Topic: sorry was Dyke/, but med question is still valid
nonna05
Frequent Contributor (1K+ posts)
Member # 33557
posted
about mycoplasma ...OK Lymedin2010 wrote it out
On Van Dyke .>>> post
it was a written summary of Dave &Ben..
Then the son..
Kinda making light of getting to doctor (Ben) with very swollen legs.
The doc said it's to much pressure and thought he would relieve pain by taking needle to pull out blood..Ben said doc had bad look on face ..Wasn't blood was infection..
If I had stuck a needle in my knee to relieve pressure, I'm sure it's not blood...but I'm not a Ben or Dave or George (Bush)
I want to know how many have Mycoplasma, wherever it is,,or get more, way more ,than normal bouts with pneumonia?
What they have gone through and maybe where else found in body.
What they did for it? How it was found?
I then had , on web, MSN < when I searched Lyme/Mycoplasma.
That took me to the article that supports that more people dealing with LD also have Mycoplasma as maybe second or third highest co infection/
Included research from Professor Garth Nicolson .
I'm just asking a medical question that I'm dealing with and would like input on from others fighting it or think they might be.
Thank you, Nonna
I'm not asking for fun. I'm asking because I'm dealing with it.
I also know others who sleep ,or try to , sitting up when all this happens , so they can breath.
Opinions please and maybe the others who replied before might chime in
nonna05
Frequent Contributor (1K+ posts)
Member # 33557
posted
It may have been a link that was highlighte(blue) on VanDyke,but I thought it was a short post mentioned Leterman or Stillman.
Posts: 2563 | From Denver,CO | Registered: Aug 2011
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nonna05
Frequent Contributor (1K+ posts)
Member # 33557
posted
Maybe if I hadn't broken two toilets because I fell, full force at them..
My knees were so swollen and painful ,they just locked up and there I went......
When I look back at it I also had the breathing, pain , pneumonia symptoms at same time.
It happened couple months between each other.
I remember having this knee issue over a year ago, not as bad.
I have had the breathing ,chest, pneumonia action from the start, along with L ear trouble ,behind it,or in deep.
Posts: 2563 | From Denver,CO | Registered: Aug 2011
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scroll down to see Ben Stiller/Letterman conversation
You can also do a search here to find the info if this is not it.
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96223 | From Texas | Registered: Feb 2001
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nonna05
Frequent Contributor (1K+ posts)
Member # 33557
posted
THANK YOU...TUTU..
.IT'S THE MEDICAL CONNECTION I'M TRYING TO GET INFO ON
I saw the one on Dyke post where Lymedin2010 actually wrote it out on that post after Otter asked @Ben,,,,
So I know where I saw It
The point is the MEDICAL part of either post..CONCERNING
MYCOPLASMA......who,what, where, why,
Chest, knees,back,
what people have gone through with this think they may have a connection been tested
wondered why two symptom events happened at same time
what treatment may have worked
the connection with the report from research
Professor I mentioned ,and how I found it..
If I knew how to make a link to it I would.
Lord ,I even copied it to word pad ,so I could look at article and refer to it.. Well, 1/2 the page is there and not original site that had link... I'm batting a 100% on this
Just does anybody have experience/knowledge/info/treatment/testing/etc. with this connection....??????????
Other post was closed that had a couple comments..
Love to hear back from you Posts: 2563 | From Denver,CO | Registered: Aug 2011
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Have you tried a search here? Hopefully someone will help you out.
I would just get a test for it the next time you see your LLMD.
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96223 | From Texas | Registered: Feb 2001
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Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- Nonna,
Do you have a LLMD? If so, THEY should be addressing the various stealth infections. You should not have to figure all this out for yourself.
Ask them if there are articles, websites or books to help you better understand all this and some supportive things you can do. But, the LLMD should be guiding your anti-infective treatments, coordinating all that.
A LL ND would also be good to have on your team. I know from personal experience, we just can't learn all there is to know about all this ourselves, when ill. We need the medical help in our LLMDs and LL NDs.
If your LLMD is not adequately taking seriously all this, it may be time to find another.
Or - if you are trying to jump or hopscotch around, doing things on your own out of synch with your LL doctor(s), that can also boomerang any attempts.
We also just can't always say this symptom is that infection. It just doesn't work that way.
It's hard not to want to know more. And hard not to pull this and that together but I get the sense that you do not have adequate medical planning - a detained plan of action - and it is of concern.
I'm not sure where this goes out of synch but, somehow, I hope your LL doctor(s) can help you OUTLINE ON PAPER the plan so you can refer back to it. -
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part of either post..CONCERNING ![[dizzy]](graemlins/dizzy.gif)
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