The Chronic Pain Solution - How To Overcome CRPS, EDS, POTS, FIBROMYALGIA [Nerve Pain]

Welcome to our webinar! If you are watching you or someone you love is suffering from chronic pain and chances are you have been down a very long road, seen a lot of doctors and you are probably to the point where you are just exhausted. That's where we come in, we are dedicated to providing hope to you guys and treating the most hopeless cases.
The Spero Clinic specializes in pain relief for symptoms some doctors consider “hopeless.” Many people report relief from symptoms like Complex Regional Pain Syndrome (CRPS), Gastroparesis, Fibromyalgia, Ehlers-Danlos Syndrome (EDS), Postural Orthostatic Tachycardia Syndrome (POTS) and more.
If you or a loved one is suffering from Neurological Dysfunction, nerve pain, complex regional pain syndrome, postural orthostatic tachycardia, ehlers danlos syndrome or fibromyalgia there is hope! Contact us, Requesting information is completely free, we're here to help. Call: 479-304-8202
Suffering from a Neurological disorder can be incredibly isolating, hopeless and frightening and we understand that. Our treatment protocols are not meant to directly treat CRPS. What we work to achieve is the rehabilitation of the central nervous system.
The nervous system is a collective of nerves stemming throughout your body with the brain as the controller. Your nervous system controls all of the information that your body transmits to communicate with your brain. In the case of CRPS, your nervous system being damaged, can severely malfunction and send signals in the extreme to simple sensory input. IE - the wind blows on your hands and it feels like a terrible burn. By relaxing and rehabilitating the nervous system, as well as correcting any other imbalances within your brain and body, we hope to reset and restore the proper functionality of the systems within your body.
** We are currently the only facility in the world offering this treatment, our expertise is constantly being developed.
Each patient brings new knowledge and a better understanding of conditions that are widely misunderstood. It enables us to consistently mold and change our treatment protocol to be the most effective that we possibly can.
Meet our dedicated team - thesperoclinic...
Connect on Social Media and See Other People's Story
Facebook: / speroclinic
Instagram: / speroclinic
Visit our website at thesperoclinic...

[@jeannettegrondin7190]

I’m in tears watching this I have fibromyalgia. thank u for what ur doing

[@DrKatinkavanderMerwe]

Jeannette Grondin thank you for your kind words❤️

[@kepazugazaga9393]

Watching from Spain. Thanks for helping loads of people around the world. ❤️❤️❤️

[@karancrane4057]

Hello from the UK. Been home for 6 weeks and still pain free 🙏🏼💕

[@dr.premlatadangi3676]

Hello Crane,how you get relief,from where you get treatment .please reply.we are in need.thsnk you .

[@karancrane4057]

@@dr.premlatadangi3676 hello I attended a clinic in Arkansas for a 3 month rehabilitation. It worked and I am now CRPS free. The clinic is called The Spero clinic I hope this helps 🙂

[@dr.premlatadangi3676]

@@karancrane4057 Hello Crane, thank you very much for your reply.please also share about there fees of treatment and where to stay durig the time of treatment. Please do not mind .This all I am asking because i have nobody in US to get to know.thank you.

[@macintoshimann9892]

Your story is so inspiring to me. Ive about lost my mind figuring out how to treat myself after 12 doctors failed and wouldn’t even give me a painkiller stronger than an antidepressant. Somehow I found the vagus nerve on my own… didn’t know what it was I just knew my system was calming down. Eventually I could bare the pain and started working to desensitize myself. Got tons of function back. Im convinced Im going to make a full recovery and once I do I am 💯% finding a way to get treatment to others with these crazy pain diseases! At one time my pain was so bad I passed out for several days except my body kept going. I woke up in the ICU being treated for drug addiction. I was very confused. Doctors didn’t listen… addiction therapists came by my room every day to harass me. Giving me a hard time because I guess I had told them I’d take their treatments while I wasn’t conscious. The doctors were really quite shocked when I “woke up” saying something about peeing out the thiamine and folate they were giving me. The doctor noticed I had finally said something intelligent! I started asking what had happened, why was I being treated like this. No answers. Quiet awkwardness. They thought I’d had a seizure and wernt interested in hearing about my full body shakes from pain. Whatever diagnostic mistakes were made wernt going to exist. Just a big fat bill. Went home worse than ever. Going through how horrible being a patient with a condition like this and finding healing on my own is a really big inspiration to make sure nobody else has to suffer through this condition. We can heal, we just need a little help!

[@jfouts1979]

I'm in Louisville, KY - 2022-04-01 - Small Fiber Neuropathy, Erythromelalgia, Fibromyalgia, Grave's Disease, Cramp Fasciculation Syndrome, Chronic Fatigue, Dysautonomia, CRPS, ... sounds like you are going to cover some topics that are of high interest to me.

[@kepazugazaga9393]

Watching from Spain. 12 horrible years with CRPS. I wish I could afford the treatment. Thanks for all your videos and work you do to help people with CRPS.

[@DrKatinkavanderMerwe]

Kepa, many of our patients do fundraising. Please also reach out to The Burning Limb Foundation - they are a nonprofit that can help with seed money as well as fundraising ideas.

[@isabella3025]

Hi how are you nowdays

[@kepazugazaga9393]

@@DrKatinkavanderMerwe Thanks for the info. God Bless you ❤️❤️❤️

[@Truerealism747]

​@@kepazugazaga9393how are you not w do you have eds

[@kimp8869]

Diagnosed a year ago after broken ankle. Miserable but can't afford treatment 😥

[@richardlarkins5187]

I am watching from Sydney Australia

[@Jomama19824]

Long Island NY.....hoping to get my daughter and wife there when its possible.....

[@lyngaffney]

Thank you for what you are doing in helping people who are without hope. You have boosted my spirits just knowing there is an option to become well again (I have EDS). I just have to look into the logistics of getting there. Any talk of setting up a clinic in Australia? I know it would be very busy from day 1 as there is nothing (as far as I know) like this here. Congratulations on your successes.

[@DrKatinkavanderMerwe]

Thanks for the kind words, Lyn! It's our dream to expand someday but no plans in the immediate future. We've had a handful of Aussie patients. :)

[@isabella3025]

I was told current could be dangerous for crps patients !! Now I know

[@velvet6187]

Can you organise online paltform where we who are unable to come and afford the treatment, could help ourselves. Unfortunately most of us had to stop working 😞

[@velvet6187]

We would pay, of course, online courses

[@iilavenderii21]

I’m not able to travel too I’m all the way on the other side of the world. I have hEDS/POTS/Fibromyalgia and other 25 stuff and really I need help but can’t get it here and this would really help I’m still 14 and I wanna live my life to the fullest. Also I’m allergic to all pain killers so I severely need help too.

[@Truerealism747]

​@@iilavenderii21how are you now pp.heds asperger's ADHD fybromyalgia cfs

[@lorrainemckenna6936]

Northern Ireland i suffer nerve damage 10/10 im crying out for help 😭i cnt go on with this pain 🙏

[@heatherelizabeth27]

Love this!!!!

[@brigittewendt8054]

What is ur thetpy treatment im not feeling left side i omn fire unable walk left leg unable move color change antidepressant destroyed me caused nerve go black unable use left side on 🔥, going crazy.drs no toudch crps dx told old cdeal lil yrs left im called damaged .

[@PEMF.Hydrogen.LLLT.Experts]

Interesting for sure!

[@jeannettegrondin7190]

This sounds amazing! Are there any areas in Canada who does this ?

[@DrKatinkavanderMerwe]

Jeannette Grondin at this time, we are the only center in the world offering this treatment system. We see many Canadian patients.

[@jeannettegrondin7190]

Dr. Katinka van der Merwe do u do online consults ? Wish I could come down there. It is weeks to accomplish this ? A Canadian would have to stay for a certain amount of time ?

[@DrKatinkavanderMerwe]

Jeannette Grondin I do! You may reach our patient care coordinator, Anna, at 479 304 8202.

[@jeannettegrondin7190]

Dr. Katinka van der Merwe ty

[@jfouts1979]

Can I still get that deal?

[@maritaskoglund193]

I’m from Norway and I am fighting CRPS.

[@ashleyslayton2695]

What all do u do for CRPS patients?

[@debrabullion3766]

From vista, California

[@kimp8869]

From Ohio

[@melissafalls5837]

Melissa from Missouri

[@TheDimachaerus]

Isn't Anna the Patient Care Coordinator?

[@kimmcmaster9172]

Watching from Dubai, where abouts are your locations? Happy to travel, have had CRPS for 6 weeks and going crazy

[@DrKatinkavanderMerwe]

Hi, Kim! We are located in Fayetteville, AR USA. Patients travel to us from all over the world. Please visit www.thesperoclinic.com to learn more about our treatment program. There is hope!

[@kimmcmaster9172]

@@DrKatinkavanderMerwe How long would a patient usually have to stay to get rid of CRPS if its caught in the early stages?

[@jonericus]

@@kimmcmaster9172 Generally 12 to 20 weeks. I have been in remission for two and a half years. I had full body CRPS for 24 years. Full remission after just 16 weeks. I now work at Spero.

[@Truerealism747]

​@@jonericusfully body corps is it fybromyalgia

[@MsPenelope52]

Hello from Australia . My daughter has CRPS in her ankle and foot. Where is your clinic ?

[@DrKatinkavanderMerwe]

Hi! We are located in Fayetteville, AR, USA, but we have had many patients from Australia.

[@DrKatinkavanderMerwe]

Hi! We're located in Fayetteville, AR, USA - but we've had many Aussies come to us for treatment!

[@1michaelgracia]

Delaware

[@s0sS1]

How can i contect you?

[@DrKatinkavanderMerwe]

You can contact Anna, our patient care coordinator, at 479-304-8202.

[@pinksocks379]

Ny