Good week again 🙏😁

Yo guys what's up I added molasses for the very first time Take a look, she's doing great I'm happy for the training we've been giving her and now we are seeing some results Alright guys let me know what's your advise I think I'm going to be adding molasses after nutes every two days ******************************** UPDATED 08/03/2021 SHE IS DOING GREAT! ID SAY SECOND WEEK OF FLOWERING ALREADY WEEK 11 FROM SEED ' DAY 1 STARTS TOMORROW! CHECK OUT THE VIDEOS AND PICS FOR BLOOM TAKE CARE GUYS PEACE OUT!

WEEK 6 (Day 36-42) My Runtz have now nicely adjusted to the flowering phase. The stretch is beginning, and the plants are slowly gaining height. However, I’m trying to keep them as small as possible since my space is somewhat limited at the moment. The two plants are in a dimly lit corner of my tent but currently receive 24-hour light because I still have other plants inside. I’ve already fertilized them a bit with everything. They’re still thriving beautifully.

My plant grew great I over don’t my veg and auto room with having way to many plants she was kinda left in the corner most of her growing life I am very happy with what she did to say I never had to do a lot basically thanks rqs for the chance .. all my other autos using rqs have a lot more space so they can actually breath

She's doing great. Beautiful Leafs and a good height for her age. Let's Go veg!🤙🏽

Tarde en subir el resumen de esta semana porque ya pensaba subir las fotos de la planta cortada, pero por el tono de los tricomas esta si es la última semana, ya el 18/11/22 subire fotos de la planta cortada lista para curar. Mas de esta semana no pasará, luego esperare para subir el resumen de la genética. Volviendo al tema de la planta esta semana solo fue regada con agua, asique el lavado de raíces se cumplió a la perfección.

The trichomes are starting to make themselves known On this one, also the smell is becoming a citrus like aroma which is one of my favorites, also No signs of deficiencies or anything yet so I hope it stays that way.

Sorry it took so long for an update. I got married in the meantime and went on a honeymoon. Before I went though I took the plants down and had a friend take care of the drying and curing. It looks like I got 2 pheno's. One is has more red hairs and is a bit more skunky and peppery. The other has bit more sativa like bud forming and smells a bitt gassy in addition to the tangieness. The yield is also definitely not disappointing. Plant 1: 76gr Plant 2: 68gr Plant 3: 65gr Total:209gr I am happy with that. Especially since it's my first LED grow.

ANTHOCYANIN production is primarily controlled by the Cryptochrome (CR1) Photoreceptor ( !! UV and Blue Spectrums are primary drivers in the production of the pigment that replaces chlorophyll, isn't that awesome! 1. Diverse photoreceptors in plants Many civilizations, including the sun god of ancient Egypt, thought that the blessings of sunlight were the source of life. In fact, the survival of all life, including humans, is supported by the photosynthesis of plants that capture solar energy. Plants that perform photosynthesis have no means of transportation except for some algae. Therefore, it is necessary to monitor various changes in the external environment and respond appropriately to the place to survive. Among various environmental information, light is especially important information for plants that perform photosynthesis. In the process of evolution, plants acquired phytochrome, which mainly receives light in the red light region, and multiple blue light receptors, including his hytropin and phototropin, in order to sense the light environment. .. In addition to these, an ultraviolet light receptor named UVR8 was recently discovered. The latest image of the molecular structure and function of these various plant photoreceptors (Fig. 1), focusing on phytochrome and phototropin. Figure 1 Ultraviolet-visible absorption spectra of phytochrome, cryptochrome, phototropin, and UVR8. The dashed line represents each bioactive absorption spectrum. 2. Phytochrome; red-far red photoreversible molecular switch What is phytochrome? Phytochrome is a photochromic photoreceptor, and has two absorption types, a red light absorption type Pr (absorption maximum wavelength of about 665 nm) and a far-red light absorption type Pfr (730 nm). Reversible light conversion between the two by red light and far-red light, respectively(Fig. 1A, solid line and broken line). In general, Pfr is the active form that causes a physiological response. With some exceptions, phytochrome can be said to function as a photoreversible molecular switch. The background of the discovery is as follows. There are some types of plants that require light for germination (light seed germination). From that study, it was found that germination was induced by red light, the effect was inhibited by subsequent far-red light irradiation, and this could be repeated, and the existence of photoreceptors that reversibly photoconvert was predicted. In 1959, its existence was confirmed by the absorption spectrum measurement of the yellow sprout tissue, and it was named phytochrome. Why does the plant have a sensor to distinguish between such red light and far-red light? There is no big difference between the red and far-red light regions in the open-field spectrum of sunlight, but the proportion of red light is greatly reduced due to the absorption of chloroplasts in the shade of plants. Similar changes in light quality occur in the evening sunlight. Plants perceive this difference in light quality as the ratio of Pr and Pfr, recognize the light environment, and respond to it. Subsequent studies have revealed that it is responsible for various photomorphogenic reactions such as photoperiodic flowering induction, shade repellent, and deyellowing (greening). Furthermore, with the introduction of the model plant Arabidopsis thaliana (At) and the development of molecular biological analysis methods, research has progressed dramatically, and his five types of phytochromes (phyA-E) are present in Arabidopsis thaliana. all right. With the progress of the genome project, Fi’s tochrome-like photoreceptors were found in cyanobacteria, a photosynthetic prokaryotes other than plants. Furthermore, in non-photosynthetic bacteria, a homologue molecule called bacteriophytochrome photoreceptor (BphP) was found in Pseudomonas aeruginosa (Pa) and radiation-resistant bacteria (Deinococcus radiodurans, Dr). Domain structure of phytochrome molecule Phytochrome molecule can be roughly divided into N-terminal side and C-terminal side region. PAS (Per / Arndt / Sim: blue), GAF (cGMP phosphodiesterase / adenylyl cyclase / FhlA: green), PHY (phyto-chrome: purple) 3 in the N-terminal region of plant phytochrome (Fig. 2A) There are two domains and an N-terminal extension region (NTE: dark blue), and phytochromobilin (PΦB), which is one of the ring-opening tetrapyrroles, is thioether-bonded to the system stored in GAF as a chromophore. ing. PAS is a domain involved in the interaction between signal transduction-related proteins, and PHY is a phytochrome-specific domain. There are two PASs and her histidine kinase-related (HKR) domain (red) in the C-terminal region, but the histidine essential for kinase activity is not conserved. 3. Phototropin; photosynthetic efficiency optimized blue light receptor What is phototropin? Charles Darwin, who is famous for his theory of evolution, wrote in his book “The power of move-ment in plants” published in 1882 that plants bend toward blue light. Approximately 100 years later, the protein nph1 (nonphoto-tropic hypocotyl 1) encoded by one of the causative genes of Arabidopsis mutants causing phototropic abnormalities was identified as a blue photoreceptor. Later, another isotype npl1 was found and renamed phototropin 1 (phot1) and 2 (phot2), respectively. In addition to phototropism, phototropin is damaged by chloroplast photolocalization (chloroplasts move through the epidermal cells of the leaves and gather on the cell surface under appropriate light intensity for photosynthesis. As a photoreceptor for reactions such as escaping to the side of cells under dangerous strong light) and stomata (reactions that open stomata to optimize the uptake of carbon dioxide, which is the rate-determining process of photosynthetic reactions). It became clear that it worked. In this way, phototropin can be said to be a blue light receptor responsible for optimizing photosynthetic efficiency. Domain structure and LOV photoreaction of phototropin molecule Phototropin molecule has two photoreceptive domains (LOV1 and LOV2) called LOV (Light-Oxygen-Voltage sensing) on the N-terminal side, and serine / on the C-terminal side. It is a protein kinase that forms threonine kinase (STK) (Fig. 4Aa) and whose activity is regulated by light. LOV is one molecule as a chromophore, he binds FMN (flavin mononucleotide) non-covalently. The LOV forms an α/βfold, and the FMN is located on a β-sheet consisting of five antiparallel β-strands (Fig. 4B). The FMN in the ground state LOV shows the absorption spectrum of a typical oxidized flavin protein with a triplet oscillation structure and an absorption maximum wavelength of 450 nm, and is called D450 (Fig. 1C and Fig. 4E). After being excited to the singlet excited state by blue light, the FMN shifts to the triplet excited state (L660t *) due to intersystem crossing, and then the C4 (Fig. 4C) of the isoaroxazine ring of the FMN is conserved in the vicinity. It forms a transient accretionary prism with the tain (red part in Fig. 4B Eα) (S390I). When this cysteine is replaced with alanine (C / A substitution), the addition reaction does not occur. The effect of adduct formation propagates to the protein moiety, causing kinase activation (S390II). After that, the formed cysteine-flavin adduct spontaneously dissociates and returns to the original D450 (Fig. 4E, dark regression reaction). Phototropin kinase activity control mechanism by LOV2 Why does phototropin have two LOVs? Atphot1 was found as a protein that is rapidly autophosphorylated when irradiated with blue light. The effect of the above C / A substitution on this self-phosphorylation reaction and phototropism was investigated, and LOV2 is the main photomolecular switch in both self-phosphorylation and phototropism. It turns out that it functions as. After that, from experiments using artificial substrates, STK has a constitutive activity, LOV2 functions as an inhibitory domain of this activity, and the inhibition is eliminated by photoreaction, while LOV1 is kinase light. It was shown to modify the photosensitivity of the activation reaction. In addition to this, LOV1 was found to act as a dimerization site from the crystal structure and his SAXS. What kind of molecular mechanism does LOV2 use to photoregulate kinase activity? The following two modules play important roles in this intramolecular signal transduction. Figure 4 (A) Domain structure of LOV photoreceptors. a: Phototropin b: Neochrome c: FKF1 family protein d: Aureochrome (B) Crystal structure of auto barley phot1 LOV2. (C) Structure of FMN isoaroxazine ring. (D) Schematic diagram of the functional domain and module of Arabidopsis thaliana phot1. L, A’α, and Jα represent linker, A’α helix, and Jα helix, respectively. (E) LOV photoreaction. (F) Molecular structure model (mesh) of the LOV2-STK sample (black line) containing A’α of phot2 obtained based on SAXS under dark (top) and under bright (bottom). The yellow, red, and green space-filled models represent the crystal structures of LOV2-Jα, protein kinase A N-lobe, and C-robe, respectively, and black represents FMN. See the text for details. 1) Jα. LOV2 C of oat phot1-to α immediately after the terminus Rix (Jα) is present (Fig. 4D), which interacts with the β-sheet (Fig. 4B) that forms the FMN-bound scaffold of LOV2 in the dark, but unfolds and dissociates from the β-sheet with photoreaction. It was shown by NMR that it does. According to the crystal structure of LOV2-Jα, this Jα is located on the back surface of the β sheet and mainly has a hydrophobic interaction. The formation of S390II causes twisting of the isoaroxazine ring and protonation of N5 (Fig. 4C). As a result, the glutamine side chain present on his Iβ strand (Fig. 4B) in the β-sheet rotates to form a hydrogen bond with this protonated N5. Jα interacts with this his Iβ strand, and these changes are thought to cause the unfold-ing of Jα and dissociation from the β-sheet described above. Experiments such as amino acid substitution of Iβ strands revealed that kinases exhibit constitutive activity when this interaction is eliminated, and that Jα plays an important role in photoactivation of kinases. 2) A’α / Aβ gap. Recently, several results have been reported showing the involvement of amino acids near the A’α helix (Fig. 4D) located upstream of the N-terminal of LOV2 in kinase photoactivation. Therefore, he investigated the role of this A’α and its neighboring amino acids in kinase photoactivation, photoreaction, and Jα structural change for Atphot1. The LOV2-STK polypeptide (Fig. 4D, underlined in black) was used as a photocontrollable kinase for kinase activity analysis. As a result, it was found that the photoactivation of the kinase was abolished when amino acid substitution was introduced into the A’α / Aβ gap between A’α and Aβ of the LOV2 core. Interestingly, he had no effect on the structural changes in Jα examined on the peptide map due to the photoreaction of LOV2 or trypsin degradation. Therefore, the A’α / Aβ gap is considered to play an important role in intramolecular signal transduction after Jα. Structural changes detected by SAXS Structural changes of Jα have been detected by various biophysical methods other than NMR, but structural information on samples including up to STK is reported only by his results to his SAXS. Not. The SAXS measurement of the Atphot2 LOV2-STK polypeptide showed that the radius of inertia increased from 32.4 Å to 34.8 Å, and the molecular model (Fig. 4F) obtained by the ab initio modeling software GASBOR is that of LOV2 and STK. It was shown that the N lobes and C lobes lined up in tandem, and the relative position of LOV2 with respect to STK shifted by about 13 Å under light irradiation. The difference in the molecular model between the two is considered to reflect the structural changes that occur in the Jα and A’α / Aβ gaps mentioned above. Two phototropins with different photosensitivity In the phototropic reaction of Arabidopsis Arabidopsis, Arabidopsis responds to a very wide range of light intensities from 10–4 to 102 μmol photon / sec / m2. At that time, phot1 functions as an optical sensor in a wide range from low light to strong light, while phot2 reacts with light stronger than 1 μmol photon / sec / m2. What is the origin of these differences? As is well known, animal photoreceptors have a high photosensitivity due to the abundance of rhodopsin and the presence of biochemical amplification mechanisms. The exact abundance of phot1 and phot2 in vivo is unknown, but interesting results have been obtained in terms of amplification. The light intensity dependence of the photoactivation of the LOV2-STK polypeptide used in the above kinase analysis was investigated. It was found that phot1 was about 10 times more photosensitive than phot2. On the other hand, when the photochemical reactions of both were examined, it was found that the rate of the dark return reaction of phot1 was about 10 times slower than that of phot2. This result indicates that the longer the lifetime of S390II, which is in the kinase-activated state, the higher the photosensitivity of kinase activation. This correlation was further confirmed by extending the lifespan of her S390II with amino acid substitutions. This alone cannot explain the widespread differences in photosensitivity between phot1 and phot2, but it may explain some of them. Furthermore, it is necessary to investigate in detail protein modifications such as phosphorylation and the effects of phot interacting factors on photosensitivity. Other LOV photoreceptors Among fern plants and green algae, phytochrome ɾphotosensory module (PSM) on the N-terminal side and chimera photoreceptor with full-length phototropin on the C-terminal side, neochrome (Fig. There are types with 4Ab). It has been reported that some neochromes play a role in chloroplast photolocalization as a red light receiver. It is considered that fern plants have such a chimera photoreceptor in order to survive in a habitat such as undergrowth in a jungle where only red light reaches. In addition to this, plants have only one LOV domain, and three proteins involved in the degradation of photomorphogenesis-related proteins, FKF1 (Flavin-binding, Kelch repeat, F-box 1, ZTL (ZEITLUPE)), LKP2 ( There are LOV Kelch Protein2) (Fig. 4Ac) and aureochrome (Fig. 4Ad), which has a bZip domain on the N-terminal side of LOV and functions as a gene transcription factor. 4. Cryptochrome and UVR8 Cryptochrome is one of the blue photoreceptors and forms a superfamily with the DNA photoreceptor photolyase. It has FAD (flavin adenine dinucle-otide) as a chromophore and tetrahydrofolic acid, which is a condensing pigment. The ground state of FAD is considered to be the oxidized type, and the radical type (broken line in Fig. 1B) generated by blue light irradiation is considered to be the signaling state. The radical type also absorbs in the green to orange light region, and may widen the wavelength region of the plant morphogenesis reaction spectrum. Cryptochrome uses blue light to control physiological functions similar to phytochrome. It was identified as a photoreceptor from one of the causative genes of UVR8 Arabidopsis thaliana, and the chromophore is absorbed in the UVB region by a Trp triad consisting of three tryptophans (Fig. 1D). It is involved in the biosynthesis of flavonoids and anthocyanins that function as UV scavengers in plants. Conclusion It is thought that plants have acquired various photoreceptors necessary for their survival during a long evolutionary process. The photoreceptors that cover the existing far-red light to UVB mentioned here are considered to be some of them. More and more diverse photoreceptor genes are conserved in cyanobacteria and marine plankton. By examining these, it is thought that the understanding of plant photoreceptors will be further deepened.

💩Holy Crap We Are Back At It And Loving It💩 Growmies we are at DAY 49 and she's just killing💀it👌 👉We are in full on flowering , gotta say the pink to redish hairs look amazing , not to mention the frost 👈 even the stems and branches are sticky icky 👈 OMG I LOVE THE PINK PISTOLS 👈 👉 BUT THE MORE IT FLOWERS THE LESS THEY ARE SHOWING 😭 So Shit , I gave them just a tad to much nutes on the first few feeding 👈 But I have since fixed it So I'm still doing some low stress training 🙃 and some defolation 😳 Lights being readjusted and chart updated .........👍rain water to be used entire growth👈 👉I used NutriNPK for nutrients for my grows and welcome anyone to give them a try .👈 👉 www.nutrinpk.com 👈 NutriNPK Cal MAG 14-0-14 NutriNPK Grow 28-14-14 NutriNPK Bloom 8-20-30 NutriNPK Bloom Booster 0-52-34 I GOT MULTIPLE DIARIES ON THE GO 😱 please check them out 😎 👉THANKS FOR TAKING THE TIME TO GO OVER MY DIARIES 👈

Day 71 - Not much going on today but is is starting to smell a bit more. Kinda sweet with a little bit of funk is the easiest way to explain it. Noticed some of her top leaves were tacoing a bit so raised the light up a little bit to try and relax her. Day 72 - She’s still chugging along and she’s packing in nicely. Other than that, not much else happening. I raised the lights a little more cause still have a few leaves up top folding like tacos. Have the high temps no higher than 78 and around 69 at night so I don’t think heat is the cause, I think I had the lights way to close. Day 73 - Nothing much to update today. She’s gonna need some more water tomorrow. Still have some tacoing of the leaves but did about all I can do now so just hoping it doesn’t bother her the last couple weeks. Day 74 - Almost waited a day to late to give her some water and nutrients. She was just starting to drop a bit but got her fed before she really had any big issues. She took 2 full gallons of water and nutes so that should hold her over for about 2-3 days. Day 75 - All looks great since watering, no more droopy leaves but man oh man the buds are getting fat and dense as hell. There’s still plenty of clear trichs and most pistils are still thick and white so still at least two week left but can’t wait for this harvest. Day 76 - Will probably be attaching some of those plant yoyo’s soon because these buds are getting fat and heavy and don’t want anything bad happening to them. This is turning out to be one of my best grows to date. The top few leaves are really tacoing and getting brittle, not a lot but a few so I raised the lights a bit more. Probably too late for the couple that are damaged but overall she should be ok. Day 77 - No major updates today, she’ll be needing some water for sure tomorrow. Other than that, I’ll be attaching some plant yo-yo’s today to support the massive buds.

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Final Report: Grow: The plants has grown very beautiful and healty without pests and diseases. They grown bushy and with medium height during all the life cycle. I had try to use LST in third veg week but i did't made correctly and after that i dicided to return to grown normally without any particolar tecnique. I used a littel more fertilizer then mine usual and that made the plants grown fast with only a littel bit of leaf margin burn which I solved by decreasing the quantity. In the first two weeks of flowering stage the plants started grow not to very tall (except for one) and the number of the branches increase, in this phase i only defoliated when the fan leaves turn yellow in late stage. During all flowering stage the flowers grown but they remained very soft, they turned dense and bigger in the last weeks and this time i waited until almost all of them were mature before harvest the plants(I waited a littel more respect OG Kush CBD). I changed the taller plant from one grow room to another(in the sixth week) when she became too high and she couldn't stay more in the smaller grow box(nothing changed in the enviroment between the two boxes). Equipment and grow box: The enviorment of grow box has been optimized every stage with the right temperature, umidity and air flow. Vegetative temp/umidity --> 23-29 °C/45-55% Flowering temp/umidity --> 20-26 °C/40-50% The air flow was created by two pc fans and one big fan. Harvest: This time the plants were full of dense buds but the lower branches had many fluffy flowers(i used them to make some hash) but the result not change too much . The result of this grow is amezing compared to my old expiriences. I harvested the flower and i made a fast curing process after i washed the crop and i let them to dry with a fan on it. After five days a take the branches which were to dry and i did the final trimmig before put all the harvest in a open jar for finishing to dry. I collected all the leaves, fluffy buds and trimming scraps in a bag and i let them dry. I harvested the taller plant before the other two because she had matured earlier(with the OG Kush ladies). Later i put the bag in the freezer and when i collect and dried all the scraps from OG Kush and Dandoverde Haze i did some Ice-O-Lator hash. I used 250g of trimming stuff and i made 11.50 g of hash, I had use a set of 5 bag and i take the resin from the 160µ - 120µ - 73µ- 25µ bags. I pressed all the resin in a great block of tasty strong hash. Always better every time 😊💪 Total harvest ---> 126g only of dense buds and 11.50g of hash.

you are God

Harvested Shiva Skunk, Zombie Kush and Sweet Love.

Finally feel like she's headed into flower, thickening of bud sights, growth has slowed, she must of shot up 2' over the last month that flower stretch is real. This will push her to mid October unless I have a miracle, I'm really banking on nice weather. I did a heavy defoliation on the inside, clean it up for better airflow and to make it easier come harvest. I have to battle mold and mildew in the fall, I used to just use a foliar spray of apple cider vinegar, which works great for mildew, but I need something stronger for mold. As such I've started a Lactobacillus Serum, that with a few drops of organic food grade cinnamon oil in a foliar spray has said to reduce instances of botrytis by 90%, anyone have experience with Lactobacillus in battling mold /mildew?

Week 8 Veg – Go Big or Go Home! 🌱💪 Hey, Grow Fam! 🌿 What an intense week it’s been in the grow room! This was one of those “go big or go home” moments, and I decided to take it to the extreme. I’m holding off on flipping to flower for just one more week because the plants are filling up the space beautifully—I can’t help but push things to their limits and see just how much these ladies can give! 😎✨ This week was all about maximizing growth and creating the best canopy I can. I did a light defoliation, just here and there to open things up a bit, and then came the bending—LOTS of bending. 🌱 I’m working hard to create an even canopy, though with all these different genetics, we’ll see how close I get! 🤞 Regardless, I’m giving it my all, and I’m super pumped to see how everything will respond in the next stage. The final touch this week? I ended it with a bold 36 hours of darkness to prepare for the big flip next week—flower mode, here we come! 🌸 What Went Down This Week: 1. Canopy Work – Bending and training all over the place to try and keep things even. It’s a real challenge with different genetics, but the payoff is going to be worth it! 2. Defoliation – Just a little bit of leaf removal here and there to help with airflow and light penetration, prepping them for that final veg stretch. 3. 36 Hours of Darkness – Closed out the week with a full day and a half of darkness. The 36 hours of darkness is a technique I like to use to help signal to the plants that it’s time to transition from veg to flower. 🌒 By giving them an extended dark period, I’m mimicking the natural shift from summer to fall, when daylight hours start to shorten. This kick-starts the plants’ flowering hormones (phytochrome), helping them shift into flower mode more smoothly and quickly. In my experience, this method helps speed up the flip, reduces early flowering stress, and often leads to a more uniform bloom across the canopy. It’s like giving the plants a little nudge to let them know, “Hey, it’s time to bloom!” 🌸 This technique is especially useful for growers like me who want to maximize the efficiency and performance of their plants. 😊 4. TrolMaster + App Love – As always, the TrolMaster app continues to blow me away. We’re going to dive deep into it below, but trust me, this app makes managing everything a breeze! 👇 Next week, we’re flipping to flower! I’m beyond excited for what’s to come, and I can already tell these plants are ready to explode with growth in flower mode. Stay tuned, because we’re about to see some serious action in the grow room! 🌸🔥 Thank you all for the continued support! 🙏 Don’t forget to check out my social media accounts for real-time updates, behind-the-scenes magic, and all the details on how this journey unfolds. Whether you’re new or have been here from the start, I appreciate every one of you. Let’s keep pushing the limits of indoor horticulture together! 🌱💚 Growers Love 💚🌱 #TrolMasterChronicles #ThinkGrowLED #SeedToHarvest #DogDoctorOfficial #AptusPlantTech #Autopots #IndoorHorticulture #ControlledEnvironment #GrowTech #PositiveVibesOnly DogDoctorOfficial P.S. – Let’s Talk TrolMaster + App If you haven’t explored the TrolMaster App yet, you’re missing out! This app gives me complete control and real-time feedback on my entire setup, from the environment to CO2 levels, humidity, light, and beyond. Every parameter is at my fingertips, and it’s all synced with the controllers. I love how easy it is to dial in the details, especially during these crucial stages. But what really gets me is the precision. 🌡️📲 With the app, I can track trends, get alerts if anything is off, and make changes on the fly—whether I’m in the room or halfway across the world. This kind of power and convenience has totally transformed how I manage my grow. Whether you’re a beginner or an expert, having this level of control is a game-changer. And as I dive deeper into flower, it’s going to be my best friend in keeping everything dialed in. Discount Codes so you can save big on your next check out 💚💚💚 Kannabia - DOGDOCTOR 30% off SeedsmanSeeds - DOGDOCTOR 10% off CannaKan- DOGDOCTOR 15% off terpyz.eu - DOCTOR 15% off The Neutralizer - PORKIT5-DOG 15% off As always thank you all for stopping by, for the love and for it all , this journey of mine wold just not be the same without you guys, the love and support is very much appreciated and i fell honored and so joyful with you all in my life 🙏
 With true love comes happiness 💚🙏 Always believe in your self and always do things expecting nothing and with an open heart , be a giver and the universe will give back to you in ways you could not even imagine so 💚 Friendly reminder all you see here is pure research and for educational purposes only Growers Love to you all 💚💚💚

I top dressed worm castings mix with more organic soil and and gave the teas ones a week other then that a I gave them just water with 3ml silica 5ml cal-mag 10ml fish’s sh!tt.