new member
 

I'm Deja, new to this site, had a rocky start here but am sticking it out cuz what I've seen I like of the threads and posts here. I hope I will be viewed as a valued member with a lot to contribute:) I have severe spondylolisthesis with severe foraminal stenosis which caused significant bilateral root nerve compression at l5/s1. After 11 months of alternative and conservative treatment, I underwent a posterior fusion with instrumentaion at this level on feb 22nd of this year. Anyway, have a great week and greatest blessings to all!|

Hi

I am glad you are settling in :)

you will find this a very welcoming and supportive community I am sure

I moved your post off that old thread to it's own as this way more members will find it to welcome you

Thank you chemar, I hope so, the ppl seem really nice:)

Hi,
I just stopped by to Welcome you to Neuro Talk. We have all wonderful, caring, people here. I hope you stay and enjoy the forum.
Nice to meet you. :)

Hi Lady, thank you for your warm reply:) I plan on sticking around, offering my support, sharing my experiences, helping others through their journeys the best I can. Have a blessed week!! *hugs*

Hi ~ I' m sorry I'm late in welcoming you to the forum! I hope you find that you enjoy it here, and meet new friends.

How are you doing now after your fusion? I hope you're doing well. That's quite an operation to undergo.

Again, welcome and take care of yourself. Peace, Lee ;)

:)Hi Squirtatioua4u
I am new to this site also and have posted in the new member section but really should have done it here by the looks of it! I have a bunch of stuff going on in the lumbar region also and looking at fusion and ADR according to neuro. I have foraminal stenosis at L5/S1 DDD bulging disc loss of height etc. I was going to ask about just doing a foraminotomy to relieve the compressed sciatic but I noticed you had fusion. can I pick your brain on how this went, what it was like and did it work. my biggest issue is the nerve, I have been managing the back pain for yrs but feel it must have gotten worse to affect the nerve now, if the nerve was sorted, i was hoping to go back to the managing bit witout further invasive surgery as I am allergic to most metals - but neuro says he has not had any probs with this. I am having allergy testing to see what the reaction is like first before deciding but hearing about what I am in for would be great as I have 4 young children and a husband who works in another country, live in oz but all my family are in ireland so no support...afraid I wont be able to manage and now have live in help (thankgod) as I cant stay on my feet!! love to hear from you.
Michelle