PLEASEHELP,Do I have MS?
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Re: PLEASEHELP,Do I have MS?
Re: PLEASEHELP,Do I have MS?
Re: PLEASEHELP,Do I have MS?
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Re: PLEASEHELP,Do I have MS?
i have been numb and dizzy all morning which is now feeling good for me but when i started doing my housework just earlier i got really dizzy and prickly all over and was burning and cold and sweating i felt so light like i couldnt feel my body i had to lie down on the floor i had this 3 times in a row while i was lying down i was very scared im feeling worse again now.
Re: PLEASEHELP,Do I have MS?
Check out the fourth post by mariesi about the thyroid. Like the others have said it could be a number of things giving you these symptoms. The first thing my doctor checked for was syphilis.
- lyndacarol
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Re: PLEASEHELP,Do I have MS?
Read, read, read. Learn as much as you can about possible diagnoses. By the way, flareups of MS are very common in a mother in the six-month period after the birth of a child; pregnancy itself and breast-feeding seem to make MS symptoms improve for a while. Breast-feeding is so good for baby and for the mother too; it is a definite topic of conversation for you and your physician. Current MS medications have no guarantees.
Just to prove the point that there are many different opinions among the members here, but we express those opinions very civilly, in general (however, emotions do run high at times – we try to keep that in mind): My opinion is just the opposite of Loriyas'… I see no urgency for getting to the doctor, unless you develop an immediate, acute symptom. And I certainly see no urgency about starting any MS meds; they are very strong, and often have their own serious side effects. Can you keep a food diary and note if your dizziness occurs after eating or eating certain foods? In my own experience, I had dizziness after eating anything with sugar (including yummy ribs with BARBECUE SAUCE). It might also be helpful to keep a Journal of your symptoms and when they occur and what you were doing. Even though I do not know you, I think your symptoms are real – they are occurring for a reason – it is only left to find that reason.
In the end, these are YOUR decisions to make, with input from your husband, doctor and the people who know you best. All the best to you.
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Re: PLEASEHELP,Do I have MS?
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Re: PLEASEHELP,Do I have MS?
Re: PLEASEHELP,Do I have MS?
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Re: PLEASEHELP,Do I have MS?

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Re: PLEASEHELP,Do I have MS?
You sound really worked up: not good for your new child, so you need to know what is wrong. So start by watching your diet and also take large amounts of vitamin D, and I mean really large: I take 5000iu a day.
Best wishes,
Sarah
Re: PLEASEHELP,Do I have MS?
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Re: PLEASEHELP,Do I have MS?
I am worried and I can't stop thinking about it but I am staying calm and not stressing because I know stress will be bad for me and also bad for my family. Im just get really scared when I have a dizzy episode and Im too scared to move around much incase it brings one on and makes me worse. Once I know whats wrong I can accept it and move forward or hopefully Im lucky enough to have something treatable/cureable.
You guys are so amazing I know you must go through hell a lot and im sitting here moaning about something that might just be nothing... thank you for listening to me.
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Re: PLEASEHELP,Do I have MS?
Re: PLEASEHELP,Do I have MS?
Serum and red blood cell magnesium levels in juvenile migraine patients.
http://www.ncbi.nlm.nih.gov/pubmed/7868328
"In comparison with normal subjects, migraineurs had significantly lower serum and red blood cell magnesium levels."
Prophylaxis of migraine with oral magnesium: results from a prospective, multi-center, placebo-controlled and double-blind randomized study.
http://www.ncbi.nlm.nih.gov/pubmed/8792038
"High-dose oral magnesium appears to be effective in migraine prophylaxis."
Oral Magnesium Load Test in Patients With Migraine
http://www.ncbi.nlm.nih.gov/pubmed/12005285
"Magnesium retention occurs in patients with migraine after oral loading, suggesting a systemic magnesium deficiency."
Intracellular and plasma magnesium in familial hemiplegic migraine and migraine with and without aura
http://www.ncbi.nlm.nih.gov/pubmed/8200020
"We found no significant differences between the magnesium levels in the five study groups. We conclude that reduced blood magnesium is unlikely to be related to migraine pathophysiology"
...without access to full text, can't get into 'table 2' to see the magnesium results in this one. would be interesting to see if the average was lower in patients but not 'statistically' so. also wondering if the controls were legit. anyone have full text access?
take control of your own health.
pursue optimal self care, with or without a diagnosis.