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desperate
I took a lot of levaquin but my entire body stings with intense electricity like electrical raindrops. and most days to the point of screaming.. My entire body is like this. even face and head.. Then I found out I have morgellans on top of this.. I did not even knew it existed. I have tons of fibers coming out my body and stool.
I have heard of people having stinging but this has an INTENSE electrical component to it.. I cant wear clothes. I just pace and cry. They even tried IVIG on me and I reacted horribly. Does ANYONE have this over entire body with such intensity you want to end it.. No one knows what is wrong with me. I have searched the internet over and NO ONE Stings to this degree with the electrical conponents.. Feels like millions of bees on me all the time.. I am beginning to think I am electronically targeted which I did not know existed but I guess it does.. I am in torture , heart pounds but is fine on tests but feels so altered with an horrific anxiety through it. |
What medications have you tried so far?
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Your symptoms sounds more like neuropathy, from what we dont know , what test have you done? |
Hi rykerjem
I agree with what Neuroproblem wrote, especially about Morgellons. What clinical tests have your care team carried out? The many knowledgeable and supportive members of NeuroTalk might be able to help you in understanding them. All the best. |
Do you think the intense electric stinging is related to the possible Morgellans, or a totally different condition?
Does your home have any possible environmental issues? Close high power lines, toxic air, radon anything ? Any other symptoms or health issues? Other meds? |
I have heard so many negative things about Levaquin.
http://www.webmd.com/drugs/2/drug-14...st-sideeffects |
I always described mine as cold stinging rain. Yours sounds more accurate. I am on low dose nalterxone. By no means does it take the symptoms away but it does not let the anxiety feelings get out of control. Hard to explain, cuz symptoms still exist but the ldn calms/stifles the screams:confused: Oh, I am diagnosed with CRPS2.
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I was wondering if something like RSD/CRPS also... relating to the stinging pain.
We do have an RSD/CRPS forum here if you want to read and compare symptoms there.. be sure to check the sticky threads- http://neurotalk.psychcentral.com/forum21.html |
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I saw the drug.com side effects, it could be a possible cause of his Neuropathy. |
Just FYI regarding Levaquin.
There are some posts in the PN Tips, Resources, Supplements & Other Treatments sub-forum on the ~Medications That May Cause Peripheral Neuropathy thread. This is one example - http://neurotalk.psychcentral.com/post661103-2.html Fluoroquinolone antibiotics~ Cipro, Levaquin, Avelox and others |
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Hi. I definitely relate to some of your description of symptoms. It sounds awful what you are going through. As someone else has said you're not alone. Have you got support and health professionals working with you to find some solutions? I think that some of the meds used for nerve pain should be able to reduce the severity of the pain. I also wondered about something to help with the very understandable level of distress and anxiety. I find strong emotions really aggravate my pain. All the best to you.
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