Welcome to my channel! My hope is that my content will be helpful. This is simply me sharing my experience and the tips and tricks that have been beneficial for me along the way. I am not a medical professional, and am not prescribing medical advice. I suggest referring back to your doctor or physician prior to implementing changes to your regimen or making personal medical decisions. Email me if you have any questions. All the best, Megan.
Primary diagnoses: CCI (Craniocervical Instability), AAI (Atlantoaxial Instability), Dysautonomia POTS (Postural Orthostatic Tachycardia Syndrome), and Lyme disease.
If you're able, do you mind making a video about how you get comfortable in the Eclipse? Problems with Eclipse for me: compression (digging) on side of neck/under ear, and under neck, after loosening it. Did you experience that?
Hi Megan, i just wanted to thankyou for making these videos. I am experiencing so many of the same symptoms and ur videos have been very reassuring to me as i await treatment. God bless 💜
Maybe try gently opening all the joints globally and breathing out full exhales when you feel any pain…that is something that is tried and true for so many conditions to resolve ☯️
Hi! Ive been experiencing necknpain upnto back of head and grating sounds on the neck. Now ive been having debilitating symptoms like difficulty swallowing, visual and hearing issues, severe panic attacks and insomnia despite xanax and ambien. Progressing to brain fog amd cognitive decline o thought im having dementia. MRI and all tests are normal.. a regenerative ortho said i havee barre liou syndrome a form of CCI and wants to try prolotherapy.. did ubhave debilitating symptoms like mine? Did prolotherapy work?
I know I have this. I almost died cause my vagus nerve was compressed. After 3 mris a technician finally noted 2 buldges and bilateral stenosis. One buldge c6 is pressing the thecal sac. Doctors wouldn't listen. Still don't. After researching for months I came àcross Dr Hauser's videos. I am hoping Los Angeles provides prolo therapy.
Hi Megan just chiming in late firstly congratulations I had a query did fixing your neck eliminate mcas Lyme I know you mentioned pots symptoms gone but what about orthostatic intolerance like passing out etc
Hi! We are twins. I’ve been living a nightmare for almost 9 years now. I KNOW I have this. I just contacted caring medical today. Were the treatments painful? I’m flying in from Utah and I’m really scared. But i literally can’t go on with life like this. So I will do anything at this point.
Thank you so much for sharing your story. I am barely finding out what is wrong with me after 3 years. I was referred to the Lift Clinic in Utah. The doctor is doing TAP treatments to move my C1 and C2 but the bones keep slipping back but slowly after 3 treatments, I'm hoping they will hold. He also developed a mouth guard that is designed to help hold your bones in place. I am a week and a half into this treatment and I feel like im in the right direction. I will be keeping prolotherapy in mind if this treatment doesn't help. My quality of life is dropping, and I think I may have CCI and POTS. It is a shame that we can't be treated with traditional medicine. 😢
Ps, your video has helped me tremendously, I have alot of the same symptoms that you had. I appreciate hearing your story. I am hopeful that feeling better is in my future ❤
I just wanna say I hope you have completely recovered! My heart went out to you how eloquently and bravely you described your tough journey. I don't even know you and I am proud of you! How amazing to have needed to drop out of school and then had the grit to go back to classes with your new lenses. Thank you for describing how they work! God bless you!
Thank you so much for providing such a valuable content. I am facing similar challenges as yours, and your videos have been a huge source of hope and inspiration for me (and probably - thousands of other people). I've a question if you don't mind: how often did you visit Dr Hauser's clinic to get injected? Were all the injections made under X-ray? The reason why I am asking is because lately a medical practitioner specialised in treating CCI has posted on a dedicated FB group that using X-ray machine for diagnosing CCI and/or injections can increase the risk of cancer. For the context: I am from Poland, my injections take place every 5-7 weeks, doctors only use PRP to inject patients here and fewer injections are made during each round, like between 8-15, but each of them implicates taking one X-ray picture, to see where the needle is placed. We do not use DMX machines (I guess they are US-specific), but instead have fairly popular devices called C-arms. I hope you are doing great and wish you excellent health!
Very helpful!, I’m a rare disease patient and advocate. It took me a long time to get diagnosed and I was gaslight because I looked normal from the outside. I was misdiagnosed with MS. I HAVE 2 rare diseases out of the over 7,000+. A lot of your symptoms were similar to mine. That is why misdiagnosis is on the rise. My health journal helped me find patters in my symptoms. It took me 12 years to get treatment as non existent when I was officially diagnosed . Only to be completely devastated to find out there was a clinical trial. The doctor explained that he did not like paperwork. I was working full time and did not know that my diagnosis of LEMS (Lambert Eaton Myastenic Syndrome) was a disability. once Googles search engine was gaining more info daily, I found a clinical trial in Phoenix, and I live in Philadelphia. I immediately had my records shipped to the my new neurologist and fired my old lazy neurologist once I knew my records were sent. With in 20:minutes of my 1st clinical trail dose, I pushed up off the wheel chair and stated to walk with confidence! Only 5% of rare diseases have FDA approved treatment. My medication is now FDA approved. And I fly to Phoenix, AZ 2x a year for check ups. ADVOCATE TODAY IF YOU DONT FEEL OKAY. @romyonrare on instagram, Facebook, X, and threads. Support groups are important once you are diagnosed. Patient wisdom is priceless. Thank you for this very important story!!
In addition to avoiding histamines (if that triggers your mast cells) other foods might not be high histamine but they are histamine liberators (cause histamines to be released) like strawberries can.
Did you get any manual adjustments on your atlas/axis with any chiro or physio during your prolo therapy? Also did you suffer from bloating at all? Thanks.
I have feeling i have cervical instability but doctor diagnose not he only did ct scan but inly in Normal posture how to determine if i have this do i need to take xray and doing flexion and extension abd after this what do you want to recommend neck prolotherapy or cervical fusion surgery hooing gor our answer coz im very depressed my symptoms the worst is my heart palpitations is so fast once im moving soes in evry hospital have a prolotherapy or in just a clinic hoping for tour answer by the way im a Filipino i got accidented i fell on trycicle hoping for you advice I'm always in house now because of this problem maam hoping gor your help
Does bracing help your POTS symptoms? My husband has bad CCI, with a ton of neurological symptoms like breathing problems, light headed, heart racing. Wondering if a brace would help. Thank you!
Hey Megan, glad to hear from you. I just want to ask did you do the neck exercise for strengthening the muscles? I have my CCI mild I hear cracking a lot specially when sleeping do I have to wear a collar?❤❤❤❤
Hello megan i’m debrina from indonesia so long from florida, i have symtoms CCI in my left upper neck because injuried, can i communicate with you, please, i need more information about florida and caring medical🥲🙏🏻
Hi Megan, Im delighted to see how well you are doing. have you ever experienced parasthesia in your face and over your ears, lips, jaw? And how did Hauser target your ligaments? You mentioned in one of your previous videos that the shift between your occiput and Atlas was over 7 mm - How did the prolotherapy target the ligaments between these bones? I am a bit confused here. Considering the treatment and trying to understand.
