(Closed) Calling Dr. Bees for Multiple Sclerosis…….very scared, please help

posted 9 years ago in Wellness
Post # 3
454 posts
Helper bee
  • Wedding: December 2012

@fishwoman: I am not a doctor but I will say, I have an autoimmune disorder as well as complex migraines (mimic stroke symptoms).  Stress WILL cause effects.  Yoga, get a massage, do something to get your mind and body off of it. 

In my experience, bad things may happen but there are ALWAYS ways of coping.  Whether it be God or serendipitous events or fate or… chance.  Whatever your cup of tea, there is always a solution or a way to manage it.  So don’t waste your time worrying about the extremes of being wheel-chair bound, collapsing, etc. 

Some of that stress could trigger a panic attack – which will make you feel worse.

Good luck. 🙂 Keep your faith up, and breathe.

Post # 4
6350 posts
Bee Keeper

I have a friend who has MS. I’m sure she would be willing to talk to you via email or facebook. She was diagnosed in her early 20s.

I’m sorry you are going through this but I promise you there are ways to cope.

Lots of prayers for you.

Post # 5
47383 posts
Honey Beekeeper
  • Wedding: November 1999

I am sorry you are feeling this way. It is only natural to be stressed when you have symptoms and a potentially scary diagnosis.

The one piece of advice  I have is to try to avoid seeking medical advice from complete strangers on the internet. There are many credible sources for medical information online but there are also many wackadoodles who can post anything they want.

I would suggest you stay off the computer, or at least focus on non- medical issues, and wait until you see your neurologist on Tuesday.

My thoughts will be with you.

Post # 6
53 posts
Worker bee
  • Wedding: January 2011

I work in the physical therapy field and I have seen a lot of patient’s with MS.  It is very hard to diagnos, but the only key symptom of MS you listed was the numbness and tingling.  I know it’s scary to not know what’s wrong, but I can tell you that stress will flair up just about anything, so just try to stay calm and please dont self-diagnos! It really may not be what you think, so don’t start worrying about 20 years down the road when you’re not sure what you have.  Rely on your doctors and I always recommend second opionions.

Post # 8
53 posts
Worker bee
  • Wedding: January 2011

Stress, caffeine, exercise, lack of sleep, diet deficiency, overreactive thyroid, and medication side effects are just some causes of twitching that are non-neurological related!

Post # 9
249 posts
Helper bee
  • Wedding: April 2011

I’m nearly a Dr. Bee, and will just tell you this. There are many things than can cause the myriad of symptoms you are experiencing. And it may take a while to figure it out. In the meantime take good care of yourself and think positively!

My thoughts will be with you for your appointment tomorrow. 

Post # 10
254 posts
Helper bee
  • Wedding: July 2012

One of my very best friends has MS. I have been with him from the very first episode that lead to his diagnosis. Numbness/tingling is a common symptom, but the other things you listed don’t say MS to me. I’d be more inclined to say that it’s stress induced, but I am a stranger on the internet. If you are really concerned the only way to get real answers is to go to a doctor.

MS is difficult to diagnose, but a neurologist should be able to give you some answers.

Take a deep breath. You’ll be in my thoughts tomorrow. Good luck!

Post # 11
1309 posts
Bumble bee
  • Wedding: December 2011

I just wanted to chime in to tell you I know what you’re going through! I had the full neurological work-up and everything came back fine. Turns out all my absolutely FREAKY symptoms (I’m talking about waking up in the middle of the night with my tongue and jaw swollen up and numb) were stress/anxiety related. It’s gone now.

If you have relatives with MS you have more experience than I do, but I know that nowadays most people with MS do NOT wind up in wheelchairs or bed bound/unable to walk! There are so many amazing medicines and treatments developed just in the last couple decades that have made this a more livable condition. It’s pretty exciting all the research going on and how close we’re getting to real progress. So even if it is the worst case scenario, there is tons of hope!!



Post # 13
249 posts
Helper bee
  • Wedding: April 2011

Good luck fishwoman!!

Post # 14
3575 posts
Sugar bee
  • Wedding: October 2010

I have two auto immune diseases and can tell you stress is a huge factor as to whether they flare up or not. 

I wish you the best and will pray for you and look for your updated posts.  Try and relax (I know, right?!!) but you’ll have some answers soon.

Post # 15
572 posts
Busy bee

I’ve experienced the same numbness and weakness on my left side for years. Many scans, tests, etc. still show nothing. One doctor made the assumption that it was MS too….not the case. Trust me weddings will bring on stress even when you think you have it all together.

I also suffer from migraines. I agree to be calm and maybe take some time to get a massage, de-stress and don’t try to diagnose yourself. Be proactive but CALM.

Ask your physician questions and take care of yourself.

My Fiance says I overreact to any illness.

Post # 16
426 posts
Helper bee
  • Wedding: March 2011

I have a Dr.’s appt on the 18th of March for some of the same things you’re listing here. Tingling, numbness, vibrations….but I also have ANXIETY and stress and so many life changes. I think stress does crazy crazy things to us and the best thing to do is relax if you can. Good luck!

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