Hello friends, sorry I haven't been on here much lately. My last post was about how my new meds were making me feel "funky" I contacted my doctor and she said since I just started taking them, I should stay on them and give them a chance to be effective. One is for depression and the other is for high blood pressure. She said it's normal to feel some side effects in the beginning but that they should subside in a few weeks. I feel totally drained and dizzy a lot, and getting sudden tingling sensations up my back and in my head but it only lasts a few seconds. Not sure if it's MS related or not since I haven't been diagnosed yet, but my journey has begun and I am now moving closer to getting some answers! I can't do much activity before I need to go rest, and that doesn't help the already "lazy" label I've been given by my unsupportive significant other! The fatigue itself isn't new to me, been having that for a long time now anyway. But now it seems like it comes on all of a sudden and it's overwhelming, like "boom" I need to sit or lay down now before I drop. I see my PCP next week on the 30th for a more thorough evaluation/follow up and have my first appointment with a neuro on July 12th at my local hospital's Neuroscience Center (MS Speciality Clinic) that was the soonest they could get me in. Sorry so long, just been off the grid lately and needed to vent and let everyone here know what's up. Thanks for all your support and well-wishes, I sure do appreciate them, it helps give me some reassurance, uplifting and positive which I need a lot of right now.
Tami
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Bamfan1442
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I hope your doctor is able to determine the cause of your most recent issues, Bamfan1442 . As for your July 12th neuro appt, I had to wait 4 months recently to see a specialist. 😳 So I know July may seem like a long wait, but it will be here before you know it. Make sure you have your list of symptoms ready! Praying you feel better today...💕
Bamfan1442 , thank you for he update. It can be difficult adjusting to new medicine, but I hope you're nearly done and can just begin to enjoy the benefits. We all hope for a quick and clear diagnosis for your issues. I hope a diagnosis will make it easier for you to find support, too.
We all know that waiting for the diagnosis is almost worse than getting the diagnosis. Hope the days go by quickly for you and that the actual diagnosis is something they can fix.
Hi Tami, fatigue is with me constantly. So I understand what you're saying. Every action you take needs "rest" following it. You are not lazy, the energy it takes to accomplish something is overwhelming. Just take each day as it comes, we are all hear to listen.
Bamfan1442 sometimes fatigue will hit me out of no where and I have to go lay down for a couple/few hours to recharge. Good luck at your new neuro's office, keep us updated on how it goes!
Thank you everyone who replied so far: Iona60 , WAshingtongirl , greaterexp , Morllyn , mrsmike , Daisuki51 , and bxrmom ! I am very greatful for the opportunity to come here and share, gripe, complain, laugh and cry with some of the most amazing and supportive people I've ever "met". It is truly a relief to know I have a place where I am accepted and can "talk" about my personal challenges and victories without judgement. You guys are awesome and words don't justify how much I appreciate your comradery and friendship!! I Just wish we could all meet somewhere and have the opportunity to see each other in person, and have a chocolate potluck! Any kind-white, dark, milk chocolate, and chocolate-coated almonds, pretzels, etc. is okay with me
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