Can you help?

  I am worried about my health. I know something is differrent. Back in July I had a reaction to a bite on my leg and soon after that I had some strange things happen to me. I had two different episodes of extreme neck pain and leg pain to the point of passing out. My husband was home and he is a paramedic and he said he thought I had a small seizer.  Since that episodes I have had a few times of strange nerves sensations that go through my body.  Extreme behind the elbow pain, ear pain, hip pain, leg pain, general all over body pain. I remember one time I had this feeling of tightness around my waist, like a paralize feeling. But it went away within a few minutes.

Itching on the skin on the left side of my neck, and the newest symptoms a strange overcast of my vision on my left side. I also had an episode of four days straight I could not go to the bathroom, with drinking fiber drink and mylalax. I was scared and thought I had colon cancer , Had a colonoscopy and all is fine.

 I have always had strange sweating issues. To the point things would be soaking wet that I touch. This has gone on for years. I had back surgery after the birth of my daughter in 2000 and I have always wondered if it was from the fact that my doctor tremendously yelled at the nurses at the hospital that they gave me the epideral in my back way into my labor. I remember he was furious at them.

 So, since all of these symptoms have been happening. I went to a neuro,  mri done, they found a small lesion on the right side of my brain. It was two small to say whether it was related to demyelination. Mri of spine and neck negative of lesions. Emg done small nerve lesion found of left side of my arm.

 Started having extreme hip pain, had a mri done. they found two cysts within my bones , but they do not think this could cause pain. I am really sick of going to each doctor , One day I have pain on one part of my body , and then another day anothe part.

 The first neuro I saw after the mri of brain, told me it could be early Ms , the other neuro, told me that MS people do not have pain. It said that he has been a neuro for 30 years and people with MS do not have pain. So, then I started thinking maybe I have fibromyagia I am just sick of this.  Now I have to go to the eye doctor and see what is going on with my left eye.

 The medical bills are really starting to effect us, but I am scared to not go and see what is wrong with me , in fear that something is being missed. I would love any advice any has. and what step to take next. Do you think it could be MS ?  Some days I feel like my big toe is immerged in hot water and I also have numbness and tingling in my legs arms and back.

I am 40 years old with three children at home. I just want to feel better. Also , my symptoms get worse right before my menstratution. My husband has been worried about me , which makes him unable to sleep , he said I wake him up with twiching of my legs at night. I feel like I sleep okay when I wake up in the morning.

Thank you for listening. I really appreciate it.

Don't return to the doctor who said MS doesn't cause pain.  He obviously doesn't know what he is doing.  MOST people with MS have pain in some fashion. 

Please post this on the lyme board here and see what you get. 

 Thank you both for answering me.

 I appreciate it.

 I am going to read more about Lyme disease. I am going to post over on the lyme board and see what others say about the lyme blood test I had.

 Thank you again.

My husband ended up taken me to the emergency room since the involuntarty twitches turned into full body jerks. It was really bad.  So, in the emergency room, I had two doctors do exams and me and they told my husband and I  that they were 99.9% sure that it was MS. I was then admitted and given Ativan to stop the body jerks. They continued through the night along with double vision and lost of some central vision on my left side. Woke up this morning and the body jerks were still there.  They did go away through the day. I have two different neurologist come in and do exams on me. I was able to do exams well. I did have a momentary problem walking on my toes and heels, but it was more of a "my brain taking a minute to registers to do it."

 Another MRI done  With and Without contrast and it was clear. The neurologist feels I DO NOT have MS. He  feels that my nerves are over reacting. and told me to take 1000 mil of Vitamin D a day. He reccommended Lexopro and Ativan if my nerves misfire again.  I am very glad that the test came back well. In the back of my mind I am wondering really what happened with me and everything that I have been going through.

 I am home now and will follow up with my family doctor? Any thoughts Thank you for your time.

 Thanks for the good thoughts  Things are getting better than last week in the hospital. The neurologist told my husband and I that we all could have Multiple Sceloris in us. It depends on how we handle stress. I am not really sure. But he seems very confident about telling us that

 I have been taking ativan and lexapro and I am starting to feel back to normal. I have not gone back to the eye doctor , in fear that the body jerks will start again, since my left eye is still showing some central vision cloudiness. It is getting better though.

 the medicine is helping and I am going to follow up with my doctor again in two weeks. Basically they will keep me on the ativan and lexapro and see if I do well. Maybe I will not have another eposide at all. Lets hope.

Thank you again,

It helps to talk with people.