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Old 02-18-2011, 09:55 AM #1
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Default We went to the PN Support Meeting last night.

What a great meeting. I thought there must have been 20 people there. Some new ones too. People come with various stages of neuropathy, various KINDS of neuropathy, (i.e. motor, small fibre, etc). and MANY questions about WHY they got neuropathy.

One interesting case was a woman aged 58. She has motor and small fiber and it's progressing so fast she doesn't understand it and she's looking for answers. I asked her 'do you know why you have this?" She said "well, my mother had it, but they say mine is idiopathic" I said "your mother had the same symptoms?" and she said "yes". I said "and they diagnosed her as idiopathic also?" and she said "Well, yeah". We all then said "well, there is definitely some genetic component going on here, an inherited neuropathy".

What a lively discussion. Lots of good info and great questions.

Glenn was there and as usual, he was his most informative self, answering question after questions and helping everyone.

Me?? I just gave out muffins. lol But I got requests for the next meeting which is on St. Paddy's Day and they want them green. Never made a green muffin but I'll try something.

Also there was this man at the meeting who had Trigeminal Neuralgia as well as PN. Now THAT is a horror story. I told him about Methyl B-12 and he said "oh I take lots of various B vitamins". I said "do you take B-6"? and he said "I think I do"

I then walked over to Glenn, passed him a note saying "Talk to that man about the dangers of too much B-6"

And Glenn did his thing. He knows SO MUCH. Thank goodness he is coming to these meetings. It's nice to pick his brain.

So we all shared what we know about PN and what we hope to know from future meetings.

Oh, we talked about clinical trials going on that are connected to PN. There are 237 clinical trials going on in the USA. Didn't know that.

We talked about how Tramadol helps certain people with burning and pain.

And want to know how good a meeting it was? When the break came midway in the meeting and everyone can stand up and walk around and leave the room for a bathroom break, well, everyone started talking to Glenn and to each other and I laughed.

It's like our brains are absorbing whatever info we have to share about PN.

We also talked about how a chronic pain sufferer deals with friends and family who do not understand PN and how it affects a person's daily interaction with people and whether or not they can participate in activities.

We found out that, it often happens, that a person thought they had a friend but in hard times, that friend turned out to be a fair weather friend.

So I do hope that anyone who lives near the NY area, well, drop in any time at one of our meetings. Next one is March 17th.

Nice group of people.

Just wanted to share .

Melody
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Old 02-18-2011, 10:27 AM #2
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Hi Melody,

That's fantastic. I was in a chronic pain support group here for a couple of years. I'll make a few calls and see if there's one for PN as well.
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Old 02-18-2011, 05:56 PM #3
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Hi Melody,

That's fantastic. I was in a chronic pain support group here for a couple of years. I'll make a few calls and see if there's one for PN as well.
Hi.

Alan and I always look forward to these meetings. Sometimes lots of people come, but if it's bad weather, then sometimes only a handful.

But there is ALWAYS something new to chat about, new opinions, various treatments, etc. We discuss what works for some and doesn't work for others. We discuss side effects.

For example, last night one of the people at the meeting had gone to his dentist and he was prescribed Prescription Toothpaste (which is essentially fluoride in big amounts). Never heard of this. And guy who got the prescription went to the pharmacy and was told "I have no idea how to fill this and his insurance would not pay for it"

So today I walked into my local pharmacy and asked "What is prescription toothpaste?" and he said "oh it hardens the enamel and some people have big issues with that so they are prescribed this toothpaste and it costs about $40 bucks or so.

I said "And it's just fluoride and nothing else?" and he said "that's right?" and I said "But isn't Fluoride dangerous"? and he said "not really".

Now I've been on the internet and I've read where it is very dangerous so who do we believe?

See what we learn at the meetings??

lol

Melody
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Old 02-18-2011, 07:43 PM #4
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Default Yes there are prescription toothpastes....

Been using them for about 4-5 years now.
What I use now is Colgate PreviDent 5000 plus a 1.1% sodium flouride formula. For a 51g tube. And costs [depending on dentist between $15-25. per tube] Only needs to be used daily, but sparingly.
It helps some? But also do consider the pain meds you are on that can leach calciums. Common from the anti-seizure meds we often take for pain.
Calcium + Vit D + Magnesium combos are also useful [per Mrs D, and also in my experiences] to help minimize damages. That I why I'm only on intermittent pain control. I like my teeth and my bones! I mite also have an asorbtion issue which the diagnosing neuro had suspected. Seems rite for me. can't speak for others tho.
There are also other major brands with similar 'prescription' pastes. Best source to find some? Your dentist! Good luck! - j
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Old 02-19-2011, 12:16 AM #5
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But also do consider the pain meds you are on that can leach calciums. Common from the anti-seizure meds we often take for pain.
This is the first I've heard of this! Assuming you mean gabapentin (Neurontin) & pregabalin (Lyrica) specifically, I did a quick search and found some mention of it, but nothing from what I'd call a credible source (or at least nothing I could understand. )

I also saw some kind of admonition about being careful not to take calcium or magnesium supplements within two hours before or after gabapentin or pregabalin. (More)

Is there some credible citation for this stuff, or is it Liberty Valance stuff? ("When the legend becomes fact, print the legend.")

Thanks,

Doc
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Old 02-19-2011, 07:12 AM #6
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Originally Posted by Dr. Smith View Post
This is the first I've heard of this! Assuming you mean gabapentin (Neurontin) & pregabalin (Lyrica) specifically, I did a quick search and found some mention of it, but nothing from what I'd call a credible source (or at least nothing I could understand. )

I also saw some kind of admonition about being careful not to take calcium or magnesium supplements within two hours before or after gabapentin or pregabalin. (More)

Is there some credible citation for this stuff, or is it Liberty Valance stuff? ("When the legend becomes fact, print the legend.")

Thanks,

Doc
We have had some posters come here who claim their teeth broke and fell out on Gabapentin or Lyrica. Some within 6mos!
They have posted also on RSD about this. Some internet websites with patient reporting, have also many posts growing in number specifically on Lyrica. (I researched this a year ago).

Antiseizure drugs commonly are listed as disrupting Vit D and calcium metabolism. Dilantin and Tegretol had this warning many years ago. So all antiseizure drugs are sort of lumped together now about this issue. But with Lyrica some of the people coming here are quite emphathic that they had sound teeth before Lyrica was prescribed!

Search "teeth" on RSD and PN and you'll find the posts.

Edit to add.... The Pfizer company is mum on this topic, like most drugs on active patent, being advertised on TV etc, we won't see the "truth" come out until patent is expired. Drug companies of late, hide things from doctors and patients. The fines they pay are chump change when discovered, and they remain laughing all the way to the bank. So no I could not find medical studies on tooth loss. That doesn't mean however that it is not happening.
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Last edited by mrsD; 02-19-2011 at 06:12 PM. Reason: fixing spelling and adding a comment...
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