Am interested in connecting with people who have this or are significant others of people who have this condition. (I'm in the latter group).
Interested in more discussions like this? Go to the Brain & Nervous System group.
Good morning and welcome to Connect..Here is a discussion group about Stiff Person Syndrome (SPS). What is the infusion that you will be getting? Is your physician a rheumatologist?
I, too, felt alone when I got my diagnosis because no one in my town had even heard of it. My brother in law, a toxicologist, sent me an article from a neurological journal that I made copies of and gave to doctors. Never hurts to do research and be your own advocate. I’m sitting here now, getting my infusion of rituxan, my wonder drug!
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Thank you so much The infusion won’t start until at least next week because they have to have a pre-authorization from my insurance so I just don’t know what to expect did you lose your eyesight in my left eye or movement
I am from Wisconsin also diagnosed with SPS in 2012 and I am getting progressively worse. I currently go to SSM Health. Would you be willing to share who your doctor is at UW? My insurance covers both. I am looking for a specialist not just a neurologist. Thank you, Michelle
I’m looking as well
Hello @colleenyoung My mobility varies from day to day. I need assistance walking in any open spaces. I wish I could say I do something to help maintain mobility but I basically try to make it through the day without having to hug the wall or asking for someone's assistance. It is purely stiffness that makes it unsafe for me walk for fear of falling. I have range of motion in my legs when I am in my home, I do stretches in the morning and at night. And I do this because it makes me feel good not so much for mobility. I have not had a lot of guidance with managing this disease accept for medication. I was trying IVIG until my insurance denied because of lack of randomized clinical trials. I have not had it in over 18 months. IVIG seemed to help me at lower doses to return to my normal.
I appreciate you inviting others into the conversation.
what meds are you taking?
@suzieflynn here is another website that may help you. Stay strong
Thank you very much Does anyone know what is going to happen to me
Hi @suzieflynn and welcome to Mayo Clinic Connect. I look forward to getting to know more about you. What treatments have you had or medications do you take for stiff person syndrome? Do you fall frequently?
low dose baclofen 5mg pt and waiting for infusion
please someone tell me what is going to happen to me, I cant find anything online I have been on every website
@suzieflynn, I have no medical background or training but I'm not sure anyone can tell you what's going to happen because the prognosis varies depending on a person’s symptoms. You can find more information here:
Stiff Person Syndrome: Outlook / Prognosis:
Here is another patient story that you may find helpful — Sharing Mayo Clinic: Diagnosed with stiff-person syndrome:
Suzie, you may also be interested in this discussion with @pattygail @sandra319 and @hammere4,
– Stiff Person Syndrome https://connect.mayoclinic.org/discussion/stiff-person-syndrom/
how do i contact them
Does anyone have stiff person syndrome? If so was oy diagnosed with gad65 blood test ?
@suzieflynn, If your question is how to do you contact Mayo Clinic, you can contact one of the appointment offices. The
contact information for Minnesota, Arizona and Florida can be found here http://mayocl.in/1mtmR63.
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