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#1 | ||
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Newly Joined
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Hi All Im new here so plz be easy on me lol
Im a 33 year old male. For years (from18) iv had problems with the left side of my body. It started off like a weak feeling in my left arm. This would come and go sometimes only once a year. In the past 18 months it started happening alot more and each time something new was coming along with it. I am now at the point where i just cant take anymore of this as feel doctors just fob me off and dont want to deal with it. I was taken into hospital sep 2013 with possable storke. That was very soon ruled out and the stroke doctor said he felt it could be ms due to what was happening and my history so sent me to see a neurologist. I waited a few weeks to get to see him and from the moment i walked in the door it was clear he had not looked at my history or anything. He would not listen to what i was saying and kept talking over me. He then said he felt it was migraine aura due to seeing colours (which i dont) I now am at a loss as my health is getting worse very fast and anytime i go to a doctor i feel fob off like they dont want to know or help. I just dont know what way to turn or what to do as im now getting very worried. Any info or help would be great i just feel so alone in all this. What I have wrong is : Heavy feeling to left arm and leg always tried even if iv had a great sleep. loss of feeling to left side also pins an needles feeling ( i find it hard to expalin) dropped foot problems with left eye poor breathing sakes that come and go muscle spasms pain Now in the last few days I can no longer lift my left leg for than 3 inches of the ground sorry for the long post and if its not wrote well i find it hard to explain what im feeling just want the doctors to start doing something |
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#2 | |||
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In Remembrance
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Welcome Cresham.
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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#3 | |||
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Grand Magnate
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oh my goodness, i'm sorry for what you're going thru.
do you live in the United States? can you get a family member or good friend to go to the dr's with you with the express purpose of being your advocate? do you have a good primary care physician; pcp? if you don't i'd try to find one and have him/her get you into a good referral for diagnosis (dx). if you have a good pcp, a dr who will listen to you and validate what's happening you will have taken a big step toward good care. have you had an MRI? any lab tests? keep in touch with us so we can offer advice and suggestions. and, welcome to NT. oh, ps...if you have eye problems, sometimes seeing an opthalmologist can help dx a problem.
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Judy trying to be New Skinny Butt ______________________ You are a child of the universe, no less than the trees and the stars; you have a right to be here. And whether or not it is clear to you, no doubt the universe is unfolding as it should. -------------------------------------- "DESIDERATA" by Max Ehrmann |
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#4 | ||
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Member
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Sometimes, drs just s***, especially specialists. They need to be reminded occasionally that THEY work for US, and they are not gods! It is very frustrating, but I encourage you to not give up. Try to find an MS support group in your area and ask for recommendations for a neuro. When I was first dx'd, I found out that there were NO good neuros in my immediate area according to other MSers. I had to go to a city about an hour away.
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msarkie "Never try to teach a pig to sing. It wastes your time, and annoys the pig." |
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#5 | |||
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Member
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MS is very hard to dx (diagnose). It mimics so many other illness'. You very well may be doctor shopping and hopping for awhile. The right one is out there it just may take time to find him/her. I say this very reluctantly because I had a horrible experience with it but so many others had a wonderful outcome, but you may want to contact the NMSS and get a name of a neuro from them. Like another poster said, you may have to travel to find a good one, but it very well may be worth the trip!
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Dx RRMS April 1992 Yearly flares from 92 to 11 MS induced seizures 2002 Flare Oct 2011 Flare Dec 2011 Left disabled after 2 previous flares Betaseron '02, Copaxone '12, Tecfidera '13 (allergic reaction to all) No longer taking any MS therapy meds |
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"Thanks for this!" says: | SallyC (06-24-2014) |
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#6 | ||
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Junior Member
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Hello
Welcome to this forum! ![]() I'm very sorry to hear about your health problems. I hope that everything resolves soon. I had similar sensations in my left arm that use to come and go every few months. Then it came back to the right arm.. I was first told that it might be RA but after many.. many many tests they finalized that it was MS. Now, I hope that MS is not your diagnosis but what I found useful with easing the symptoms in my hands was Dr. Terry Wahls diet. I CANT STRESS ENOUGH HOW THIS DIET HELPED MY LIFE. I'm not getting paid or anything to promote this diet.. it just changed my life sooooo much that I want everyone with a chronic condition to try it.. It's worth to try.. at least for a week. CUT OFF GLUTTEN, DAIRY and CARBS & have a lot of vegetables, and fresh leafy greens & high quality proteins. Hope you will feel better soon. Charie |
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"Thanks for this!" says: | SallyC (06-24-2014) |
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