Hi, I'm an 18 year old. Everything started in January with what I thought was a sinus infection, but I don't think it was. Anyways my symptoms were dizziness, stiff neck, fatigue, vertigo, weakness. I than noticed sudden weight loss, and I feared cancer, so I got a blood test, and they said it was all good. A few weeks later I started experiencing hot flashes, tingling in hands and feet, trouble breathing, sweating. Other symptoms I had were stuff muscles(sometimes it would be hard to walk). I than had tremors in my hands and feet, heavy head, stiff fingers, occasional trouble swallowing, muscle twitching all over, vision change, and a bad memory. My original doctor thought it was "just a virus." We got a new doctor and he was concerned, so he sent me to a neurologist, and she thought it was ms, so I got an MRI of the brain and spine, which came back normal. She gave up on me after another round of blood tests, and said it was anxiety. I have no idea what to do now, I feel hopeless. Some of these symptoms have subsided, but some I still have, and others come and go. I'm here tonight because I suddenly noticed I can't feel much throughout my whole body, including in my throat. I worry everyday that I have als or some awful disease. Someone have any symptoms like these? Thanks in advance!
Yes, all my symptoms eventually went away. But, not until I calmed down after taking some anti-anxiety meds and allowimg time to go by, which then let me know I was OK. I did get off the meds since anti-anxiety/anti-depressants can have a lot of side effects. They definitely helped and do have a place in a person's well-being if the situation is severe enough, like mine was. I hope each of you are doing well, as I know you haven't posted here in quite a while.Please be reassured that all is well and things are totally normal and fine, and I hope for the best for you!!
I just came across your post today.I've been having a lot of what you described in this post for the last nine weeks... including a severe sinus infection & all the twitching... did you ever find out what it was... how long did it take to subside? I've had a CT, MRI, EKG, chest X-ray, blood work... all come back great :/ all that we have found is I'm gluten intolerant and have a little low potassium, b12 and vitamin D... all of which I have been treating for the past two months... I'm 25 & had to quiet my job due to all of this... I put a post today explaining everything. I would just love to feel normal again. I'm very healthy aside from this. I watch everything I eat... right on target for weight and before this worked out at least three times a week...Thank you advance for taking the time to read this comment. Hope you are doing well.
I am a healthy 48 year old male with few medical problems. Around June 25th this year after a very stressful situation, my right thumb began to twitch. This continued and finally I went to my Dr. on July 12th. His diagnosis was stress and tendonitis of the flexon muscle of the right thumb. He ordered Prednisone and Naproxen as well as a spika splint to immoblize the thumb. The next day parathesis of both legs developed (timgling in the front upper legs and shins). I had a reaction to the Prednisone and was hospitalized on July 12th with a very high B/P and an immediate CT was ordered to rule out a stroke. Prior to hospitalization and being a nurse, I thought I would do my own research. Bad mistake since the internet leads you from thumb twitching to things like MS and ALS. That thought along with the psycosis the Prednisone brought on sent me over the edge.
While hospitalized, my neurologist who is also a friend ordered an MRI of the brain, neck and cervical spine, carotid ultrasounds, and a series of bloodwork, (with the RA panel negative and thyroid within range, plus all other test normal). Before discharge he came in and told me I do not have MS, ALS, Parkinson's and anything to worry about. He ordered Xanax as needed and Trazadone nightly to sleep.
Since all this began, I have had thumb twitching (now resolved for about 36 hours after experiencing for almost a month), soreness in my right wrist, forearm and bicep area, soreness in my left arm and bicep, continued tingling in my legs, more so around my knees and slightly higher, loss of about 14 lbs. in 3 weeks, insomnia, popping or pulling feeling in the arch of my right foot. I have started Chiropractic care and counseling. Since reading your post on here, I have asked my neurologist for a follow up visit to look into PVS since I am a chronic sufferer of Sinus infestions (2-3 a year), and also to look into GBS. I did have Mono years ago and also have had HSV (Herpes Simplex Virus) for alomst 30 years, although that has presented no problems for almost 15 years with taking a prophylaxis.
I appreciate your post and it appears whatever is causing these symptoms are more widespread than I imagined. Have you had any new news since your last post (symptoms subsided, treatments, etc?)
Spenies Dad
I have been going through everything that both of you have been going through since July of 2008. It started off with a rash and a virus. It went from that to a sinus like infection, aches and pains in muscles and joints, numbness, tingling, and muscle twitches all over, eye floaters and blurriness. I have had 2 brain mris, 1 cervical mri, bone scan, EMG/NCS, spinal tap (high myelin protein), and have gone to 13 doctors. All I have so far are high EBV titers ( all 3 numbers), low Vitamin D, 2 ct scans of the abdomen, EGD on yesterday, and just took an Igenix lyme test. I also know that I have a low CD57, which is indicative of chronic lyme disease. I have no idea what I have. I have never heard of anything post viral going on this long. I want answers and don't have them. I would certainly advise you both to make sure that you get full and complete workups. If you have to go to 1000 doctors before you get answers, do so because your health is not worth it!
I am sorry for everything that you are going through too. It is really scary and so easy to worry when you know that you are not yourself. It is so hard waiting for that neuro appt. too. My doctor cancelled mine on the day I was scheduled (family emergency) and even though I then only had to wait 2 more days to be rescheduled, it is so hard waiting. Even now, that the doctor told me not to worry and that it was post viral, sometimes without having had an MRI I still find myself worrying. I have to keep reminding myself that I have been to a few different specialists and my primary care doctor many times, and everyone keeps saying that this will go away, they just don't know exactly when. I have to keep telling myself that I am fine.
I hope that you are feeling a little better knowing that weird symptoms do not mean the end of the world. I hope that you will get a simple explanation from the neuro and that it is indeed something that will eventually go away. Be hopeful and try to think positive. It's so hard, going through this, I know. It's something you don't think could happen, to get a virus and then be so sick afterwards. Write anytime and I am thinking of you.
Thanks for your reply! I'm so sorry you had to go thru pneumonia and the bronchitis. What a rough time you were through. It really helps to know there are things that can explain odd symptoms. That was interesting how your eye doctor was the one who mentioned PVS first. And, it's a good thing your eyes are in such great shape! I wish I didn't have to wear contacts but I am nearsighted so they are a must ;) You are a real trooper with all you went through and then with some neurological things... wow! I agree that it's so hard when you have children. You try to keep your "game face" on but inside you are so frustrated and worried, as well as tired.
I'm grateful for people like you who respond. It helps me in ways I can't really explain. Just reaching out to people in times of need takes the edge off a bit and I thank you again.
I hope you continue to feel much better!! Take care.
I was diagnosed with post viral syndrome a couple of weeks ago. It sounds so similar to what you are experiencing and it is very scary to have so many neurological symptoms. I too was worried that I had some horrible disease. Mine started with pneumonia in November followed by asthmatic bronchitis. While I was still sick with the bronchitis I started experiencing all kinds of odd symptoms that were hard to explain since they seemed to vary day by day and even hour by hour. I started with feeling like something was crawling in my back (I assume muscle spasms) and then my muscles would twitch. Sometimes my arms, legs even my back and stomach. Then I felt extreme weakness in both my arms and sometimes in my legs. Sometimes it felt like my arms were glued to the bed. I was so tired too. The symptoms would travel. Sometimes they were in my arms, sometimes my legs, sometimes just one arm or leg. I would feel a burning or almost a cold sensation go through my muscles too. At times I completely lost my appetite. My fingers would go numb and my hands and feet tingle. Sometimes my fingers were so stiff it felt like they didn't work right and they would get tired just holding a pen. My vision felt off for awhile (although I went to an eye doctor and they said my eyes were great and they do feel better now). It was actually the eye doctor that first mentioned post viral. I saw a rheumatologist and they said I had fribromyalgia (which was something I already thought I had before I have even gotten sick because I have experienced years of achiness). They ordered aquatic physical therapy for me. I then saw a neurologist who said that she could find nothing neurologically wrong with me. She assessed me in her office and said that she did not even need to order further testing. She said that the post viral can take awhile to go away, there is no time line on how long it will last. She told me to try to relieve any stress that I may have and she even recommened bath salts that help relieve muscle pain and stress. She asked me if I had ever had mono (I did) because she said that post viral is more commom in people who have had mono or Epstein Barr. She said that the post viral is your body reacting. I didn't really fully understand, reacting to what. I have 3 young children at home and it's really hard to be a mom when you feel so bad. Some days are bad and some are good. I wish that there was more information out there for us. It is really scary. I hope that your neuro appt goes well.
I forgot to add that on some days the muscles were sore to the touch (localized pain)