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rivergem
Member
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Posted: Wed Jul 4th, 2007 07:44 am |
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Aw Lauren, I'm so sorry that you've "joined the club" of lyme. It IS scary, but you now have a positive identifier of your problems, and hopefully, a starting point to you feeling better! Always get a copy of your results, it will help you to see how far you've come and help you to stay the course. I need to reference my results, periodically, because my memory is so slow.
I am curious how your doctor identified you have low B-12. I have had a few shots from my doctor over the years, not because anything that showed up specifically (that I am aware of) on my blood work, but because I was so run down. Eventually, I added it to my routine care. I was already giving myself injections for chronic fatigue (diagnosed before lyme disease was found), and I asked my doctor if I could add the B-12 to the same syringe.
How did your treatment options meeting with your doctor go?
Vicki
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remingtonbo
Member
| Joined: | Sat Jan 26th, 2008 |
| Location: | |
| Posts: | 1 |
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Offline
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| Mana: |   |
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Posted: Sun Jan 27th, 2008 03:24 am |
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Hello,
I found an intresting topic related to the rife and wave frequencies on CD, so I decided to go ahead and join. This would be my first lyme board membership. While I don't have lyme, my mother does and I have been trying to help her find treatments which might be effective. She has been diagnosed with lyme for some time now. I had my own battles with mono and fibromalgia ( I was diagnosed with mono 4 times in a 5 year period). Fortunately, I was able to get relatively well through exercise and diet. I did some VIBE treatments and HBOT which were very beneficial. Anyways, I'm from the San Antonio area and hopefully will be able to contribute to the discussions.
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rivergem
Member
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Posted: Fri Feb 15th, 2008 09:34 am |
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Hey Rem,
Hopefully you've found a better site than this one to get some answer's. I put a lot of time (and hope) on this site, to my disappointment. It may have started out strong but...try yahoo's lyme site.
I'm not familiar with the treatment you are talking about...sorry.
Vicki
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Eve Avent
Member
| Joined: | Thu Apr 12th, 2007 |
| Location: | Lubbock |
| Posts: | 27 |
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| Mana: |  |
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Posted: Mon Nov 3rd, 2008 04:31 am |
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Hi Lauren!
How bout those Raiders???
Did you ever go in to Dr. Dalton? He will draw your blood and send it to the ONLY lab that can definatively tell you if you have the disease. But honey, at 21 and you feelin like an old woman.... Join our group. You wrote me a while back, but my memory is SO bad that I can't recall if you ever got tested or not?? Don't wait to start treatment until this stuff invades your brain.
Listen, there is a documentary out called "Under Our Skin" that you simply MUST buy. It's kind of expensive ($29.00 online only), but I watch mine over and over so I don't feel so alone. Beside the fact that it is an EXCELLENT documentary, you will really be able to get a grip on what has happened to you and your health and your life. You need to know this stuff because you can make your husband ill (as I have) and your kids if you're not really careful.
I've told you that you can call me any time if you need to. I find myself more and more isolated as this stuff progresses. It's a bad thang.
Take care hon
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