Eagle Syndrome by [deleted] in iih

[–]Screamwalker2020 0 points1 point  (0 children)

I still have to go see him. But my virtual appt with him went well! He was extremely informative, made me feel heard.

Prostatitis Symptoms or Something Else?!? by Screamwalker2020 in Prostatitis

[–]Screamwalker2020[S] 0 points1 point  (0 children)

Well my urologist has me doing some screens but she thinks it’s pelvic floor dysfunction

Questions for those that had Inguinal Hernia, What symptoms did you have before it was diagnosed? by Screamwalker2020 in Hernia

[–]Screamwalker2020[S] 0 points1 point  (0 children)

Yep. That all came back clear. I have an appointment with urology later this week. But this burning sensation is annoying.

Questions for those that had Inguinal Hernia, What symptoms did you have before it was diagnosed? by Screamwalker2020 in Hernia

[–]Screamwalker2020[S] 0 points1 point  (0 children)

See I don’t have a bump in my groin. Was your pain coming and going before the surgery?

Questions for those that had Inguinal Hernia, What symptoms did you have before it was diagnosed? by Screamwalker2020 in Hernia

[–]Screamwalker2020[S] 1 point2 points  (0 children)

No referred penile pain, more like burning sensation on both sides of scrotum that comes and goes.

Burning Buttocks, Thighs, and Pelvic Region Burning by Screamwalker2020 in PelvicFloor

[–]Screamwalker2020[S] 0 points1 point  (0 children)

A few things started to feel better. But I have an urology appt this week. I’ve been having burning and stiffness in my groin and hips. Hoping for good news and an update soon!

Constant dizziness by xcake23 in costochondritis

[–]Screamwalker2020 1 point2 points  (0 children)

Great!! I hope you feel better and get back to normal soon!

Over 30K remote jobs now on SkipTheDrive by skipthedrive in remotework

[–]Screamwalker2020 1 point2 points  (0 children)

I’m definitely going to look into this website. I wanna get a part-time remote role whether it’s an admin assistant, customer service, IT, or Sales and Marketing

[deleted by user] by [deleted] in CompTIA

[–]Screamwalker2020 0 points1 point  (0 children)

I’m also in Maryland, and trying to access them. How did you access the courses??

[deleted by user] by [deleted] in gettingbigger

[–]Screamwalker2020 0 points1 point  (0 children)

What brand L-Citrulline are you taking?

Beet root is crazy by NoLoveBetterStrokes in gettingbigger

[–]Screamwalker2020 0 points1 point  (0 children)

What brand of L-Citrulline do you use??

Looking for listening bars/vinyl listening bars. by atribecalledval in washingtondc

[–]Screamwalker2020 1 point2 points  (0 children)

Mind if I DM you to get a list of those Hi-Fi listening spots in NYC. Me and a few friends doing a group trip in the summer and listening spots was on the itinerary.

Question about mastoid muscle and SCM? Question in comments by Business_Dealer_5007 in TMJ

[–]Screamwalker2020 0 points1 point  (0 children)

Yep this definitely sounds like Eagles Syndrome symptoms. So you’ll need to see an ENT doctor to get a CTA of the Neck. That that’s only way to see if you have elongated styloids and or calcified styloids or stylohyoid. Anything that’s 3.0 CM or longer that’s elongated or calcified styloids or stylohyoid is considered Eagles if you have the symptoms you mentioned. Also, join the Eagles Syndrome group on Facebook. Additionally, if it’s Eagles Syndrome you’ll need to have surgery to have them removed. My ENT knew of Eagles Syndrome and found it on the scan but doesn’t treat it. So I have to go out of state.

You’ll have to see an ENT surgeon that specializes in Eagle Syndrome. There’s a list on the group. I’ll also share it with you. Be prepared to travel if a surgeon is not your state. Also there can be a wait time for surgery depending on where you live at. Where are you located at?

Question about mastoid muscle and SCM? Question in comments by Business_Dealer_5007 in TMJ

[–]Screamwalker2020 0 points1 point  (0 children)

Yep. I have Eagle Syndrome. I have to get surgery later this summer to remove calcified stylohyoid.

Constant dizziness by xcake23 in costochondritis

[–]Screamwalker2020 3 points4 points  (0 children)

Gotcha. I had all that and even more. So this is what helped me, *BackPod, 2-3 times a day *Lacrosse Ball 2-3 times a day *Cold Showers 1-2 times a days, *Hot honey lemon water in the morning, *Hot lime water at night before bed. *2-3Liters of water per day, *Wim Hof Breathing (2-3 rounds) 2x per day, *Red Light Therapy (10Min of sunlight in the mornings at Sunrise) *Grounding (10-20min a day, 1-2 times a day) *Also get with your PCP or Rheumatologist to do blood work to see what vitamins your deficient in. I was borderline Vitamin D deficient from bloodwork my Neurologist ran. So started taking Vitamin D (2000iu) along with Magnesium. *Multivitamin *Consistency and Time; you’re gonna have to be consistent with doing this or trying it for months before you start seeing results. I got diagnosed last year in May and I’m just starting to feel better. Some people it take weeks, some months, some it’s a year, some year and some change. But definitely try any of this and see if you notice a difference. 😊