The doctor agreed with me that I am getting worse with spasticity and that the high doses of Baclofen cause such miserable size effects and the drugs managing the side effects have side effects of their own.
So, I am going to try the pump. Will take time to get this lined up. They test you, and if you pass, they do outpatient surgery where they install a small pump in your abdomen, it then has a tube that goes into your spinal cord . They can put necessary Baclofen dose into the spinal canal, thereby not getting all the systemic side effects by taking pills. Plus, you can get higher doses of Baclofen that way, theoretically less spasticity and less spasms.
Its a bit scary, but my life has become so limited and impaired and filled with pain and fear, that I am willing to try it. Many SPS patients go this route.
You then have to refill the pump every 5 weeks to 3 months depending on your needs. Its dangerous to run out, you can die or have seizures, so you always keep pills on you just in case, and take the Baclofen orally. The device lasts 5 to 7 years.
It has come to this.
So, I am going to try the pump. Will take time to get this lined up. They test you, and if you pass, they do outpatient surgery where they install a small pump in your abdomen, it then has a tube that goes into your spinal cord . They can put necessary Baclofen dose into the spinal canal, thereby not getting all the systemic side effects by taking pills. Plus, you can get higher doses of Baclofen that way, theoretically less spasticity and less spasms.
Its a bit scary, but my life has become so limited and impaired and filled with pain and fear, that I am willing to try it. Many SPS patients go this route.
You then have to refill the pump every 5 weeks to 3 months depending on your needs. Its dangerous to run out, you can die or have seizures, so you always keep pills on you just in case, and take the Baclofen orally. The device lasts 5 to 7 years.
It has come to this.


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