Chronic fatigue with pressure headaches
Posted , 6 users are following.
hi I have had m e Cfs for about 3 years it started off from respitary infection then pressure like headaches and a other host of symptoms I had a follow up with neurologist see how I was doing I still bitterly complain about the feeling that my head is blocked not so much like the pressure headaches I started with but still lots of pulsing sensations clicking sensations.
anyway my neurologist suggested yoga I had tried earlier in year when I was in a worse place than now and it caused spasms so was a bit hesitant and the fact I tried graded exercise for 2 weeks which completely floored me for months I have been cautious on what I do .
i tired the yoga last night I found that when I would bend my head forward on the ground pressure would build and throb a bit and was a lot of tension in the neck and shoulders now I am wondering if there is a problem with my blood supply to my head I know pots can cause these sensations has anyone suffered with similar symptoms and does this sound like a symptom of m e ?I enjoyed the yoga but wasn't sure whether to continue maybe I should let my doctor know.
1 like, 21 replies
Retriever russ151
Posted
Good luck you are the best judge on what to do.
russ151 Retriever
Posted
mike76241 russ151
Posted
Hi Russ, just a couple of suggestions,
at the end of the day many CFS sufferers experience pain in
neck and shoulders, try a massage, better still a chiropractic
session, which will determine area of muscle tension,(around £30)
for severe headaches a self massage of face muscles can reduce
pain by up to 15%, and reduce dependance on painkillers,
you never seem to feel the of benefits from yoga, but always
well worth doing,
russ151 mike76241
Posted
hi mike yes I do self massage and have a good chiropractic which helps a great deal I jus didn't realise how bad the tension was there I have a constant feeling my head is blocked the theory that it is a build up of toxins definatley makes sense you have to keep trying things I suppose thanks for advice
Patrickgeoffrey russ151
Posted
Personally I don't think it has anything to do with toxins in the system,mtine is directly link to the flu, I am 58 I first had problems at 17, I have had many relapses over the years.the longest was 6 years,but I always recover
russ151 Patrickgeoffrey
Posted
Well it's good to hear you recover but unfortunately relapse it's certainly a devastating illness whatever it is that causes it mine was a viral infection initially then had respitary infections I have gradually got worse but now found kind of a base line but seems I can't progress now maybe I will recover like yourself realistically I think it could take years if I do it's took 3 years to get to this point thanks have to keep being positive
Patrickgeoffrey russ151
Posted
russ151 Patrickgeoffrey
Posted
I'm not sure on my recovery to be honest you mention not trying to get flu now the thing with me is yes I had infections until the last infection which completely wiped me out stopped me from working and haven't worked for 2 years since had seizures headaches no sleep symptoms go on and on but since that happened I have not had 1 infection it's like my immune system has changed it doesn't let anything in that's why I wonder about my recovery I suppose everyone is different with m e I see I Norway they stumbled across a cancer drug which helped not that I would use it but it re routes the immune system and has helped people meditation has been the best thing I used keeping positive tho at times it is hard take care
Patrickgeoffrey russ151
Posted
Yes exactly it is like your immune system is too strong.when I have a relapse I do get colds or the flu. I suspect the viral infection or flights your immune system in overdrive,it is when I recover I have have to avoid getting the flu as it causes a relapse.When I am having a replaces I have flu like symptoms sore and aching muscles and I don't feel well like I am fighting virus but it is not the flu it feel different. I suspect my immune system is causing the problems so I agree with you you only have to be careful if you recover. I think I get better when the immune system stops causing the problems
Patrickgeoffrey russ151
Posted
I actually think post viral syndrome better describes my condition as I don't suffer from fatigue. I sleep well and wake up rested,dont feel exhausted or tired but I always feel stiff and sore like I just ran a marathon and Have a hard time walking even short distances like a 100 metres,post viral syndrome is related to cfs but without the fatigue
artistmike Patrickgeoffrey
Posted
" post viral syndrome is related to cfs but without the fatigue "
I'm afraid that's just not true. Plenty of people who have developed ME, CFS, Fibromyalgia etc. originally had infections, like Glandular Fever, Flu etc.. That is why what you are talking about is correctly known as Post Viral Fatigue Syndrome.
What I agree with and so would many others with these conditions is that the term "fatigue" is a bit of a misnomer. I was in the army for many years and know what fatigue is and I don't recognise that as part of the condition,I just feel permanently ill and like you, have trouble doing much and walking any distance becomes virtually impossible.
Patrickgeoffrey artistmike
Posted
Patrickgeoffrey artistmike
Posted
I googled the definition of fatigue fa·tigue/f?'teg/nounextreme tiredness, typically resulting from mental or physical exertion or illness. I felt that was the meaning I don't suffer from fatigue but I do have a hard time walking my muscles are always sore and stiff,my condition is directly caused by the flu, I aways sleep well wake up rested,never feel tired or exhausted I do get pressure headaches,flu like symptoms I have never been diagnosed with EM or CFS as I don't suffer from fatigue the way most people describe it and by the definition above so the post viral syndrome better describes my condition,fatigue by definition is very specific but is sometimes used vaguely
Patrickgeoffrey artistmike
Posted
I googled CFS definition of symptoms
]SymptomsEditThe most commonly used diagnostic criteria and definition of CFS for research and clinical purposes were published by the United States Centers for Disease Control and Prevention (CDC).[5] The CDC recommends the following three criteria be fulfilled:[19]A new onset (not lifelong) of severe fatigue for six consecutive months or greater duration which is unrelated to exertion, is not substantially relieved by rest, and is not a result of other medical conditions.The fatigue causes a significant reduction of previous activity levels.Four or more of the following symptoms that concurrently last six months or longer:impaired memory or concentrationpost-exertional malaise, where physical or mental exertions bring on "extreme, prolonged exhaustion and sickness"unrefreshing sleepmuscle pain (myalgia)pain in multiple joints (arthralgia)headaches of a new kind or greater severitysore throat, frequent or recurringtender lymph nodes (cervical or axillary)The CDC states other common symptoms include the following:[17]brain fog (feeling like one is in a mental fog)difficulty maintaining an upright position, dizziness, balance problems or faintingallergies or sensitivities to foods, odors, chemicals, medications, or noiseirritable bowel syndrome-like symptoms such as bloating, stomach pain, constipation, diarrhoea and nauseachills and night sweatsvisual disturbances (sensitivity to light, blurring, eye pain)depression or mood problems (irritability, mood swings, anxiety, panic attacks)The CDC proposes that persons with symptoms resembling those of CFS consult a physician to rule out several treatable illnesses: Lyme disease,[19] "sleep disorders, major depressive disorder, alcohol/substance abuse, diabetes, hypothyroidism, mononucleosis (mono), lupus, multiple sclerosis (MS), chronic hepatitis and various malignancies."[20] Medications can also cause side effects that mimic symptoms of CFS.[19]
Patrickgeoffrey artistmike
Posted
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1710789/
jackie00198 Patrickgeoffrey
Posted
Last year, the U.S. Institute of Medicine (IOM) was tasked by several U.S. departments to write a report on ME/CFS. These report includes new guidelines for symptoms to diagnose the illness. For this report, Google "IOMs Report Guide for Clinicians." This report is considered a major step in the U.S. for getting ME/CFS to be taken seriously.