Topic pentru aspirantele la titlul de mamica-45-157

mikado a scris:

Mada   un test nu faci?vad ca la CM-ul trecut nu ai spoting deloc   

Mika, fac maine dimineata test, daca nu vine azi, desi eu cred ca va veni! Nu am avut spotting cm-ul trecut, dar mi-a venit direct in ziua 29. Acum sunt in ziua 30. Nu am avut niciodata cm-uri de 30 de zile, erau de maxim 29. Deci, daca nu vine nici azi, maine am voie sa sper!

Mayya, daca era o luna normala si as fi urmarit ovulatia sau macar as fi prestat in perioada ei, mi-as fi facut si eu test, dar asa sansele sunt foarte mici sa fie, d-aia nu ma grabesc cu testul
Ziua 10 la tine ar fi sambata, 

sonia30 a scris:

almisor,ce frumosi sunt!sa iti iasa!  

ms ... să sperăm, de obicei c?nd gătesc ceva pentru prima dată am noroc.. sper să am și de data asta

mika, smart, cmin

mădă, chiar așa... tu c?nd faci test??
LE: așa, dacă nu vin azi ca lumea pui m?na și de dimi faci test..

mika ms ... cred că o las pe m?ine cu milușeii... azi mai fac ordine prin casă și să-mi fac lista cu ce-mi trebuie pentru ce am eu de g?nd să bucătăresc eventual dau o fugă la supermarket să fac cumpărături.. să vedem

vin cu vesti



am vb la cabinet , pap-ul a iesit foarte bine, mi-a zis ca as putea sa il repet linistita la 2 ani iar la analiza de secretie nu am nici o lighioana doar filamente de candida prezente ..asta stiu ..de ani buni imi iese la fel ..
simptome deranjante oricum nu am dar mi-a zis sa iau flucovim preventiv si eu si sotul, si daca apare vreo mancarime ceva sa pun clotrimazol crema ( la fel stiam si asta ) si ne vedem dupa pasti sa vedem cu bebele cum facem

sunt fooooarte bucuroasa ca nu am vreo ligioana

  hello fete dragi

maya 

n-am apucat sa citesc din urma. Am avut probleme dimineata cu hidroforul si am venit tarziu la servici, iar acu intru in 2 sedinte. Deci nu apuc sa citesc.

mada, cand faci test?

mayya     
poate faci tratamentul pentru candida ca mine .. astepti sa iti vina  si pe urma        

Mayya, ma bucur mult pentru tine Bravo!  Sa dea Domnul sa fie ca la cmin

Diri, buna Nu cred ca apuc sa fac test ca vin uratii azi

gata pe ziua de azi 

maya,ce bine ca nu ai nimic!

mikule,multumesc ma saturai.maine mai am de spalat covoarele si spalat parchetu,ca nu mai pot de spate si ma ustura nasu...

mada,da,am ajutoare nu asa vrednice ca atunci cand s-a insurat,da nici de aruncat

diri  

maya

al meu pleca sa plateasca facturi si o banca si sa imi ia spaghete si ardei gras pt sos inca nu mancaram nimic,le fac mai tarziu,mai avem supica si cu branza,nu murim de foame

Maya    eu sper sa nu ai locatari 

Sonia , mai este si maine o zi     acum odihna
eu n-am covoare ...doar o mochetuta mica in dormitor

buna Diri 

legat de locatari:
MTHFR Gene Mutation

What is it?
The gene MTHFR (Methylenetetrahydofolate Reductase) encodes the protein MTHFR. Its job is to convert one form of folate (5,10-Methylenetetrahydofolate) to another form of folate (5-Methyltetrahydrofolate). 5-Methyltetrahydrofolate is used to convert Homocysteine (a "bad" amino acid) to Methionine (a "good" amino acid). Therefore, if MTHFR is not doing its job as well, homocysteine will not be converted to Methionine and will be elevated in plasma. Elevated Homocysteine has been associated with a variety of multi-factorial diseases.

Essentially what this means is that the genes that instruct MTHFR to convert homocysteine to Methionine are mutated and may not be capable of doing this important function. MTHFR is an enzyme that converts Homocysteine to an essential amino acid (Methionine). When the genes are mutated you may be lacking this enzyme. Your Homocysteine levels can possibly climb making the blood clot. Some doctors don't check for the MTHFR mutations and rely only on homocysteine levels. This isn't as reliable as testing for the mutations, because Homocysteine levels fluctuate (if you catch your level on a normal day, you may go undiagnosed).

What Type Do I Have?
With MTHFR, there are two different genes identified for this mutation, and it's possible to be "heterozygous," "compound heterozygous," or "homozygous." The MTHFR gene mutation has varying degrees of possible implications. The order of potential severity from most to least is:
1. C677T & C677T (Two C Copies - C677T Homozygous)
2. C677T & A1298C (One Copy of Each The C & A - Compound Heterozygous)
3. C677T (One C Copy - C677T Heterozygous)
4. A1298C & A1298C (Two A Copies - A1298C Homozygous)
5. A1298C (One A Copy - A1298C Heterozygous)

The MTHFR mutation is fairly common in the general population. Approximately 44% of the population is heterozygous and another approximate 12% are homozygous for the MTHFR mutation. Compound heterozygous and homozygous MTHFR have the highest incidences of being linked to implantation failure, late term miscarriages, specific birth defects and overall vascular health. Whichever type of MTHFR you have, it should not be discounted, particularly if there is a personal or family history of any such incidences.

What Are the Implications?
Any and all of the mutations can affect homocysteine levels, but there is much dispute as to whether elevated homocysteine levels are actually needed in order for MTHFR to cause medical complications. Many other MTHFR patients have normal homocysteine levels; yet have had implantation problems, m/c(s), and/or stillbirth(s) due to clotting problems. So it is important to find out your Homocysteine levels (although again, normal doesn't necessarily mean all is well). This is a serious field and MTHFR is a serious condition, so consulting an expert is wise.

Research shows that high homocysteine levels and/or those with the mutation show a higher propensity for thrombosis (blood clots), arteriosclerosis (hardening of arteries), Alzheimer's, stroke, heart attack, Fibromyalgia, migraines (especially with "Aura" migraines), osteoporotic fractures, bone marrow disorders and for those of child bearing years, it has found to be connected to higher incidences of down's syndrome, spina bifida, other neural tube defects, trisomy, miscarriage, stillbirth, implantation failure, placental abruption, preeclampsia, higher incidences of autism, amongst others. Additionally, if you test positive you may want to have your parents, siblings, and any children you may already have tested, as well. There are a few positives to this disorder. Because folate is necessary for cellular division, there is support that shows having this disorder can actually help keep certain types of cancer cells from multiplying as rapidly, so there are some benefits from having this mutation.

Treatment?
Many doctors prescribe Folgard, which is a prescription vitamin supplement containing high levels of folic acid, B12 and B6. These vitamins are what the body essentially needs to convert Homocysteine to Methionine. To put this into perspective, the average multivitamin contains 400 mcgs , most prenatals have 800mcgs of Folic Acid (200% of the normal daily value). Those that are compound heterozygous and those that are homozygous for the mutation are recommended taking 5 mgs. of Folic Acid/B vitamins (12 times the average multi-vitamin and 6 times more than prenatals). It is also recommended to begin taking a low dose (LD) aspirin (81 mgs) once a day, every day, for the rest of your life.

For those undergoing fertility treatments, often times the treatment includes Lovenox (low molecular weight heparin) or Heparin (both are anti-coagulants) during the cycle. If you have a history of implantation failure or early miscarriage, it is becoming more acceptable to use the protocol established by the well-respected Reproductive Immunologist Dr. Beers by beginning Lovenox (40mg/once a day) on cycle day 6 and continuing throughout the cycle. If pregnancy is confirmed, this dosage is likely increased (Typically up to 40mg/twice a day, but potentially higher doses are prescribed dependent upon blood work results since homocysteine levels tend to increase with pregnancy) and usage continues throughout your pregnancy. Approximately two to four weeks prior to birth, the patient is converted to Heparin and continues to take an anti-coagulant for another 6 weeks postpartum (typically switched back to Lovenox). During that time, you will typically be directed to take additional Calcium and Vitamin D, as anti-coagulants can cause bone loss (Heparin more so than Lovenox). Some doctors will recommend a bone scan after use is discontinued to ensure there are no bone density issues. While being treated with an anti-coagulant, you will typically be asked to discontinue taking the 81 mg. baby aspirin since the anti-coagulants will replace the need for the thinning property of the LD aspirin. The FDA has placed Lovenox in the pregnancy category B. Lovenox is not expected to be harmful to an unborn baby. It is not known whether Lovenox passes into breast milk or if it could harm a nursing baby. Do not use Lovenox without telling your doctor if you are breast-feeding a baby. However, many doctors believe it is fine to breastfeed for the 6 weeks postpartum while still receiving Lovenox.

mika multumim de info

eu am reluat acidul folic de luna trecuta , scrie acolo ca ajuta in caz ca e

astept ziua de sambata sa vad ce se imtampla si oricum dupa pasti o iau de la inceput cu analize si tot si o sa fac mutatiile asta e clar..