. We all must chose can our bodies tolerate these powerful drugs? Do the benefits of taking the hormone therapy of 3-5% less chance of cancer reoccurrence out weigh the detrimental full body effects? I hasten to add if we chose not to take these drugs make sure you get a bi-annual MRI to spot any small cell cancers that may have returned. Side Effects impact on cardio-sensitive individuals: Extreme exhaustion A-fibrillation 3 Nausea Muscular-joint pain Higher lipid count Raised out of controlled range Blood Glucose A-1C levels previously balanced Extremely wide ranging high to low BP swings. Diastolic plunged many times to under 50 causing dizziness just shy of unconsciousness Angina frequency increased to daily and grew more intense in pain BUN and Creatinine Levels now ranging high off normal. Tried Taxoxifen but this will not work out either apparently. Was on a 30 Day Trial. Stopping yesterday, June 7 at Day 15. Developed extreme **neuropathy** of feet spreading into legs to knees. Letrozole Side Effects https://search.brave.com/search?q=Letrozole+Side+Effects&source=desktop Tamoxifen Side Effects https://search.brave.com/search?q=Tamoxifen+Side+Effects&source=web ~ MabelLean Surgery 1/12;/2024; 1/26/2024 DX 1/2024, Right, Intrusive Ductal and Lobular Carcinoma, Stage IA, Grade 2, ER+, PR+, HER2+, ISH Treatment → * NEED: MRI Bi-annually along with 3D Mammography and Sonogram UPDATE: June 1, 2024: MRI Results → * NO Cancer Reoccurrence! ~ 1 Corinthians 16:13 Final Exhortations Watch, stand fast in the faith, be brave, be strong.

Coping with Pudendal Neuralgia and Anxiety

Dealing with Chronic Pain: My Story

Pinched Nerve in Ankle: Seeking Advice

Living with Nerve Entrapment: Seeking Support and Advice

my **neuropathy** started as a teen in my thighs, so far there are no signs of MS. My hands and feet are numb. I can't work with buttons or small items. I have terrible sciatica. My taste has altered in the past 2 years and nothing tastes good. My whole digestive tract isn't working so well just found dismotility in my esophagus after 10 years of troubles and testing. Just found auditory processing disorder that also began 2 or 3 years ago. My memory has gotten bad and either I stumble when I speak or I throw out the wrong words for what I mean or both. My legs are giving out and I am working out in hopes to help everything. That's a pinch. Just looking to see if anyone else has the same things going on.