FirstFirst progesterone mc10
First progesterone mc5
First-progesterone vgs 200
First-progesterone vgs 400 of all, sorry about my english. It's been four weeks I've been experencing strange symptoms. It started when I was exercising in a bike late at night (by that time I was having four hours
exerciseAerobic exercise
Aging and exercise
Asthma
Benefit of regular exercise
Bone-building exercise
Diabetes and exercise
Exercise - a powerful tool
Exercise - dress appropriately
Exercise and age
Exercise and weight loss
Exercise can lower blood pressure a day) and felt a strange
chillChills on my entire left side. I thought was just the cold of night. But in the morning, my I was feeling
weaknessWeakness/
painAbdominal pain
Abdominal pain diagnosis
Acupuncture and pain
Ankle pain
Anterior knee pain
Back pain - low
Bone pain or tenderness
Breast pain
Causes of painful intercourse
Chest pain
Chronic pain - resources in my left
legLeg lengthening/shortening
Leg pain
Leg pain (osgood-schlatter)
Shin splints, I couldn't make
exerciseAerobic exercise
Aging and exercise
Asthma
Benefit of regular exercise
Bone-building exercise
Diabetes and exercise
Exercise - a powerful tool
Exercise - dress appropriately
Exercise and age
Exercise and weight loss
Exercise can lower blood pressure. Two days later I was still feeling it, plus a low
backBack pain - low
Back strain treatment painAbdominal pain
Abdominal pain diagnosis
Acupuncture and pain
Ankle pain
Anterior knee pain
Back pain - low
Bone pain or tenderness
Breast pain
Causes of painful intercourse
Chest pain
Chronic pain - resources. I went to ER thinking about a discal
herniaBrain hernia
Brain herniation
Diaphragmatic hernia repair - series
Femoral hernia
Hernia
Hernia repair
Herniated disk repair
Herniated lumbar disk
Herniated nucleus pulposus
Herniated nucleus pulposus (slipped disk)
Hiatal hernia, but the exams and x-ray were normal. Still, I was feeling my
legLeg lengthening/shortening
Leg pain
Leg pain (osgood-schlatter)
Shin splints strange. In that day, later, I started to realize that when I touched (light touch) my body in the left side (specially abdomen) I felt that same
chillsChills pass through my left side, specially in the
legLeg lengthening/shortening
Leg pain
Leg pain (osgood-schlatter)
Shin splints, abdomen and
backBack pain - low
Back strain treatment of my
headHead and face reconstruction
Head injury
Head lice
Indications of head injury
Radial head injury. I've been then to a neurologist. I told her I have a history of
fasciculationsMuscle twitching too and she ordered EMG and
MRIAbdominal mri
Chest mri
Heart mri
Lumbosacral spine mri
Melanoma of the liver - mri scan
Mri
Mri of the brain
Mri of the head
Mri scans
Spine mri, to rule out
ALSAls - resources
Amyotrophic lateral sclerosis
Animal bites
Bell's palsy
Cerebral palsy
Cerebral palsy - resources
Genital sores - female
Genital sores - male
Indigestion
Marine animal stings or bites
Parkinson’s disease and MS. All came normal, but I saw on Internet it doesn't means I really don't have MS and I'm desperate. The
weaknessWeakness in
legLeg lengthening/shortening
Leg pain
Leg pain (osgood-schlatter)
Shin splints seems to have gone, but I feel even more the
chillsChills on my left side, sometimes even without a touch. I'm very
nervousAged nervous tissue
Central nervous system
Central nervous system and peripheral nervous system
Irritable bowel syndrome
Nervous system
Neurosarcoidosis
Primary lymphoma of the brain about diseases since I have suspected of
CushingCushing syndrome Syndrome (what have been ruled out). I can't stop thinking about MS. What are your thoughts? What's the possibilitys besides this symptoms? And there's something else I can do to rule this out? Thank you very much.
Best of luck!
i have had ms symptoms for many years and it started with bladder problems. thanks.
About 10 years ago I had recurrent bladder infections, or so I thought. Horrible painful ones. Following urine testing, no infection would be found. I was sent to a urologist and went through alot of testing, including having a procedure at hospital where the urologist used a scope and camera to examine inside my bladder. Nothing was found to explain the bladder problems I was having, but he was able to see I could not fully empty my bladder and also that it was severely spastic. It would just come and go. Sometimes it would be a year or two between flares. Then I could go months off/on again with problems. It has not been fun let me tell you.
I need to use the bathroom upwards of 20-30 times per day, no exaggeration. I only ever can manage to empty my bladder a very little bit. I get bladder spasms. About a year and a half ago the spasms were so severe it felt like a abdominal organ was rupturing, I didn't realize even that it was the bladder, it was severe. Until I tried to urinate. Not a drop could come out. Had a rush trip to ER screaming with pain and unable to stand. It has continued pretty steady since then, with a few periods of relief but they don't last. Ironically just last night it got out of control nearly as bad as that experience a year and a half ago. I should really have gone to the ER but I am just so sick of being in that place, the wait, etc. I took 2 strong pain pills that would make me so loopy I wouldn't care, just to fall asleep and avoid ER. This morning I was able to pass urine and the spasms are bearable at least, although not gone. I can't stand pain meds, take them next to never, I am developing a disconcerting level of pain tolerance so sometimes I have to be doubled over in agony before I even pay attention to just how bad a shape I am in.
I have had 2 episodes in the past 2 months where I lost all control of the bladder. I had no sensation it was emptying at all until my pants were wet. I cried hard those 2 days let me tell you. I am only 32 years old. Now I am having some mild leaking of urine from time to time, only when I stand up from a sitting position.
Still, the biggest issue for me is the spasms, they can take my breath right away and I have been bedridden from the pain several times.
I have MS dx 7 years now, but thinking back probably had it way before then. I am fully mobile and they have given me the prognosis of bengn/RR.
From what your saying about feeling a coldness I have not heard of that before, normally it's a burning type sensation especially when moving your head - this is called "l'hermittes" sign and means that you have lesions on the spinal cord.
Are you sure it's a cold feeling and not a burning sensation?? When they gave you the MRI did you have the drug