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Old 12-21-2015, 09:17 AM #21
Ragtop262 Ragtop262 is offline
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Madisongrrl - I'm glad you have finally found an avenue to pursue regarding the cause of all your issues. It's just amazing how many different things can cause the crazy neurological symptoms that all of us experience to one degree or another. And how hard it is to identify what the cause (or causes) are.

Best of luck in your ongoing treatment. Lyme disease is a tough nut to crack, especially if you've had it for a decade. But based on all your posts, it seems you are very tough and resilient - and will never give up. If anyone can beat lyme, I think you can.
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Old 12-25-2015, 04:59 PM #22
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Madisongrrl - I just wanted to tell you that I had the unknown rashes for 2 or 3 years (Lyme symptoms for decades), and I had an Integrative doctor tell me that supplementing with 50 to 100 mg of zinc would help the rashes. I was supplementing, but only 15 mg of zinc. When I upped my dose of zinc, the rashes went away!
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Old 12-25-2015, 05:11 PM #23
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Zinc is overlooked I believe. I never had rash type issues until all the topicals I use and supports on my knee and ankle which cause some abrasions. I started taking 25-50mg Zinc Picolinate daily not that long ago and glad I did. I also LOVE zinc oxide for healing rashes/abrasions.
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Old 01-15-2016, 02:15 AM #24
MAT52 MAT52 is offline
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Maddisongirl well done you for tracking down and proving Lyme. My cousin, who lives in France has Lyme. Hers was confirmed by an excellent primary care doctor where she lives who has a special interest in Lyme. Unfortunately it crossed the placenta of both of her young sons while in vitro so they have to take treatment too I believe. She does very well on the treatment - some sort of antibiotic along with a herbal medicine she gets supplied from Scotland where her family are from.

I was investigated for Lyme a year ago although I felt it very unlikely because I've never lived in a Lyme area. The test came back negative anyhow and it was one run by my neurologist who dies see Lyme disease in his area of Scotland where it is increasing. I am interested in the fungal causes David mentions here. My small fibre neuropathy seemed to start prior to my RA symptoms starting. I'm getting nowhere with investigations however but your news has inspired me to persist badgering my doctors to get to the cause as its progressing slowly but surely and I have this horrible ache in my pelvis now which means it has risen from my groin and seems to be getting worse in my face now too.

I hope you have great success with treatments. Mat X

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Originally Posted by DavidHC View Post
Madisongrrl,

Thank you for all this. Where to start...

First off, I hope you had a good weekend, though it must have been strange given the bomb that was dropped on your lap. But, again, I'm glad you have some answers.

You've had quite a few twists and turns. I am really rooting for you to improve, and wish I could do more than just hope and wish.

I asked about the herbal antibiotics, because I've done months of research on them and intend to begin introducing a series of them over a two-month period. If I can be of use, let me know please.

I'm convinced that in my case it was some sort of bacterial or fungal infection, or that's my strong suspicion, and that it leaked through my gut, to was worsened by my gut health and poor diet. We'll see what happens in a few months, but one thing you're journey and your efforts have led me to do is to think long and hard about my own past and history. I don't think it was Lyme in my case, though who knows, and thankfully you've provided us with some great resources if any of us suspect it. I think mold or bacteria or yeast are more likely and not via a bite. But who knows.

What else? There's so much here. Well, it made me sad to hear about that nurses poor daughter. But you will definitely have a sympathetic person there, who will actually care. Why is it that more often than not it's nurses who care and are helpful and even knowledgeable, rather than, say, physicians? Rhetorical...

BTW I get night sweats too, but usually after a night of eating very heavily and eating lots of carbs. I was too stupid to stop and realize how I was damaging my body. Now I can't touch carbs, or grains to be more precise.

Well, again, I'm rooting for you. Please let us know how you're doing.
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If you get lemons, make lemonade

Sjögren’s, Hashimoto’s and Systemic Sclerosis with Raynaud’s, Erythromelagia and small fibre polyneuropathy, GI problems top to tail, degenerative disc disease and possible additional autoimmune diseases
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Old 01-15-2016, 12:24 PM #25
DavidHC DavidHC is offline
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Mat, just in case you haven't seen this thread, if you're interested as it seems you are:

http://neurotalk.psychcentral.com/thread230382.html


Quote:
Originally Posted by MAT52 View Post
Maddisongirl well done you for tracking down and proving Lyme. My cousin, who lives in France has Lyme. Hers was confirmed by an excellent primary care doctor where she lives who has a special interest in Lyme. Unfortunately it crossed the placenta of both of her young sons while in vitro so they have to take treatment too I believe. She does very well on the treatment - some sort of antibiotic along with a herbal medicine she gets supplied from Scotland where her family are from.

I was investigated for Lyme a year ago although I felt it very unlikely because I've never lived in a Lyme area. The test came back negative anyhow and it was one run by my neurologist who dies see Lyme disease in his area of Scotland where it is increasing. I am interested in the fungal causes David mentions here. My small fibre neuropathy seemed to start prior to my RA symptoms starting. I'm getting nowhere with investigations however but your news has inspired me to persist badgering my doctors to get to the cause as its progressing slowly but surely and I have this horrible ache in my pelvis now which means it has risen from my groin and seems to be getting worse in my face now too.

I hope you have great success with treatments. Mat X
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