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raynaud’s brain

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Q: My son was recently diagnosed with Raynaud’s, he is 4 years old and has other health problems!?
I was wondering how often it is that a young child ends up with this disorder. My son has brain damage, Autism, A silent asperation, and some unknown syndrome. I can figure ouy if the raynaud’s has anything to do with all of this other stuff. Does anyone out there know if it is truly rare for a young child to have Raynaud’s?

A: You might try reading through this site for ideas on autism

http://www.shirleys-wellness-cafe.com/autism.htm

omega fatty acid is essential.

For Raynaud’s try vitamin E and magnesium
also the omega fatty acid.

Use sea salt instead of table salt and check for a nutritious diet for autism. Some foods, junk foods, diet soda, etc… are better to avoid.

Q: I need help explaining all of these symptoms?
Light sensitivity/photophobia
occasional blurred vision — sunglasses tend to help with these two a little bit
occasional to frequent brain fog
raynaud’s phenomenon (particularly cyanosis, but all three stages occur)
constant peripheral numbness (left ulnar, specifically)

once in awhile there is lip numbness as well, but it generally goes away, and it’s never really severe. it also happens when i give blood, so this doesn’t concern me much.

at first, a b12 deficiency seemed plausible, though b vitamins have helped some symptoms improve on occasion, i don’t think that’s the answer.

early stages of MS is a possibility, but i’m a male, and a lot less likely to get MS than a female, based on statistics.
Diabetes has crossed my mind, but I don’t show any other typical symptoms of unregulated BGLs

hypothyroidism is also possible.

Migraines recently crossed my mind, but I don’t get any severe headaches. I do experience what could be described as similar to a sensory migraine aura but i never get an attack. But other than the light sensitivity, and the brain fog, i don’t know how much migraines really explain. I’m not particularly sensitive to auditions or olfactory sensations

i don’t currently have insurance, but i’m still looking for an answer. knowing is better than not knowing. my doctors are not helpful anyway, and when i do get new insurance, i will find new doctors.

A: Try to get a job with some sort of insurance. You need to see a doctor. Raynauds can be associated with some types of autoimmune disorders such as Lupus. You are right that some vitamin deficiencies can cause this along with some types of anemias (B-12 deficiency would cause a certain type of anemia, but there can be iron deficiency anemia or other anemias that can cause this). Also, a heart condition could cause this. Anxiety can exacerbate any other illness symptoms, so try not to focus so much on your illness and instead, focus on being well and feeling good.

A doctor would really need to examine you. If you don’t have insurance, there are usually free medical clinics for poor people or the uninsured, but the extent of testing that they would do without any insurance would probably be quite limited.

Q: Pulse of numbness/tingling throughout my body?
OK, I am a 20 yr old female. I was diagnosed with Systemic Lupus this past April, but apparently I’ve had it for 6 years now. For the past year I have been experiencing intermittent pulsations of numbness/tingling throughout my body. It comes on every few weeks and lasts anywhere from 3-5 days, nonstop. It’s about an average of 2 pulses a second. It mostly occurs when I move or change direction. I know it is SOMEHOW linked to my antidepressant, Pristiq. Every time I miss a dose, or stop taking it for a medical test, the pulses come back, usually about 12 hours after the missed dose, but this last time it took 3 days to start happening. They start out faintly and get worse and stronger as time passes. When they happen I have trouble walking, talking, anything. I can’t feel where my limbs are because I lose feeling during the pulses. I was actually drinking a glass of water once and the pulse came and I couldn’t feel the cold water in my mouth anymore. The numbness only lasts when the shocks are occuring, as I stated about 2 a second. You can imagine how difficult this has made my life. I went to work today and ran into customers all day! I try to go through my everyday tasks but they’re so much more difficult when the pulses come.

I went to the doctor and they did a VNG on me. I have a vertical nystagmus of the eyes, but I do not have vertigo. I even went to physical therapy because they thought it was vertigo but I never got dizzy with the shocks when I was there, they said I was wasting my time doing physical therapy. I now have an appointment with my cardiologist tomorrow (I also have mitral valve prolapse) to see if maybe my heart is the problem. I am getting an Auditory Brainstem Analysis later this week (MRI of my ear canals and the surrounding brain tissue) and I have been told by my doctor I also need to schedule an appointment with a neurologist.

I just want to get this over with and fix whatever’s wrong. I already went through all the doctor stuff THIS YEAR! I had to fly to Pittsburgh to the Lupus Center to find out if I had Lupus. I am open to any thoughts anyone has as to what the heck this could be. They said I had a mild cause of lupus. I am taking 200mg of plaquenil a day, no steriods. I also take Yasmin, and 50 mg of Prisitq. I have stopped taking the Prisitq for the last 4 days to make sure this isn’t some weird addiction thing. So far the pulsations are still going strong. I looked up SSRI Discontinuation Syndrome, but that sounds like it’s just the effects of depression after you discontinue the SSRI, plus vomiting and chills. I don’t have that. Honestly I haven’t even felt depressed since I stopped the medication. I haven’t felt nauseous, but I always cold (I’m about 115 lbs.)

Here’s my medical history:
My aunt has Lupus, and another aunt has Multiple Sclerosis. My cousin has Epstein Barr. I had a hermangioma under my eyes when I was younger which rarely acts up now. I used to have high cholesterol that was induced by acutane (acne medication) but that was about 4 years ago. I had to take Lipitor for about a year. During that time I also had issues with high triglycerides, but that has since been resolved. About a year and a half ago I had issues with low blood sugar and that was fixed by just eating often. I developed a tic in my shoulder around 3 years ago because of Zoloft. I discontinued with medication and still have the tic a few times a week (it was about 60 times a day). When that was an issue I had a EEG done which showed a few abnormal results but nothing to be worried about because abnormal firings of the brain was normal in adolescents. I discovered I had mitral valve prolapse one day when I was about to fall asleep and my heart started racing and my left arms started hurting. I do have regurgitation but it’s very little. Along with Lupus I also have Raynaud’s Phenomenon which causes my feet to turn purple in normal temperature rooms. I have had an MRI with and without contrast, they said there were no brain lesions because of the lupus. I have been on numerous antidepressants for the past 6 years.

I don’t know if the Pristiq is what has been causing these horrible sensations or it has been acting as the TREATMENT for something else I didn’t even know was wrong, so when I stopped taking the treatment, the problem came back. I know some of you must be thinking, ‘hello, they’re gone when you take your meds just keep taking them!’ but I can’t do that, I don’t know if the meds are causing this and hurting me or not. Maybe if I keep taking the Pristiq the symptoms will just keep getting worse when I have to stop taking it and maybe even hurt my body more.

I need help! I was planning to move out of my mother’s house to go away to college next semester and I’ve had to put off my plans for another day because I’m not well enough to live on my own! I’m still stuck at my community college! These health issues are building up and slowly destroying what little life I h

A: Emily,

I honestly can’t believe that you’ve been going through this hell for all this time. I have MS, so some of these things sound familiar to me, but your MRI results came back negative for lesions on the brain which would have been able to confirm MS. However it is common to use a spinal tap to assist the diagnosing of MS when MRIs come back negative. MRIs are not the only way to detect MS. Check this out: http://tr.im/spinaltapms

Unfortunately, since I have MS, that is really the only thing I’m familiar with on this level. Although is has not been proven yet, it hasn’t been disproven either, but there are thoughts of the possibility that MS can be genetic, and because Multiple Sclerosis is already in your family, that would expose you to a higher chance of having it yourself. There is also a similar possibility of the Epstein Barr virus that may have a link to MS. http://tr.im/epsteinbarr_ms

Ugh, it hurts me to not have an answer for you. If I come across any information that even remotely has a possibilty of having to do with your situation, I will email it to you.

Prayers go out for your health and sanity as you try to figure this out.

God Bless.

Q: Can anyone help with diagnosis of health issue described below?
I am 29yrs old mother or 3, have definitive dx of congenital bilateral dislocating hips (need dbl rplcmt), narcolepsy, cataplexy, interstitial cystitis w/ hunner’s ulcers, brain dysautonomia from CO poisoning. I also have the following chronic sx: neuropathy in my finger tips and feet, pain n muscles and joints (early onset of osteoarthritis), nodules on skin, extreme sensitivity to smells, low range bp around 108/60, dizziness upon standing, motion sickness, raynaud’s phenom, recurrent shingles, sob, easily contract staph and strep skin infections, slow to heal, fatigue w/ intermittent insomia, memory loss both some st & lt, also had pelvic organ prolapse resulting in surgical repair such as hysterectomy, tvt, etc. which my body rejected the graphs used and cause numerous problems.

I am at a loss of what to do, I had to switch family dr and when I go to dr or any medical facility other than my specialist I am treated like a drug seeker and hypochondriac! I know my sx are real th major onset was 8yrs and over the past 6months my sx are so severe I can no longer ignore them. I have tried to research syndromes and diseases because I know that all these sx have to fall into something or maybe I’m a case study all alone. Its very frustrating to live like this at 29 and I just don’t know what to do anymore. I also seem to have adverse reactions to almost every medication so I try to steer clear of those also. (Sorry if seems like rambling…also adding details as I think of them. will gladly answer any ? to further detail) Anyway, hope someone out there might have some insight and help point me in right direction….Thx!
Saw neuro at onset but not since, they didn’t find anything at the time but since that time have found out med hx ie co poisoning and sx have become mush more severe.

Currently see urologist weekly for bladder tx, ortho for hips, fam dr is internist but a crappy one & sleep specialist. Someone rec rheum’gist & ortho suggest genetic testing his concern is connective tissue disorder like ehlers danlos on wait list but growing impatient…need to find shorter avenue for dx if there is one…give this further info anymore suggestions?? thx again for any and all insight!

A: I would suggest that you see an internist and an infectious disease doctor. Keep your chin up, you are physically ill, don’t let yourself think anything but. Do you get migraines or headaches with nausea? Have you had a heart echogram with bubble injection? Have you been tested for lyme? There is a retro virus XMRV similar to HIV that was discovered some 18 years ago but left to spread in our blood supply. It is the third known retro virus. Please check out the whittemore institute, they are also on facebook where you can talk to others with similar illnesses .http://www.wpinstitute.org/

god bless

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