Has anyone ever had a migraine w/ numbness? I have had 2, both in March, one 05 and one this year. It starts out with my hand going numb, then up my arm and then my face (right side). That happens for about 10 mins, then the massive pain starts and the numbness goes away. I also had an aura before my last one but not the first one.
Hi Zan, Yes, I have had the numbness, vision auras, and could not balance, or speak until "it" passed. I do not always get the aura, and sometimes get the aura and no pain, but the weak, sick feeling, and be unable to function.
For me, these episodes usually are a day after a time of great stress. It is very frightening, and I hope you get some help soon.
Hey there.... I have those too and my neurologist diagnosed them as Hemiplegic migraines -- My arm stays weak for 5 to 7 days afterwards though. Due to the hemiplegia, people that are diagnosed with them cannot take vasoconstrictors such as triptans and ergots -- Imitrex, DHE etc.....because of the higher stroke risk.
My arm stayed week for a few days after this last one too. How scary. Couldn't just have the regular old migraine, now could we? UGH. How many have you had? May i ask you age too? They are very scary. I am so afraid of having a stroke since they are so similar.
I looked up hemiplegic migraine, but I don't think that is what I am having becaue I could completely move my arm, it was just numb and from what I've read, I am pretty sure with these you can't move your arm. Was that your case? My neuro has never diagnosed this way, just as complex migraine.
I have had many -- lost count! My family on my mother's side has a history of these so mine is "familial" due to it being genetic but there are also what they call "sporadic hemiplegic migraine". I could move my arm with my shoulder if that makes sense. They are scary - the first time it happened and I went to the ER they all thought I was having a stroke, which the CT scan cleared. I just had a consult with a "staff" neurologist at Mayo Clinic and we talked about the lasting weakness and he wasn't convinced it wasn't a hemiplegic migraine due to that. With numbness only you would be able to return to normal when that goes away and not have the lasting weakness. It's so complicated!!! And a lot of docs I have noticed fall back on the complex migraine when they aren't totally sure what to call them. I am 28 years old and have both hemiplegic and classic with aura migraines. It's hell and very scary.
Are you on any preventative meds? What do you take when you get a migraine? I am getting BOTOX next month and am supposed to start atenolol in addition to the Topamax I am already on. I get migraines a couple times a week now and have taken pretty much everything they can offer at this point. The hemiplegic migraines I get a couple times a month.
Wow, we are about the same age (I'm 29). Too weird. My mom gets Migraine w/ aura but never the numbness. With mine, I could move my fingers, hand, etc, just couldn't feel them. So, I guess I don't know if they are the hemiplegic or not. The only reason I worry is they say not to take Triptans if you are having those types. I don't take a preventative med because I have only had 2 in my life, but the neuro gave me scripts of midrin and topamax if I need them. What do you take for prevention?
I have tried midrin and it didn't work for me but that's not saying much seeing as MOST meds haven't worked! I am currently taking Topamax 200mg daily for prevention. Do you ever get the "aura" (numbness, vision loss, etc..) without the pain following? I wasn't documenting those occurences and my neuro said that those are migraines too so I needed to!
Yes, the midrin was supposed to be for the pain, but I haven't used it yet as they just gave it to me when I had the last one in March. I haven't filled the Topamax but will if I need too. No, I don't get the aura w/o pain, but my mother does. I think I will ask to see a new neurologist to see what they think and be properly diagnosed. I have had a hard time finding good doctors lately.
My family has had this type of migraine for years. We have been followed by the Mayo Clinic for over thirty years and researchers may have isolated the chromosome where this is carried. Incidence in our family is one out of three has this type of migraine with numbness, pain, sickness, etc. It is very scary, however, the docs have said that we are at no greater risk of having a stroke than the general population. I am 44 and had one last week but had not had one in six years, prior to that it had been 12 years. My 20 year old daughter has had a half a dozen in the last 4 months. Was hospitalized several years ago for 5 days with paralysis, swallowing difficulty, etc. Took her a while to be able to read, tie her shoes, use her right hand, but everything did come back eventually with no residuals. opie
I am followed by the Mayo Clinic also. Are you diagnosed with complex migraine or hemiplegic migraine. I just wanted to be clear with the stroke risk -- being diagnosed doesn't raise the stroke risk but taking triptans and other vasoconstrictors does. It is well documented that if diagnosed with Hemiplegic migraines triptans and other vasoconstrictors are contraindicated due to the risk of stroke.
We have been diagnosed with atypical familial hemipelegic migraines. My father actually takes nitroglycerin at the onset of a migraine. It does leave him with a headache but the paralysis and the length of the migraine seems to be shortened. He is going back to Mayo in August to see if there is anything new as the frequency of his headaches is increasing.
I also get Hemiplegic migraines with aura. I have the familiar type, and I have gotten this since I was 12. It wasn't until I was 23 that I was able to get a succesful diagnosis.
I have been on a preventative for the bast year now, Inderal, and it has worked very well. I went from 4 migraines a month to none at all. Until today. It's possible that I need to get a stronger dosage.
My symptoms are loss of vision, spots, dumbness starting at my fingers and travels up my right arm to my face. My nose, mouth, throat, teeth, and eyes goes numb. I get severely confused and can not speak normally. Everything takes incredible effort, like dialing the phone - it takes several times to get it right.
I have been very considered about the possibly of stroke, I was basically told that if there is any change in the migraine to get to ER right away.
I've only been getting migraines for 6 months or so, but the symptoms seem to shift around the gamut. Today was the first time I ever had a migraine with numbness (hand and foot) Also, my face felt the opposite of numb, kind of ultrasensitive, especially my nose.
Yeah... I have something similiar. I will suffer a gnawing numbness in my upper lip or my right cheek, which disappears, then it feels like somebody just slammed a rock into my head. I also feel an incredible sense of vertigo for hours, and my eyes feel heavy and I feel somewhat disoriented. I have CFS so I am not too surpised by the latter of my symptoms (vertigo, heavy eyes, disorientation) but they still scare me.Current Confirmed Diseases :Eczema, Chronic Fatigue Syndrome, Chronic Constipation (which varies by time, and is rather emberassing) Chronic Migraine, Minor Asthma
Meds: Aquaphilic Cream (eczema) Non perscription, Albuteror perscription Inhaler
I had no idea there were other people out there that had this same exact thing going on. My migraines were so strange that I didn't even want to tell teachers what was going on with me b/c they would look at me like I was nuts.
I have had migraines with numbness that begins in my right hand or right side of my face. It can travel up my arm, into my mouth and throat (at that point I feel like I can't breathe right...but I think it's just that the numbness feels so weird). The numbness can be just tingling or so numb you could chop a finger off and I don't think I would feel it!. I usually get very confused. SOmetimes I can't speak or if I can my words come out messed up. I forget important things like my own phone number. ONe time I almost fell over from weakness on the right side of my body. Rarely I have vision disturbances. One time my right arm felt so weird I couldn't even look at it....it was like it wasn't my arm (strange). ONe time I had messed up hearing....people sounded as if they were talking to me out of synch or from another room or something. I used to have very bad light sensitivity. I used to throw up too. During really bad migraines, sometimes I experienced strange mood swings. After the pain and everything is gone, I still have pain if I sneeze or cough or move my head to suddenly. I also used to get what I call, "flash" headaches.....where for several weeks after a migraine I wouild experience a few brief but extremely sharp flashes of pain in a specific part of my head.
Oh...has anyone experienced this part.....after the migraine you are really hungry and have to eat right away? My mom and I are both like this. Also...it takes me two or three days to feel like my body is back to normal. I can't describe it well. But after a migraine, it's like I'm wiped out for the next couple of days
They were really bad in my teens and through highschool. Sometimes I got them every other day for a week. Now I am 30 and can go two years without one. The last one was when I was pregnant (3rd trimester). THat was aweful b/c for the first time I got the numbness on the left side and the headhache on the right (reversed from all of my other headaches). I thought that b/c of this reversal that maybe something was wrong in the pregnancy and wasn't sure it was a migraine....ended up calling 911. The headache before that was the day I went home from the hospital after giving birth. I am thinking that pregnancy and childbirth are triggers for me now....hormonal?
The worst thing of all is that every time I am about to get a migraine the first symptom I have is this feeling like, "oh crap...here it comes" It's just this really uncomfortable feeling that I can't explain. There is nothing like it. I just feel it coming on. The only way I can try to communicate it to others is that it's like every inch of my body is sick....all the sudden I feel it everywhere.
SOmetimes I get the numbness and other symptoms and get no headache at all.
As I have gotten older, the painful part of the headache is more easily managed with over the counter stuff (never could have done that before).
My mom had this very same kind of migraine too. My brother and dad are prone to headaches also, but not this kind.
DOes anyone know if the mayo clinic is looking for ppl with these types of headaches still?
Does anyone have these same symptoms with a diagnosis? I have never had a diagnosis for what type of migraine I have. I saw two neurologists when I was a teenager.
oh yeah...and I had a stupid doctor prescribe imitrex (back when it was only available as an injection). I took that stuff a few times and started to think I might fall over dead. I just stopped taking it on my own. Later, another doctor told me that I shouldn't be taking vaso constrictors. If you read about the stages of a migraine, yuou could see why this would be bad.
At the very beginning, when you have aura or other strange sensations but no pain....the blood vessels in your head are constricting. the constrict so much that you don't get enought oxygen to parts of your brain....the is when strange things start to happen. THen, dilation begins and those blood vessels begin to get inflamed....this is when the pain starts.
SO just imagine how BAD it would be to take any type of vaso constrictor when your blood vessels are already so constricted that you are experienceing stroke like symptoms.
I had a doctor tell me that if I waited until the pain started to take the vaso constrictor that that would be good....but I opted not to do this because sometimes I could go from aura to pain and back to aura/numbness again. It was impossible for me to predict wether or not the constriction would start again. Anyway, I don't care what any doctor says to me now....there is NO WAY I woudl take a vaso constrictor with the severity of my symptoms.
Hi I have been reading about your headaches and you are describing my daughter's episodes perfectly. It always starts with numbness/heavy feeling in leg, foot and arm then to her nose,mouth and speech. Words come out wrong. She is not herself after for a day orso. At first her neurologist told us to give her advil, and now we are using Excedrin at the onset and she is not having a headache at all. Just the Aura as described above, so a 2-3 hour ordeal instead of a 12 hour ordeal with the headache and nausea/vomiting. What are some preventatives that are successful? How did some of you manage through school, etc? These started out as one every six months and now she has had two this weekend.
I get this as well, however I also have a seizure Dx. Usually when I get numbness with my migraine, I am on the lookout for an impending seizure. It has yet to happen in conjunction with a migraine, but it always makes me think that it's what is about to burst. It's all very frightening, especially when you aren't able to sort one issue out from the other.
On top of all that, I use Topamax to control both, which gives paresthesia anyway, plus I'm a partial hemiplegic from having had a brain tumor and subsequent stroke already! I a mess, isn't I. I really don't know if I can offer much insight into this discussion, but I know that I have similar presentation with about a third of my migrain onsets. about 2/3 of my migrain onsets are visual deprivation ( I lose vision in both eyes within about 30-60 seconds) followed by gradual onset of discomfort, then actual agony over about 20-30 minutes. My bail out med, Imitrex nasal, gives pretty good relief about 70% of the time if I catch symptoms very early. I have noticed though that it seems to briefly make the numbness on my hemiplegic side get vastly worse for about 30 minutes after use. My neurologist has told me that this is a perception on my part and not a "T.I.A." as I have had multiple MRA's that do not show any vascular anomolies beyond surgical ones(which are substantial).
hi i no exactly what you mean , its not nice at all. i get really paranoid when mine starts as i had a migraine indused stroke they think i was 13 when it happened but not detected till i was 25. i am now 35 and still suffering the headaches. i was really lucky as the stroke only affected 1/4 of my feild vission. but i now get scared when my headaches start incase it causes another. this time my face started with a strange sensation just on one side it almost feels numb i should know go back to my GP but am to scared.