Prolotherapy & PRP Round 5 // Caring Medical Trip
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- Опубліковано 8 сер 2022
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#Prolotherapy
You gave me so much hope here Rachel. I’ve been suffering for years and I finally got the CCI diagnosis. I also have Eagle syndrome and hypermobility. Going to start prolotherapy and PRP soon. Thank you ❤
You’re so lucky to have someone who can travel and attend your treatment. For awhile now, I’ve been convinced that I need get a workup and hopefully neck treatment. But it’s a cross country trip, and I can’t find a person who can commit to going with me, which Caring Medical requires. Thanks for the update, it’s encouraging regardless.
Oh no I didn't know they required this either.. I'd definitely be alone
caring medical is so dumb in that regard. I've gotten posterior injections plenty of times elsewhere and it's not a big deal. Like regenexx does not require you to have a baby sitter. But caring medical does really help people. I'm not saying they dont. But that rule is dumb. I think somethin crazy must have happened and they got sued or something.
He does 3x more injections that's probably why
@@feoleb Was Peak in Orlando a place you would recommend? And does your tentative plan to go to Colorado involve Regenexx? It sounds to me as if you have researched and found alternatives to Caring. My cranial condition has been so bad that I can’t properly do web research to locate alternatives around the country. If you were willing to pass along what alternatives you’ve found, it would help me out. I’m still hoping to find someone to commit to attending appointments with me at Caring, but it’s not looking good.
@@matthaines8136 My wife had injections from another practitioner and ended up with an irritated vagus nerve. 36 hours of nausea, dizziness and vomiting. Having someone around to help is important but that said, wonder if you can get a nurse for hire for the day of prolotherapy. Looks to be cheaper to do that than even pay for a second plane ticket for a companion to fly with you across the country. We'd planned to check into that for her only to have me end up needing treatment from Caring Medical as well. We now do a two-fer with us both getting treatment and alternating days
Thank you for posting this , I was considering seeing dr hauser as my symptoms are causing me to feel suicidal. I have been to so many specialists and doctors. They have labeled me as just anxious cause my bloodwork is fine. I am so scared and I've lost trust in doctors. This gives me hope that maybe someone can really get better from this. The only reason why I even know I have cervical instability is because my chiropractor told me that my c curve is backwards and I have degeneration in my neck. Please keep us updated when you can I want to see you succeed!
My son will be getting his 3rd prolotherapy treatment soon for cervical instability, intracranial hypertension, curve correction, etc. Dr. Hauser and Dr. Hutchison are amazing. Don't lose hope! I understand how doctors place the label of anxious because they simply have no answers as to what to diagnose you with. But that doesn't mean there isn't there isn't a diagnose for you. We've had similar issues. Caring Medical may have answers/help for you. Praying for you.
same situation. was told i have stiff spine.
@@sharonmccauley4134 That's what happened to me too just bc I have some irrational fears and panic attacks in the past but I never needed meds and it never interfered with my life then all of a sudden I started getting heart attack symptoms and getting injured very easily just being diagnosed with anxiety and stiff trap muscles... well I was a dancer so why is my neck stiff and I had a ton of neurological symptoms out of nowhere? I was nearly disabled in Oct and Nov. Had my first consultation with Dr Hauser a few days ago and I have cervical instability causing internal jugular vein and vagus nerve compression. How did your son get instability and what were his symptoms if you don't mind sharing? I'm so glad the prolo is working I didn't start mine yet
@@JacksonStar4757 i underwent prolo 3 years ago. It costs like almost new car and no effect.
@@Pavel_Franta Aw I'm sorry it didn't work for you was it your neck or another area you had treated and did you do all the treatments? Some people have said they didn't get better till their 3rd or 4th treatment or even 5th
Hi Rachael, This is so great to see. You are making a tangible positive difference in peoples' lives, through your willingness to share this journey, doing so in a way that works with the DNRS. And huge respect also to your husband. What a team you guys are. God bless.
Happy to see u doing good 💯
I am so overjoyed to see your progress! Love you ❤
Thanks for the update. You look healthier.
Great news! ❤🙏🏻 Please keep updating every once in a while.
Am glad that you are getting better and stronger as each day pass!GOD bless you!
Thank you so much for all the information I’m going through similar symptoms and this info has been so helpful 💐
So glad I found you! I was just diagnosed with hEDS, POTS, and MCAS and one of my subscribers sent me your channel.
You're in our hearts...
Love from Renee and Leo.
It is good to see that this therapy is working, and that it is an option for people. I wish I could afford to visit the clinic :(
So glad you updated! My neck looks like the before picture (I have heds). Also my neck pain is giving me diastolic hypertension 😞
Happy for you! =)
Glad to see you are seeing some improvements. I know this can be so hard. Thanks for sharing. So few doctors and people in general know about this kind of thing and really helps to see the details, especially directly after getting injections. That's really important for accurate observations and records.
Lookin Great Rachael.
My chronic illness journey seems similar to yours, although I haven't had a fusion. I also have three sons that have the same issues. I am convinced by all the research I have done, that Dr. Hauser and Dr. Hutcheson could really help us; but I am left bewildered not understanding how we could ever afford to all go ... so, we all continue to just exist, rather than live. It brought tears to my eyes, to see Caring Medical's treatments help you so much that you said you were starting to feel like you could live again. It's something I'd like to hear everyone with these conditions say, but especially my sons.🥲🤧🥺
Hey!
No suggestions but I wanted to say thanks for your videos whenever you can do it. I can’t always watch every video because I can barely manage anything now but I always love watching (either channel). I have an amazing physio here but other than her, really YOU and your journey is actually what gives me the most hope (which is in small supply right now for all sorts of random reasons). Besides I agree that things can be healed. For me because I have been unwell since birth, I am unsure I can heal EVERYTHING, BUT I absolutely think I can definitely heal a fair bit and also improve quality of life in everything else!! Currently leaving a lot up to God but thanks for your willingness to share and encouragement. Keep it up! (And one year of strengthening, given all you’ve been through…it’ll fly by!) xo
I’m so happy for you!!! ❤ Have your POTS improved?
Yes! But truthfully I think brain retraining / DNRS has been the most helpful thing for my POTS :)
Hi Rachel, I just came across your video and I must say you are such a positive beautiful person. I'm glad you are recovering. I'm thinking of seeing Dr. Hauser is the injection painful? I'm one of those people who can't take pain medication. You are in my prayers.
My daughters symptoms started JUST LIKE YOURS!!! And doctors here tell her nothing is wrong with her neck. She was sick for about a month 3 to 6 months before all the POTS symptoms started. They have slowly progressed, worsening. Headaches, facial pain, right side of head pain. A broad range of symptoms that doctors in state of Tennessee refuse to listen to, admit are related to her neck. WE are so frustrated!!!!!
Did she get burning and pins and needles in feet? Along with ankle pain ?
@@matthaines8136 Not that I am aware of. New neurologist is currently thinking that she could have IIH and is pursuing that. She will probably have a LP to check for it after return visit on 23rd this month. Currently on Daimox to see if it relieves any of her symptoms, so far no.
Very inspiring! Our son has gotten PRP at Centeno Clinic in Colorado. We've yet to have Prolo. He has tremendous CCJ instability along with Os Odontoideum. Very difficult journey. We live in Florida and get regular Chiro treatment in Clearwater.
Does he have EDS?
Did it work?
How long and often do you do neck weights, and what weight do you do? Also I've done that stiff neck walk on the beach. Both beautiful and a little frustrating :p
Hi Rachel, I was wondering where did you get your neck weights from? :)
Rachel i am so happy you are doing well! Because of you i found dr. Gilete in Barcelona and get diagnosed with AAI i stability, EDS and POTS:) Also getting prolotherapy in UK with dr. Mo Akmal in September. Wish me luck:) Best regards from Croatia
Hi did you have your treatment for your neck xx
@@jodiemaplesden3270 Hello, yes I had it. Dr. Akmal gave me 10 prolo injections to the neck, also epidural and steroids in my protrusions(C4-C5 and C5-C6) , i am a little bit better,about 10-15%, I will get another round PRP prolo in December.
@@anjaplesa4549 thank you for getting back to me.Glad you are a bit better .Do you have cci and aai. I am going to book soon xxx
@@jodiemaplesden3270 I have AAI diagnosed by dr. Gilete in Barcelona.
@@anjaplesa4549 think i will have prp xxxx
Was wondering how many rounds of prolo they will do ? I might go to caring medical
Hey Rachel! Sorry to bother you but you can elaborate on what the brain training program is? And where can i do it?
It's so awesome to see you doing so well, Rachel! You are so so right! Healing from chronic illness IS possible! Going through chronic Lyme Treatment finally, and have made such huge leaps and bounds! God always makes a way ♥️
Did your neck problem ever affect the muscles at the base of your skull the suboccipital muscles ?
Can i ask why you get prolo when you had fusion? Did The fusion not help or make it worse?
Hi Racheal...lovely to hear you are doing well...just wanted too know how your pusitile tinnitus is doing?..do you experience headaches with it?
Hey Rachael,
it‘s nice to see, that things are going right now in a good direction. I wish you all the best and god‘s blessing for your journey.
I have a question, because I have also a Neck Instability caused by EDS and my symptoms getting worse over the last months. I live im Germany and there aren‘t similiar treatments or the knowledge about these conditions like Caring Medical does.
In the worst case, i would fly to Florida and get a Prolotherapy there, but i don‘t know, how to raise the money.
Maybe you can tell me, if you have to pay for it by yourself or do you have the possibility of meeting the cost from a health insurance and how much should i expect to pay?
Would you approve it in the case of EDS ?
I hope you read my message an you can give me an advice! 🙏
Thank you for sharing your story with us. 😘
Ich kenne eine Arzt in Deutschland der prolotherapie durchführt und dies auch sehr gewissenhaft. Kann man auf Yt irgendwie privatnachrichten schreiben ?
@@maries8802 Danke für deine Nachricht. Nein, das ist glaube ich nicht möglich. Aber wir könnten es so machen, dass du mir hier den Namen schreibst, wenn du willst und wir löschen es im Anschluss wieder? Wäre das okay für dich?
How do you afford this ,, it’s just me on this journey and no ability to afford these treatments? No family to
Help either can’t find anyone near by to help or help to tell me what’s going on
I do dnrs too but still greatly loop about symptoms and what to do cuz I’m not doing any other treatments because I’m not rich travel and have 16,000 to afford them to
seriously - the prolotherapy is so far out of reach for so many who would benefit from it.
Do you still take LDN?
glucosamine and chondroitin can help too. 👍👍
Do you (or anyone reading this!) know of any places in the UK that offer prolotherapy or similar for CCI/AAI? It doesn't seem like we have any options similar to caring medical. (I looked into regenexx here but unfortunately they don't treat CCI patients). Thank you for sharing your journey, it does give me hope 💛
Dr. Mo Akmal
Also dr. John Tanner
@Floyd. B thanks for your reply. I have had the upright scans and diagnosis already. I was told algocells don't treat CCI? Will look into it further, thanks
@@anjaplesa4549 thanks for your reply
@Floyd. B you mean Rolandas Janusas in Belgium? I could not reach him.
Did you get burning or tingling feet and ankle pain?
Yes I did. Bad nerve pain in my feet and legs too! It’s improving a lot
@@HealingWithRachael my issues got bad after a wreck and I keep wondering if there's some instability in the lower part worsening it, but maybe this reassures it's all neck, thanks for replying!
Do you still take Low-Dose Naltrexone? :)
I do not! I found that other methods of healing were more helpful for me and I no longer needed it :)
how much all this cost please
A lot - 1 prolotherapy neck injection session is $1400 - add on the cost for the new patient consult and additional consults and travel expenses, etc. Many thousands of dollars
😓 𝓟Ř𝔬𝓂𝔬𝐒ϻ