Chronic Fatigue Syndrome :: Numbness In Face, Neck Legs And Around My Wrists
Jan 20, 2015
All been having a few new symptoms . numbness in face just one side and neck legs and around my wrists anyone else have these symptoms . also lent on my elbow its really gone sore very red and skin coming off something that has never happened before i used to bruise very easily before but nothing like this . i,ve been trying to find out what sort of help out there for me and not really getting anywhere i was wondering what sort of help others where getting.
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I've suffered from CFS for a good few years now, I've just started with numbness in the arms and sometimes my legs. Has anybody had the same experience?
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I was told I had post viral fatigue in 1997 - in 2004 I was diagnosed with Chronic Fatigue Syndrome. I had to give up on my career but made a new one, working part-time hours. I've been lucky enough to scrape by.
This January however, I started to get symptoms new to me. Walking and veering to the one side, tingling in my hands and feet and numbness too. Also a terrible stiffness that affects my walking and my ability to pick things up. The worst new thing is terrible problems swallowing.
I had to give up work completely - I just couldn't do it and I am back to sleeping 14 hours a day.
My GP sent me to a neurologist. After a 13 week wait in pain and discomfort I finally saw neuro 2 days ago.
Her attitude really pissed off. Chronic Fatigue was talked about the whole time. I couldnt feel pin pricks on my face, feet or hand. I had a positive reaction to the Babinski sign (I know about it as I have a friend who is a GP). She told me, it's not MS, it's CFS.
BUT, I am being sent for an MRI, to see a speech therapist for the swallowing problems, a physiotherapist for the stiff legs, a psychologist for my memory problems and I am being put on pregabalin painkillers. (The NHS is great once you are in the system).
What I would like to ask, after years of CFS, I didn't think numbness and tingling were part of CFS symptoms.
How many of you have these types of symptoms?
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I feel mostly well but lately my only annoyance has been shoulder neck and back of head ache. This is mainly located at the right side of my body but occasionally spreads to the other side. It's more of a constant dull ache which is relieved temporarily by icing it. Does anyone else get this? Sometimes I feel like the pain is also in my left ear. saw my gp a week or so ago and he didn't seem concerned. I just wondered If anyone else experiences this. Yesterday I felt like it hurt to swallow in my throat but only at the side where im getting the rest of the head pain.
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I'm a 20 year old university student struggling to cope with the constant pain and irritation of my eczema.
I get it all over my arms, armpits, neck, chest, the back of my legs and my wrists. Its scabby, sore and irresistible to scratch at. I have on too many occasions scratched it until i bleed but i really cant help it. I have had severe eczema all my life but in the past two years, it has really started to get me down. I have applied prescribed steroid creams, Hydrocortisone, E45, Doublebase.. showered and bathed in prescribed shower and bath gels and swallowed countless anti-histamine tablets in the hope of them taking away the itch and the urge to scratch.
I'm writing this as i am so fed up, just like the millions of others suffering from eczema out there, and hope that one of you out there can help me, or atleast give me some tips to reduce the irritation.
Currently i am applying Aveeno Skin Relief Moisturising Lotion after i shower. It does reduce the itch and calm my skin, but the redness and dryness returns when the cream is absorbed or whenever i start to sweat. I can't partake in exercise or sporting activities as i am scared, actual fear, of how itchy and sore my whole body becomes.
As i sit here repeatedly itching up and down my arms i'm hoping there is someone out there who can give me some advice, i've had enough of being embarrassed and fed up of my skin.
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Last month i had a very bad bout with the flu. My whole body was paining. It started with my upper legs. Almost like someone gave me charlie horse in my muscles. Then my feet and bottom of my feet started paining. I could not even walk. I wore memory foam slippers on my feet the few times out of bed. My hands had the same painful sensitive sensations as my feet. a few days later my lungs started to hurt and I had something pneumonia. When i started recovering, the pain and numb sensations stayed on the bottom of my feet, my hands legs and arms. Not to mention the weakness that still exist in my limbs. Also, which is confusing and worrying me most now is the numbness on my face and in my mouth, it feels like dental freezing leaving my mouth. It's been at least a month since i recovered from the flu. I have seen my Dr. and have been scheduled for a CT scan. Has anyone had these symptoms before?
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I'm a 30 year old female who lately has been going through a tough time. I have always been a worrier, especially when it comes to health. Since I was 9 years old I've worried about different diseases (especially after googling) which made me convinced my life would end several times in my life. Right now I'm going thru a bad phase which I don't know what to do. It all started last year when I started getting lots of numbness and tingling in face and legs. Then in November I started getting left sided chest pain which is 24/7 stabbing pains. I've been to emergency twice since Feb. And they did EKG, xray and blood tests which supposedly came out fine. Then, in February I started getting heart palpitations, skipping beats. At this point I was convinced I have heart disease. 3 weeks ago the mild dizziness started where I felt I was gonna faint. During the time it started I remember going out to eat with my hubby and kids and I literally felt like I was not there, as if I was in another planet, everything felt unreal. I've been really tired too. I've been seeing a cardiologist who did an EKG, heart Echo. And tomorrow I'm having a stress test and a holter monitor for 24 hours. He thinks its anxiety. But I am not convinced. I'm just extremely scared of dying because I have 3 children who are all under 7 years old. By the way, I did want to mention that from October thru March I was going thru a big worry with the law. Don't want to get into details but I was very worried for 5 months that I was going to go to jail. Everything turned out fine however, I don't know if that worry triggered physical anxiety symptoms.
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I am just wondering whether anyone has had genetic testing to rule out causes of fatigue? Myself and my brother both suffer with extreme tiredness and I'm wondering if it's worth asking for it to be investigated down the genetic route.
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I was just diagnosed as being hypothyroid, Tsh 10.65, my question is does anyone else experience tingling/numbness in your face, arms and legs and also have head pressure?? I've had some anxiety and I think maybe its the cause any thoughts?
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I have Primary Sjogren's Syndrome but was born Hypermobile. It was only after my present Rheumatologist diagnosed that I have scoliosis that I started to research. I found the Beighton Scale and the Brighton criteria which I match completely. I explained my research to my consultant and she agrees. However while she and another consultant both agree I do have POTS so far I don't have an appointment to see anyone to help me. I have had ECGS and a bubble ECG but they have been taken while lying down. Now the POTS I really noticed post the birth of my last son 29 years ago is getting much worse, can anyone advise me as it has taken decades to get this far, I don't feel time is on my side
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I was a raving hypochondriac, have suffered cs for 5 years,had mr scans,ct scans,myelograms and lumbar punctures,see my specialist regularly and just given different medication,vi suffer neck pain, headaches,numbness in arms and hands,but also have severe numbness in legs and feet,my hands and feet are permanently icy while the rest of my body burns up,feel permanently dizzy and nauseous,i have vision problems and incontinence problems,for past few months i have got steadily worse and not able to walk more than few yards,and cant get outdoors without aid of wheelchair,as pain in my joints and muscles is so bad,the nerves that are trapped have moved down my spine which is causing the leg pain,i have seen 3 specialists and a professor of m.s,i have meltdowns every so often as i always have been so active and cs can just bring you to your knees,i find that the specialists i see seem to think i am neurotic,i asked him to have my pain for a week and then come back and tell me how he feels...i feel people just don't understand how debilitating cs is and because outwardly you look ok and you do your hair and put some slap on your face,but walk a mile in my shoes when at 3am im walking the floor counting the hours till can have another pain killer,my last visit to my specialist i was given morphine patches,but suffering from ibs and gall stones was warned by my doctor that they would have adverse effects and they were so addictive.
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I'm a thirteen year old girl with an unhelpful doctor who literally doesn't want anything to do with me because I'm 'hard work' to diagnose. My family believes it's chronic fatigue syndrome, fibromyalgia or both. So that's the home treatment path I'm taking. My symptoms have been going for 6 months now and they are diarrhea, nausea, joint aches, headaches, fatigue, confusion, dizziness brain fog, tenderness, weakness and muscle pain. I've been tested for crohn's, ulcerative colitis, hypothyroidism, hyperthyroidism, parasites, dysbiosis, virus, infections and celiac disease. I also have eczema, restless legs, irritable bowel, anxiety and gastroesophageal reflux disease. I'm not under any stress at the moment.
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Just wondered how other people cope with the family holiday. Being out of your normal routines and in a new place perhaps. What do you put in place to help you cope?
Being at home knackered is one thing but being in a caravan, apartment or hotel etc. is much different. Having to be mobile and do holiday stuff with the kids, can and is an overload for my system. Do you avoid going away because of things like this or is it just me?
The last 10-day holiday we took has taken me 4 months to get over! (Moreover, I was still feeling rough after 4 months…) I know I am lucky to be able to grab a family holiday, but I do wonder at times, if it’s more harm than good taking a holiday with ME/CFS.
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I am currently applying for jobs, but I am unsure answer yes or no to the do you have a disability? question. I do have CFS, which does impact my life, although I am able to work. What do you think?
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Went to see my gp yesterday and told her about my heart beat readings I've been having recently of 115 just to walk downstairs, 124 to walk upstairs, 135 to walk downstairs on a bad day. My heart rate goes up from 74 to 105 when laying down to standing. She took my heart rate as a sat there and it was 98. She's now sending me for an ECG. She thinks it might be to do with the sack or lining around the heart? She told me the official names but I was silly and didn't get her to write it down. Now I can't remember what she called. She said she has seen cases before.
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I was wondering if anyone else diagnosed with ME is constantly thirsty? I've had all the blood tests (and have been diagnosed with ME), so diabetes is omitted. It seems to be worse on an evening and I'm always topping up my fluids with water and herbal teas-so plenty hydrated! It's not my worse symptom, but just wondering if it was common?
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Just wondering whether people get any unexplained bruising or get easily bruised? I get them quite often and it's worrying me. My rheumatologist said that it can happen as our body is over sensitive.
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I am a 32 year old female. My question relates to Exercise Intolerance. I am very unfit and am wanting to get fit for the first time in my life but whenever I start even an easy exercise program, I get really wiped out. I usually feel okay after my "workout" (barely a plausible term) session, but feel extremely fatigued the next day. Which interrupts my program. This can be very irregular tho, sometimes I can do quite a bit and feel fine the next day. I had bulimia, starting at age 17 for 10 years and am wondering if this is still the effects on my body. I have no other side effects from the bulimia. Apart from that I have suffered Chronic Fatigue Syndrome, but these symptoms disappear if I don't exercise. I have had my heart and lungs checked out, blood tests etc, all come back fine. Can someone please, please shed some light as to why I get so exhausted following even a small amount of exercise. It doesnt seem to matter be it cardio or weights.
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Anyone smoke with CFS? I dislike drinking a ton so I was wondering if anyone smokes marijuana? I've seen online it's good for it and it doesn't make it worse... Anyone ?
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Hi everyone, I was diagnosed with CFS/ME a year ago and since having surgery last November it has got so bad that I am unable to return to my job I am only 22 and it's really making me upset.
I have had all the blood tests available and all came back negative apart from today my doctor called and said I have a vitamin D deficiency and has given me 3 months worth of medication. Has anyone else with CFS/ME got a vitamin D deficiency? Also did supplements help your CFS? Or even cure it? How long did it take for you to feel better?
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I had stuff to do today that I could not leave. I have since had several dizzy spells. I get these when I do the school run. Has anyone fully passed out?
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