Stiff Person Syndrome: Want to connect with others
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 Support Group.
So sorry to hear all this. I work at Mayo Clinic and my husband was diagnosed at Mayo Clinic in Rochester, Minnesota. That is actually where this condition was first identified and one of the key diagnostic tools is a blood test. My husband did not find baclofen to help, and is on a variety of meds, including neurotin. He tried plasma exchange as an experimental treatment, but that did not help him. Everybody responds differently to meds and treatments. He finds keeping his back really warm helps him, so he wears lots of jackets all the time, even in the summer, he wears fleece sweatshirts. As for dystonia, he does not have that, but a dear friend does and has turned to alternative medicine for much of her support to try to strengthen her neck, etc. She wears a neck brace that helps a lot. I have not heard her mention botox injections and I would have expected she would have told me if she had tried that. I am guessing that placement of those injections can make a difference, similar to when a steroid injection is given for a bad knee, it has to get put in the right place to really help. I am not a doctor or any type of professional care giver and what I'm saying is not anything official from Mayo Clinic. I just happen to work there, in the communications department. All the best and happy to talk more if that helps.
Thank you @suzanneleafbrock for providing some first-hand experience. I'm glad that your husband found help at Mayo in Minnesota. I hope @maritakelly is able to find some help for her sister soon.
@maritakelly Would your sister be able to travel to Mayo in Minnesota if they had appointments available?
Teresa
@maritakelly It sounds as if your sister has really been trying to come up with the correct diagnosis and treatment. I can certainly understand how difficult it must be not to find a treatment that works well for her.
Will you keep in touch and let us know how she is doing?
Teresa
Darlene
Hi @msdee004, welcome to Connect. We look forward to getting to know you. Do you have stiff person syndrome?
Hello. My sister was diagnosed with stiff persons syndrome about 4 years ago at Houston Methodist in Houston Texas, and it is hard to get a physician to help her. She has tremors that last for hours and will only be helped with Valium. I called John Hopkinsin Baltimore to ask for help, they said they would make an appointment to see her, let's hope that works out.. Right now she is trached because she has trouble breathing and they won't see her until she is released from therapy. We live in Louisiana in a rural area so our options are limited. I read on many sites medicinal marijuana helps allot. Praying for everybody with this disease !!
Hi I'm trying to send the following information to Marita Kelly but it won't go! Can you help me? Thanks
We have a support group for Ataxia in Tampa at USF Morsani center which I am the president of. We meet every other month on the third Saturday. But for this month we are meeting on March 24th (Bcas I will be out of town on 17th) and we are meeting at a different location for this month only.
St Joseph’s Hospital North
Twiggs Cafe
4211 Van Dyke Rd
Lutz, FL 33558
12:30-3:00pm
I could go on & on but if you want to contact me please feel free to do so by sending me a private message.
Respectfully,
Darlene
Hi Martha my name is Darlene, I live in Tampa, FL and I was diagnosed with SPS in August 2011 by my wonderful doctor, Theresa Zesiewicz (a neurologist at USF) 813-974-5909. I was referred to her by my son neurologist for Ataxia (a degenerative nerve disorder) similar to MS. Yes I have a double whammy. Ataxia/SCA5 & SPS! Dr.Z (what she is often called) did a thorough examination on me for Ataxia, and she noticed my gait so she said that she wanted to test me for SPS. And her notion was correct the test came back positive for SPS.
Dr. Z put me on IVIg treatment for about 2 years and it really helped me, but I had an allergic reaction to it so she stopped it. So she went to work looking for me something else that would help me and she came up to Plasmapheresis. I get it every 3 months at TGH where I'm hospitalized for 10 days Bcas I receive the treatment once every other day for 5 days. And let me tell you that it really helps it gives me a boost of energy!
Hi Marita my name is Darlene, I live in Tampa, FL and I was diagnosed with SPS in August 2011 by my wonderful doctor, Theresa Zesiewicz (a neurologist at USF) 813-974-5909. I was referred to her by my son neurologist for Ataxia (a degenerative nerve disorder) similar to MS. Yes I have a double whammy. Ataxia/SCA5 & SPS! Dr.Z (what she is often called) did a thorough examination on me for Ataxia, and she noticed my gait so she said that she wanted to test me for SPS. And her notion was correct the test came back positive for SPS.
Dr. Z put me on IVIg treatment for about 2 years and it really helped me, but I had an allergic reaction to it so she stopped it. So she went to work looking for me something else that would help me and she came up to Plasmapheresis. I get it every 3 months at TGH where I'm hospitalized for 10 days Bcas I receive the treatment once every other day for 5 days. And let me tell you that it really helps it gives me a boost of energy!
We have a support group for Ataxia in Tampa at USF Morsani center which I am the president of. We meet every other month on the third Saturday. But for this month we are meeting on March 24th (Bcas I will be out of town on 17th) and we are meeting at a different location for this month only.
St Joseph’s Hospital North
Twiggs Cafe
4211 Van Dyke Rd
Lutz, FL 33558
12:30-3:00pm
I could go on & on but if you want to contact me please feel free to do so by sending me a private message.
Respectfully,
Darlene
Significant other here; just found this blog and would like to talk, but time prevents me. Just wanted to get this website out to anyone in need; will be back here as soon as I can. (just found out this board won't let me give out links) Google " NORD " (National Organization for Rare Disorders) and "Stiff Person Syndrome" Hope this is helpful.