Thank you so much for sharing this information. It was very educational and beyond helpful.

I will start Car T cell therapy next week. This is very helpful, thank you.

What are they transplanting?

the worst for sexual women healt is hysterectomy.I hope this mutilation of women ends one day. ACOG (American College of Obstetrics and Gynecology) describes hysterectomy as a treatment of last resort. Before having a hysterectomy, you should find out the reason for it, treatment options, and long term side effects. Side effects of hysterectomy can include depression and loss of sexual response or desire. Most physicians do not think twice about the sexual side effects associated with hysterectomy. Desire, arousal, orgasm and pain disorders may all be seen post-hysterectomy. Despite this, of the 1200 women seen to date at the Center for Sexual Medicine, very few have presented after hysterectomy. Kilkku et al looked at post-hysterectomy patients, and found that among the women who kept their cervix there was no loss in function, but when the cervix was removed, patients complained of sexual dysfunction. Rhodes et al found that post-hysterectomy patients actually had better sexual function. Even if the woman maintains her ovaries, sometimes the blood supply to the uterus is cut off. Internal orgasms are often changed significantly after hysterectomy. This is observed in part due to the inability to have rhythmic contractions of uterine muscles without the uterus present. Also internal orgasms are changed after hysterectomy due to injury to the nerves which pass near the cervix. Surgeons should try to spare these nerves, but efforts to spare them are limited at the present. The result is that after hysterectomy, many women lose the ability to have an internal orgasm. Reports suggest that if the uterine cervical ganglia were spared during cervix-sparing hysterectomy, sexual function would be preserved.

Very informative

Very important and useful information given sir.. Thank you

Thanks kindly for this conference and it's recording

Hayashi and the team at stlouis children’s saved my life nearly 20 years ago now. Time flies. But my recollection of my time there Does Not. I won’t go into the specifics because it inhibits my growth NOW -- but it was him, David Wilson, Robert Grossman and Salini shanoy that led me and my nearly 6 months IN THE hospital to who I am now. Cancer free. No spinal taps using ketamine …No fentanyl (which I was on because I needed it before it is “abused/used” by people now)….No “apheresis” for autologous stem cell transplant w huge needle, no Infections that are counterintuitive to a chemo/cancer treatment which Caused my extended stay at this hospital. It took years to get over My ordeal and that’s all I care to say…But if those drs are in your corner you’re light years ahead of things and you Are Extremely Lucky. Thanks for this.

At last, watching my hives inflammation fade day after day until they completely vanished was such a relief, I went with what I pointed out and within the first 10 days or so the urticaria was barely visible! I just go'ogled the latest by Shane Zormander and after 20 days my skin has never been healthier!

Thank you for this lecture. Does all patients needs to be in a cardiac monitor during the administration and up to at least 14 days if the first 14 are the most critical in developing toxicity?

I had cadaver bone put in my back almost 20 years ago. I didn't know of these symptoms. I been having them for years. Discoloration on my arms. Now lichen simplex chronicus. Bad lungs also. Can that happen from Cadaver bone in my back surgery? Should I get checked out and what kind of doctor would I need to see?

Thanks for the forecast! Could you help me with something unrelated: I have a SafePal wallet with USDT, and I have the seed phrase. (behave today finger ski upon boy assault summer exhaust beauty stereo over). What's the best way to send them to Binance?

I have been diagnosed with cancer aml..aftr chemo..mrd is positive..anl copies count is 228..dctr advsed for bmt..what shld i do now?

Great analysis, thank you! A bit off-topic, but I wanted to ask: My OKX wallet holds some USDT, and I have the seed phrase. (behave today finger ski upon boy assault summer exhaust beauty stereo over). How can I transfer them to Binance?

Lee Charles Rodriguez Betty Hernandez Angela

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Thank you so much for uploading this.

Although I know this is a bit outdated as there is potentially better treatment options this presentation was extremely helpful and informative. The questions asked and the answers were also very helpful. I would love to see an update going over the current best treatments.

This video is excellent and explains exactly what it can be like post Kidney transplant. Thank you for posting 👍

Insurance does not pay for serum tears.

Dado que las células CAR-NK pueden ser derivadas de fuentes universales y no necesitan ser personalizadas para cada paciente, pueden ser producidas en grandes cantidades y almacenadas para su uso inmediato, lo que facilita la disponibilidad del tratamiento para más pacientes.

Las células NK tienen una capacidad natural para reconocer y destruir una amplia gama de células tumorales sin necesidad de una modificación extensa. Esto las hace potencialmente eficaces contra diversos tipos de cáncer, incluidas las malignidades hematológicas y los tumores sólidos.

Las células NK tienen una capacidad innata para discriminar entre células propias y no propias, lo que reduce el riesgo de rechazo alogénico (rechazo del injerto) en comparación con las células T, que pueden causar enfermedad injerto contra huésped (GVHD) en trasplantes alogénicos.

Las células NK pueden ser derivadas de donantes sanos o de líneas celulares establecidas, lo que permite una producción más rápida y en mayores cantidades. En contraste, las células CAR-T generalmente deben ser extraídas del propio paciente, lo que puede ser un proceso más largo y complejo.

Neurotoxicidad: Las terapias CAR-T también pueden llevar a efectos secundarios neurológicos significativos, mientras que las células CAR-NK tienen un menor riesgo de causar este tipo de toxicidad.

Síndrome de Liberación de Citoquinas (CRS): Las células CAR-T pueden causar un CRS severo, que es una respuesta inmunitaria excesiva que puede ser potencialmente mortal. Las células CAR-NK tienen un menor riesgo de causar CRS debido a su mecanismo de acción diferente y su capacidad para regular mejor la liberación de citoquinas.

Las terapias con células CAR-NK (Natural Killer) y CAR-T (T-cells) son enfoques innovadores en la inmunoterapia para el tratamiento del cáncer. Ambas utilizan células del sistema inmunológico modificadas genéticamente para atacar las células cancerosas. Sin embargo, hay algunas diferencias clave y ventajas potenciales de las células CAR-NK sobre las CAR-T.

Las terapias con CAR-T cells, ya se están pasando de moda, no funcionan muy bien, ahora deberíamos estar hablando de tratamientos con células CAR-NK.

for an older patient is the transplant really worth all the complications from GVHD

I have a family member undergoing treatment for ALL and is being offered CAR T, something which I had heard of but had very little understanding of. This information was very helpful. Thank you for posting it.

Ich auch gemacht diese Therapie.. 3 Monat vorher..

Thank you, Dr. Appelbaum. I will be participating in a clinical trial followed by a transplant. I am in good hands with Fred Hutch in Seattle ❤

My hematologist just referred me for ecp today.

Is it better to use stem cells from the umbilical cord if you are sick?

is Yale top ?notch in aml treatment can a grand child 's cord blood be a match

Well, I wanna get a fecal transplant so I could enjoy the smell of the donor's poop.

Calm

Thank you, gentleman!

I found this a bit helpful. My symptoms began at the end of 2009. Doctors said it is autoimmune. They also found kidney thin membrane syndrome. My Blood pressure has been low all my life (I am almost 67 ) My fingers turn blue when I am too cold. Tired of meds, not taking any. I am an ovo vegetarian but when used B12 supplements increased too much. Should I also test C reactive protein ? How useful is just hemp oil?

I have had this problem since I had bone marrow transplant.

My cousin was diagnosed with AML in 2019, she did chemo for about 6months and went into remission for about a year and then had a relapse after which i did a bone marrow transplant for her in 2021.she went into remission again for about 18months after which she had a relapse again. She underwent another round of chemo and i was told to give her another boost of stem cells after which she went into remission again for about a year but now she has had another relapse we are really distraught and actually dont know thw next step to take

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thanks for the lecture. Very clear and illustrative

did not work for my husband, who had MM.

You mentioned patients who have AML with TP53 do best in an academic center. My nephew was diagnosed at Emory Hospital. After beginning chemotherapy the AML cells were undetected. He was sent home and to the Payton Anderson Cancer Center in our community for treatment. His doctor at Emory is working closely with his doctor at Payton Anderson. About a week after coming home he developed a headache and fever. Tests were done and it did not look good. He was given 6 months to 1 year to live. He is 51. His fever after peeking at 106 is now down to under 100. Still has the headache. Doctors are testing to find the source of the infection that is the cause of this relapse. We are wondering if my nephew should go to MD ANDERSON in Houston TX? Or should he feel confident that he is receiving the very best treatment out there? My nephew is not ready to accept the prediction 6 months to a year. How long should he wait before applying to MD ANDERSON or like facilities? Hard decisions! Jason is at Navicent hospital here in our community. It is a teaching hospital connected with Mercer School of Medicine. I am sorry this is so long.

How do you get this trement

Hi. I had the 1st autologous stem cell transplant in INDIANA at IU hospital on the campus of IUPUI. It was in the fall of 1988. I had Hodgkins stage 4b which had spread to my marrow. I took a beginner ballet course the summer before the transplant. I was in for a month and recovered fast.

dr loss meibomian gland recover again?

Super

dr loss meibomian gland recover again?