Well today I met with my new neurologist and she is a keeper. I like her personality...... She knows the specialist in Houston I saw and she says he has no personality...I agree. She seems to be a stright forward type person which I like to have in a doctor!
Anyway, she is running an EEG on July 21st, sometime I will have another MRI of the lumbar region on my back, and she wants to do an MRA, and several tests called Evoked Potentials. She is also going to have some congitive evaluation done so we can get a good baseline of where I am at now, and have a comparison for the future.
Currently she gave me a few more meds (whoooopppeeeee) and says to stay on the Betaseron. She wants to follow me on this for a while. She thinks my MS is an aggressive form, but it is still classifed as Relasping Remitting MS. She wants more MRI's done but does not think my insurance will pay for some since I had some done back in May.
I am off to see the LLMD tomorrow. New Neuro thinks I do have both MS and Lyme and she wants me to keep up on the treatment with LLMD. I also have to get him to look into the Thyroid issues and talk about my blood pressure. It was 153/107 today when they checked it in the office. last night it was 104/68 which is (low) normal for me......don't know what today was about!
She is also talking about a treatment called IVIg. I think she will talk more about that after I get through all these tests mentioned above.
Just a girl interested in learning more about these horrible diseases, and just maybe help some one else out along the way!
Showing posts with label LLMD. Show all posts
Showing posts with label LLMD. Show all posts
Thursday, June 26, 2008
Wednesday, June 4, 2008
CONFUSION!!
So, I fly to Houston today to see the MS Specialist that is supposed to know about Lyme. He started in on the "no lyme in Texas" spiel. Frustrating.......
He says all he sees is pointing to MS.....he looks at the Igenex reports and says there is not enough there to consider Lyme, that I needed to have the CSF checked for Lyme titer, which had never been done(so I/we thought); he also said the MRI's are showing him seriously active MS lesions (LLMD says he is seeing NOTHING but Lyme, no MS). I got home and read up on some things and spoke to the local neuro and he told me he did have the b Lyme checked on the CSF and it was negative(want to talk that over with the LLMD). I found a site today that had some info I think is interesting. It also points more towards a definite MS diagnosis.
I thought I may have found a local neuro that used to be a Lyme specialist who I could run some of this by for possible help or direction, but I do not know if she will see me. Waiting, in limbo.....
Also called the LLMD also today to see what his thought was on the CFS being nefgative and the aforementioned site info as well. Still waiting on him to call back as well. Limbo......again......
I do not want a definite diagnosis of anything debilitating, but I just want to know what the heck my body is doing.......it is so frustrating to be caught between 2 diseases that have no 100% diagnositic tests to tell you what is going on. I feel pulled between 2 doctors who are routing for their specialty to be the "winner" and I am stuck in the middle of it all not knowing what to do. The LLMD says do not do steroids as it is a trigger for Lyme, and NN(new neuro) says I should start steroids right away. ON(old neuro) says I should start Avonex treatment ASAP, and NN says he thinks it is not that great and I should start Betaseron ASAP,.......what to do, what to do????
He says all he sees is pointing to MS.....he looks at the Igenex reports and says there is not enough there to consider Lyme, that I needed to have the CSF checked for Lyme titer, which had never been done(so I/we thought); he also said the MRI's are showing him seriously active MS lesions (LLMD says he is seeing NOTHING but Lyme, no MS). I got home and read up on some things and spoke to the local neuro and he told me he did have the b Lyme checked on the CSF and it was negative(want to talk that over with the LLMD). I found a site today that had some info I think is interesting. It also points more towards a definite MS diagnosis.
I thought I may have found a local neuro that used to be a Lyme specialist who I could run some of this by for possible help or direction, but I do not know if she will see me. Waiting, in limbo.....
Also called the LLMD also today to see what his thought was on the CFS being nefgative and the aforementioned site info as well. Still waiting on him to call back as well. Limbo......again......
I do not want a definite diagnosis of anything debilitating, but I just want to know what the heck my body is doing.......it is so frustrating to be caught between 2 diseases that have no 100% diagnositic tests to tell you what is going on. I feel pulled between 2 doctors who are routing for their specialty to be the "winner" and I am stuck in the middle of it all not knowing what to do. The LLMD says do not do steroids as it is a trigger for Lyme, and NN(new neuro) says I should start steroids right away. ON(old neuro) says I should start Avonex treatment ASAP, and NN says he thinks it is not that great and I should start Betaseron ASAP,.......what to do, what to do????
Wednesday, May 21, 2008
Today's appointment.....
went well. I mean I guess there was not much to talk about since the other MRIs are tomorrow. LLMD was just gauging how I was doing on my meds and supplements. I do not think I have seen much change yet, which it has only been 3 weeks on most of it so it is still early. He thinks I did have a "herx" reaction and that is good. Although it sucks when it is going on.....hard to deal with 2 kids when you do not want to get out of the bed because everything hurts and is tired. I was prodded at more today and more blood sucked out. He still has not heard from the last igenex test for the co-infections. That should come in any day.......
Tomorrow I will be poked (literally) for the spinal and prodded for more blood and more lovely shots of the neck and upper back.
Tomorrow I will be poked (literally) for the spinal and prodded for more blood and more lovely shots of the neck and upper back.
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