Stumbled on your ACDF videos through watching your art videos. So much food for thought. I’ve always struggled with nerve numbness in my hands while doing transcription, always stopping, standing up, shaking my hands out, eventually quitting transcription. I’ve seen doctors and chiropractors and was recently diagnosed with cervical degenerative disc disease…no one seemed to think I should do anything more, even tho I have days where I have to literally hold my head with both hands to bend over because otherwise I can’t bend over…it’s like a bowling ball atop my shoulders I can’t control. I guess my point is this - thank you for sharing your story. Sometimes it’s like stumbling through the dark without a guide …maybe you’re that guide. Best wishes in your recovery.
I hear exactly what you are saying and I empathize with what you are experiencing. The body can definitely get in the way of living life to the fullest and problems with the cervical spine are hard to ignore. Please don’t give up! These days you have to be your own advocate in healthcare and do what’s right for you. Blessings to you!
I really appreciate this video on many levels. I had ACDF plus discectomy, 3 levels fused, in May of this year. I am now almost 6 months out. I have the same kinds of feelings you do as far as would I do it again. I was desperate with horrible nerve pain and as an artist/creator my life stopped. It's been worse than the whole pandemic stuff. I'm struggling with the feeling of a lump in my throat that gets progressively worse as I go about my days. It's a special club we are in. I don't think I could ever put on my cervical collar without experiencing extreme claustrophobia or ptsd. It was just awful for 2 months. plus I lost 755 of my voice for 10 weeks. I had no warning of that issue! They said a few days!!! Yeah, thanks for making this and being honest.
Thank you so much for sharing your story. I definitely understand what you are still going through. I was told of the possibility of losing my voice, even permanently, but I was lucky that did not happen. Any physical stress including working on my art and channel can aggravate my neck, shoulders and back still. I am familiar with the lump feeling and stress and even allergies make it worse. For me, old school Benadryl helped, which calms so many systems (Disclaimer: I am not a medical doctor 😊 😂). Anyway, I wish you the best and hope you continue to heal!
Hi, I know this conversation was two years ago, but I just had surgery two weeks ago and do have a lot of muscle pain because of not exercising my neck while it’s in this brace but the numbness I had before in my index finger and thumb are still there and seem to be worsebut I do appreciate all you’ve talked about and you have made me feel better
A friend of mine had that surgery like 20 years ago, and when I went to go see her in the hospital afterward, I bawled when I saw her. Bless your heart. What a scary predicament. Big hugs to you🤗
Just working my way through your timeline series of ACDF surgery. I too had the very same surgery, c6 to c7. I also am having issues with my insurance company paying for the overnight hospital stay. It has been 3.5 months since surgery for me and so far I can’t say that I am any better off as a result of the surgery. Like you I am concerned about my future. I weld for a living and have been doing this work for nearly 40 years and now I am thinking it might be time to hang it up. The stress of it all is worse than the physical pain at this point. However, I am an optimistic and certainly hopeful, time will tell. Now on to your one year.
@@mrprjarrettjarrett2285 It definitely took a long time for me to feel relatively better than before surgery. I’m not going to lie, anything using my arms extensively still causes pain that lingers. Hopefully, you will feel better in time because it is still “early”in your case. The worst part is knowing you can’t do what you did before. Best of luck to you in your recovery.
@@TheWellEducatedArtist Thank you for your reply and sharing your journey, it is greatly appreciated. We all have to adapt to our situation and just do the best that we can and I do hope that you continue to get better with time. I look forward to checking out your art as well. I also love art and like to paint . I am an amateur at best but my grandchildren love the paintings that I do for them and inspires them to be creative and to enjoy art.
Hi I’m glad that I founded someone that I can relate,I had the same procedure done on 11/2023 ,after that my life completely changed for the worse ,I’m in pain 24/7 ,I can’t work like I used to ,I had a great cleaning business but I can’t do my job as before 😢.I hate to complain how I feel ,because until now nothing positive to say .My husband and family are tired to see me complaining,they make me feel like I’m faking.I’m very depressed because I was so fun and happy most the time and very positive about life ,this surgery was a life changer,sometimes I feel miserable,doctor said can take it up to 3 years to feel better .But I need to be able to go back to work ,clean my on house ,sleep again without so much pain ,doctors don’t prescribe pain killer because we can get addicted to it and I don’t want that .thank you for your video ,I have hope that things will get better 🙏 My name is Aline God bless you
So sorry to hear you are in so much pain. I understand what that is like. Give yourself more time to heal because it has taken over a year for me to see some relief. You will be in my prayers.
I just had ACDF (C6-C7) 2 weeks ago yesterday! No insurance issues (yet). My arm and shoulder pain is GONE! Only remaining issue is numbness in my pointer finger, but I understand that should fade over time. I'm back at work, back at the gym (limited) and actually feel great! I'm sorry to hear about your struggles and that your recovery has been less than ideal. I'm 53 (that can't be right!), not young, but I really, really take care of myself and always have, so maybe that helped. Glad to see your scar looks good, mine is still nasty and I can see people staring at it like I was in a knife fight or something lol.
I had ACDF (3 levels) 3 months ago and even though my surgeon came highly recommended he turned out to be anything but good due to his profound apathy. I saw him once before surgery and again on the day of surgery and I’ve not seen nor spoken with him since, despite having significant medical problems following the surgery. If I had it to do over again I would still have the surgery because I honestly didn’t have a choice. What I would do differently however, is get two or more opinions and ask a lot more questions and challenge some of the answers, especially regarding disk replacement vs fusion. I was allowed one follow-up visit at 6 weeks and that was with the nurse and I have been refused any further visits, and I am NOT a problem patient. I can certainly relate to the problems you have had as well as to having to deal with a very unpleasant and apathetic staff. I decided to try physical therapy which is helping, but it has not resolved my problems, but I’m hopeful I will get better in time. I wish you well and hope in time things will improve for you as well.
So sorry for what you have been through with your surgeon. That is very strange that you have not seen your surgeon after the surgery at all since they need to make sure your fusion is taking. Hopefully things will improve over time with the problems. At 3 months I was definitely having my doubts about the surgery. I wish you the best!
we are the same. We didn't have a choice, and had 3 levels done. I'm glad yours worked out well too. Mine was a lifesaver, I couldn't even get out of bed, I had zero strength in my arms. It was very scary.
I’m 58, I understand why people get surgery, I will never do surgery, Gyrotonics has made a huge difference, I do chiropractic when I feel I need it and I have saved money for an amazing medical massage therapist who has changed everything. I pray you have miracles and divine healing 🙏🏽♥️
I had 5-6-7 done in July. I had very good results. My left hand is still numb but praying it comes back. My pain is all gone but do have esophageal issues now. Not bad but certainly hope it doesn’t get worse with age. I’m 66. I wish you the best and hope it has gotten better with time.❤
@@kathyrippyfleming7277 Thanks so much! I wish you the best in your recovery. My numbness got better after about a year so hopefully your will go away. 🙏
If you were having trouble walking then your spine was probably being impinged which suggests that surgery was mandatory. Hopefully you'll continue to improve as the fusion progresses and gets stronger like real bone. Wishing you only the best in your recovery!
I just recently found your channel.. I'm really enjoying your videos and I am so sorry you're having so much pain after your surgery. To have pain every day can really bring you down but you keep on going. I'm hoping it will get better for you soon 🙏🙏🙏
Wow how smiley ☺️ even after this much stress and pain you give tons off positive energy to people's God bless By the way you look 35 Hard to blive you said you're 50 😲 😮
Thank you for the information. I had an ACDF approximately six weeks ago and have been experiencing pain from the base of my neck down to my left shoulder, extending to my left hand’s pinky, ring, and middle fingers. According to my surgeon, I have permanent nerve damage, but the pain should subside over time. To put it bluntly, I am in burning pain, and have weaknesses in my left arm and I suffer from severe migraines. God bless you and be well. 🙏🏽🙏🏽🙏🏽
Wishing you a speedy recovery! I still have to work to keep my muscles from getting tight in my back and neck to avoid migraines and burning in the shoulders. Massage and a lacrosse ball have really helped, as well as, staying hydrated. Anything to relieve nerve compression and/or spasms.
16 months from my C5-6-7 ACDF. Mandatory for me to prevent paralysis. Still with symptoms and disability. You are not alone. Many facebok groups for support. Update please.
Thank you for your comment, Linda. Have continued to improve slowly and I recently posted a 1 year update. I wish the best on your journey and hope you find some relief.
The health care system sucked way before the plandemic hit . Get you in make there money then kick you to the curb after a few months. They don't want to hear that your still having issues
@@TheWellEducatedArtist I am 3 yrs post surgery & symptoms have very much decreased !!! I am doing my best compared to my last 6 years. Minimum symptoms despite Myelomalacia “bruising of the spinal cord”
I had mine about 2 years ago 3 disk they went threw front It has helped me alot with the neck but I now am having trouble with food sticking in my throat had swallow test the other day said it was due to my neck hardware narrowing as my food goes threw my question is your scar looks great mine dont look near as good as yours what did u use to help the scar by the way I do art as well so Ill be checking you channel out just let me know what u used for the scar Im 59 I dont know what to do bout swallowing therapist try to use pudding etc to take with my pills ty for your video😊
@@marygirl8291 thanks so much for your comment. I used Mederma for the scar. Sorry about your throat. I actually know a guy who can move his esophagus from one side to another after ACDF.
@@TheWellEducatedArtist I was just watching one of your art videos I used merderma when I first had it done but I was bad and did not stick with it maybe Ill get back on it lol
I had ACDF C6-7 in 1991. I had severe pain in my upper back. Misdiagnosed for 2 yrs because symptoms weren’t typical. Drugs and PT didn’t help. Finally MRI showed need for surgery. Took a piece of bone from my hip to fuse disk. My relief was immediate. I knew as soon as I woke up that pain was gone. Recovery was slow, i had lingering back pain and PT was very hard. Muscles in my upper back had been so triggered from constant pain that it took a year to slowly calm down. Now, so many years later i have degenerative damage to disks above fusion but not the pain. Would I do it again…..yes! Edited to say choose your surgeon wisely. I would only go with a highly qualified and highly recommended neurosurgeon.
On 6/5 I had anterior and posterior cervical fusion 4 levels. I am 70 yrs old and still suffering from muscular pain and headaches. I know this is early in my recovery process.
Hi I just came across your video as I was trying to find others & experiences with acdf surgery. Thank you for this video. I had acdf surgery C5-7 3 months ago, I’ve worn the collar for all 3 months, but my Dr allowed me to take it off the last few weeks in my home, no driving yet. My concern is- I am a RN, I see my surgeon next week & the plan has been for me to go back to working FT. I’m so scared & stressed out. I haven’t been able to do much exercise because with no driving I can’t get out and do a lot. And if I overdo it, I get a lot of neck pain which causes me migraines. I am worried I will go back to work full-time and get burnt out right away. When did you feel like you were able to work & be on your feet for long periods? Thank you
@@CharissaRascoe-if2qu I would say after 3 months I could be on my feet for a few hours and be ok. However I was by no means back to 100 percent and neck mobility was limited. Picking up heavy items was, and still is, a no go for me if I don’t want to be in pain. My muscles in my back and shoulders still haven’t acclimated and my back and neck are easily strained. may find you have to take it easy at first as an RN depending on where you work and your duties. It took me a full year to really find a new normal. I wish you luck as you move forward in your healing process.
Had four level ACDF fusion surgery 11 months ago. Most of my pain is gone. The nerves going to my arms were damaged, and slowly healing. Still taking Gabapentin. Had to do the surgery, as pain was intense.
Thank you for sharing your story. I so enjoy your honesty and hope that you continue to improve over time. I’m 10 weeks post op ACDF C4-7 & can empathize with you. I see from your comments that you are feeling better. Do you mind sharing what you attribute that too? Sending you wishes of wellness and happiness
Thank you so much! I guess I can attribute feeling better to just the process of healing over time and muscle relaxers helped with the cycle of spasms. When they said it takes a year for your body to heal and adjust I think that is the truth and I am not a very patient person. I wish you the best in your recovery and I will put out my 1 year update soon!
Thank you so much for your response. I’m experiencing much of the same - I started PT a month ago & the spasms were so severe I was unable to sleep. Dr. prescribed a Medrol pack and asked me to rest for a week. I was in so much pain yesterday it scared me, but am feeling 100% better today. You are an inspiration and I agree, the body takes 1-2 years to heal from this. Looking forward to your next update. And your artwork is beautiful.
Interesting question whether you would do it again. I just had c6-c7 fusion 3 days ago. I had no choice, I had a trapped nerve from a herniated disk. If I did not have surgery, I definitely would have slowly lost most of my physical stamina. I choice the best hospital (hss) and selected a highly credentialed surgeon. I expect to be back to where I was before my injury, time will tell.
@@Lord_Don surgery was well worth it. I had a very good surgeon, had no issues with anything he did. No blood in the throat, no issues with incision, neck and arm feel good.
Hi. I can relate so much to these videos. I feel the same way. My life took a wrong turn 2 years ago. I did want to say after my revision surgery last week I am feeling more hopeful that I will get back to my life, maybe not as active but definitely more active than 2020. I wanted to mention to you that non-union or lack of fusion is only detected using CT scan and the flexión X-rays. I don’t know if your doctor has sent this to you. Also, any additional surgeries have to be done with the best spine surgeon there is for revision. I am still early in my recovery, but so far way better than before.
I truly hope your feeling better however I kind of feel this topic is a moot point . If someone has cord compression and the beginning of myelopathy like myself a discectomy and fusion is unavoidable. If I don’t have the surgery my symptoms will only worsen and permanent cord damage will be inevitable. Anyway best wishes to you and I hope I perhaps have a better outcome after my 3 level fusion 🙏
Did you have pain in the throat or bad congestion before the surgery...have c5-7 stenosis and have had throat pain and constriction of the throat muscles and hoarseness... hope things improve
I definitely had problems with my nose from from the neck but my soreness was always around my head, across my face, and down the sides of the throat into the shoulders and shoulder blades and later down the left arm and leg. I did have a swallowing test that said that my throat muscles weren’t functioning properly but they did not realize it was from the neck muscles at the time….doctors don’t tend to communicate well and the cervical spine affects a lot more than the neck….
@@TheWellEducatedArtist I have an appointment with my surgeon Wednesday, I’m kinda in a better situation my injury was work related so I’m only paying in blood and pain..
I’ve been in neck pain for the last 5 years since a car accident. Makes doing artwork more difficult. I have a single level cervical fusion scheduled for the end of the month. A little nervous but excited to have the procedure.
My boyfriend has the exact same issue as you. He’s scheduled for surgery this Friday. I hope your surgery goes well 🥰 Totally off topic, but one time he ran out of gas on the Q street off ramp and had to walk to get gas. Has this ever happened to you?
I would get some more opinions. There are countless websites where you can have a free MRI review on line. One is Dr Daniel Lieberman in Phoenix. He is a retired neurosurgeon. Deuk spine is another. Don't mess around with this--if you need it get it but make sure you absolutely need it. Good luck.
I had it done on c4,5,6. For 3 months I kept saying I had trouble swallowing my own saliva. The dr didn’t see me he said it was normal and gave me more pain medication. I’m one of 23 siblings. This is significant because unless you are bleeding out you don’t complain. 3 months after my surgery I spiked a fever of 104 I was going septic from an abscess around my esophagus from where they had punctured three holes in my esophagus using the wrong instrument. Surgery, iCU, and a month hospital stay and being sent home with a feeding tube for a year and no food or drink by mouth while they hoped the third hole that they missed would heal. It did. I don’t trust doctors, our bodies are miraculous, they do want to heal. It’s been five years and I realized when I was told I couldn’t cry or the hole might not close I guess I boxed up the trauma and all I lost and moved forward. As I slowly unpack things mentally now and a NDE that occurred during that time as well, it occurred to me that others must be struggling out there as well and stumbled onto your story. I’m an art major and looking forward to checking out your channel. Thanks for sharing your story, it’s nice to know I’m not alone in my struggles. Grateful to still be here and trying to find my way back to a creative and fulfilled life again.
@@agingsisterhood Thanks so much for your comment! I believe it is important for people going into this surgery to know that everyone’s experience with ACDF is different and most surgeons don’t tell the stories like yours. I am so sorry you had to go through all of that. I wish you the best as you continue to heal.
I believe true healing begins when you move beyond fear and realize that disconnecting isn’t the answer-it’s time to reconnect. The soul always knows, and I believe the universe is intentional in how it guides us. Finding your channel on RUclips felt like one of those intentional moments. Not only are you an incredibly talented artist, but your tutorials are so well done and inviting-they really encourage that creative spark to come alive again. On top of that, hearing you openly share your experience with your ACDF made it feel safe to start speaking up about my own journey. The universe reminded me that I’ve been silencing my creativity for too long, and it’s been crushing my spirit. Thank you for inspiring me to reconnect with that part of myself. I’m really looking forward to trying one of your tutorials! 🦋👐🦋
My husband has bone spurs and they are wanting to ACDF on C4-C7. I’m very hesitant as I’ve heard it’s not a surgery that comes without post surgery issues. I’m hoping an epidural injections and PT to hold off on the surgery.
My prayers for healing are being sent your way. I’m turning 60 in October. I also struggle with chronic pain. My back is the worst and I have any ailments. It all mainly started when I had a brain aneurysm in 1996. I slowly fell apart after that. I wish all the best for you and pray that you find some relief. 😘🤟❤️
Hi, I hope you are recovering well. I also have disc degeneration since 2010, and have had several epidural injections over the last 12 years. Just a few months ago, I started feeling severe pain in both my shoulders and right arm. After an MRI scan, I am diagnosed with severe disc degeneration on C5-6-7. I had 2 epidural injections done in the last 2 months, but there’s still pain and numbness in my both shoulders and my right arm. My neuro-surgeon suggested for ACDF since the injections didn’t seem to help anymore. I didn’t want to rush for surgery, so I asked him to let me try for a third epidural this month. Based on my own research, I am quite confused with all the information I found. I looked at trusted resources from university hospital, spine health, etc. There’s an obvious consensus on 90% success rate of ACDF and that we should consider the benefits vs risks. After hearing your story, I am quite hesitant and not sure if I should go for it. I’m 52, not sure if it’s worth the risks. Anyway, I wish you all the best and complete recovery very soon. Thanks for sharing your story.
I totally understand. I only decided to do surgery as a last resort. It didn’t solve all the issues I was having but I think it did help. It did take an entire year to see the benefits, though. I wish you the best!
any neurosurgeon will tell you pain is not a reason for this surgery. I am sorry you are going through this. My advice is this--having had now 4 levels fused----(2 surgeries )---STAY ACTIVE. Yoga will be a lifesaver. I work hard doing air conditioning work, I lift heavy things, I climb ladders, I use a lot of heavy tools and equipment. If I didn't, I would be 10x worse. GOOD LUCK TO YOU---DO YOGA please---start slow.
@@mtsaz100 I just had my 2-level ACDF yesterday. I am discharged from the hospital today. I have to agree with @TheWellEducatedArtist that this decision was my last resort. I made a video on my RUclips channel sharing my thought process leading towards this surgery. It was a tough decision.
They just did what I would call is a manual nerve test for strength and not one with needles which I have had before ….and yes I do have a cage and screws.
I had a ACDF surgery at c5 c6 level 2.5 months back. My neck movement has gotten better but I still have some stiff muscles in my upper shoulder. My main concern is with the tingling feeling that I still have in my legs. How long did the tingling feeling last for you and did it go away completly?
Hi, Ankit. For some reason I did not see your comment…The tingling got better after about 9 months but still comes back off and on when my muscles get tight.
@@TheWellEducatedArtist I’m 3 months out. I had c2-T1 fusion. I was told if I didn’t have the surgery I would be paralyzed as well. It had already started effecting my balance. I’m 43. did u have any balance (walking) issues? If so, how long did it take to see improvement??? I feel so discouraged at times.
@@spin2643 Wow - 6 levels! I've been told I need a 5 level ACDF (C4 to T2). My cord is now only 5mm AP. I'm really concerned about adjacent disc disease (ADD). I know it's an issue with bigger fusions and I also have EDS which would make me more prone to ADD. How are you doing now? Did you get any advice re ADD?
I am 4 weeks out 3 levels. I think you are just lovely and I am still not sure where I will go. I’m 56. Fitness has been my career for 25 years. I am doing 3 hrs a day virtual, but don’t think I can ever do the hard core in person again. How is your work going?
Blessings to you! It’s taken a year for things to get back to normal but just be careful not to overdo it at first. I wish you the best as you recover. ❤️
I had the same surgery in 2014 and it disabled me can’t work cause I can’t sleep can’t bend over can’t stand very long I would really say do your home work before I would do it
Mine is work related...meant postop 7 weeks. It's not been fun. I start PT on neck and arm, and OT for my arm and arm related to loss of fine motor skills. I I still have numbness from below my shoulder down to fingertips. I tire out easy, it's like my head gets hard to hold up. I was working full time as a hospice RN, now retired from being a hands on nurse. Would I do again, as a nurse I say Yes because there is permanent problems if surgery wasn't done. Like permsnent ataxia and myelopathy. This has to do with balance and gait. My best nonpill medication is icepacks. It's going to take a long time....😢 to heal. Taking one day at a time. Pain in bu#@ waiting on everything to be approved! My myelopathy will never go away but the surgery will prevent it from progression.
My journey has been hard so far my physical therapy)and OT therapy been hard? And I'm starting them over plus additional occupationional therapy. Okay my pain med has kicked in. I have to keep correcting what I wrote
I found out almost 2 years ago that I have a slipped disc in my neck c6-7 he said I also have mylophy and spinal stenosis at c3-4 and arthritis been about 2 years since I found out but the lasts week it’s got so bad I fell like I’m dying I have chronic neck pain I suffer with bad head also that won’t go away and I fell lost of pressure in the back on my head I suffer with dizziness and off balance also and my neck fills flimsy I can’t look up it hurts to bad I have never pain all the way to my finger and legs also it’s like it’s messing with my brain saying oh you can’t do this just looking at my arms to me is weird I have a 4 out 5 weeekness in my arms I know I need this surgery I fell like if I don’t somtbig bad gonna happen but I’m also scared something bad happening with surgery I have a 3 year old and I fell so lost I wanna get better beofre she goes to school I fell lost 😭 how bad was the pain did you have any of these symptoms I also have trouble breathing which also scars me about surgery
@@autumn3035 I had many of the same symptoms including headaches, weakness, pain etc. you have. I also had trouble breathing. The anxiety of the unknown will get the best of you. I remember feeling hopeless and helpless and feeling impending doom for the surgery. I was scared but did not know what else to do because I was miserable. I also really feel for you having a 3 year old because if you decide to have this surgery you will need lots of help. You cannot pick up anything including children for a while. Honestly, I still have problems if I pick up things with any weight. You will have good days, or even weeks ,and bad ones if you are like me. I understand your struggle and I wish you the best no matter your decision. Be kind to yourself, you are going through a lot.
@@TheWellEducatedArtist thank you so much for replying back to me ❤️ and I’m so glad that your doing some better and may god watch over you and help you get better also ❤️ and yeah I just fell so helpless and lost I’m so depressed there not 1 day that I don’t cry and yeah she my little angel but she wants me to pick her her up all the time and it’s gonna hurt me not being able to pick her up but I need to get better beofre she has to go to school but I shouldn’t have to worry about not having help I have my fiancée and his mom and his Mawmaw and pawpaw also live with me just the thought of having my neck cut open terrifies me there all not wanting me to do it but I don’t think I have much of a choice is messing with my hole body 😭
Also did your neck ever fells very flimsy ? Was you ever light head or dizzy I stay dizzy and do you ever regret getting the surgery? Or you glad you did
I’m around 6 months post op and in agony the last 3 days out of nowhere . I only had one level done despite needing 3, surgeon felt 3 at once was too aggressive but I’m 6 months on with issues from the untreated levels now, miserable , upset, frustrated. I’m 37, what is life going to look like in 5 years never mind 30 years. This is hard surgery !! Would love to speak to anyone else in a similar position as I’ve no one to talk to who’s had the surgery
@@charlottewaudby7258 I’m so sorry you are in so much pain. I will say that it is my understanding that a lot of people have set backs around 5-6 mos. I know I did. There were a lot of ups and downs the first year. I’m honestly surprised that your surgeon was so conservative if you needed more levels done since they usually aren’t. I was told that once one level was done that it was likely that the other levels that showed deterioration would deteriorate more quickly? There are so many schools of thought on this so who really knows. I am assuming that your surgeon says everything looks ok on your X-rays at 6 mos? Failed fusions do happen more than they like to admit so hopefully that is not the case. I can say that I would never want to go through this surgery again if it could be avoided. It took me over a year to feel like maybe the surgery was somewhat beneficial. I hope that in time your pain will improve as the fusion completes.
Three vertebrae ACDF will limit neck mobility. I don’t know what kind of art you do but don’t be afraid to wear your cervical collar when you work if you have to lean forward to take off the stress off the neck. I still use mine so I can work on a project longer without muscle spasms. Just be kind to yourself and don’t overdo it. Thanks for watching.
My first and second opinions both recommended ACDF rather than disc replacement. I believe it was due to the state of the facet joint. The condition was too bad.
For over 18 months I had tingling followed by strong muscle pains along the right side of my neck that extended out to the end of my shoulder and down to my right breast as well as down to my right shoulder blade. It got to the point using my right hand to control a mouse and to type on my computer slowed down markedly. I went through months of physical therapy, injections and ablations. No relief that lasted more than a few hours. At the end of March 2023 I underwent an ACDF of my C3-C4-C5. I was out of the hospital in under 24 hours. I noticed immediately I was out of pain and there was no more tingling. I took it easy for over a month and then started doing the exercises and stretches I learned when I was undergoing PT. Now, after over 6 months post surgery, I am feeling great. No tingling. No pain. I have great mobility with my neck. GOD forbid I should ever have to do it again, but if I started suffering what I went through pre-surgery I would definitely do it again. I had a great surgeon who was/is supported by a great staff in a great hospital. Insurance was a big help even though at times I felt they were slowing down my access to the surgery. There was a reason for the slowdown. Overall, if anyone should ask me where to go and what to do should they suffer what I suffered, I would send them to the surgeon who did my ACDF.
I’m scheduled for ACDF surgery on c4-c5 and c5-c6 in November. I’m in North Dallas and wondering which doctor you saw and the hospital you had surgery at. I hope it’s not the same doctor 😬
I had posterior cervical laminectomy with fusion 10 weeks ago. I have numb feet and hands. My feet hurt. So far no better. I’m a young 68 and very discouraged. The surgery is a bear. I’m a retired physician and I don’t trust doctors either.
Im still paying on two fusions and 4 MRIs from 2015😂 Now they're saying i have an other disc completely blown in to the sciatic right above where they fysed L5,S1 🥶🥳 ive been suffering for 4 year's now😂🤣🤪🤢
@@johnmitchell8925 I am so sorry. I know they said if you have one vertebrae fused you are likely to have more above or below. I wish you the best of luck with a solution and pain relief.
I had my surgery due to a pinched nerve at C 6-7 but I do have arthritis in another vertebrae at C 4-5 for years. Actually, evidence suggests that ACDF surgery on one vertebrae can be a contributor of inflammation and arthritis later, so that is a tough call. Depends on how much pain you are in right now and if nothing else has helped. With any surgery there is always risks.
@TheWellEducatedArtist I can live with the symptoms now. They suck but i can manage. But I'm scared it's going to progress and progress fast and I'll be in a wheelchair or something soon. :( but I guess maybe the acdf couldn't stop that anyway. :(
Recently i had ACDF surgery, i had accident and my C3,C5,C6 was broken, my both hands was not working properly as there was numbness and power loss. Its been almost 8 weeks now still im struggling to get back on track. But this technology is live saving for me. Now im doing all day to day activities but dont know when i can behave normally? Can any one tell me how much time it takes to cure and when i can jump, run and do my gyming?
@@swapnilpowar7432 for everyone it is different. Early on you have to be careful as the bones are not fused fully so things like lifting heavy weights are generally not recommended. Fusion usually occurs after a year but nerves may take 2 years to fully heal. Eight weeks is still early so don’t be too hard on yourself. Your surgeon should advise you as to what activities are okay to do for your particular surgery and situation. Good luck in your recovery!
@@TheWellEducatedArtist I want all the people that had this surgery to be better because i might need it for myself because i have three protruding discs in my neck.
I dont think acdf is "elective". You shouldn't have any surgery like this unless you have no other options. I couldn't get up--I had zero strength in my arms, and couldn't get up out of bed. I was dropping things, I was falling. That is not elective. I had 3 levels, and now- I'm perfect. I can do my job which is a trade and I lift heavy things and work hard. So ----its not an elective thing unless you want to live in bed. I hope you get better. IF YOU NEED THIS SURGERY: ---GO TO A NEUROSURGEON OR ORTHOPEDIC SURGEON WHO ONLY DOES SPINAL SURGERY. If you live in a rural area, go to a major medical center. This is not something to mess around with. In my particular case, my neurosurgeon wont even make an appointment until they have records and MRI to see if you have to have the surgery. Its not "well if he wants it he can have it"---no. This isn't like a nose job. This is not elective in my opinion unless you want no life. I was instantly cured when I woke up from surgery, spent 3 days in the hospital and am now perfect, but I went to the right dr---which is absolutely key. GOOD LUCK.
I agree with you that ACDF should not be considered an elective surgery but that is how INSURANCE sees it and codes it as such. They don’t care that it is the only option for some people. I know that seems absurd but that is the terminology they use.
@@TheWellEducatedArtist I never considered that. One thing- my handwriting is unreadable since this---but it was so scary basically having 10% of the strength in my arms---very scary. I have a large painting I started and cant finish (becasue of this neck thing) . I need someone to finish it. Is this something you would be interested in? Its like 4 feet by 5 feet. I have the background laid out- its a photo of the grandcanyon/colorado river near lees ferry. I usually put the background down inaccrylic and finish in oil but thats me. Acrylic, oil, whatever is fine. I can send a photo and if you are interested I can send the canvas. Thanks
Stumbled on your ACDF videos through watching your art videos. So much food for thought. I’ve always struggled with nerve numbness in my hands while doing transcription, always stopping, standing up, shaking my hands out, eventually quitting transcription. I’ve seen doctors and chiropractors and was recently diagnosed with cervical degenerative disc disease…no one seemed to think I should do anything more, even tho I have days where I have to literally hold my head with both hands to bend over because otherwise I can’t bend over…it’s like a bowling ball atop my shoulders I can’t control. I guess my point is this - thank you for sharing your story. Sometimes it’s like stumbling through the dark without a guide …maybe you’re that guide. Best wishes in your recovery.
I hear exactly what you are saying and I empathize with what you are experiencing. The body can definitely get in the way of living life to the fullest and problems with the cervical spine are hard to ignore. Please don’t give up! These days you have to be your own advocate in healthcare and do what’s right for you. Blessings to you!
I really appreciate this video on many levels. I had ACDF plus discectomy, 3 levels fused, in May of this year. I am now almost 6 months out. I have the same kinds of feelings you do as far as would I do it again. I was desperate with horrible nerve pain and as an artist/creator my life stopped. It's been worse than the whole pandemic stuff. I'm struggling with the feeling of a lump in my throat that gets progressively worse as I go about my days. It's a special club we are in. I don't think I could ever put on my cervical collar without experiencing extreme claustrophobia or ptsd. It was just awful for 2 months. plus I lost 755 of my voice for 10 weeks. I had no warning of that issue! They said a few days!!! Yeah, thanks for making this and being honest.
Thank you so much for sharing your story. I definitely understand what you are still going through. I was told of the possibility of losing my voice, even permanently, but I was lucky that did not happen. Any physical stress including working on my art and channel can aggravate my neck, shoulders and back still. I am familiar with the lump feeling and stress and even allergies make it worse. For me, old school Benadryl helped, which calms so many systems (Disclaimer: I am not a medical doctor 😊 😂). Anyway, I wish you the best and hope you continue to heal!
Hi, I know this conversation was two years ago, but I just had surgery two weeks ago and do have a lot of muscle pain because of not exercising my neck while it’s in this brace but the numbness I had before in my index finger and thumb are still there and seem to be worsebut I do appreciate all you’ve talked about and you have made me feel better
A friend of mine had that surgery like 20 years ago, and when I went to go see her in the hospital afterward, I bawled when I saw her. Bless your heart. What a scary predicament. Big hugs to you🤗
Just working my way through your timeline series of ACDF surgery. I too had the very same surgery, c6 to c7. I also am having issues with my insurance company paying for the overnight hospital stay. It has been 3.5 months since surgery for me and so far I can’t say that I am any better off as a result of the surgery. Like you I am concerned about my future. I weld for a living and have been doing this work for nearly 40 years and now I am thinking it might be time to hang it up. The stress of it all is worse than the physical pain at this point. However, I am an optimistic and certainly hopeful, time will tell. Now on to your one year.
@@mrprjarrettjarrett2285 It definitely took a long time for me to feel relatively better than before surgery. I’m not going to lie, anything using my arms extensively still causes pain that lingers. Hopefully, you will feel better in time because it is still “early”in your case. The worst part is knowing you can’t do what you did before. Best of luck to you in your recovery.
@@TheWellEducatedArtist Thank you for your reply and sharing your journey, it is greatly appreciated. We all have to adapt to our situation and just do the best that we can and I do hope that you continue to get better with time. I look forward to checking out your art as well. I also love art and like to paint . I am an amateur at best but my grandchildren love the paintings that I do for them and inspires them to be creative and to enjoy art.
Hi I’m glad that I founded someone that I can relate,I had the same procedure done on 11/2023 ,after that my life completely changed for the worse ,I’m in pain 24/7 ,I can’t work like I used to ,I had a great cleaning business but I can’t do my job as before 😢.I hate to complain how I feel ,because until now nothing positive to say .My husband and family are tired to see me complaining,they make me feel like I’m faking.I’m very depressed because I was so fun and happy most the time and very positive about life ,this surgery was a life changer,sometimes I feel miserable,doctor said can take it up to 3 years to feel better .But I need to be able to go back to work ,clean my on house ,sleep again without so much pain ,doctors don’t prescribe pain killer because we can get addicted to it and I don’t want that .thank you for your video ,I have hope that things will get better 🙏
My name is Aline
God bless you
So sorry to hear you are in so much pain. I understand what that is like. Give yourself more time to heal because it has taken over a year for me to see some relief. You will be in my prayers.
I hope you are doing better now!🙏
Bless both of you.
Dang, my friend I didn’t know that. My thought’s and prayers are with you. I love watching your videos. Hang in there, you can do it.
Thanks, Ray!
I just had ACDF (C6-C7) 2 weeks ago yesterday! No insurance issues (yet). My arm and shoulder pain is GONE! Only remaining issue is numbness in my pointer finger, but I understand that should fade over time. I'm back at work, back at the gym (limited) and actually feel great! I'm sorry to hear about your struggles and that your recovery has been less than ideal. I'm 53 (that can't be right!), not young, but I really, really take care of myself and always have, so maybe that helped. Glad to see your scar looks good, mine is still nasty and I can see people staring at it like I was in a knife fight or something lol.
@@johnaroach that’s great news! Good luck with your continuing recovery!
I had ACDF (3 levels) 3 months ago and even though my surgeon came highly recommended he turned out to be anything but good due to his profound apathy. I saw him once before surgery and again on the day of surgery and I’ve not seen nor spoken with him since, despite having significant medical problems following the surgery. If I had it to do over again I would still have the surgery because I honestly didn’t have a choice. What I would do differently however, is get two or more opinions and ask a lot more questions and challenge some of the answers, especially regarding disk replacement vs fusion. I was allowed one follow-up visit at 6 weeks and that was with the nurse and I have been refused any further visits, and I am NOT a problem patient. I can certainly relate to the problems you have had as well as to having to deal with a very unpleasant and apathetic staff. I decided to try physical therapy which is helping, but it has not resolved my problems, but I’m hopeful I will get better in time. I wish you well and hope in time things will improve for you as well.
So sorry for what you have been through with your surgeon. That is very strange that you have not seen your surgeon after the surgery at all since they need to make sure your fusion is taking. Hopefully things will improve over time with the problems. At 3 months I was definitely having my doubts about the surgery. I wish you the best!
we are the same. We didn't have a choice, and had 3 levels done. I'm glad yours worked out well too. Mine was a lifesaver, I couldn't even get out of bed, I had zero strength in my arms. It was very scary.
I’m 58, I understand why people get surgery, I will never do surgery, Gyrotonics has made a huge difference, I do chiropractic when I feel I need it and I have saved money for an amazing medical massage therapist who has changed everything.
I pray you have miracles and divine healing 🙏🏽♥️
uhmmm never say never.
I had 5-6-7 done in July. I had very good results. My left hand is still numb but praying it comes back. My pain is all gone but do have esophageal issues now. Not bad but certainly hope it doesn’t get worse with age. I’m 66. I wish you the best and hope it has gotten better with time.❤
@@kathyrippyfleming7277 Thanks so much! I wish you the best in your recovery. My numbness got better after about a year so hopefully your will go away. 🙏
If you were having trouble walking then your spine was probably being impinged which suggests that surgery was mandatory. Hopefully you'll continue to improve as the fusion progresses and gets stronger like real bone. Wishing you only the best in your recovery!
I just recently found your channel.. I'm really enjoying your videos and I am so sorry you're having so much pain after your surgery. To have pain every day can really bring you down but you keep on going. I'm hoping it will get better for you soon 🙏🙏🙏
Thanks, Lori!
i hope you get better soon. thanks for posting
Wow how smiley ☺️ even after this much stress and pain you give tons off positive energy to people's
God bless
By the way you look 35
Hard to blive you said you're 50 😲 😮
You are so kind!
@@TheWellEducatedArtist
Love the background wall to look beautiful paint work
I have lost my positive vibe and smile. I hope it returns 😢
Thank you for the information. I had an ACDF approximately six weeks ago and have been experiencing pain from the base of my neck down to my left shoulder, extending to my left hand’s pinky, ring, and middle fingers. According to my surgeon, I have permanent nerve damage, but the pain should subside over time. To put it bluntly, I am in burning pain, and have weaknesses in my left arm and I suffer from severe migraines. God bless you and be well. 🙏🏽🙏🏽🙏🏽
Wishing you a speedy recovery! I still have to work to keep my muscles from getting tight in my back and neck to avoid migraines and burning in the shoulders. Massage and a lacrosse ball have really helped, as well as, staying hydrated. Anything to relieve nerve compression and/or spasms.
16 months from my C5-6-7 ACDF. Mandatory for me to prevent paralysis. Still with symptoms and disability. You are not alone. Many facebok groups for support. Update please.
Thank you for your comment, Linda. Have continued to improve slowly and I recently posted a 1 year update. I wish the best on your journey and hope you find some relief.
Had to get neck and back fused at 55. Now at 63 I ha e another degenerative disc
The health care system sucked way before the plandemic hit . Get you in make there money then kick you to the curb after a few months. They don't want to hear that your still having issues
@@TheWellEducatedArtist I am 3 yrs post surgery & symptoms have very much decreased !!! I am doing my best compared to my last 6 years. Minimum symptoms despite Myelomalacia “bruising of the spinal cord”
I had mine about 2 years ago 3 disk they went threw front It has helped me alot with the neck but I now am having trouble with food sticking in my throat had swallow test the other day said it was due to my neck hardware narrowing as my food goes threw my question is your scar looks great mine dont look near as good as yours what did u use to help the scar by the way I do art as well so Ill be checking you channel out just let me know what u used for the scar Im 59 I dont know what to do bout swallowing therapist try to use pudding etc to take with my pills ty for your video😊
@@marygirl8291 thanks so much for your comment. I used Mederma for the scar. Sorry about your throat. I actually know a guy who can move his esophagus from one side to another after ACDF.
@@TheWellEducatedArtist I was just watching one of your art videos I used merderma when I first had it done but I was bad and did not stick with it maybe Ill get back on it lol
I had ACDF C6-7 in 1991. I had severe pain in my upper back. Misdiagnosed for 2 yrs because symptoms weren’t typical. Drugs and PT didn’t help. Finally MRI showed need for surgery. Took a piece of bone from my hip to fuse disk. My relief was immediate. I knew as soon as I woke up that pain was gone. Recovery was slow, i had lingering back pain and PT was very hard. Muscles in my upper back had been so triggered from constant pain that it took a year to slowly calm down. Now, so many years later i have degenerative damage to disks above fusion but not the pain. Would I do it again…..yes! Edited to say choose your surgeon wisely. I would only go with a highly qualified and highly recommended neurosurgeon.
You are a beautiful person! ✨
On 6/5 I had anterior and posterior cervical fusion 4 levels. I am 70 yrs old and still suffering from muscular pain and headaches. I know this is early in my recovery process.
Hi I just came across your video as I was trying to find others & experiences with acdf surgery. Thank you for this video. I had acdf surgery C5-7 3 months ago, I’ve worn the collar for all 3 months, but my Dr allowed me to take it off the last few weeks in my home, no driving yet. My concern is- I am a RN, I see my surgeon next week & the plan has been for me to go back to working FT. I’m so scared & stressed out. I haven’t been able to do much exercise because with no driving I can’t get out and do a lot. And if I overdo it, I get a lot of neck pain which causes me migraines. I am worried I will go back to work full-time and get burnt out right away. When did you feel like you were able to work & be on your feet for long periods? Thank you
@@CharissaRascoe-if2qu I would say after 3 months I could be on my feet for a few hours and be ok. However I was by no means back to 100 percent and neck mobility was limited. Picking up heavy items was, and still is, a no go for me if I don’t want to be in pain. My muscles in my back and shoulders still haven’t acclimated and my back and neck are easily strained. may find you have to take it easy at first as an RN depending on where you work and your duties. It took me a full year to really find a new normal. I wish you luck as you move forward in your healing process.
Had four level ACDF fusion surgery 11 months ago. Most of my pain is gone. The nerves going to my arms were damaged, and slowly healing. Still taking Gabapentin. Had to do the surgery, as pain was intense.
@@richardfoltz4351 glad to hear the pain in gone. Wish you the best!
Thank you for sharing your story. I so enjoy your honesty and hope that you continue to improve over time. I’m 10 weeks post op ACDF C4-7 & can empathize with you. I see from your comments that you are feeling better. Do you mind sharing what you attribute that too? Sending you wishes of wellness and happiness
Thank you so much! I guess I can attribute feeling better to just the process of healing over time and muscle relaxers helped with the cycle of spasms. When they said it takes a year for your body to heal and adjust I think that is the truth and I am not a very patient person. I wish you the best in your recovery and I will put out my 1 year update soon!
Thank you so much for your response. I’m experiencing much of the same - I started PT a month ago & the spasms were so severe I was unable to sleep. Dr. prescribed a Medrol pack and asked me to rest for a week. I was in so much pain yesterday it scared me, but am feeling 100% better today. You are an inspiration and I agree, the body takes 1-2 years to heal from this. Looking forward to your next update. And your artwork is beautiful.
Interesting question whether you would do it again. I just had c6-c7 fusion 3 days ago. I had no choice, I had a trapped nerve from a herniated disk. If I did not have surgery, I definitely would have slowly lost most of my physical stamina. I choice the best hospital (hss) and selected a highly credentialed surgeon. I expect to be back to where I was before my injury, time will tell.
How are you doing now?
Damned if you do Damned if you dont😢
@@Lord_Don surgery was well worth it. I had a very good surgeon, had no issues with anything he did. No blood in the throat, no issues with incision, neck and arm feel good.
I've been told I need a 5 level fusion (C4 to T2). My spinal cord is compromised and now 5mm AP diameter. Really thinking about holding off.
Keep up the great work, I’m rooting for you and your family on a safe recovery ❤️🩹
Hi. I can relate so much to these videos. I feel the same way. My life took a wrong turn 2 years ago. I did want to say after my revision surgery last week I am feeling more hopeful that I will get back to my life, maybe not as active but definitely more active than 2020. I wanted to mention to you that non-union or lack of fusion is only detected using CT scan and the flexión X-rays. I don’t know if your doctor has sent this to you. Also, any additional surgeries have to be done with the best spine surgeon there is for revision. I am still early in my recovery, but so far way better than before.
I truly hope your feeling better however I kind of feel this topic is a moot point . If someone has cord compression and the beginning of myelopathy like myself a discectomy and fusion is unavoidable. If I don’t have the surgery my symptoms will only worsen and permanent cord damage will be inevitable. Anyway best wishes to you and I hope I perhaps have a better outcome after my 3 level fusion 🙏
It has truly taken a full year but things are going better. It is definitely a journey! Best wishes to you for your surgery!
Hi friend sending you a pm
Thank you for sharing praying for you
I hope things are better for you now(or at least improving)
Things are not perfect but are much better. Thank you!
I had a medical massage therapist, deep tissue massages got me through the post op, the muscle spasms were bad.
Wonderful idea! Medical massage definitely helps if you live where you can find one!
Did you have pain in the throat or bad congestion before the surgery...have c5-7 stenosis and have had throat pain and constriction of the throat muscles and hoarseness... hope things improve
I definitely had problems with my nose from from the neck but my soreness was always around my head, across my face, and down the sides of the throat into the shoulders and shoulder blades and later down the left arm and leg. I did have a swallowing test that said that my throat muscles weren’t functioning properly but they did not realize it was from the neck muscles at the time….doctors don’t tend to communicate well and the cervical spine affects a lot more than the neck….
@@TheWellEducatedArtist indeed it does... it's very complex.. I'm staying on the sideline for now... Stay well
Was there anything they could do?@@TheWellEducatedArtist
C4-c7 4 months since my ACDF but now I have constantly pain in my back pt done my neck any else pain disappear after surgery
try a nucca chiropracter had 5,6 and 7 in 2017 have a lot more problems than before .been doing the nucca chiro has made a big differences
@@AprilTavis I’ll have to check into it. Thanks!
I’ve had ACDF level 3 surgery 7 months ago and I’m in more pain now then after the surgery.., SMH
I’m so sorry. I’m better than I was at 7 mos, so I pray that it your pain gets better with time.
@@TheWellEducatedArtist I have an appointment with my surgeon Wednesday, I’m kinda in a better situation my injury was work related so I’m only paying in blood and pain..
Is it really worse or are you trying to milk the system since it was at work?
What a clown response it’s called nerve damage.. Please be stupid someplace else , Thaanks
Same here 3 level 6 mths ago my issue is back neck pain is killing me don’t know why
I’ve been in neck pain for the last 5 years since a car accident. Makes doing artwork more difficult. I have a single level cervical fusion scheduled for the end of the month. A little nervous but excited to have the procedure.
I totally understand. May you have a speedy recovery and a relief from your pain in the near future!
My boyfriend has the exact same issue as you. He’s scheduled for surgery this Friday. I hope your surgery goes well 🥰
Totally off topic, but one time he ran out of gas on the Q street off ramp and had to walk to get gas. Has this ever happened to you?
@@hjong8830 🦌
I would get some more opinions. There are countless websites where you can have a free MRI review on line. One is Dr Daniel Lieberman in Phoenix. He is a retired neurosurgeon. Deuk spine is another. Don't mess around with this--if you need it get it but make sure you absolutely need it. Good luck.
How are you doing now?
I had acdf surgery c3 thru c7 its been 2 years im still recovering i still have pain and neck movement is not good horrible maybe I waited to long
I hear you! The recovery and results are mixed for many but I hope it gets better. Neck pain is the worst!
I had it done on c4,5,6. For 3 months I kept saying I had trouble swallowing my own saliva. The dr didn’t see me he said it was normal and gave me more pain medication. I’m one of 23 siblings. This is significant because unless you are bleeding out you don’t complain. 3 months after my surgery I spiked a fever of 104 I was going septic from an abscess around my esophagus from where they had punctured three holes in my esophagus using the wrong instrument. Surgery, iCU, and a month hospital stay and being sent home with a feeding tube for a year and no food or drink by mouth while they hoped the third hole that they missed would heal. It did. I don’t trust doctors, our bodies are miraculous, they do want to heal. It’s been five years and I realized when I was told I couldn’t cry or the hole might not close I guess I boxed up the trauma and all I lost and moved forward. As I slowly unpack things mentally now and a NDE that occurred during that time as well, it occurred to me that others must be struggling out there as well and stumbled onto your story. I’m an art major and looking forward to checking out your channel. Thanks for sharing your story, it’s nice to know I’m not alone in my struggles. Grateful to still be here and trying to find my way back to a creative and fulfilled life again.
@@agingsisterhood Thanks so much for your comment! I believe it is important for people going into this surgery to know that everyone’s experience with ACDF is different and most surgeons don’t tell the stories like yours. I am so sorry you had to go through all of that. I wish you the best as you continue to heal.
I believe true healing begins when you move beyond fear and realize that disconnecting isn’t the answer-it’s time to reconnect. The soul always knows, and I believe the universe is intentional in how it guides us.
Finding your channel on RUclips felt like one of those intentional moments. Not only are you an incredibly talented artist, but your tutorials are so well done and inviting-they really encourage that creative spark to come alive again. On top of that, hearing you openly share your experience with your ACDF made it feel safe to start speaking up about my own journey.
The universe reminded me that I’ve been silencing my creativity for too long, and it’s been crushing my spirit. Thank you for inspiring me to reconnect with that part of myself. I’m really looking forward to trying one of your tutorials! 🦋👐🦋
My husband has bone spurs and they are wanting to ACDF on C4-C7. I’m very hesitant as I’ve heard it’s not a surgery that comes without post surgery issues.
I’m hoping an epidural injections and PT to hold off on the surgery.
I wish you and your husband the best.
Don't do it. Seek doctor Deuk spine institute. You can find him on RUclips
My prayers for healing are being sent your way. I’m turning 60 in October. I also struggle with chronic pain. My back is the worst and I have any ailments. It all mainly started when I had a brain aneurysm in 1996. I slowly fell apart after that. I wish all the best for you and pray that you find some relief. 😘🤟❤️
Thank you so much! I wish the same to you. God bless!
Hi, I hope you are recovering well.
I also have disc degeneration since 2010, and have had several epidural injections over the last 12 years. Just a few months ago, I started feeling severe pain in both my shoulders and right arm.
After an MRI scan, I am diagnosed with severe disc degeneration on C5-6-7. I had 2 epidural injections done in the last 2 months, but there’s still pain and numbness in my both shoulders and my right arm. My neuro-surgeon suggested for ACDF since the injections didn’t seem to help anymore. I didn’t want to rush for surgery, so I asked him to let me try for a third epidural this month.
Based on my own research, I am quite confused with all the information I found. I looked at trusted resources from university hospital, spine health, etc. There’s an obvious consensus on 90% success rate of ACDF and that we should consider the benefits vs risks. After hearing your story, I am quite hesitant and not sure if I should go for it. I’m 52, not sure if it’s worth the risks.
Anyway, I wish you all the best and complete recovery very soon. Thanks for sharing your story.
I totally understand. I only decided to do surgery as a last resort. It didn’t solve all the issues I was having but I think it did help. It did take an entire year to see the benefits, though. I wish you the best!
❤
any neurosurgeon will tell you pain is not a reason for this surgery. I am sorry you are going through this. My advice is this--having had now 4 levels fused----(2 surgeries )---STAY ACTIVE. Yoga will be a lifesaver. I work hard doing air conditioning work, I lift heavy things, I climb ladders, I use a lot of heavy tools and equipment. If I didn't, I would be 10x worse. GOOD LUCK TO YOU---DO YOGA please---start slow.
@@mtsaz100 I just had my 2-level ACDF yesterday. I am discharged from the hospital today. I have to agree with @TheWellEducatedArtist that this decision was my last resort. I made a video on my RUclips channel sharing my thought process leading towards this surgery. It was a tough decision.
Did they do a nerve test prior to surgery? And did they replace your vertebrates withe still parts and screws?
They just did what I would call is a manual nerve test for strength and not one with needles which I have had before ….and yes I do have a cage and screws.
I had a ACDF surgery at c5 c6 level 2.5 months back. My neck movement has gotten better but I still have some stiff muscles in my upper shoulder. My main concern is with the tingling feeling that I still have in my legs. How long did the tingling feeling last for you and did it go away completly?
Hi, Ankit. For some reason I did not see your comment…The tingling got better after about 9 months but still comes back off and on when my muscles get tight.
@@TheWellEducatedArtist I’m 3 months out. I had c2-T1 fusion. I was told if I didn’t have the surgery I would be paralyzed as well. It had already started effecting my balance. I’m 43. did u have any balance (walking) issues? If so, how long did it take to see improvement??? I feel so discouraged at times.
@@spin2643 Wow - 6 levels! I've been told I need a 5 level ACDF (C4 to T2). My cord is now only 5mm AP. I'm really concerned about adjacent disc disease (ADD). I know it's an issue with bigger fusions and I also have EDS which would make me more prone to ADD. How are you doing now? Did you get any advice re ADD?
I'm very hopeful, that after a year your body will be healed better ♡ I will be posted for that video
Thank you, Mauricio!
Very informative! Thanks for sharing! ☺️
I am 4 weeks out 3 levels. I think you are just lovely and I am still not sure where I will go. I’m 56. Fitness has been my career for 25 years. I am doing 3 hrs a day virtual, but don’t think I can ever do the hard core in person again. How is your work going?
Blessings to you! It’s taken a year for things to get back to normal but just be careful not to overdo it at first. I wish you the best as you recover. ❤️
I had the same surgery in 2014 and it disabled me can’t work cause I can’t sleep can’t bend over can’t stand very long I would really say do your home work before I would do it
I'm 6 weeks our from my ACDF surgery at C5-C6 and C6-C7 herniations. I've got a long road ahead
Lot of pain, also have a partial rotator cuff surgery
Mine is work related...
@@sharonlowery8958 Best of luck in your journey!
Mine is work related...meant postop 7 weeks. It's not been fun. I start PT on neck and arm, and OT for my arm and arm related to loss of fine motor skills. I I still have numbness from below my shoulder down to fingertips. I tire out easy, it's like my head gets hard to hold up. I was working full time as a hospice RN, now retired from being a hands on nurse. Would I do again, as a nurse I say Yes because there is permanent problems if surgery wasn't done. Like permsnent ataxia and myelopathy. This has to do with balance and gait. My best nonpill medication is icepacks. It's going to take a long time....😢 to heal. Taking one day at a time. Pain in bu#@ waiting on everything to be approved! My myelopathy will never go away but the surgery will prevent it from progression.
My journey has been hard so far my physical therapy)and OT therapy been hard? And I'm starting them over plus additional occupationional therapy. Okay my pain med has kicked in. I have to keep correcting what I wrote
I found out almost 2 years ago that I have a slipped disc in my neck c6-7 he said I also have mylophy and spinal stenosis at c3-4 and arthritis been about 2 years since I found out but the lasts week it’s got so bad I fell like I’m dying I have chronic neck pain I suffer with bad head also that won’t go away and I fell lost of pressure in the back on my head I suffer with dizziness and off balance also and my neck fills flimsy I can’t look up it hurts to bad I have never pain all the way to my finger and legs also it’s like it’s messing with my brain saying oh you can’t do this just looking at my arms to me is weird I have a 4 out 5 weeekness in my arms I know I need this surgery I fell like if I don’t somtbig bad gonna happen but I’m also scared something bad happening with surgery I have a 3 year old and I fell so lost I wanna get better beofre she goes to school I fell lost 😭 how bad was the pain did you have any of these symptoms I also have trouble breathing which also scars me about surgery
@@autumn3035 I had many of the same symptoms including headaches, weakness, pain etc. you have. I also had trouble breathing. The anxiety of the unknown will get the best of you. I remember feeling hopeless and helpless and feeling impending doom for the surgery. I was scared but did not know what else to do because I was miserable. I also really feel for you having a 3 year old because if you decide to have this surgery you will need lots of help. You cannot pick up anything including children for a while. Honestly, I still have problems if I pick up things with any weight. You will have good days, or even weeks ,and bad ones if you are like me. I understand your struggle and I wish you the best no matter your decision. Be kind to yourself, you are going through a lot.
@@TheWellEducatedArtist thank you so much for replying back to me ❤️ and I’m so glad that your doing some better and may god watch over you and help you get better also ❤️ and yeah I just fell so helpless and lost I’m so depressed there not 1 day that I don’t cry and yeah she my little angel but she wants me to pick her her up all the time and it’s gonna hurt me not being able to pick her up but I need to get better beofre she has to go to school but I shouldn’t have to worry about not having help I have my fiancée and his mom and his Mawmaw and pawpaw also live with me just the thought of having my neck cut open terrifies me there all not wanting me to do it but I don’t think I have much of a choice is messing with my hole body 😭
Also did your neck ever fells very flimsy ? Was you ever light head or dizzy I stay dizzy and do you ever regret getting the surgery? Or you glad you did
Did you have trouble walking I’m so weak it’s messing with my legs now and this just started a few days ago
I am in the Dallas area and lookng at doing this surgery. Who is your Dr. and What was your hospital?
@@tpbarron MDMC
@@tpbarron Surgeon was young but good and very pleasant, Katzen.
I’m around 6 months post op and in agony the last 3 days out of nowhere . I only had one level done despite needing 3, surgeon felt 3 at once was too aggressive but I’m 6 months on with issues from the untreated levels now, miserable , upset, frustrated. I’m 37, what is life going to look like in 5 years never mind 30 years. This is hard surgery !! Would love to speak to anyone else in a similar position as I’ve no one to talk to who’s had the surgery
@@charlottewaudby7258 I’m so sorry you are in so much pain. I will say that it is my understanding that a lot of people have set backs around 5-6 mos. I know I did. There were a lot of ups and downs the first year. I’m honestly surprised that your surgeon was so conservative if you needed more levels done since they usually aren’t. I was told that once one level was done that it was likely that the other levels that showed deterioration would deteriorate more quickly? There are so many schools of thought on this so who really knows. I am assuming that your surgeon says everything looks ok on your X-rays at 6 mos? Failed fusions do happen more than they like to admit so hopefully that is not the case. I can say that I would never want to go through this surgery again if it could be avoided. It took me over a year to feel like maybe the surgery was somewhat beneficial. I hope that in time your pain will improve as the fusion completes.
Im an artist, and they say i need c5c6c7 fusion. Any advice?
Three vertebrae ACDF will limit neck mobility. I don’t know what kind of art you do but don’t be afraid to wear your cervical collar when you work if you have to lean forward to take off the stress off the neck. I still use mine so I can work on a project longer without muscle spasms. Just be kind to yourself and don’t overdo it. Thanks for watching.
Why didn't you do disc replacement
My first and second opinions both recommended ACDF rather than disc replacement. I believe it was due to the state of the facet joint. The condition was too bad.
@@TheWellEducatedArtist thanks for your prompt reply. I hope you are feeling better and managing the pain. Stay strong 💪 ✨️
For over 18 months I had tingling followed by strong muscle pains along the right side of my neck that extended out to the end of my shoulder and down to my right breast as well as down to my right shoulder blade. It got to the point using my right hand to control a mouse and to type on my computer slowed down markedly. I went through months of physical therapy, injections and ablations. No relief that lasted more than a few hours. At the end of March 2023 I underwent an ACDF of my C3-C4-C5. I was out of the hospital in under 24 hours. I noticed immediately I was out of pain and there was no more tingling. I took it easy for over a month and then started doing the exercises and stretches I learned when I was undergoing PT. Now, after over 6 months post surgery, I am feeling great. No tingling. No pain. I have great mobility with my neck. GOD forbid I should ever have to do it again, but if I started suffering what I went through pre-surgery I would definitely do it again. I had a great surgeon who was/is supported by a great staff in a great hospital. Insurance was a big help even though at times I felt they were slowing down my access to the surgery. There was a reason for the slowdown. Overall, if anyone should ask me where to go and what to do should they suffer what I suffered, I would send them to the surgeon who did my ACDF.
I’m scheduled for ACDF surgery on c4-c5 and c5-c6 in November. I’m in North Dallas and wondering which doctor you saw and the hospital you had surgery at. I hope it’s not the same doctor 😬
Hope everything goes well for you!!! The doctor was actually OK as far as skill so no worries, but the hospital is, let’s say, on the south side…
I had posterior cervical laminectomy with fusion 10 weeks ago. I have numb feet and hands. My feet hurt. So far no better. I’m a young 68 and very discouraged. The surgery is a bear. I’m a retired physician and I don’t trust doctors either.
Im still paying on two fusions and 4 MRIs from 2015😂 Now they're saying i have an other disc completely blown in to the sciatic right above where they fysed L5,S1 🥶🥳 ive been suffering for 4 year's now😂🤣🤪🤢
@@johnmitchell8925 I am so sorry. I know they said if you have one vertebrae fused you are likely to have more above or below. I wish you the best of luck with a solution and pain relief.
They want me to do this surgery due to arthritis in my neck. Should i do it?
I had my surgery due to a pinched nerve at C 6-7 but I do have arthritis in another vertebrae at C 4-5 for years. Actually, evidence suggests that ACDF surgery on one vertebrae can be a contributor of inflammation and arthritis later, so that is a tough call. Depends on how much pain you are in right now and if nothing else has helped. With any surgery there is always risks.
@TheWellEducatedArtist I can live with the symptoms now. They suck but i can manage. But I'm scared it's going to progress and progress fast and I'll be in a wheelchair or something soon. :( but I guess maybe the acdf couldn't stop that anyway. :(
Recently i had ACDF surgery, i had accident and my C3,C5,C6 was broken, my both hands was not working properly as there was numbness and power loss. Its been almost 8 weeks now still im struggling to get back on track. But this technology is live saving for me. Now im doing all day to day activities but dont know when i can behave normally? Can any one tell me how much time it takes to cure and when i can jump, run and do my gyming?
@@swapnilpowar7432 for everyone it is different. Early on you have to be careful as the bones are not fused fully so things like lifting heavy weights are generally not recommended. Fusion usually occurs after a year but nerves may take 2 years to fully heal. Eight weeks is still early so don’t be too hard on yourself. Your surgeon should advise you as to what activities are okay to do for your particular surgery and situation. Good luck in your recovery!
The operation killed my stamina and will
I hope you are okay now.
Thank you! Doing better and will post update soon!
@@TheWellEducatedArtist I want all the people that had this surgery to be better because i might need it for myself because i have three protruding discs in my neck.
Bless you, but I received nothing from this.
So, sorry! 😞 Wish you the best! It’s been several years now and things are better than they were.
I dont think acdf is "elective". You shouldn't have any surgery like this unless you have no other options. I couldn't get up--I had zero strength in my arms, and couldn't get up out of bed. I was dropping things, I was falling. That is not elective. I had 3 levels, and now- I'm perfect. I can do my job which is a trade and I lift heavy things and work hard. So ----its not an elective thing unless you want to live in bed. I hope you get better. IF YOU NEED THIS SURGERY: ---GO TO A NEUROSURGEON OR ORTHOPEDIC SURGEON WHO ONLY DOES SPINAL SURGERY. If you live in a rural area, go to a major medical center. This is not something to mess around with. In my particular case, my neurosurgeon wont even make an appointment until they have records and MRI to see if you have to have the surgery. Its not "well if he wants it he can have it"---no. This isn't like a nose job. This is not elective in my opinion unless you want no life. I was instantly cured when I woke up from surgery, spent 3 days in the hospital and am now perfect, but I went to the right dr---which is absolutely key. GOOD LUCK.
I agree with you that ACDF should not be considered an elective surgery but that is how INSURANCE sees it and codes it as such. They don’t care that it is the only option for some people. I know that seems absurd but that is the terminology they use.
@@TheWellEducatedArtist I never considered that. One thing- my handwriting is unreadable since this---but it was so scary basically having 10% of the strength in my arms---very scary. I have a large painting I started and cant finish (becasue of this neck thing) . I need someone to finish it. Is this something you would be interested in? Its like 4 feet by 5 feet. I have the background laid out- its a photo of the grandcanyon/colorado river near lees ferry. I usually put the background down inaccrylic and finish in oil but thats me. Acrylic, oil, whatever is fine. I can send a photo and if you are interested I can send the canvas. Thanks
She has a very southing voice , lol I almost wanted to rest my eyes , lol
You unkowningly swivel, tilt, turn and twist your neck all around when you talk. I'm sure that isn't helping you.
Get on with it already