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Old 01-15-2012, 07:04 PM #1
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Since you mentioned "intense dryness of the sinuses", I'm curious if you have dry eyes or mouth? Sjogren's is an autoimmune disease that is not only common to include neuropathy, but 40% of patients have negative blood work. Have they run SSA & SSB for Sjogren's? If you have dry eyes or mouth, I would request they run these labs. If they are negative, then you might request a lip biopsy.

Also, did they diagnose neuropathy just from temperature & tuning fork? Did they do a skin biopsy for small fiber neuropathy? If not, it might be worth asking for.

BTW, iron deficiency anemia is also common with autoimmune disease. There are options to increase ferritin if supplements are not working. One is Ferrlecit (iron) by IV...if your doctor thinks it's bad enough. Do you know your ferritin level?
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Old 01-16-2012, 06:18 PM #2
whitechinacat whitechinacat is offline
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Quote:
Originally Posted by en bloc View Post
Since you mentioned "intense dryness of the sinuses", I'm curious if you have dry eyes or mouth? Sjogren's is an autoimmune disease that is not only common to include neuropathy, but 40% of patients have negative blood work. Have they run SSA & SSB for Sjogren's? If you have dry eyes or mouth, I would request they run these labs. If they are negative, then you might request a lip biopsy.

Also, did they diagnose neuropathy just from temperature & tuning fork? Did they do a skin biopsy for small fiber neuropathy? If not, it might be worth asking for.

BTW, iron deficiency anemia is also common with autoimmune disease. There are options to increase ferritin if supplements are not working. One is Ferrlecit (iron) by IV...if your doctor thinks it's bad enough. Do you know your ferritin level?
Thank you for your thoughts. I don't have dryness anywhere other than my nose. Occasionally my eyes too, but I just attribute that to wearing contact lenses - I've had that for years. I was tested for the Sjogren's antibodies and was negative (twice) though many of symptoms fit and I know it's possible to be seronegative.

Yes, he did diagnose neuropathy just from the temperature and tuning fork. I will ask the new neurologist if he thinks a biopsy would be advisable.

My ferritin is always about 20. I think I've seen it in the 18-22 range whenever it's been tested. The neurologist said it's not horribly low, but low enough to cause some symptoms and it would be a good idea to try to increase it. He said he likes to see a minimum of 45 and would rather it be over 65.
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Old 11-02-2013, 11:29 PM #3
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whitechinacat, Maybe you will not see this, but that sounds scary. I hope you get something figured out soon. Maybe this is some kind of food sensitivity. I know I keep mentioning this book, but it is a good one--Foods That Fight Pain has some great info on foods that trigger various ailments such as migraines, joint pain, digestive problems, & fibromyalgia. For example he lists the common triggers for migraine, in order of importance: dairy products, chocolate, eggs, citrus fruits, meat, wheat (bread, pasta, etc.), nuts, tomatoes, onions, corn, apples, bananas.
Ron
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Old 01-16-2012, 06:25 PM #4
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Well, the new neurologist had a cancellation today so I got to see him right away.

It was a good appointment. I am used to walking away from appointments with my family doctor or rheumatologist feeling that I've learned nothing and have no plan for moving forward. It's frustrating to say the least. The neurologist listened to my history and did a neuro exam. The only abnormality there is that my knee reflexes are quite uneven, but he said he wasn't sure why. He said that my story is quite complex and he can't think of any particular neurological disease that would account for my symptoms, but he is willing to investigate and try to help me feel better. That's a wonderful thing to hear! He admitted that it would be sort of a fishing expedition, but he was willing to cast a wide net and see what he could find.

I am having my MRI of brain and spine repeated (it's been a year) to see if there have been any changes. Depending what it looks like he may also redo the NCV/EMG at a later point. He also wants me to do a sleep study and to wear a holter monitor (because of the palpitations/fainting).

I am going to try Lyrica as well starting at 75 mg at bedtime and then 75mg twice a day. I am quite interested to see if it will make a difference.

I'm just relieved to have some direction here.
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Old 10-31-2013, 12:50 AM #5
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Hi My name is Danielle and i know it was last year that you wrote this blog but i was wondering if you can help me. My daughter who is 14years old has been experiencing the same symptoms that you describe. Unfortunately it has got so bad she now has a feeding tube and often needs to use a wheel chair to move around. She also has a nodule on right side of thyroid too that has not as yet been removed.
Reading your post i am wondering if you have any more answers to your condition or if you have found out anything that may help with your symptoms. My daughter is using a drug called mestinon which is the only thing that has given a bit of relief. I would really appreciate it if you could email me and give me an update on your progress.
I hope you are doing well and look forward to hearing from you.
Danielle






Quote:
Originally Posted by whitechinacat View Post
Well, the new neurologist had a cancellation today so I got to see him right away.

It was a good appointment. I am used to walking away from appointments with my family doctor or rheumatologist feeling that I've learned nothing and have no plan for moving forward. It's frustrating to say the least. The neurologist listened to my history and did a neuro exam. The only abnormality there is that my knee reflexes are quite uneven, but he said he wasn't sure why. He said that my story is quite complex and he can't think of any particular neurological disease that would account for my symptoms, but he is willing to investigate and try to help me feel better. That's a wonderful thing to hear! He admitted that it would be sort of a fishing expedition, but he was willing to cast a wide net and see what he could find.

I am having my MRI of brain and spine repeated (it's been a year) to see if there have been any changes. Depending what it looks like he may also redo the NCV/EMG at a later point. He also wants me to do a sleep study and to wear a holter monitor (because of the palpitations/fainting).

I am going to try Lyrica as well starting at 75 mg at bedtime and then 75mg twice a day. I am quite interested to see if it will make a difference.

I'm just relieved to have some direction here.
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Old 10-31-2013, 04:31 PM #6
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Danielle, whitechinacat hasnt been here since may of 2012. try sending her a message, maybe she will get notification if her email is the same.
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