I had my fusion on March 25, after a month of being so fatigued they finally figured out I was on to many narcotics. Since then I will find my self crying for no reason at all. Sometimes I will cry for an entire day off and on. I am still in some pain and just started going to physical therapy. I a 42 and never had a surgery in my life. My doctor said that it is common and my therapist upped my Cymbalta from 60 mg to 90 mg and it helped for 2 weeks. I had blood work done and my vitamin D is very low, They told me surgery to the vertebrae does different things to women, even can cause menopause. Has anyone else had the depression/crying like I have?View Thread
I just had c5-6-7 fusion on Dec. 29. The ruptured disc actually "exploded" the week of Oct. 21, and my MRI shocked my surgeon. Since it was so bad, and I am a teacher, and we never sit, or have a break,constant testing, etc. he put me on leave as of Oct. 27. He wanted me to get a new disc, I got to see it, and it was supposed to be the latest and greatest, but the insurance company wouldn't approve it. After all of the insurance mess,they approved another fusion My fusion finally happened on Dec. 29. This time they needed to used cadaver bone and a sponge to fill the cage, last cage, which I still have, has only my bone fragments.
I'm healing better than my last fusion, but just started getting teary again, but not as bad I have good days and bad like we all have. One thing my surgeon did this time was put a steroid solution on my throat so it would be easier to swallow and eat. My 1-1/2 hour surgery ended up being 45 min. longer with all of the tiny bits from the exploded disc. I am still very weak, and sleeping is very hard. This time my meds are Percocet and Soma (muscle relaxer). My arm is much better and have no pain. This time my pain is in my shoulders and spine.
Let me know if anyone has had another fusion like me and the length of recovery time. Last time .I know I went to work to soon. I want to take it slower this time. My last fusion was March 25 2013. I'm now44. .View Thread
I'm not that same person. I'm sorry . I live in Colorado. An update though , I'm a teacher and last August on bus duty I fell backwards from stepping in a sprinkler hole that the summer crew never filled in. I continued to work, but I was on Workmans comp due to the tea curing complications I was having.i had X-rays done by my surgeon and my fusion was in tact but no MRI was done. Workmans Comp is a bitch!! I had less strength in my arm again and my headaches were getting worse. I went through Physical Therapy and saw my Workmans Comp dr every week or so. Even had to get a cat scan once because the pain was so intense since all the pressure after a fall is taken by c4 or c7 now since C5c6 are fused. After 3 months of Workmans comp I was released. At my year checkup my spine surgeon gave me a prescription to see a chiro for my headaches. After seeing him for about 6 weeks twice a week my headaches were gone but I was getting numbing and tingling in my right arm. I saw my surgeon last week, he had me have an MRI, and I have a ruptured disc between C6c7. He gave me an epidural shot in the area for the symptoms . I am now on a pain log for weeks to see if it will work . Since my surgery 15 months ago, I still can't wear lanyards around my neck or heavier necklaces due to a choking type sensation in my throat. I do use special oil on my neck to exercise my esophagus to decrease scar tissue, but it still hasn't helped as much as the dr thought. They now make cute stretchy lanyard bracelets that I wear for my school is and keys.
Let me know how you are doing! I know I wrote a book ! But spinal surgery is so different. It shocks the entire body. One thing I learned from my chiro is that every year after surgery, there is a 3% chance that the disc above or below will have some sort of problem .
My blood test showed my vit D is back up to the normal range. I still get emotional, but not as often. I still have tremors in my right arm when I am having a tough day. I go back to my surgeon tomorrow. I have been going to my physical therapist regularly, and started walking. I am a school teacher and school starts Aug. 9, and I want to have the energy and the oomph I used to have. I realized the other day that it has only been a little bit more than 4 months since the surgery, and with the busy summer I have had, I have been told that I am still going to have good and bad days. My physical therapist had one of those"Easy Readers" for sale and told me that it would work well for me since I have had trouble reading material during the classes I have been taking. It is like an easel with a clipboard. I'm excited to try it out at my next class. I also learned that I need to use my special oil that I put on my scar and move my esophagus and all the other stuff in my neck around daily so the soft tissue will spread so I don't always feel like I have a big knot in my throat. I still have trouble with hard foods; buy it's getting better
Do, or Did you all have good and bad days for the first year?View Thread
I did have a blood test and my vitamin d was very low. I go back in July to get another blood test done. My doctor also increased my Cymbalta to 120 mg. I am definitely crying less. I started physical therapy but since my vit. d is low, I am still lethargic. I just don't have the energy like I used to, but then again, I'm still in the healing process. Thank you so much for your commentsView Thread