I don't usually do this, because I read most of the posts and can usually answer my questions. But, I need to know if any of you with definite MS feel the way I often do.
I feel carppy. Therre is no other way to say it. I feel crummy, almost all of the time. My head roars, I feel weak, so fatigued that a trip to the store has me in bed. Along with it I'm irritable and impatient. I'm running to the BR with bladder cramps and everything down under feels strained and raw and achey (no UTI). It's not nausea, or sweating, or anything that I can relate to a specific illness, like I don't feel like the flu, or a cold or alleriges, or GERD. In fact, eating is one of my few pleasures. I have felt this way for the last few months.
My brain is working okay.
Other than the urinary, I have little pain, except for what breaks through with the TN - lots of little jaw pains recently and I see the dentist Monday, but no teeth are tender, gums are good. My gait has slowed and I'm tripping alot and it just makes me mad. Well, I am having really bad eye pain in both eyes intermittently for the last couple months and I am staying in a humidified room and using moisturizeing drops all the time and it is better today.
So, I hate going to the doctor and saying "I feel crummy" and not having anything to tell him specifically about why.
So sorry this is how you are feeling. I think an overwhelming combination of sx's can create a windfall of pain and depression.
Then it becomes a vicious cycle and we begin to just feel crappy like you stated.
How do you describe it. Ask your Dr if he/she has ever had MS and tell them it is kinda like that??
I have been in so much pain the last couple days and feel like the MonSter has grabbed both ends of my spine and decided to twist. Then I start thinking...am I feeling this way because I don't exercise enough? Am I making this worse for myself by trying to exercise?
Soon negative feelings seep in and the tumble begins. Not as fun as the roll down a grassy knoll when you were young.
I think Lulu is right if you have changed/stopped your DMD's you are going to be on a roller coaster.
We still think you are wonderful and wish you all the best with your funk and telling your Dr.
My sincere thoughts and prayers go out to you <3
And "NO" you do not have a bad attitude! You are entitiled to these feelings and emotions....They belong to you! They are REAL!
As you know I too have been "Going Through it!" I finally told the doctor this week (the Electophysiologist) when he asked, I said straight up "I feel like sh*t!" I feel like "How can someone who is NOT terminally ill feel this bad?????" is there something else worse than MS wrong w/ me? Then I get the new dx of NCS (autonomic dysfunction) to go along with this beast from "Hell"
Oh how I know how you feel. And I have had a mental relapse again......I guess you could call it an acceptance (sp) issue once again. But you know what...We will be OK! We are strong.....(hey isn't that some words from a Pat Benetar song..lol)
Be good to yourself. And cheers for happier, non-crappy days, or I would settle for at least one day a week....Is that to much to ask?
Did you have to go off your Provigil along with your DMDs? I remember that you were taking this medicine because it's the one I'm taking and it helps me so much. Regardless, though, I've been feeling crummy almost all of the time as of When I feel cra ppy, I am seriously grumpy. :(
I wonder if this correlates to disease activity . . . Maybe it has to do with spasticity . . . I don't know, but I'm sure everyone with MS can relate.
I'm sorry you're feeling like this. It pi ss*s me off to feel like this, too! LOL
Yes, I do have days/weeks where I feel crummy. Nothing specific considering the dx. I do have breakthrough TN pain, muscle weakness and cramping and assorted sensory symptoms. Some weeks it just seems to hit me harder than others.
A "spell" can go on for a few days to a few weeks. I have questioned my docs and my therapist about depression, they respond with "no". Usually a spell includes some new symptom that further impacts my day to day functioning. The current one includes balance and falling issues, a new involvement in upper extremities instead of just lower extremities. I have no energy nor desire to participate in routine daily duties and events but do so because of my kids.
The closest thing I can relate to this feeling is similar to recovery from the flu or an exhausting vacation trip with the entire family where I overdo everything since "I look so good" no one can see I carppy I feel .
My local neuro calls it a relapse every time but my MS neuro not necessarily so. My local neuro, whom I have been seeing for 5 years now takes one look at me and says, You don't feel good , do you?" He 'gets it' but has no magic remedy for it. He apologizes for not being able to fix it and tells me its just the nature of the beast.
So, you are NOT alone. I have gone to my local neuro and said bluntly I don't feel good. Usually this involves a change in my drugs to control symptoms but nothing more except a sympathetic pat on the shoulder.
you sound like the way I feel about 4 days of the week... if I rest for a day or two I might have a good day...then of course I might go to the store for groceries, and it starts all over again.
I called the MS Clinic about my mouth, they said DO NOT GET YOUR TEETH PULLED, not yet.. they want to see me first as the pain is not constant and it's not just one tooth or an infection that is causing this pain.... so I'm glad I called them.
hope you feel better soon, but I know how you feel.. rest up and try not to do to much. Its hard to change your lifestyle this much is't it.
i feel crappy most of the time, which i why for me i have sledomed planned much of anything. do most things on the fly, when i am feeling decent. so much during free time or wanting to be around folks is a totally hit or miss thing for me. and has been fro years.
i still drip pee after peeing. i shake it, squeeze it, everything, but i have to roll some tissue around me there so i don't drip on my leg. i HATE this. this has been going on for years.
i have the constatn R-eye dull throbbing pain and the R-lower-jaw-hinge area pain.
sleep quality affects my moods i know. the other night i just lay & toss and turn and the aches and pain is counters a good nites sleep.
my body just has a hard time getting "comfortable". and i mean my physical body. is it ms or my spinal issues or both or what? beats me. but some pains i know exactly where they are coming from, but that doesn't mean it [is] that area. a funky nerve thing could be causing it.
can't exercise like i used too which adds to my frustrations.
all this affects how my mind is doing or it takes up a lot of mental energy that i would prefer to have been spent on something else.
i hate walking with other people because i have to walk slow. and of course i appear outwardly as being ok, most people say, "hurry up" etc.
so yes, i feel something like you do, crappy a lot of the time. more so than say, feeling good.
and what to say to the doctor? you and i have it a bit different there. the doctors i see, the burden of proof is on my shoulders. instead of a doctor trying to find out what is actually wrong and writing a diagnosis, i'm talking to the wind. you know that because you have seen some of my paperwork -- non-va versus va writings.
they aren't really there to help you due to health rationing.
though i probably tell them them the same things you and others here tell the doctors you all see. but i have such a frustrating time expressing myself verbably i know i myself cause some of the confusion with my doctors.
i dunno Quix, wrapping it up here, sure, i too feel more crappy most of the time versus not. as i've said before i can put on a happy face, etc for a few hours most days.
I feel generally lousy for one reason or another about every day. I know there is nothing the Doctors can do. Also there are specialist and tests I just do not want to deal with so I with hold information from the doctors.
The thing that helps the most is I buddied up with someone who was diagnosed and started the DMD at the same time. That has been a God Send.
I also have one Doctor I call once a week for five minutes. Just being able to say I am in pain helps even if it is to his answering machine. He will call me back if I need him. He asks if he can help I usually say no but thank you.
I wrote on my health care blog this week about how much healing there is from a doctor who does not have all the answers but cares.
For me I can stand anything if I know people care.
My message to you Quix. is I care that you are in pain and feel crummy.
We care about U2, Alex. And Wobbles, I am happy to hear that you're hanging onto the wobbly teeth, at least so far. That's a choice that's hard to undo.
My dear Dr. Quizzles, you and everyone on this thread -- everyone in this forum, really -- have been lifted before the throne of the almighty Creator of heaven and earth, with a request for relief as well as clarity. I don'tknow how He'll answer, but I know He will.
I do not have an answer as to why, all I know is that you are an amazing and generous lady who has helped so many of us on this forum. I am so sorry you are having to endure so much. I can only pray for you to have peace admist your "personal storm" to reach out to others, friends , family, and stay involved. It sounds like a lot of things could be causing this since you have so much going on. Hang in there...you are lifted up..God does care...you are not alone
Hi Quix!!! I hope you are feeling better!! I know you want to be the one here to support everyone and carry there beasts for them all while dealing with your own syptoms!!! Just hang in there!!! you are human and you are allowed to have your time too!!! I too have been feeling crappy everyday for too many months to count!!! I come here for soooo much, it's support, validation and wisdom!!! We all owe you sooo much!!! Give and take and I'll scratch your back and you scratch mine!!! We're all in this together!!! So always ask the forum family when you need help !!! Thank you Quixf all for all you do and to everyone here!!! I hope you feel better real soon!!
I couldn't understand any better if we were twins, I don't think. If you recall my situation, it is different than most, but, to answer your basic qualifying question - I have definite MS. I believe I survive by not thinking about much as far as symptoms - little ones anyway. It is very hard to know which disease is causing which symptom, so I don't try to see specialists - though Medicaid won't let me see many outside the hospital anyway.
I've noticed lately, though, that I have felt more and more "BAD". Fatigue has hit like a freight train - reminds me of when I first became ill. I always described it as periodic times when my fatigue was so overwhelming - I couldn't rise above it. All my joints hurt - my body was inflamed everywhere, with joints swollen. Eyes hurt and so dry and blurry. And my GI and Lung problems all seem to flare up. There is a mood change as well. I always prided myself in being able to stay mostly filled with joy - looking at the humor in life and enjoying my kids and my Lord, and delighting in learning new things. But more and more, depression and irritability are creeping in with nothing offering relief.
I know my doctor is thinking I won't live that much longer, which means I don't get pep talks from him. He's sympathetic, but although he's always been the optimist, I don't see it in his eyes anymore. I don't mean to bring you down - I know you have a lot of life to live and are still able to be active. BUT, I hear you saying you're getting less and less able to keep your activity up. I want you to know I understand that transition (hopefully temporary for you) and change and how difficult it is.
Denial - even though not really real denial - in other words - we both are aware of the truth of what's going on! Allowing yourself to not focus on the seriousness or permanence of the illness sometimes is what keeps us going. No one with the dx of MS knows for sure the path their disease will take. I do know a bit more because of all the other diseases and problems, but still don't know for sure. Miracles happen, and I don't know exactly how things will play out.
I do want to say to you, though, and to myself - I think its OK to mourn and take a moment to be angry with your circumstance. Life isn't what you wanted nor is it always easy to accept. When we try to always wear a smile - it isn't being truthful to ourselves and the grief backs up and becomes poison. Let it out and THEN move on and think how you can use the latest crappy thing to help others or yourself.
I don't know if I can say anything right now to be helpful but I am very down right now. I have a son who is suffering terribly, horrific financial problems, nothing works in my home - nor cars. My body breaks down more and more each day and I can't bear my children seeing their sole support dying before their very eyes. I can't even make food or clean up my surroundings. I don't even want to bathe or see anyone - except for church, which I still try to make it to almost every week. I felt myself thinking iffy thoughts about it too lately.
OK - point is. GET your FEELINGS out. Tell us - or someone. Be vulnerable and honest about your fear and disappointment. You'll be more help to yourself and others as well if you don't pretend to always be strong. I've always been the strong one. People expect it from me, which makes it hard sometimes. I'm working on being more honest with myself and everyone else. Hey - I can't do it all (or even much or any of it). I have a strong faith in Christ and so I try daily to give my concerns to Him - and then try to not take them back!!! lol
I apologize for rambling and hope you know I'm just trying to make you realize you're not alone and that it's a good thing to express your down times. I'm thinking of you, and want you to know it. Blessings, Jan
You don't know me, but you have, in the past, answered to desperate posts of mine in a very warm-hearted and truly helpful way.
I just wanted to say I'm sorry you feel like this so often- and probably right now, too, and I definitely don't think it's a bad attitude- of all people, you are the least I could possibly imagine they would just whinge around, even by just having read your posts and a lot of the great stuff you've written here, I get the powerful impression of a VERY strong person- maybe that's what makes it even harder when you feel like that.
I really hope you will have more good days soon- my thoughts are with you!
Wow, you just described me! I pretty much feel crappy all the time too. Somedays less crappy than others but still crappy. Thursday night I went out with my daughter and we did a little shopping and then on to a movie. Well I bet you can guess where I was for the next 2 days. That's right, in bed.
I think that's one of the things I hate the most is knowing that if you try to enjoy yourself a little your gonna pay for it a lot. It's damned if you do and damned if you don't. Needless to say I choose to stay in most of the time for this very reason.
Quix, you have inspired me in so many ways. You always seem to have something positive to tell us when we are down and out and you very seldom complain to us even though we know that you suffer a lot. I just wish there was something I could say or do to help you like you have always helped me.
One thing I do want you to know and that is, I value our friendship very deeply. You have went above and beyond for me in many different ways, and now I will try and do the same for you by lifting you up to my GOD and praying for you every day. I will also pray for your doctors so that they may understand what your telling them and also know how to help you. I wish I could do more but you do know I'm just a phone call away or a post away. I love you dearly and we all need you to be a part of our lives. Hang in there my friend I know the LORD is going to bless you.
You were one of the first to post to my MS Question yesterday, while I do not have an actual dx of MS (yet?) I too experience many of these exact same symptoms.
I have come up with ways to tell my GP, like I have this feeling of extreme exhaustion just wash over me without warning, I can be just sitting in a chair watching TV and this occurs and I have to go and lie down and then I sleep for hours even if I have only been up for a couple of hours, how do I tell him what that feels like, simple. Doc this feeling of exhaustion feels like I've just run a 32 mile marathon without getting up out of my chair and no rest breaks.
Feeling crappy? Hard to explain that one I know, I try to pull together some of those crappy feelings into some semblance of order, like do I ache all over, do I feel weak, unsteady today, more jittery than usual, is my heart racing today, etc. Then I come up with something to kind of paint a picture of what I feel like, also sometimes I just start up the web cam on my laptop and take a photo of myself feeling "crappy" and compare it to a photo of myself on a "good day" and share those pics with him.
Sometimes you know pictures speak louder than words. I don't know if this helps, but I do realize what you are going through, even though I personally haven't truly been diagnosed with this MonSter I really believe that it is what has been going on with me since August of 2007, that's when this MonSter started it attack on my person. (Not sure I can really say that without (I can't think of the word, but it means that I have been diagnosed with it) I know now, confirmation!) confirmation, see I told you I had mental problems! :)
Keep your head up, don't give up, I and many others here need your guideance and support and I know I'll be here to support you.
Hoo, boy, Quix. I feel for you! The roar (mine's pretty dull, thank goodness!), the exhaustion, the weakness, etc.,etc.,
I'm an avowed Fun Hog. I do the fun stuff, anyway, knowing full well I'll pay for it the next two days or weeks. But the fun is worth it, even if it's something as mundane as drawing up the next couple of day's menus and shopping for the ingredients. Yes, this to me is fun, and yes, I'm a goofball, too. I'll come home from the store, put the stuff away, and collapse in bed for the afternoon, utterly exhausted.
I don't participate in the same dangerous sports I used to (anybody want to buy a surfboard?), but there's this sick desire to push the fun envelope and hope I don't cause myself another relapse.
I'm so grateful I can still work 3 days a week. I get to help other people come to diagnosis in the Cardiology world, so they can take their own plan of action. It gets me out of my own head and personal medical problems. I get the feeling your work here and on other forums is fulfilling, too. You're still using your brilliant mind!
Yes, I feel cruddy, weak, spastic, stiff, buzzy, shocky, leaky, and depressed because I'm not performing my music any more for awhile, all on a daily basis. I'm trying to make lemonade from the lemons the Universe is throwing me. Some days, I don't have the energy to do even that.
Hi I am new to the forum today and have read many of your posts and have felt drawn to your wamth, honesty and giving to other people. Sometimes it is good to receive and look how many friends you have made, so in spite of feeling horrible, I am sure that you will feel some well deserved support in return for all that you have offered to others. Live in the moment and find something to make you smile :)
Seems like pretty much everyone here is feeling about the same as you. I like Guitar_grrrrl's attitude though!! She does what she can, when she can regardless of the repercussions but of course we can't all do that either.
You are so helpful to everyone Quix and it just doesn't seem justfied that you of all people are feeling so crappy!
You know that I haven't been around too much lately but I am doing my best to exercise daily and it really seems to be helping with the little icky feelings that I can't seem to explain. I have the added problem of asthma and chronic bronchitis that slows me down some but I do what I can to get er done! I recently underwent a MIBI test and echocardiogram due to a glitch on my last EKG and get my results back on Tuesday. Then I had blood tests and an ultrasound on my thyroid due to pain in my neck as well as other symptoms that seem to point toward Hashimoto's (I hope not) but perhaps the results of these tests will tell me why I feel crappy most days (especially since most of my docs çan't accept my MS diagnosis). You know how long I have been having a problem of getting up in the morning after 10 hours of sleep and having to go directly back to bed cause I can't keep my eyes open...well, it's still here 4 days out of 7 and the Amantadine isn't helping. I have to agree with whoever said..."bottom line, MS S*CKS!!!
I certainly hope that you start to feel better soon and maybe once the weather gets sunnier and it gets easier to get out regularly for some fresh air and natural Vitamin D! I hope your symptoms give you a break soon and I DO NOT believe it is a bad attitude, rather perhaps it's because you are not doing enough for yourself because you are too busy doing so much for others??? Maybe a change in your schedule and the time you spend on the computer needs to be thought about??? Just a suggestion but I really hope you start to feel better soon!!
Seems as if its a majority vote...I too totally relate to feeling just plain lousy a lot of the time...I am always trying to move on and away from it though.
I haven't been on here as much as I was, after I get thru reading I am too tired to type it seems or I put it off til I feel better.
I have had some good and bad days. I have had cateract surgery on both eyes now, the right eye was a cup of tea and the left eye just gave us trouble. I had to go back to the OR once more but its doing well now. My eye Dr has been there almost every day to see me. What a great Dr he is.
I lost my headaches with the right eye surgery and now I am having pain with the left but it should get better.
I have made some plans and I want to be able to enjoy myself, they are on the 29th and 30th, i am planning on some fun !!
Oh, Quix, i hope you have some better days coming up. And all of us really. I have to stay positive, its all I have and it works well.
yeh every day its hard to try to feel better-- when every day is a challenge. there isnt a day that we arent reminded or scared of whats going to happen newxt???
i have even resented people that try 2 help urgg shouldnt feel that but its there!!! wish you the best!! tick
... and the rest of you... Your strength and perserverence inspires me. To feel as bad as you do and still find the energy to come here and reach out - to give love and support and answers to the frightened newbies (and long-timers). That alone SHOULD be enough to allow you to be lifted above your suffering, if the world were a fair playing field. I wish you a speedy recovery and a lightened load. Take care of yourself.
Well if sadness and euphoria can be MS sx then why can't feeling as you do. I think the fact that so many of us feel as you do shows that MS is so totally complex it doesn't really matter whether the MS is actually causing it in a biological sense or if the MS sx are the source (if you see what I mean) the fact remains that we feel dreadful a lot of the time and that needs to be addressed - and soon.......
OK - lecture over - now go take care of yourself and get some help.
I'm in remission right now, so it's been a while since I felt that bad.
Even in remission, I had four days of bowel-twisting cramps and diarrhea. Sorry for the TMI, but it was so weird - it was like I had a flu bug or something. But I was perfectly healthy, and even had plenty of energy when I wasn't running to the bathroom. My abdomen felt painful and tender, too.
What to tell the doc? I would just tell him you feel terrible - fatigued, cranky, and more symptomatic than usual. This would elicit a "That's MS!" comment from my neuro, but I think yours is a little more hands-on.
You all are so sweet and remind me why the only thing I really want to do with a day is spend it here! Thank you for your kind words, sharing your feelings, and letting me know that I was not just a loser who got a bad attitude and gave up.
Somehow, I felt like with the MS I should feel pretty normal except for the symptoms. I really mean that. Kinda silly.
Clearly part of my overall crumminess is depression, so my PCP and I doubled my Effexor. I don't think that being off the DMD is part of it except the anger that I was forced off of it, and any other, by the cost. My neuro doesn't think any of the DMDs are going to help me, as he feels that the bulk of my disease is in direct axonal death. I have very little evidence of inflammation: Steroids never had an effect, I have very few T2 lesions, and I only had one O-Band, yet I have a lot of disability (EDSS about 5.5) He's waiting for an oral med. We'll discuss this in May.
So, I am much happier this afternoon. I saw the dentist - nice, kind, friendly guy. After three years without a cleaning (I know, 'mybad) I very little tartar and only two tiny areas of mild gingivitis. The "extruding molar" is doing just that. It's a healthy molar which is "super-erupting." I guess that's only fitting for someone living near Mt. St. Helens. Two years ago I freakishly fractured the virgin molar below it, and it had to be extracted. Then this molar had nothing to contact and began erupting right out of my gum - so now I have to have another healthy tooth extracted. I guess, it can't be just pushed back in.
Given that I am congenitally missing 14 permanent teeth anyway, and now will have lost 2 more, I only have 16 teeth (of my own) left in my mouth. Bummer. Now I get to look forward to the extraction next month. yippee.
In a fit of defiant perversity, I stopped by the ice cream shoope on the way back home and had a chocolate chip mint hot fudge sundae. So there! Now I am giddily smiling in a sugar high and expecting a crash in 2 or 3 hours. So, getting rid of the dental dread (plus enough sugar to hype a small soccer team) has improved my mood immensely.
Thanks for the words that kept me afloat. Next stop my urogyne and begging for meds for the bladder spasms. Return the census, pay JCPenney, and fill out my MS survey for the Pacific Northwest Registery.
Are all of you signed up for NARCOMS??? Let's be heard. Every one please do this!
I'm so glad that things seem a bit better. This dental issue has been weighing on your mind for a good while now, and probably has added to the depression factor. Just one more #$#$% way your body is betraying you.
But now that's on its way to being resolved. I'm hoping the urogyn will come up with something that works for you too. Lulu has had great results from Sanctura, and with the huge :-( $250 the feds will give you on the donut hole issue you might be able to afford that.
Let us know how you do on more Effexor. So many here need antidepressants, and the meds are such an individual thing that finding the right med and dosage is tough.
I just wanted to encourage you to keep telling the forum how you're doing, both the good and the bad. You have helped all of us more than you can ever know.
PS Ice cream, esp a Hot Fudge Sundae? Mahhhvelous!
Sorry I am late on your post. Well, you sound better, or possible relieved that the dentist appt is over. I am sure that was a heavy weight on you. Seems like the outcome was better than expected. (Although not the extraction next month :( )
Yes, "most" days I feel crummy. I actually can't recall a perfectly "normal" day in at least 1 1/2 years. Some days I have a bit more energy, until I start walking around, then the leg hurts and it is over. This makes me pretty angry.
I have a bit of a depression cycle, or perhaps maybe more than a bit ?! When my mood is better, I am better.
I need to focus on what I have and not what I lost, or don't have any longer. I went to a cub scout tour of a military base, and 1st time I thought, I can not do this. A walker would have been perfect for me that day. It was awfully hard to get through it. I am really having lots of trouble just standing, walking is easier for me. I dont even though if that makes sense. (standing in lines..etc.)
Anyway, dear Q, I think we are all in this together. So glad to be in a place where people "get it", and I don't feel that I am complaining. Just living this life with this awful disease.
I just got out of the hospital tonight. I escaped early due to not tolerating a procedure I needed to prep for a colonoscopy. They're looking for a bleed - two fecal blood positive. Plus my hemoglobin was 8.2, so had 2 units of blood and an infusion of iron. Also found a new nodule in my upper right lobe (lung) as well as atelectasis bilaterally in bases. I'd been told it was only the right, but both? Oh boy. So many issues. Walking around the hall once dropped my O2 sat to 88, so that's not good. My spleen lesion is same size, but bile duct is still dilated and a possible mass at pancreatic head is there - causing ? My osteoporosis is so bad I'm very worried. I've lost 20% in my spine in 1 year. BAD. And 9% in right hip. BAD I'm very concerned about fracture. I've already lost almost an inch and have such severe pain in my back and hips I can't take it some times. My problem is that I have so many problems that the doctors are overwhelmed and don't know what to do. I would love to have someone to help with the MS. I really don't have anyone except a neurologist who has given up.
I'm glad you're feeling a bit better, cause I need a lift. I spoke to a psychiatrist about some help. I've been on effexxor and he wants me to try a SSRI only again - so I'm changing to prozac. Never tried it so what do I have to lose. I do feel better having my hemoglobin up some. Man - I felt like an emotional wet noodle!
I too feel like you and i am off to the neuro cause insurance wants an update....well here's your update i feel like crap...lol
Always tired, bruised from clumsiness, disorganized, emotional, no libido, stressed, pain, numbness,and much much more. This week i start getting all but 6 of my bottom teeth taken out...not to mention the whole top is coming out too!
So what do i tell the guy..hey call that lady at the insurance and tell her to get off my back?
i want to rest but they try to make you feel guilty for being sick IMO...
Quix: This is very late, but I do go through periods of feeling vaguely under the weather where I’m tired and dragging and vaguely achey and generally lousy for no obvious reason without being all out sick. I was never really sure if these episodes were caused by the MS or not. Once I did try to get to the bottom of it by going to the walk-in clinic at work, but they said I didn’t have a UTI or a sinus infection or anything else that they could identify so I gave up on that.
I do notice that I sometimes get really psychologically and emotionally tired of dealing with the MS. I know what you mean when you say “Somehow, I felt like with the MS I should feel pretty normal except for the symptoms” because I’ve thought that, too. And yet it doesn’t quite work out that way.
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