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Asking for opinions
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1
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331
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February 6, 2024
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To much b6 in my blood work
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2
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262
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January 18, 2024
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Looking Your Stories - How has this site benefited you?
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0
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232
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January 9, 2024
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Is it healthy to allow symptoms to persist? (and what worked for my symptoms)
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2
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825
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December 14, 2023
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EM symptoms but only in winter?
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2
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395
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October 23, 2023
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Lipoprotein A
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0
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297
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October 21, 2023
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ADHD, sensory integration issues and erythromelalgia
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20
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2147
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July 2, 2023
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Medication that works
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44
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3729
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June 23, 2023
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My history of EM
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9
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435
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June 22, 2023
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Preparing for Your Doctor’s Appointment
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1
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209
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June 22, 2023
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Bobs protocol
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28
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5597
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June 22, 2023
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EM and other neurological disorders
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3
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751
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June 14, 2023
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7 Things to Look for When Choosing a Doctor
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0
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306
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May 18, 2023
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For everybody who has nerve pain and dont know why
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1
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402
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May 14, 2023
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Spotlight on Our ModSupport Member: Sharon a.k.a Stoney
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0
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304
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April 26, 2023
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Spotlight: Ben’s Friends former Intern, Dr. Melissa Jones, MD
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0
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271
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April 13, 2023
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Diagnosed with CRPS
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2
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327
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March 27, 2023
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Low blood pressure! Experiences? Anyone on meds for it?
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11
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388
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March 11, 2023
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Do you think EM is the most painful and the most terrible disease of the world?
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2
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456
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March 11, 2023
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Wheelchair and disability
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32
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2079
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March 10, 2023
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Ben’s Friends inks partnership with ClozTalk
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0
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200
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March 9, 2023
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Rare Disease Diagnosis: Difficulties and Advancements
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0
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256
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March 8, 2023
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Pain,pain,pain!
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20
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604
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February 28, 2023
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How Frequent Are Your EM Flares?
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22
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934
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February 28, 2023
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Looking for Ways to cope
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10
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1320
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February 28, 2023
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Global Genes’ Rare Daily website features Ben Munoz
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0
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155
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February 23, 2023
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Some of Ben’s Friends secrets to maintaining healthy communities
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0
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164
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February 21, 2023
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What’s Your And? Podcast features Scott Orn
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0
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183
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February 9, 2023
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Benefits of Having a Rare Disease and Chronic Illness Support Group
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0
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174
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February 6, 2023
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Once Upon a Gene podcast Features Ben’s Friends
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0
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205
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January 31, 2023
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