- Raj - Spondylolisthesis Story (Grade 1)
Hi Everyone, This is my story about Spondylolisthesis. Every thing was going good in my life; I just got married in December 2010. Life was looking beautiful. But then I was diagnosed in July 2011 with a grade 1 Spondylolisthesis at L5 S1. I was 26. At that time I took rest from my office and went to many doctors for consultation. I was hoping it was not a big problem, but when I came to know about Spondylolisthesis, and it's effects on daily life, I went into a depression for the first three months after learning this. I was a very active person and I was running my own business, so for this I had to do a lot of meetings, sometimes I had to do more than 4-5 meetings in a day. At that time I was confused as to how to manage everything and what to do next. But, my business partner is my wife, and family supports me a lot. It's helped me a lot recovering from the depression. I've tried the medications, physical therapy and a back brace. After two months my back pain was less. The only thing that hurts me a lot, is that sometimes my mom and dad have to lift heavy weight instead of me, because I can no longer do the lifting. But I am happy that I was diagnosed at an earlier stage.
The condition effects my daily activities now, so I have to do less activity. I feel more pain when I sleep on left side, so I can't sleep on left side anymore. At work I usually take a break after 1 hour of being seated. If I work more then 7-8 hours a day, then it hurts. I'm not taking medicine for pain, just doing regular PT. Doing exercise daily has really helped a lot of the pain and so does heat. I love long drives with family and lots of other activities, which I can't do now. I always have fear of long traveling and bumpy roads. I feel pain in my lower back and buttocks when I do longer traveling of more than 1 hour. Truly speaking, I'm not in such real pain now. As for surgery, I'm not thinking of that. I want to spent my life without doing any surgery. Went to the doctor and he said it's not moving forward ... it is stable. But I have to do a x-ray every 90 days.
It's Life. Sometimes God gives us lots of happiness, and sometimes we are on the other side.
- Raj
Raj Prajapati Pre-Op X-Ray Grade 1
About Spondylolisthesis Stories ...
Welcome! Spondylolisthesis Stories is a compilation of personal stories involving individual's diagnoses, experiences, surgeries, and life with Spondylolisthesis.
My hope is that this site may offer a voice and platform for those with the spine condition to share their personal stories with the medical community, fellow Spondyo patients, and the world as a whole. Spondylolisthesis Stories also provides a wide array of information, personal knowledge, support and ideas for those with Spondylolisthesis. Whether you were recently diagnosed, learning to live with the condition, making difficult decisions regarding surgical interventions, in the early phase of recovery following an operation, or further into your journey, this site covers it all!
In addition to general stories about this spine condition, personal stories which focus on the subject of Spondylolisthesis & Pregnancy may also be found. These shared experiences detail the matter of labor and delivery, and include women with both unfused slips and those whom have had surgery prior to pregnancy. It has been my experience that this topic is one which is shrouded in some mystery. By sharing these stories I hope we may be able to shed some light on the subject; offering guidance and ideas to those females with Spondyo who would like to become pregnant but fear the unknowns which this condition can create.
I am always seeking new stories and would love to hear yours! Let your story and voice be heard! Please contact me (Brenna), at spondyostories@gmail.com, in order to share your story here. If you are seeking additional help and support from others with Spondyo, please ask to join the "Spondylolisthesis and Retrolisthesis Support Group" on Facebook. *This group is closed, and therefore, offers a higher level of privacy and comfort for all members to share openly and without fear of judgement. It is open to anyone with Spondylolisthesis (or a family members of those with Spondylolisthesis) to join.
Below the Spondylolisthesis stories you will find several survey questions. If you have Spondylolisthesis, please take a moment to review these questions and select your answer(s). You are also encouraged to join in and participate by interacting in the "Community Answers" board, located at the bottom of the page. Feel free to post questions and comments, share stories, answer the questions already presented, and ask your own questions! I greatly appreciate your participation and look forward to reading your answers and comments!
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