Ive been experiencing exactly what you described! Last month had this tingling feeling in my leg and foot before my period, and now this month its back again with my period. Did you ever find out whats going on? Are you still going through this??
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Hormones! All
Of this I have experienced and still occasionally do. It’s smack around my
Menstration time.
Of this I have experienced and still occasionally do. It’s smack around my
Menstration time.
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I too have been having pins and needles feeling in my feet, legs, fingers and arms and sometimes even my face! Its been going on for about a month now! I had blood work done and the doctor said my blood work was normal! I haven’t had any xrays or any other kinds of test yet bet i will have too! Like you said this makes you scared about what could be going on!
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There are two types of hemiplegic migraine (HM), which are distinguished based on the family history in affected people: familial hemiplegic migraine (FHM, in which at least one other close family member has the condition) and sporadic hemiplegic migraine (SHM, in which there is no family history).[1]
FHM may be caused by changes (mutations) in the CACNA1A, ATP1A2, SCN1A, and PRRT2 genes. The first three of these genes give the body instructions for making proteins involved in moving charged atoms (ions) across cell membranes. This process is important for for normal signaling between nerve cells (neurons) in the brain and other parts of the nervous system. Researchers think that mutations in these genes may upset the balance of ions in neurons, affecting the release and uptake of certain neurotransmitters in the brain. The exact function of the PRRT2 gene is not yet understood but is also thought to play a part in controlling signals between neurons. When the genes involved in FHM do not work correctly, the signaling abnormalities between neurons lead to the development of severe headaches and auras in affected people.[4] The genetic cause in many families with FHM remains unknown.[3]
While SHM occurs in people with no history of the condition in their family, most cases are due to new (de novo) mutations that occur for the first time in the affected person. Some people with SHM do inherit a mutation from a parent who has the mutation but is not affected. The ATP1A2 and CACNA1A genes have been found to cause SHM in addition to FHM. Many people with SHM do not have a mutation in one of these genes; however, researchers think that mutations in other, unidentified genes are also involved in the condition.
The known types of familial hemiplegic migraine (FHM) that are due to a mutation in the CACNA1A, ATP1A2, or SCN1A genes are inherited in an autosomal dominant manner.[6] When a person with an autosomal dominant condition has children, each child has a 50% (1 in 2) risk to inherit the mutated gene from the affected parent. FHM due to a mutation in one of these genes accounts for some, but not all, cases of FHM. It is likely that there are additional types of FHM caused by mutations in other genes.[6]
People who are the first member of their family to have hemiplegic migraine are classified as having sporadic hemiplegic migraine (SHM). Some cases of SHM are caused by one of the genetic mutations that cause familial hemiplegic migraine (FHM), due to either having a new mutation, or from inheriting the condition from a parent with no signs or symptoms.[6] In these cases, a person with SHM can still pass the condition on to a child.
I jave had these all my life andnow my kids and grands also have this. Blessings.
FHM may be caused by changes (mutations) in the CACNA1A, ATP1A2, SCN1A, and PRRT2 genes. The first three of these genes give the body instructions for making proteins involved in moving charged atoms (ions) across cell membranes. This process is important for for normal signaling between nerve cells (neurons) in the brain and other parts of the nervous system. Researchers think that mutations in these genes may upset the balance of ions in neurons, affecting the release and uptake of certain neurotransmitters in the brain. The exact function of the PRRT2 gene is not yet understood but is also thought to play a part in controlling signals between neurons. When the genes involved in FHM do not work correctly, the signaling abnormalities between neurons lead to the development of severe headaches and auras in affected people.[4] The genetic cause in many families with FHM remains unknown.[3]
While SHM occurs in people with no history of the condition in their family, most cases are due to new (de novo) mutations that occur for the first time in the affected person. Some people with SHM do inherit a mutation from a parent who has the mutation but is not affected. The ATP1A2 and CACNA1A genes have been found to cause SHM in addition to FHM. Many people with SHM do not have a mutation in one of these genes; however, researchers think that mutations in other, unidentified genes are also involved in the condition.
The known types of familial hemiplegic migraine (FHM) that are due to a mutation in the CACNA1A, ATP1A2, or SCN1A genes are inherited in an autosomal dominant manner.[6] When a person with an autosomal dominant condition has children, each child has a 50% (1 in 2) risk to inherit the mutated gene from the affected parent. FHM due to a mutation in one of these genes accounts for some, but not all, cases of FHM. It is likely that there are additional types of FHM caused by mutations in other genes.[6]
People who are the first member of their family to have hemiplegic migraine are classified as having sporadic hemiplegic migraine (SHM). Some cases of SHM are caused by one of the genetic mutations that cause familial hemiplegic migraine (FHM), due to either having a new mutation, or from inheriting the condition from a parent with no signs or symptoms.[6] In these cases, a person with SHM can still pass the condition on to a child.
I jave had these all my life andnow my kids and grands also have this. Blessings.
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Hi all, three months ago I had a bleed on the brain, at the time it was unexplained the reason why. At the time my face drop headache, could not speak or walk. I am now left with a headache, what I was told about. It was not said I would get pin needle in my arm's hand feet and side of my neck,I have not had a follow-up appointment because of COV 19. Do anyone know of this happening to anyone else. because I am thinking what wrong now. Holly
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Late to the party but, did you find out what it is? I was thinking maybe hypoparathroidism. It’s rare but can happen after thyroid surgery.
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I'm feeling constant pins and needles, but I don't have nerve issue or diabetes. The Doctor said it is anxiety. Can it be true?
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I have the same symptoms. I am vita d deficient my vita d went down to a 7 or 11. My numbers were coming up last we checked BUT I have something called chairai malformations and when i read about it the headaches , vision problem and a lot of other symptoms. I’m actually stinging abs burning all over today . I did have blood work done for d and b12 today.
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I would like it if anyone could assist me. for the past week I have been experiencing pins and needles in my hands and feet, but for some reason at night while trying to sleep I get a dead right arm and then it goes through my chest back and left arm. I am woken up so It gets very uncomfortable. I have to do blood tests I am low in iron
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I have same past 3 months I just keep getting told its carpul tunnel and stress blood pressure high I too am worried still if its symptoms of heart attack or stroke!
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