FND & RHS symptoms 7 months after treatment...

If you haven't seen my videos detailing my treatment, watch them here: • MORE TREATMENT??? [PAR...
To find a doctor in your area: iafnr.org/member-referral-dir...
Under 'keyword search' type the area where you live.
Ottawa Performance Care: www.ottawaperformancecare.com
Dr. Isaiah Redfern: [e-mail]

[@estuchedepeluche2212]

Glad to see you are so much better!

[@franzcesar]

I am very happy for you, my best wishes to you, you deserve the best, thank you for sharing your courage!!!

[@bcolocha86]

Thank you, seeing your video has given given me hope I can recover from FND. Febuary is 3 year from when I got diagnosed. I had accepted that I was going to learn to live it, but your video gave me resources and hope. So I made an appointment to see a biofeedback specialist.

[@TanyatasticTalks]

Let me know how it goes!! I’m sitting now at 98% recovered- no symptom relapse whatsoever. The doctor I saw is trained in Functional Neuroscience and Rehabilitation- the association website is in the description box, you can always email him - he may know of clinics where you live

[@babyhands251]

Yes, amazing 🧠✊🏻☺️

[@electrikwayz6634]

I am really grateful for your videos. i just got RHS a week ago. I saw you mentioned around 2 weeks or so you started to get some facial response back. Wsa that really about the time? I hope it does for me as well. I got on all my meds 24 hours after getting it and been doing acupuncture for 3 days now. Hoping for the best. TY

[@TanyatasticTalks]

Hope you’re feeling better this week!! It took a few weeks to get my face back- although my eye was the last thing to recover - still have some issues with that same eye - it twitches when I’m in any sort of pain now. You caught it right away, that is a very good thing. Every case is different though, just depends how your body handles it all. Let me know if you have any other questions!

[@electrikwayz6634]

@@TanyatasticTalks Thank you for the response. My neurologist said it takes time to just relax and we will go from there. Thanks again

[@selenacolon880]

Was there treatment that you did to help with any facial switching and dropping? And did you mouth and smile function return on its own?

[@TanyatasticTalks]

With RHS my movement in my face and mouth came back within a month and a half after the onset of symptoms. My facial contractions developed afterwards since my brain was caught in a loop. The treatment I had in October helped and come mid-January they have completely stopped which was amazing to see because I thought I was going to have to live with that.

[@snowyskylar8821]

May I ask your thoughts on something? I had shingles severely when I was 13 years old, that was forty years ago, and developed dreadful FND at the onset of menopause. I'm almost certain this herpes virus lays in your system and attacks the vagus nerve. Your thoughts please ?

[@TanyatasticTalks]

It might! I know my nervous system was just on red alert after my shingles outbreak/ RHS and then progressed into FND from there because my brain didn’t know what to do anymore. It does lay dormant and then pops out when it wants (which is awful)

[@snowyskylar8821]

@@TanyatasticTalks I too had shingles on my left side of my neck near my ear....my FND is all left sided...🌷⚘

[@TanyatasticTalks]

@@snowyskylar8821 oh interesting - I know of some other people who have it on one side more so than the other

[@brianbordenkircher52]

I have had this 2 years now. Head hurts so bad from the jolts and yelping, a Tourette’s like tic

[@TanyatasticTalks]

I found treatment in October of 2019! It’s on my channel under playlists. I went to see a chiropractor who specializes in neuroscience. I have my life back. I’m 98% recovered which is still unbelievable! The mimicking, tremors, difficulty walking, severe chronic fatigue, hearing hypersensitivity, sensory overload, numbness in my arms and legs (which was starting up more frequently before I found treatment), intense reactions to things - they’re all gone. The only thing left is that I still get scared easily but that’s pretty much it. I’d recommend trying to find someone in your area that can maybe help with all of what you’re experiencing. I was starting to lose hope in thinking I’d be like this for forever.

[@TeamKerIGold]

Can I ask how much was this treatment and do they take insurance?

[@TanyatasticTalks]

They’re based in Canada, and when I had insurance (as that works differently here) I had coverage for this. www.Ottawaperformancecare.com

[@carmenchoong339]

Can the treatment you had cure severe pain hyperacusis and tinnitus?

[@TanyatasticTalks]

Carmen Choong it helped lower my hearing hypersensitivity I can be out in public and not have to wear my noise cancelling headphones anymore, it also helped with my tinnitus too, it also helped lower the nerve pain I felt on a daily basis. The nerve pain now still acts up with the weather, stress, fatigue but it’s a good barometer at times for me to slow down

[@carmenchoong339]

@@TanyatasticTalks Thank you for your reply. I am trying to seek help for my daughter who is 18. She has severe pain hyperacusis and tinnitus. She is overprotecting her ears by wearing ear muffs and isolating in her room. I can't find such treatment in Malaysia. If you can help me to find out from your doctor? Thanks.

[@TanyatasticTalks]

Carmen Choong I’ll get back to you! Im just on holiday right now but I’ll check back in a few days! I know it’s very difficult and isolating. That was my life for 3 years

[@carmenchoong339]

@@TanyatasticTalks Thank you. I appreciate your help. My daughter suffers a lot of pain from any sound. Her prolonged isolation is affecting her mental health too.